Accès à distance ? S'identifier sur le proxy UCLouvain
Guidelines for the use and interpretation of assays for monitoring autophagy.
Primary tabs
Document type | Article de périodique (Journal article) – Article de recherche |
---|---|
Access type | Accès restreint |
Publication date | 2012 |
Language | Anglais |
Journal information | "Autophagy" - Vol. 8, no. 4, p. 445-544 (2012) |
Peer reviewed | yes |
Publisher | Landes Bioscience ((United States) Austin) |
issn | 1554-8627 |
e-issn | 1554-8635 |
Publication status | Publié |
Affiliations |
UCL
- SSS/IONS/CEMO - Pôle Cellulaire et moléculaire UCL - SST/ISV - Institut des sciences de la vie UCL - SST/LIBST - Louvain Institute of Biomolecular Science and Technology |
MESH Subject | Animals ; Autophagy ; Biological Assay ; Humans ; Models, Biological |
Links |
- Klionsky Daniel J., Abeliovich Hagai, Agostinis Patrizia, Agrawal Devendra K., Aliev Gjumrakch, Askew David S., Baba Misuzu, Baehrecke Eric H., Bahr Ben A., Ballabio Andrea, Bamber Bruce A., Bassham Diane C., Bergamini Ettore, Bi Xiaoning, Biard-Piechaczyk Martine, Blum Janice S., Bredesen Dale E., Brodsky Jeffrey L., Brumell John H., Brunk Ulf T., Bursch Wilfried, Camougrand Nadine, Cebollero Eduardo, Cecconi Francesco, Chen Yingyu, Chin Lih-Shen, Choi Augustine, Chu Charleen T., Chung Jongkyeong, Clark Robert S.B., Clarke Peter G.H., Clarke Steven G., Clave Corinne, Cleveland John L., Codogno Patrice, Colombo María Isabel, Coto-Montes Ana, Cregg James M., Cuervo Ana Maria, Debnath Jayanta, Dennis Patrick B., Dennis Phillip A., Demarchi Francesca, Deretic Vojo, Devenish Rodney J., Di Sano Federica, Dice J. Fred, Distelhorst Clark W., Dinesh-Kumar Savithramma P., Eissa N. Tony, DiFiglia Marian, Djavaheri-Mergny Mojgan, Dorsey Frank C., Dröge Wulf, Dron Michel, Dunn, Jr. William A., Duszenko Michael, Elazar Zvulun, Esclatine Audrey, Eskelinen Eeva-Liisa, Fésüs László, Finley Kim D., Fuentes José M., Fueyo-Margareto Juan, Fujisaki Kozo, Galliot Brigitte, Gao Fen-Biao, Gewirtz David A., Gibson Spencer B., Gohla Antje, Goldberg Alfred L., Gonzalez Ramon, González-Estévez Cristina, Gorski Sharon M., Gottlieb Roberta A., Häussinger Dieter, He You-Wen, Heidenreich Kim, Hill Joseph A., Høyer-Hansen Maria, Hu Xun, Huang Wei-Pang, Iwasaki Akiko, Jäättelä Marja, Jackson William T., Jiang Xuejun, Jin Shengkan V., Johansen Terje, Jung Jae U., Kadowaki Motoni, Kang Chanhee, Kelekar Ameeta, Kessel David H., Kiel Jan A.K.W., Kim Hong Pyo, Kimchi Adi, Kinsella Timothy J., Kiselyov Kirill, Kitamoto Katsuhiko, Knecht Erwin, Komatsu Masaaki, Kominami Eiki, Kondo Seiji, Kovács Attila L., Kroemer Guido, Kuan Chia-Yi, Kumar Rakesh, Kundu Mondira, Landry Jacques, Laporte Marianne, Le Weidong, Lei Huan-Yao, Levine Beth, Lieberman Andrew P., Lim Kah-Leong, Lin Fu-Cheng, Liou Willisa, Liu Leroy F., Lopez-Berestein Gabriel, López-Otín Carlos, Lu Bo, Macleod Kay F., Malorni Walter, Martinet Wim, Matsuoka Ken, Mautner Josef, Meijer Alfred J., Meléndez Alicia, Michels Paul, Miotto Giovanni, Mistiaen Wilhelm P., Mizushima Noboru, Mograbi Baharia, Moore Michael N., Moreira Paula I., Moriyasu Yuji, Motyl Tomasz, Münz Christian, Murphy Leon O., Naqvi Naweed I., Neufeld Thomas P., Nishino Ichizo, Nixon Ralph A., Noda Takeshi, Nürnberg Bernd, Ogawa Michinaga, Oleinick Nancy L., Olsen Laura J., Ozpolat Bulent, Paglin Shoshana, Palmer Glen E., Papassideri Issidora S., Parkes Miles, Perlmutter David H., Perry George, Piacentini Mauro, Pinkas-Kramarski Ronit, Prescott Mark, Proikas-Cezanne Tassula, Raben Nina, Rami Abdelhaq, Reggiori Fulvio, Rohrer Bärbel, Rubinsztein David C., Ryan Kevin M., Sadoshima Junichi, Sakagami Hiroshi, Sakai Yasuyoshi, Sandri Marco, Sasakawa Chihiro, Sass Miklós, Schneider Claudio, Seglen Per O., Seleverstov Oleksandr, Settleman Jeffrey, Shacka John J., Shapiro Irving M., Sibirny Andrei A., Silva-Zacarin Elaine C.M., Simon Hans-Uwe, Simone Cristiano, Simonsen Anne, Smith Mark A., Spanel-Borowski Katharina, Srinivas Vickram, Steeves Meredith, Stenmark Harald, Stromhaug Per E., Subauste Carlos S., Sugimoto Seiichiro, Sulzer David, Suzuki Toshihiko, Swanson Michele S., Tabas Ira, Takeshita Fumihiko, Talbot Nicholas J., Tallóczy Zsolt, Tanaka Keiji, Tanaka Kozo, Tanida Isei, Taylor Graham S., Taylor J. Paul, Terman Alexei, Tettamanti Gianluca, Thompson Craig B., Thumm Michael, Tolkovsky Aviva M., Tooze Sharon A., Truant Ray, Tumanovska Lesya V., Uchiyama Yasuo, Ueno Takashi, Uzcátegui Néstor L., van der Klei Ida J., Vaquero Eva C., Vellai Tibor, Vogel Michael W., Wang Hong-Gang, Webster Paul, Xi Zhijun, Xiao Gutian, Yahalom Joachim, Yang Jin-Ming, Yap George S., Yin Xiao-Ming, Yoshimori Tamotsu, Yue Zhenyu, Yuzaki Michisuke, Zabirnyk Olga, Zheng Xiaoxiang, Zhu Xiongwei, Deter Russell L., Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes, 10.4161/auto.5338
- Klionsky Daniel J., Autophagy: from phenomenology to molecular understanding in less than a decade, 10.1038/nrm2245
- Klionsky Daniel J., Cuervo Ana Maria, Seglen Per O., Methods for Monitoring Autophagy from Yeast to Human, 10.4161/auto.3678
- Mizushima Noboru, Methods for monitoring autophagy, 10.1016/j.biocel.2004.02.005
- Mizushima Noboru, Yoshimori Tamotsu, Levine Beth, Methods in Mammalian Autophagy Research, 10.1016/j.cell.2010.01.028
- Rubinsztein David C., Cuervo Ana Maria, Ravikumar Brinda, Sarkar Sovan, Korolchuk Viktor I., Kaushik Susmita, Klionsky Daniel J., In search of an “autophagomometer”, 10.4161/auto.5.5.8823
- Klionsky Daniel J, The autophagosome is overrated!, 10.4161/auto.7.4.14730
- Eskelinen Eeva-Liisa, Reggiori Fulvio, Baba Misuzu, Kovács Attila L., Seglen Per O., Seeing is believing: The impact of electron microscopy on autophagy research, 10.4161/auto.7.9.15760
- Seglen PO. Regulation of autophagic protein degradation in isolated liver cells. In: Glaumann H and Ballard FJ, eds. Lysosomes: Their Role in Protein Breakdown. London: Academic Press, 1987:369-414.
- de Duve Christian, Wattiaux Robert, Functions of Lysosomes, 10.1146/annurev.ph.28.030166.002251
- Dunn William A., Autophagy and related mechanisms of lysosome-mediated protein degradation, 10.1016/0962-8924(94)90069-8
- Gordon Paul B., Seglen Per O., Prelysosomal convergence of autophagic and endocytic pathways, 10.1016/0006-291x(88)90556-6
- Dice J. Fred, Klionsky Daniel J., Artophagy: The art of autophagy—Macroautophagy, 10.4161/auto.6.3.11263
- Kovács János, Fellinger Elizabeth, Kárpáti Anna P., Kovács Attila L., László Lajos, Réz Gábor, Morphometric evaluation of the turnover of autophagic vacuoles after treatment with Triton X-100 and vinblastine in murine pancreatic acinar and seminal vesicle epithelial cells, 10.1007/bf02890242
- Kovács J, Biomed Biochim Acta, 45, 1543 (1986)
- Kovács János, László Lajos, kovács Attila L., Regression of autophagic vacuoles in pancreatic acinar, seminal vesicle epithelial, and liver parenchymal cells: A comparative morphometric study of the effect of vinblastine and leupeptin followed by cycloheximide treatment, 10.1016/0014-4827(88)90158-9
- Chu Charleen T., Autophagic Stress in Neuronal Injury and Disease, 10.1097/01.jnen.0000229233.75253.be
- Fass Ephraim, Shvets Elena, Degani Ilan, Hirschberg Koret, Elazar Zvulun, Microtubules Support Production of Starvation-induced Autophagosomes but Not Their Targeting and Fusion with Lysosomes, 10.1074/jbc.m607031200
- Kovács Attila L., Reith Albrecht, Seglen Per O., Accumulation of autophagosomes after inhibition of hepatocytic protein degradation by vinblastine, leupeptin or a lysosomotropic amine, 10.1016/0014-4827(82)90020-9
- Tóth Szilveszter, Nagy Krisztina, Pálfia Zsolt, Réz Gábor, Cellular autophagic capacity changes during azaserine-induced tumour progression in the rat pancreas, 10.1007/s00441-001-0506-7
- Loos Benjamin, Engelbrecht Anna-Mart, Cell death: A dynamic response concept, 10.4161/auto.5.5.8479
- Seglen PO, Acta Biol Med Ger, 40, 1587 (1981)
- Ktistakis Nicholas T., Andrews Simon, Long Joshua, What is the advantage of a transient precursor in autophagosome biogenesis?, 10.4161/auto.7.1.13697
- Kovács Attila L., Réz Gábor, Pálfia Zsolt, Kovács János, Autophagy in the epithelial cells of murine seminal vesicle in vitro, 10.1007/s004410000275
- Mizushima Noboru, Yoshimori Tamotsu, How to Interpret LC3 Immunoblotting, 10.4161/auto.4600
- Nishida Yuya, Arakawa Satoko, Fujitani Kenji, Yamaguchi Hirofumi, Mizuta Takeshi, Kanaseki Toku, Komatsu Masaaki, Otsu Kinya, Tsujimoto Yoshihide, Shimizu Shigeomi, Discovery of Atg5/Atg7-independent alternative macroautophagy, 10.1038/nature08455
- Kanki Tomotake, Kang Dongchon, Klionsky Daniel J., Monitoring mitophagy in yeast: The Om45-GFP processing assay, 10.4161/auto.5.8.9854
- Grandér Dan, Kharaziha Pedram, Laane Edward, Pokrovskaja Katja, Panaretakis Theoharis, Autophagy as the main means of cytotoxicity by glucocorticoids in hematological malignancies, 10.4161/auto.5.8.10122
- Welter Evelyn, Thumm Michael, Krick Roswitha, Quantification of nonselective bulk autophagy inS. cerevisiaeusing Pgk1-GFP, 10.4161/auto.6.6.12348
- Raju Deepa, Jones Nicola L., Methods to monitor autophagy inH. pylorivacuolating cytotoxin A (VacA)-treated cells, 10.4161/auto.6.1.10222
- Geng Jiefei, Klionsky Daniel J., Determining Atg protein stoichiometry at the phagophore assembly site by fluorescence microscopy, 10.4161/auto.6.1.10249
- Swanlund Jamie M., Kregel Kevin C., Oberley Terry D., Investigating autophagy: Quantitative morphometric analysis using electron microscopy, 10.4161/auto.6.2.10439
- Zhang Ji, Ney Paul, Reticulocyte mitophagy: Monitoring mitochondrial clearance in a mammalian model, 10.4161/auto.6.3.11245
- Seglen Per O., Brinchmann Monica Fengsrud, Purification of autophagosomes from rat hepatocytes, 10.4161/auto.6.4.11272
- He Congcong, Klionsky Daniel J., Analyzing autophagy in zebrafish, 10.4161/auto.6.5.12092
- Calvo-Garrido Javier, Carilla-Latorre Sergio, Mesquita Ana, Escalante Ricardo, A proteolytic cleavage assay to monitor autophagy inDictyostelium discoideum, 10.4161/auto.7.9.16629
- Xu Fei, Liu Xiao-Hong, Zhuang Fei-Long, Zhu Jun, Lin Fu-Cheng, Analyzing autophagy inMagnaporthe oryzae, 10.4161/auto.7.5.15020
- Klionsky DJ. Autophagy: Lower Eukaryotes and Non-Mammalian Systems, Part A. Amsterdam: Academic Press/Elsevier, 2008.
- Klionsky DJ. Autophagy in Mammalian Systems, Part B. Amsterdam: Academic Press/Elsevier, 2008.
- Klionsky DJ. Autophagy in Disease and Clinical Applications, Part C. Amsterdam: Academic Press/Elsevier, 2008.
- Zhu Jianhui, Dagda Ruben K., Chu Charleen T., Monitoring Mitophagy in Neuronal Cell Cultures, Methods in Molecular Biology (2011) ISBN:9781617793271 p.325-339, 10.1007/978-1-61779-328-8_21
- Ylä‐Anttila Päivi, Vihinen Helena, Jokitalo Eija, Eskelinen Eeva‐Liisa, Chapter 10 Monitoring Autophagy by Electron Microscopy in Mammalian Cells, Methods in Enzymology (2009) ISBN:9780123745477 p.143-164, 10.1016/s0076-6879(08)03610-0
- Eskelinen Eeva-Liisa, Maturation of Autophagic Vacuoles in Mammalian Cells, 10.4161/auto.1.1.1270
- Eskelinen Eeva-Liisa, To be or not to be? Examples of incorrect identification of autophagic compartments in conventional transmission electron microscopy of mammalian cells, 10.4161/auto.5179
- Eskelinen Eeva-Liisa, Kovács Attila L., Double membranes vs. lipid bilayers, and their significance for correct identification of macroautophagic structures, 10.4161/auto.7.9.16679
- Eskelinen E-L. Fine structure of the autophagosome. In: Deretic V, ed. Autophagosome and Phagosome. Totowa, NJ: Humana Press, 2008:11-28.
- Berg Trond Olav, Fengsrud Monica, Strømhaug Per Eivind, Berg Trond, Seglen Per O., Isolation and Characterization of Rat Liver Amphisomes : EVIDENCE FOR FUSION OF AUTOPHAGOSOMES WITH BOTH EARLY AND LATE ENDOSOMES, 10.1074/jbc.273.34.21883
- Eskelinen E-L. Macroautophagy in mammalian cells. In: Saftig P, ed. Lysosomes. Georgetown, TX: LandesBioscience/Eurekah.com, 2005.
- Rabouille C., The differential degradation of two cytosolic proteins as a tool to monitor autophagy in hepatocytes by immunocytochemistry, 10.1083/jcb.120.4.897
- Kovács Attila L., Pálfia Zsolt, Réz Gábor, Vellai Tibor, Kovács János, Sequestration Revisited: Integrating Traditional Electron Microscopy, De Novo Assembly and New Results, 10.4161/auto.4590
- Gao Wentao, Kang Jeong Han, Liao Yong, Ding Wen-Xing, Gambotto Andrea A., Watkins Simon C., Liu Yong-Jian, Stolz Donna B., Yin Xiao-Ming, Biochemical Isolation and Characterization of the Tubulovesicular LC3-positive Autophagosomal Compartment, 10.1074/jbc.m109.054197
- Baba Misuzu, Osumi Masako, Ohsumi Yoshinori, Analysis of the Membrane Structures Involved in Autophagy in Yeast by Freeze-Replica Method., 10.1247/csf.20.465
- Réz G, Lab Invest, 43, 269 (1980)
- Punnonen Eeva-Liisa, Pihakaski Kaarina, Mattila Kari, Lounatmaa Kari, Hirsim�ki Pirkko, Intramembrane particles and filipin labelling on the membranes of autophagic vacuoles and lysosomes in mouse liver, 10.1007/bf00239447
- FENGSRUD M, Ultrastructural characterization of the delimiting membranes of isolated autophagosomes and amphisomes by freeze-fracture electron microscopy, 10.1078/0171-9335-00125
- Rao V. Ashutosh, Klein Sarah R., Bonar Spencer J., Zielonka Jacek, Mizuno Naoko, Dickey Jennifer S., Keller Paul W., Joseph Joy, Kalyanaraman Balaraman, Shacter Emily, The Antioxidant Transcription Factor Nrf2 Negatively Regulates Autophagy and Growth Arrest Induced by the Anticancer Redox Agent Mitoquinone, 10.1074/jbc.m110.133579
- Krick Roswitha, Mühe Yvonne, Prick Tanja, Bredschneider Monika, Bremer Sebastian, Wenzel Dirk, Eskelinen Eeva-Liisa, Thumm Michael, Piecemeal microautophagy of the nucleus: Genetic and morphological traits, 10.4161/auto.5.2.7639
- Meschini Stefania, Condello Maria, Calcabrini Annarica, Marra Manuela, Formisano Giuseppe, Lista Pasquale, De Milito Angelo, Federici Elena, Arancia Giuseppe, The plant alkaloid voacamine induces apoptosis-independent autophagic cell death on both sensitive and multidrug resistant human osteosarcoma cells, 10.4161/auto.6952
- Proikas-Cezanne Tassula, Robenek Horst, Freeze-fracture replica immunolabelling reveals human WIPI-1 and WIPI-2 as membrane proteins of autophagosomes, 10.1111/j.1582-4934.2011.01339.x
- Kovács J, Acta Biol Med Ger, 41, 131 (1982)
- Hirsimäki Y, Eur J Cell Biol, 27, 298 (1982)
- Cheong H., Atg17 Regulates the Magnitude of the Autophagic Response, 10.1091/mbc.e04-10-0894
- Xie Z., Nair U., Klionsky D. J., Atg8 Controls Phagophore Expansion during Autophagosome Formation, 10.1091/mbc.e07-12-1292
- Sigmond Timea, Fehér Judit, Baksa Attila, Pásti Gabriella, Pálfia Zsolt, Takács‐Vellai Krisztina, Kovács János, Vellai Tibor, Kovács Attila L., Chapter Twenty‐Eight Qualitative and Quantitative Characterization of Autophagy in Caenorhabditis elegans by Electron Microscopy, Methods in Enzymology (2008) ISBN:9780123745484 p.467-491, 10.1016/s0076-6879(08)03228-x
- Kovács AL, Vellai T, Müller F. Autophagy inCaenorhabditis elegans. In: Klionsky DJ, ed. Autophagy. Georgetown, Texas: Landes Bioscience, 2004:217-23.
- Weibel ER. Practical Methods for Biological Morphometry. Academic Press, New York, 1979.
- Williams MA. Quantitative methods in biology: Practical methods in electron microscopy. Amsterdam, New York, Oxford: North-Holland Publishing Company, 1977.
- Howard V, Reed MG. Unbiased stereology; three dimensional measurement in microscopy. U Bios Scientific Publishers, 1998.
- Punnonen Eeva-Liisa, Reunanen Hilkka, Effects of vinblastine, leucine, and histidine, and 3-methyladenine on autophagy in ehrlich ascites cells, 10.1016/0014-4800(90)90061-h
- Kovács A.L., László L., Fellinger E., Jakab A., Orosz A., Réz G., Kovács J., Combined effects of fasting and vinblastine treatment on serum insulin level, the size of autophagic-lysosomal compartment, protein content and lysosomal enzyme activities of liver and exocrine pancreatic cells of the mouse, 10.1016/0305-0491(89)90189-2
- Shelburne JD, Am J Pathol, 73, 641 (1973)
- Reyes Francisca C., Chung Taijoon, Holding David, Jung Rudolf, Vierstra Richard, Otegui Marisa S., Delivery of Prolamins to the Protein Storage Vacuole in Maize Aleurone Cells, 10.1105/tpc.110.082156
- Dunn, Jr. William A., Cregg James M., Kiel Jan A.K.W., Klei Ida J. van der, Oku Masahide, Sakai Yasuyoshi, Sibirny Andrei A., Stasyk Oleh V., Veenhuis Marten, Pexophagy: The Selective Autophagy of Peroxisomes, 10.4161/auto.1.2.1737
- Wang Ke, Klionsky Daniel J, Mitochondria removal by autophagy, 10.4161/auto.7.3.14502
- Bélanger Myriam, Rodrigues Paulo H., Dunn, Jr. William A., Progulske-Fox Ann, Autophagy: A Highway for Porphyromonas gingivalis in Endothelial Cells, 10.4161/auto.2828
- Birmingham Cheryl L., Brumell John H., Autophagy Recognizes Intracellular Salmonella enterica serovar Typhimurium in Damaged Vacuoles, 10.4161/auto.2825
- Colombo María Isabel, Gutiérrez Maximiliano G., Romano Patricia S., The Two Faces of Autophagy: Coxiella and Mycobacterium, 10.4161/auto.2827
- Ogawa Michinaga, Sasakawa Chihiro, Shigella and Autophagy, 10.4161/auto.2829
- Vergne Isabelle, Singh Sudha, Roberts Esteban, Kyei George, Master Sharon, Harris James, Haro Sergio de, Naylor John, Davis Alex, Delgado Monica, Deretic Vojo, Autophagy in Immune Defense Against Mycobacterium tuberculosis, 10.4161/auto.2830
- Yoshimori Tamotsu, Autophagy vs. Group A Streptococcus, 10.4161/auto.2822
- Lynch-Day Melinda A., Klionsky Daniel J., The Cvt pathway as a model for selective autophagy, 10.1016/j.febslet.2010.02.013
- Birmingham Cheryl L., Canadien Veronica, Gouin Edith, Troy Erin B., Yoshimori Tamotsu, Cossart Pascale, Higgins Darren E., Brumell John H., Listeria monocytogenesEvades Killing by Autophagy During Colonization of Host Cells, 10.4161/auto.4450
- Klionsky D.J., Protein Transport from the Cytoplasm into the Vacuole, 10.1007/s002329900220
- Dini Luciana, Pagliara Patrizia, Carlà Emanuela C., Phagocytosis of apoptotic cells by liver: A morphological study : Phagocytosis of Apoptotic Cells, 10.1002/jemt.10107
- Kroemer G, El-Deiry W S, Golstein P, Peter M E, Vaux D, Vandenabeele P, Zhivotovsky B, Blagosklonny M V, Malorni W, Knight R A, Piacentini M, Nagata S, Melino G, Classification of cell death: recommendations of the Nomenclature Committee on Cell Death, 10.1038/sj.cdd.4401724
- Réz G, Acta Biol Hung, 42, 133 (1991)
- Giammarioli Anna Maria, Gambardella Lucrezia, Barbati Cristiana, Pietraforte Donatella, Tinari Antonella, Alberton Manuela, Gnessi Lucio, Griffin Roger J., Minetti Maurizio, Malorni Walter, Differential effects of the glycolysis inhibitor 2-deoxy-D-glucose on the activity of pro-apoptotic agents in metastatic melanoma cells, and induction of a cytoprotective autophagic response, 10.1002/ijc.26420
- Mayhew Terry M., Quantitative Immunoelectron Microscopy, Methods in Molecular Biology (2007) ISBN:9781588295736 p.309-329, 10.1007/978-1-59745-294-6_15
- Mayhew T. M., Lucocq J. M., Griffiths G., Relative labelling index: a novel stereological approach to test for non-random immunogold labelling of organelles and membranes on transmission electron microscopy thin sections, 10.1046/j.0022-2720.2001.00977.x
- Schmid Dorothee, Pypaert Marc, Münz Christian, Antigen-Loading Compartments for Major Histocompatibility Complex Class II Molecules Continuously Receive Input from Autophagosomes, 10.1016/j.immuni.2006.10.018
- Kovács János, Regression of autophagic vacuoles in seminal vesicle cells following cycloheximide treatment, 10.1016/0014-4827(83)90460-3
- Réz G, Eur J Cell Biol, 71, 341 (1996)
- Kovács Attila L., Grinde Bjørn, Seglen Per O., Inhibition of autophagic vacuole formation and protein degradation by amino acids in isolated hepatocytes, 10.1016/0014-4827(81)90336-0
- Mortimore G. E., Hutson N. J., Surmacz C. A., Quantitative correlation between proteolysis and macro- and microautophagy in mouse hepatocytes during starvation and refeeding., 10.1073/pnas.80.8.2179
- Mortimore GE, J Biol Chem, 263, 2506 (1988)
- Zhu Jian-hui, Horbinski Craig, Guo Fengli, Watkins Simon, Uchiyama Yasuo, Chu Charleen T., Regulation of Autophagy by Extracellular Signal-Regulated Protein Kinases During 1-Methyl-4-Phenylpyridinium-Induced Cell Death, 10.2353/ajpath.2007.060524
- Bjørkøy Geir, Lamark Trond, Brech Andreas, Outzen Heidi, Perander Maria, Øvervatn Aud, Stenmark Harald, Johansen Terje, p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death, 10.1083/jcb.200507002
- Razi Minoo, Tooze Sharon A., Chapter 17 Correlative Light and Electron Microscopy, Methods in Enzymology (2009) ISBN:9780123745477 p.261-275, 10.1016/s0076-6879(08)03617-3
- Shu Xiaokun, Lev-Ram Varda, Deerinck Thomas J., Qi Yingchuan, Ramko Ericka B., Davidson Michael W., Jin Yishi, Ellisman Mark H., Tsien Roger Y., A Genetically Encoded Tag for Correlated Light and Electron Microscopy of Intact Cells, Tissues, and Organisms, 10.1371/journal.pbio.1001041
- Castillo Karen, Rojas-Rivera Diego, Lisbona Fernanda, Caballero Benjamín, Nassif Melissa, Court Felipe A, Schuck Sebastian, Ibar Consuelo, Walter Peter, Sierralta Jimena, Glavic Alvaro, Hetz Claudio, BAX inhibitor-1 regulates autophagy by controlling the IRE1α branch of the unfolded protein response : Bax inhibitor-1 controls autophagy, 10.1038/emboj.2011.318
- Ylä-Anttila Päivi, Vihinen Helena, Jokitalo Eija, Eskelinen Eeva-Liisa, 3D tomography reveals connections between the phagophore and endoplasmic reticulum, 10.4161/auto.5.8.10274
- Hayashi-Nishino Mitsuko, Fujita Naonobu, Noda Takeshi, Yamaguchi Akihito, Yoshimori Tamotsu, Yamamoto Akitsugu, Electron tomography reveals the endoplasmic reticulum as a membrane source for autophagosome formation, 10.4161/auto.6.2.11134
- Schneider EM, Lorezn M, Walther P. Autophagy as a hallmark of hemophagocytic diseases In: Gorbunov N, ed. Autophagy: Principles, regulation and roles in disease: Nova Science Publishers, 2012.
- Massey A. C., Kaushik S., Sovak G., Kiffin R., Cuervo A. M., Consequences of the selective blockage of chaperone-mediated autophagy, 10.1073/pnas.0507436103
- Bosco Daryl A, Morfini Gerardo, Karabacak N Murat, Song Yuyu, Gros-Louis Francois, Pasinelli Piera, Goolsby Holly, Fontaine Benjamin A, Lemay Nathan, McKenna-Yasek Diane, Frosch Matthew P, Agar Jeffrey N, Julien Jean-Pierre, Brady Scott T, Brown Robert H, Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS, 10.1038/nn.2660
- Sou Yu-shin, Tanida Isei, Komatsu Masaaki, Ueno Takashi, Kominami Eiki, Phosphatidylserine in Addition to Phosphatidylethanolamine Is anin VitroTarget of the Mammalian Atg8 Modifiers, LC3, GABARAP, and GATE-16, 10.1074/jbc.m505888200
- Le Grand Jaclyn Nicole, Chakrama Fatima Zahra, Seguin-Py Stéphanie, Fraichard Annick, Delage-Mourroux Régis, Jouvenot Michèle, Boyer-Guittaut Michaël, GABARAPL1 (GEC1): Original or copycat?, 10.4161/auto.7.10.15904
- Kabeya Y., LC3, GABARAP and GATE16 localize to autophagosomal membrane depending on form-II formation, 10.1242/jcs.01131
- Weidberg Hilla, Shvets Elena, Shpilka Tomer, Shimron Frida, Shinder Vera, Elazar Zvulun, LC3 and GATE-16/GABARAP subfamilies are both essential yet act differently in autophagosome biogenesis, 10.1038/emboj.2010.74
- Kovsan Julia, Blüher Matthias, Tarnovscki Tanya, Klöting Nora, Kirshtein Boris, Madar Liron, Shai Iris, Golan Rachel, Harman-Boehm Ilana, Schön Michael R., Greenberg Andrew S., Elazar Zvulun, Bashan Nava, Rudich Assaf, Altered Autophagy in Human Adipose Tissues in Obesity, 10.1210/jc.2010-1681
- Tanida Isei, Minematsu-Ikeguchi Naoko, Ueno Takashi, Kominami Eiki, Lysosomal Turnover, but Not a Cellular Level, of Endogenous LC3 is a Marker for Autophagy, 10.4161/auto.1.2.1697
- Huang Wei-Pang, Scott Sidney V., Kim John, Klionsky Daniel J., The Itinerary of a Vesicle Component, Aut7p/Cvt5p, Terminates in the Yeast Vacuole via the Autophagy/Cvt Pathways, 10.1074/jbc.275.8.5845
- Cai Qian, Lu Li, Tian Jin-Hua, Zhu Yi-Bing, Qiao Haifa, Sheng Zu-Hang, Snapin-Regulated Late Endosomal Transport Is Critical for Efficient Autophagy-Lysosomal Function in Neurons, 10.1016/j.neuron.2010.09.022
- Castino Roberta, Fiorentino Ilaria, Cagnin Monica, Giovia Antonino, Isidoro Ciro, Chelation of Lysosomal Iron Protects Dopaminergic SH-SY5Y Neuroblastoma Cells from Hydrogen Peroxide Toxicity by Precluding Autophagy and Akt Dephosphorylation, 10.1093/toxsci/kfr179
- Michiorri S, Gelmetti V, Giarda E, Lombardi F, Romano F, Marongiu R, Nerini-Molteni S, Sale P, Vago R, Arena G, Torosantucci L, Cassina L, Russo M A, Dallapiccola B, Valente E M, Casari G, The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy, 10.1038/cdd.2009.200
- Ahlberg J, J Biol Chem, 260, 5847 (1985)
- McLeland Christopher B., Rodriguez Jamie, Stern Stephan T., Autophagy Monitoring Assay: Qualitative Analysis of MAP LC3-I to II Conversion by Immunoblot, Methods in Molecular Biology (2011) ISBN:9781603271974 p.199-206, 10.1007/978-1-60327-198-1_21
- Chakrama Fatima Zahra, Seguin-Py Stéphanie, Le Grand Jaclyn Nicole, Fraichard Annick, Delage-Mourroux Régis, Despouy Gilles, Perez Valérie, Jouvenot Michèle, Boyer-Guittaut Michaël, GABARAPL1 (GEC1) associates with autophagic vesicles, 10.4161/auto.6.4.11819
- Kim John, Huang Wei-Pang, Klionsky Daniel J., Membrane Recruitment of Aut7p in the Autophagy and Cytoplasm to Vacuole Targeting Pathways Requires Aut1p, Aut2p, and the Autophagy Conjugation Complex, 10.1083/jcb.152.1.51
- Shu Chih-Wen, Drag Marcin, Bekes Miklos, Zhai Dayong, Salvesen Guy S., Reed John C., Synthetic substrates for measuring activity of autophagy proteases-autophagins (Atg4) : Autophagins (Atg4), 10.4161/auto.6.7.13075
- Li Min, Chen Xi, Ye Qi-Zhuang, Vogt Andreas, Yin Xiao-Ming, A high-throughput FRET-based assay for determination of Atg4 activity, 10.4161/auto.18777
- Ketteler Robin, Seed Brian, Quantitation of autophagy by luciferase release assay, 10.4161/auto.6401
- Li Min, Hou Yifeng, Wang Jinsong, Chen Xiaoyun, Shao Zhi-Ming, Yin Xiao-Ming, Kinetics Comparisons of Mammalian Atg4 Homologues Indicate Selective Preferences toward Diverse Atg8 Substrates, 10.1074/jbc.m110.199059
- Klionsky Daniel J, For the last time, it is GFP-Atg8, not Atg8-GFP (and the same goes for LC3), 10.4161/auto.7.10.15492
- Mizushima N., In Vivo Analysis of Autophagy in Response to Nutrient Starvation Using Transgenic Mice Expressing a Fluorescent Autophagosome Marker, 10.1091/mbc.e03-09-0704
- Castino Roberta, Lazzeri Gloria, Lenzi Paola, Bellio Natascia, Follo Carlo, Ferrucci Michela, Fornai Francesco, Isidoro Ciro, Suppression of autophagy precipitates neuronal cell death following low doses of methamphetamine, 10.1111/j.1471-4159.2008.05488.x
- Matsui Y., Takagi H., Qu X., Abdellatif M., Sakoda H., Asano T., Levine B., Sadoshima J., Distinct Roles of Autophagy in the Heart During Ischemia and Reperfusion: Roles of AMP-Activated Protein Kinase and Beclin 1 in Mediating Autophagy, 10.1161/01.res.0000261924.76669.36
- Suzuki K., The pre-autophagosomal structure organized by concerted functions of APG genes is essential for autophagosome formation, 10.1093/emboj/20.21.5971
- Hanson Hugo H., Kang Semie, Fernández-Monreal Mónica, Oung Twethida, Yildirim Murat, Lee Rebecca, Suyama Kimita, Hazan Rachel B., Phillips Greg R., LC3-dependent Intracellular Membrane Tubules Induced by γ-Protocadherins A3 and B2 : A ROLE FOR INTRALUMINAL INTERACTIONS, 10.1074/jbc.m109.092031
- Sanjuan Miguel A., Dillon Christopher P., Tait Stephen W. G., Moshiach Simon, Dorsey Frank, Connell Samuel, Komatsu Masaaki, Tanaka Keiji, Cleveland John L., Withoff Sebo, Green Douglas R., Toll-like receptor signalling in macrophages links the autophagy pathway to phagocytosis, 10.1038/nature06421
- Sanjuan Miguel A., Milasta Sandra, Green Douglas R., Toll-like receptor signaling in the lysosomal pathways, 10.1111/j.1600-065x.2008.00732.x
- Florey Oliver, Kim Sung Eun, Sandoval Cynthia P., Haynes Cole M., Overholtzer Michael, Autophagy machinery mediates macroendocytic processing and entotic cell death by targeting single membranes, 10.1038/ncb2363
- Martinez J., Almendinger J., Oberst A., Ness R., Dillon C. P., Fitzgerald P., Hengartner M. O., Green D. R., Microtubule-associated protein 1 light chain 3 alpha (LC3)-associated phagocytosis is required for the efficient clearance of dead cells, 10.1073/pnas.1113421108
- Gong Lan, Cullinane Meabh, Treerat Puthayalai, Ramm Georg, Prescott Mark, Adler Ben, Boyce John D., Devenish Rodney J., The Burkholderia pseudomallei Type III Secretion System and BopA Are Required for Evasion of LC3-Associated Phagocytosis, 10.1371/journal.pone.0017852
- Dupont Nicolas, Lacas-Gervais Sandra, Bertout Julie, Paz Irit, Freche Barbara, Van Nhieu Guy Tran, van der Goot F. Gisou, Sansonetti Philippe J., Lafont Frank, Shigella Phagocytic Vacuolar Membrane Remnants Participate in the Cellular Response to Pathogen Invasion and Are Regulated by Autophagy, 10.1016/j.chom.2009.07.005
- Reggiori Fulvio, Monastyrska Iryna, Verheije Monique H., Calì Tito, Ulasli Mustafa, Bianchi Siro, Bernasconi Riccardo, de Haan Cornelis A.M., Molinari Maurizio, Coronaviruses Hijack the LC3-I-Positive EDEMosomes, ER-Derived Vesicles Exporting Short-Lived ERAD Regulators, for Replication, 10.1016/j.chom.2010.05.013
- English Luc, Chemali Magali, Duron Johanne, Rondeau Christiane, Laplante Annie, Gingras Diane, Alexander Diane, Leib David, Norbury Christopher, Lippé Roger, Desjardins Michel, Autophagy enhances the presentation of endogenous viral antigens on MHC class I molecules during HSV-1 infection, 10.1038/ni.1720
- Plowey Edward D., Cherra Salvatore J., Liu Yong-Jian, Chu Charleen T., Role of autophagy in G2019S-LRRK2-associated neurite shortening in differentiated SH-SY5Y cells, 10.1111/j.1471-4159.2008.05217.x
- Nicotra Giuseppina, Mercalli Francesca, Peracchio Claudia, Castino Roberta, Follo Carlo, Valente Guido, Isidoro Ciro, Autophagy-active beclin-1 correlates with favourable clinical outcome in non-Hodgkin lymphomas, 10.1038/modpathol.2010.80
- Tanida Isei, Ueno Takashi, Kominami Eiki, LC3 and Autophagy, Autophagosome and Phagosome (2008) ISBN:9781588298539 p.77-88, 10.1007/978-1-59745-157-4_4
- Chu Charleen T., Plowey Edward D., Dagda Ruben K., Hickey Robert W., Cherra Salvatore J., Clark Robert S.B., Chapter 11 Autophagy in Neurite Injury and Neurodegeneration, Autophagy in Disease and Clinical Applications, Part C (2009) ISBN:9780123749369 p.217-249, 10.1016/s0076-6879(08)04011-1
- He Hua, Dang Yongjun, Dai Fangyan, Guo Zekun, Wu Jiaxue, She Xinyu, Pei Yuan, Chen Yongjing, Ling Wenhai, Wu Chaoqun, Zhao Shouyuan, Liu Jun O., Yu Long, Post-translational Modifications of Three Members of the Human MAP1LC3 Family and Detection of a Novel Type of Modification for MAP1LC3B, 10.1074/jbc.m303800200
- Shpilka Tomer, Weidberg Hilla, Pietrokovski Shmuel, Elazar Zvulun, Atg8: an autophagy-related ubiquitin-like protein family, 10.1186/gb-2011-12-7-226
- Zois Christos E., Koukourakis Michael I., Radiation-induced autophagy in normal and cancer cells: Towards novel cytoprotection and radio-sensitization policies?, 10.4161/auto.5.4.7667
- Xin Yurong, Yu Long, Chen Zheng, Zheng Lihua, Fu Qiang, Jiang Jianmin, Zhang Pingzhao, Gong Romu, Zhao Shouyuan, Cloning, Expression Patterns, and Chromosome Localization of Three Human and Two Mouse Homologues of GABAA Receptor-Associated Protein, 10.1006/geno.2001.6555
- Novak Ivana, Kirkin Vladimir, McEwan David G, Zhang Ji, Wild Philipp, Rozenknop Alexis, Rogov Vladimir, Löhr Frank, Popovic Doris, Occhipinti Angelo, Reichert Andreas S, Terzic Janos, Dötsch Volker, Ney Paul A, Dikic Ivan, Nix is a selective autophagy receptor for mitochondrial clearance, 10.1038/embor.2009.256
- Gassmann Max, Grenacher Beat, Rohde Bianca, Vogel Johannes, Quantifying Western blots: Pitfalls of densitometry, 10.1002/elps.200800720
- Kirisako Takayoshi, Ichimura Yoshinobu, Okada Hisashi, Kabeya Yukiko, Mizushima Noboru, Yoshimori Tamotsu, Ohsumi Mariko, Takao Toshifumi, Noda Takeshi, Ohsumi Yoshinori, The Reversible Modification Regulates the Membrane-Binding State of Apg8/Aut7 Essential for Autophagy and the Cytoplasm to Vacuole Targeting Pathway, 10.1083/jcb.151.2.263
- Chung Taijoon, Phillips Allison R., Vierstra Richard D., ATG8 lipidation and ATG8-mediated autophagy in Arabidopsis require ATG12 expressed from the differentially controlled ATG12A AND ATG12B loci : Arabidopsis autophagy requires ATG12, 10.1111/j.1365-313x.2010.04166.x
- Chung T., Suttangkakul A., Vierstra R. D., The ATG Autophagic Conjugation System in Maize: ATG Transcripts and Abundance of the ATG8-Lipid Adduct Are Regulated by Development and Nutrient Availability, 10.1104/pp.108.126714
- King Jason S., Veltman Douwe M., Insall Robert H, The induction of autophagy by mechanical stress, 10.4161/auto.7.12.17924
- Ju Jeong-Sun, Varadhachary Arun S., Miller Sara E., Weihl Conrad C., Quantitation of "autophagic flux" in mature skeletal muscle, 10.4161/auto.6.7.12785
- Degtyarev Michael, De Mazière Ann, Orr Christine, Lin Jie, Lee Brian B., Tien Janet Y., Prior Wei W., van Dijk Suzanne, Wu Hong, Gray Daniel C., Davis David P., Stern Howard M., Murray Lesley J., Hoeflich Klaus P., Klumperman Judith, Friedman Lori S., Lin Kui, Akt inhibition promotes autophagy and sensitizes PTEN-null tumors to lysosomotropic agents, 10.1083/jcb.200801099
- Klionsky Daniel J., Elazar Zvulun, Seglen Per O., Rubinsztein David C., Does bafilomycin A1block the fusion of autophagosomes with lysosomes?, 10.4161/auto.6845
- Xie Rui, Nguyen Susan, McKeehan Wallace L, Liu Leyuan, Acetylated microtubules are required for fusion of autophagosomes with lysosomes, 10.1186/1471-2121-11-89
- Gonzalez-Polo R.-A., The apoptosis/autophagy paradox: autophagic vacuolization before apoptotic death, 10.1242/jcs.02447
- Cuervo A. M., Impaired Degradation of Mutant -Synuclein by Chaperone-Mediated Autophagy, 10.1126/science.1101738
- Trincheri Nicol F., Follo Carlo, Nicotra Giuseppina, Peracchio Claudia, Castino Roberta, Isidoro Ciro, Resveratrol-induced apoptosis depends on the lipid kinase activity of Vps34 and on the formation of autophagolysosomes, 10.1093/carcin/bgm271
- Sarkar Sovan, Ravikumar Brinda, Rubinsztein David C., Chapter 5 Autophagic Clearance of Aggregate‐Prone Proteins Associated with Neurodegeneration, Autophagy in Disease and Clinical Applications, Part C (2009) ISBN:9780123749369 p.83-110, 10.1016/s0076-6879(08)04005-6
- Shintani Takahiro, Klionsky Daniel J., Cargo Proteins Facilitate the Formation of Transport Vesicles in the Cytoplasm to Vacuole Targeting Pathway, 10.1074/jbc.m404399200
- Karim Md. Razaul, Kanazawa Takumi, Daigaku Yasuhiro, Fujimura Shinobu, Miotto Giovanni, Kadowaki Motoni, Cytosolic LC3 Ratio as a Sensitive Index of Macroautophagy in Isolated Rat Hepatocytes and H4-II-E Cells, 10.4161/auto.4615
- Farkas Thomas, Høyer-Hansen Maria, Jäättelä Marja, Identification of novel autophagy regulators by a luciferase-based assay for the kinetics of autophagic flux, 10.4161/auto.5.7.9443
- Frankel Lisa B, Wen Jiayu, Lees Michael, Høyer-Hansen Maria, Farkas Thomas, Krogh Anders, Jäättelä Marja, Lund Anders H, microRNA-101 is a potent inhibitor of autophagy : miR-101 regulates autophagy, 10.1038/emboj.2011.331
- Farkas Thomas, Daugaard Mads, Jäättelä Marja, Identification of Small Molecule Inhibitors of Phosphatidylinositol 3-Kinase and Autophagy, 10.1074/jbc.m111.269134
- Szyniarowski Piotr, Corcelle-Termeau Elisabeth, Farkas Thomas, Høyer-Hansen Maria, Nylandsted Jesper, Kallunki Tuula, Jäättelä Marja, A comprehensive siRNA screen for kinases that suppress macroautophagy in optimal growth conditions, 10.4161/auto.7.8.15770
- Sarkar Sovan, Korolchuk Viktor I., Renna Maurizio, Winslow Ashley R., Rubinsztein David C., Methodological considerations for assessing autophagy modulators: A study with calcium phosphate precipitates, 10.4161/auto.5.3.7664
- Iwata J.-i., Excess Peroxisomes Are Degraded by Autophagic Machinery in Mammals, 10.1074/jbc.m512283200
- Narendra Derek, Tanaka Atsushi, Suen Der-Fen, Youle Richard J., Parkin is recruited selectively to impaired mitochondria and promotes their autophagy, 10.1083/jcb.200809125
- Nogalska Anna, Terracciano Chiara, D’Agostino Carla, King Engel W., Askanas Valerie, p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis, 10.1007/s00401-009-0564-6
- Hosokawa Nao, Hara Yukichi, Mizushima Noboru, Generation of cell lines with tetracycline-regulated autophagy and a role for autophagy in controlling cell size, 10.1016/j.febslet.2006.04.008
- Ni Hong-Min, Bockus Abigail, Wozniak Ann L., Jones Kellyann, Weinman Steven, Yin Xiao-Ming, Ding Wen-Xing, Dissecting the dynamic turnover of GFP-LC3 in the autolysosome, 10.4161/auto.7.2.14181
- Gutierrez M. G., Saka H. A., Chinen I., Zoppino F. C. M., Yoshimori T., Bocco J. L., Colombo M. I., Protective role of autophagy against Vibrio cholerae cytolysin, a pore-forming toxin from V. cholerae, 10.1073/pnas.0601437104
- Suttangkakul A., Li F., Chung T., Vierstra R. D., The ATG1/ATG13 Protein Kinase Complex Is Both a Regulator and a Target of Autophagic Recycling in Arabidopsis, 10.1105/tpc.111.090993
- Balgi Aruna D., Fonseca Bruno D., Donohue Elizabeth, Tsang Trevor C. F., Lajoie Patrick, Proud Christopher G., Nabi Ivan R., Roberge Michel, Screen for Chemical Modulators of Autophagy Reveals Novel Therapeutic Inhibitors of mTORC1 Signaling, 10.1371/journal.pone.0007124
- Patterson George H, Lippincott-Schwartz Jennifer, Selective photolabeling of proteins using photoactivatable GFP, 10.1016/j.ymeth.2003.10.006
- Hamacher-Brady Anne, Brady Nathan R., Gottlieb Roberta A., Enhancing Macroautophagy Protects against Ischemia/Reperfusion Injury in Cardiac Myocytes, 10.1074/jbc.m603783200
- Noda Takeshi, Klionsky Daniel J., Chapter 3 The Quantitative Pho8Δ60 Assay of Nonspecific Autophagy, Methods in Enzymology (2008) ISBN:9780123745484 p.33-42, 10.1016/s0076-6879(08)03203-5
- Klionsky Daniel J., Monitoring Autophagy in Yeast, Protein Targeting Protocols (2007) ISBN:9781588297020 p.363-371, 10.1007/978-1-59745-466-7_24
- Patterson G.H., Knobel S.M., Sharif W.D., Kain S.R., Piston D.W., Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy, 10.1016/s0006-3495(97)78307-3
- Kimura Shunsuke, Noda Takeshi, Yoshimori Tamotsu, Dissection of the Autophagosome Maturation Process by a Novel Reporter Protein, Tandem Fluorescent-Tagged LC3, 10.4161/auto.4451
- Shaner Nathan C, Campbell Robert E, Steinbach Paul A, Giepmans Ben N G, Palmer Amy E, Tsien Roger Y, Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein, 10.1038/nbt1037
- Strack Rita L., Keenan Robert J., Glick Benjamin S., Noncytotoxic DsRed Derivatives for Whole-Cell Labeling, Flow Cytometry Protocols (2011) ISBN:9781617379499 p.355-370, 10.1007/978-1-61737-950-5_17
- Gurskaya Nadya G, Verkhusha Vladislav V, Shcheglov Alexander S, Staroverov Dmitry B, Chepurnykh Tatyana V, Fradkov Arkady F, Lukyanov Sergey, Lukyanov Konstantin A, Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light, 10.1038/nbt1191
- Ryhänen Tuomas, Hyttinen Juha M. T., Kopitz Jürgen, Rilla Kirsi, Kuusisto Erkki, Mannermaa Eliisa, Viiri Johanna, Holmberg Carina I., Immonen Ilkka, Meri Seppo, Parkkinen Jussi, Eskelinen Eeva-Liisa, Uusitalo Hannu, Salminen Antero, Kaarniranta Kai, Crosstalk between Hsp70 molecular chaperone, lysosomes and proteasomes in autophagy-mediated proteolysis in human retinal pigment epithelial cells, 10.1111/j.1582-4934.2008.00577.x
- Rekas Agata, Alattia Jean-René, Nagai Takeharu, Miyawaki Atsushi, Ikura Mitsuhiko, Crystal Structure of Venus, a Yellow Fluorescent Protein with Improved Maturation and Reduced Environmental Sensitivity, 10.1074/jbc.m209524200
- Kabeya Y., LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing, 10.1093/emboj/19.21.5720
- Badr Christian E., Wurdinger Thomas, Nilsson Jonas, Niers Johanna M., Whalen Michael, Degterev Alexei, Tannous Bakhos A., Lanatoside C sensitizes glioblastoma cells to tumor necrosis factor–related apoptosis-inducing ligand and induces an alternative cell death pathway, 10.1093/neuonc/nor067
- Melendez A., Autophagy Genes Are Essential for Dauer Development and Life-Span Extension in C. elegans, 10.1126/science.1087782
- Otto Grant P., Wu Mary Y., Kazgan Nevzat, Anderson O. Roger, Kessin Richard H., Macroautophagy Is Required for Multicellular Development of the Social AmoebaDictyostelium discoideum, 10.1074/jbc.m212467200
- Liu Xiao‐Hong, Liu Tong‐Bao, Lin Fu‐Cheng, Chapter 19 Monitoring Autophagy in Magnaporthe oryzae, Methods in Enzymology (2008) ISBN:9780123745484 p.271-294, 10.1016/s0076-6879(08)03219-9
- Pinan-Lucarré Bérangère, Paoletti Mathieu, Dementhon Karine, Coulary-Salin Bénédicte, Clavé Corinne, Autophagy is induced during cell death by incompatibility and is essential for differentiation in the filamentous fungus Podospora anserina : Autophagy, differentiation and cell death in Podospora, 10.1046/j.1365-2958.2003.03208.x
- Veneault-Fourrey C., Autophagic Fungal Cell Death Is Necessary for Infection by the Rice Blast Fungus, 10.1126/science.1124550
- Kikuma T., Ohneda M., Arioka M., Kitamoto K., Functional Analysis of the ATG8 Homologue Aoatg8 and Role of Autophagy in Differentiation and Germination in Aspergillus oryzae, 10.1128/ec.00024-06
- Nolting Nicole, Bernhards Yasmine, Pöggeler Stefanie, SmATG7 is required for viability in the homothallic ascomycete Sordaria macrospora, 10.1016/j.fgb.2009.03.008
- Baghdiguian Stephen, Martinand-Mari Camille, Mangeat Paul, Using Ciona to study developmental programmed cell death, 10.1016/j.semcancer.2006.11.005
- Rusten Tor Erik, Lindmo Karine, Juhász Gábor, Sass Miklós, Seglen Per O., Brech Andreas, Stenmark Harald, Programmed Autophagy in the Drosophila Fat Body Is Induced by Ecdysone through Regulation of the PI3K Pathway, 10.1016/j.devcel.2004.07.005
- Scott Ryan C., Schuldiner Oren, Neufeld Thomas P., Role and Regulation of Starvation-Induced Autophagy in the Drosophila Fat Body, 10.1016/j.devcel.2004.07.009
- Denton Donna, Shravage Bhupendra, Simin Rachel, Mills Kathryn, Berry Deborah L., Baehrecke Eric H., Kumar Sharad, Autophagy, Not Apoptosis, Is Essential for Midgut Cell Death in Drosophila, 10.1016/j.cub.2009.08.042
- Yoshimoto K., Processing of ATG8s, Ubiquitin-Like Proteins, and Their Deconjugation by ATG4s Are Essential for Plant Autophagy, 10.1105/tpc.104.025395
- Besteiro Sébastien, Brooks Carrie F., Striepen Boris, Dubremetz Jean-François, Autophagy Protein Atg3 is Essential for Maintaining Mitochondrial Integrity and for Normal Intracellular Development of Toxoplasma gondii Tachyzoites, 10.1371/journal.ppat.1002416
- Williams Roderick A., Tetley Laurence, Mottram Jeremy C., Coombs Graham H., Cysteine peptidases CPA and CPB are vital for autophagy and differentiation in Leishmania mexicana, 10.1111/j.1365-2958.2006.05274.x
- Williams Roderick A.M., Woods Kerry L., Juliano Luiz, Mottram Jeremy C., Coombs Graham H., Characterization of unusual families of ATG8-like proteins and ATG12 in the protozoan parasiteLeishmania major, 10.4161/auto.5.2.7328
- Elsässer Albrecht, Vogt Achim M, Nef Holger, Kostin Sawa, Möllmann Helge, Skwara Woitek, Bode Christoph, Hamm Christian, Schaper Jutta, Human hibernating myocardium is jeopardized by apoptotic and autophagic cell death, 10.1016/j.jacc.2004.02.053
- Knaapen Michiel W.M., Davies Michael J., De Bie Martine, Haven Aldwyn J., Martinet Wim, Kockx Mark M., Apoptotic versus autophagic cell death in heart failure, 10.1016/s0008-6363(01)00290-5
- Kostin S., Myocytes Die by Multiple Mechanisms in Failing Human Hearts, 10.1161/01.res.0000067471.95890.5c
- Perez-Perez M. E., Florencio F. J., Crespo J. L., Inhibition of Target of Rapamycin Signaling and Stress Activate Autophagy in Chlamydomonas reinhardtii, 10.1104/pp.109.152520
- Koike Masato, Shibata Masahiro, Waguri Satoshi, Yoshimura Kentaro, Tanida Isei, Kominami Eiki, Gotow Takahiro, Peters Christoph, von Figura Kurt, Mizushima Noboru, Saftig Paul, Uchiyama Yasuo, Participation of Autophagy in Storage of Lysosomes in Neurons from Mouse Models of Neuronal Ceroid-Lipofuscinoses (Batten Disease), 10.1016/s0002-9440(10)61253-9
- Tanak Hasan, Yavuz Metin, Density functional computational studies on (E)-2-[(2-Hydroxy-5-nitrophenyl)-iminiomethyl]-4-nitrophenolate, 10.1007/s00894-009-0539-5
- Tang Daolin, Kang Rui, Livesey Kristen M., Cheh Chun-Wei, Farkas Adam, Loughran Patricia, Hoppe George, Bianchi Marco E., Tracey Kevin J., Zeh Herbert J., Lotze Michael T., Endogenous HMGB1 regulates autophagy, 10.1083/jcb.200911078
- Gniadek Thomas J., Warren Graham, WatershedCounting3D: A New Method for Segmenting and Counting Punctate Structures from Confocal Image Data, 10.1111/j.1600-0854.2007.00538.x
- Decuypere Jean-Paul, Welkenhuyzen Kirsten, Luyten Tomas, Ponsaerts Raf, Dewaele Michael, Molgó Jordi, Agostinis Patrizia, Missiaen Ludwig, De Smedt Humbert, Parys Jan B., Bultynck Geert, Ins(1,4,5)P3receptor-mediated Ca2+signaling and autophagy induction are interrelated, 10.4161/auto.7.12.17909
- Amer Amal O., Swanson Michele S., Autophagy is an immediate macrophage response to Legionella pneumophila, 10.1111/j.1462-5822.2005.00509.x
- Gutierrez Maximiliano G., Master Sharon S., Singh Sudha B., Taylor Gregory A., Colombo Maria I., Deretic Vojo, Autophagy Is a Defense Mechanism Inhibiting BCG and Mycobacterium tuberculosis Survival in Infected Macrophages, 10.1016/j.cell.2004.11.038
- Ogawa Michinaga, Sasakawa Chihiro, Intracellular survival of Shigella, 10.1111/j.1462-5822.2005.00652.x
- Kamentsky Lee, Jones Thouis R., Fraser Adam, Bray Mark-Anthony, Logan David J., Madden Katherine L., Ljosa Vebjorn, Rueden Curtis, Eliceiri Kevin W., Carpenter Anne E., Improved structure, function and compatibility for CellProfiler: modular high-throughput image analysis software, 10.1093/bioinformatics/btr095
- Wu J.-Q., Counting Cytokinesis Proteins Globally and Locally in Fission Yeast, 10.1126/science.1113230
- Geng Jiefei, Baba Misuzu, Nair Usha, Klionsky Daniel J., Quantitative analysis of autophagy-related protein stoichiometry by fluorescence microscopy, 10.1083/jcb.200711112
- Brady Nathan R., Hamacher-Brady Anne, Yuan Hua, Gottlieb Roberta A., The autophagic response to nutrient deprivation in the hl-1 cardiac myocyte is modulated by Bcl-2 and sarco/endoplasmic reticulum calcium stores : Bcl-2 and calcium control of autophagy, 10.1111/j.1742-4658.2007.05849.x
- Qadir M. A., Kwok B., Dragowska W. H., To K. H., Le D., Bally M. B., Gorski Sharon M., Macroautophagy inhibition sensitizes tamoxifen-resistant breast cancer cells and enhances mitochondrial depolarization, 10.1007/s10549-007-9873-4
- Dolloff Nathan G., Ma Xiahong, Dicker David T., Humphreys Robin C., Li Lin Z., El-Deiry Wafik S., Spectral imaging-based methods for quantifying autophagy and apoptosis, 10.4161/cbt.12.4.17175
- Phadwal Kanchan, Alegre-Abarrategui Javier, Watson Alexander Scarth, Pike Luke, Anbalagan Selvakumar, Hammond Ester M., Wade-Martins Richard, McMichael Andrew, Klenerman Paul, Simon Anna Katharina, A novel method for autophagy detection in primary cells : Impaired levels of macroautophagy in immunosenescent T cells, 10.4161/auto.18935
- Lee H. K., Lund J. M., Ramanathan B., Mizushima N., Iwasaki A., Autophagy-Dependent Viral Recognition by Plasmacytoid Dendritic Cells, 10.1126/science.1136880
- Kuma Akiko, Matsui Makoto, Mizushima Noboru, LC3, an Autophagosome Marker, Can be Incorporated into Protein Aggregates Independent of Autophagy: Caution in the Interpretation of LC3 Localization, 10.4161/auto.4012
- Szeto Jason, Kaniuk Natalia A., Canadien Veronica, Nisman Rozalia, Mizushima Noboru, Yoshimori Tamotsu, Bazett-Jones David P., Brumell John H., ALIS are Stress-Induced Protein Storage Compartments for Substrates of the Proteasome and Autophagy, 10.4161/auto.2731
- Kaniuk N. A., Kiraly M., Bates H., Vranic M., Volchuk A., Brumell J. H., Ubiquitinated-Protein Aggregates Form in Pancreatic -Cells During Diabetes-Induced Oxidative Stress and Are Regulated by Autophagy, 10.2337/db06-1160
- Fujita K.-i., Maeda D., Xiao Q., Srinivasula S. M., Nrf2-mediated induction of p62 controls Toll-like receptor-4-driven aggresome-like induced structure formation and autophagic degradation, 10.1073/pnas.1014156108
- Pierre Philippe, Dendritic cells, DRiPs, and DALIS in the control of antigen processing, 10.1111/j.0105-2896.2005.00300.x
- Pankiv Serhiy, Clausen Terje Høyvarde, Lamark Trond, Brech Andreas, Bruun Jack-Ansgar, Outzen Heidi, Øvervatn Aud, Bjørkøy Geir, Johansen Terje, p62/SQSTM1 Binds Directly to Atg8/LC3 to Facilitate Degradation of Ubiquitinated Protein Aggregates by Autophagy, 10.1074/jbc.m702824200
- Hara Taichi, Nakamura Kenji, Matsui Makoto, Yamamoto Akitsugu, Nakahara Yohko, Suzuki-Migishima Rika, Yokoyama Minesuke, Mishima Kenji, Saito Ichiro, Okano Hideyuki, Mizushima Noboru, Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice, 10.1038/nature04724
- Komatsu Masaaki, Waguri Satoshi, Chiba Tomoki, Murata Shigeo, Iwata Jun-ichi, Tanida Isei, Ueno Takashi, Koike Masato, Uchiyama Yasuo, Kominami Eiki, Tanaka Keiji, Loss of autophagy in the central nervous system causes neurodegeneration in mice, 10.1038/nature04723
- Calvo-Garrido Javier, Escalante Ricardo, Autophagy dysfunction and ubiquitin-positive protein aggregates in Dictyostelium cells lacking Vmp1, 10.4161/auto.6.1.10697
- Bjørkøy Geir, Lamark Trond, Johansen Terje, p62/SQSTM1: A Missing Link between Protein Aggregates and the Autophagy Machinery, 10.4161/auto.2.2.2405
- Matsumoto Gen, Wada Koji, Okuno Misako, Kurosawa Masaru, Nukina Nobuyuki, Serine 403 Phosphorylation of p62/SQSTM1 Regulates Selective Autophagic Clearance of Ubiquitinated Proteins, 10.1016/j.molcel.2011.07.039
- Köchl Robert, Hu Xiao Wen, Chan Edmond Y. W., Tooze Sharon A., Microtubules Facilitate Autophagosome Formation and Fusion of Autophagosomes with Endosomes : Role of Microtubules in AV Formation, 10.1111/j.1600-0854.2005.00368.x
- Eng Kai Er, Panas Marc D., Hedestam Gunilla B. Karlsson, McInerney Gerald M., A novel quantitative flow cytometry-based assay for autophagy, 10.4161/auto.6.5.12112
- Ciechomska Iwona A., Tolkovsky Aviva M., Non-Autophagic GFP-LC3 Puncta Induced by Saponin and Other Detergents, 10.4161/auto.4843
- Tsvetkov A. S., Miller J., Arrasate M., Wong J. S., Pleiss M. A., Finkbeiner S., A small-molecule scaffold induces autophagy in primary neurons and protects against toxicity in a Huntington disease model, 10.1073/pnas.1004498107
- Joo Joung Hyuck, Dorsey Frank C., Joshi Aashish, Hennessy-Walters Kristin M., Rose Kristie L., McCastlain Kelly, Zhang Ji, Iyengar Rekha, Jung Chang Hwa, Suen Der-Fen, Steeves Meredith A., Yang Chia-Ying, Prater Stephanie M., Kim Do-Hyung, Thompson Craig B., Youle Richard J., Ney Paul A., Cleveland John L., Kundu Mondira, Hsp90-Cdc37 Chaperone Complex Regulates Ulk1- and Atg13-Mediated Mitophagy, 10.1016/j.molcel.2011.06.018
- Fujita N., Hayashi-Nishino M., Fukumoto H., Omori H., Yamamoto A., Noda T., Yoshimori T., An Atg4B Mutant Hampers the Lipidation of LC3 Paralogues and Causes Defects in Autophagosome Closure, 10.1091/mbc.e08-03-0312
- Decuypere Jean-Paul, Bultynck Geert, Parys Jan B., A dual role for Ca2+ in autophagy regulation, 10.1016/j.ceca.2011.04.001
- Nyfeler B., Bergman P., Triantafellow E., Wilson C. J., Zhu Y., Radetich B., Finan P. M., Klionsky D. J., Murphy L. O., Relieving Autophagy and 4EBP1 from Rapamycin Resistance, 10.1128/mcb.05430-11
- García-Martínez Juan M., Moran Jennifer, Clarke Rosemary G., Gray Alex, Cosulich Sabina C., Chresta Christine M., Alessi Dario R., Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR), 10.1042/bj20090489
- Pereira Gustavo J. S., Hirata Hanako, Fimia Gian M., do Carmo Lúcia G., Bincoletto Claudia, Han Sang W., Stilhano Roberta S., Ureshino Rodrigo P., Bloor-Young Duncan, Churchill Grant, Piacentini Mauro, Patel Sandip, Smaili Soraya S., Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) Regulates Autophagy in Cultured Astrocytes, 10.1074/jbc.c110.216580
- Serra V., Markman B., Scaltriti M., Eichhorn P. J.A., Valero V., Guzman M., Botero M. L., Llonch E., Atzori F., Di Cosimo S., Maira M., Garcia-Echeverria C., Parra J. L., Arribas J., Baselga J., NVP-BEZ235, a Dual PI3K/mTOR Inhibitor, Prevents PI3K Signaling and Inhibits the Growth of Cancer Cells with Activating PI3K Mutations, 10.1158/0008-5472.can-08-1385
- Liu T.-J., Koul D., LaFortune T., Tiao N., Shen R. J., Maira S.-M., Garcia-Echevrria C., Yung W.K. A., NVP-BEZ235, a novel dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor, elicits multifaceted antitumor activities in human gliomas, 10.1158/1535-7163.mct-09-0160
- Vingtdeux Valérie, Giliberto Luca, Zhao Haitian, Chandakkar Pallavi, Wu Qingli, Simon James E., Janle Elsa M., Lobo Jessica, Ferruzzi Mario G., Davies Peter, Marambaud Philippe, AMP-activated Protein Kinase Signaling Activation by Resveratrol Modulates Amyloid-β Peptide Metabolism, 10.1074/jbc.m109.060061
- Puissant Alexandre, Auberger Patrick, AMPK- and p62/SQSTM1-dependent autophagy mediate Resveratrol-induced cell death in chronic myelogenous leukemia, 10.4161/auto.6.5.12126
- Vingtdeux V., Chandakkar P., Zhao H., d'Abramo C., Davies P., Marambaud P., Novel synthetic small-molecule activators of AMPK as enhancers of autophagy and amyloid- peptide degradation, 10.1096/fj.10-167361
- Gordon PB, J Biol Chem, 268, 26107 (1993)
- Ganley Ian G., Wong Pui-Mun, Gammoh Noor, Jiang Xuejun, Distinct Autophagosomal-Lysosomal Fusion Mechanism Revealed by Thapsigargin-Induced Autophagy Arrest, 10.1016/j.molcel.2011.04.024
- Thoreen Carson C., Kang Seong A., Chang Jae Won, Liu Qingsong, Zhang Jianming, Gao Yi, Reichling Laurie J., Sim Taebo, Sabatini David M., Gray Nathanael S., An ATP-competitive Mammalian Target of Rapamycin Inhibitor Reveals Rapamycin-resistant Functions of mTORC1, 10.1074/jbc.m900301200
- Sarkar Sovan, Davies Janet E., Huang Zebo, Tunnacliffe Alan, Rubinsztein David C., Trehalose, a Novel mTOR-independent Autophagy Enhancer, Accelerates the Clearance of Mutant Huntingtin and α-Synuclein, 10.1074/jbc.m609532200
- Casarejos M.J., Solano R.M., Gómez A., Perucho J., de Yébenes J.G., Mena M.A., The accumulation of neurotoxic proteins, induced by proteasome inhibition, is reverted by trehalose, an enhancer of autophagy, in human neuroblastoma cells, 10.1016/j.neuint.2011.01.008
- Carpenter J. E., Jackson W., Benetti L., Grose C., Autophagosome Formation during Varicella-Zoster Virus Infection following Endoplasmic Reticulum Stress and the Unfolded Protein Response, 10.1128/jvi.00281-11
- Seglen P. O., Gordon P. B., 3-Methyladenine: Specific inhibitor of autophagic/lysosomal protein degradation in isolated rat hepatocytes, 10.1073/pnas.79.6.1889
- Wu You-Tong, Tan Hui-Ling, Shui Guanghou, Bauvy Chantal, Huang Qing, Wenk Markus R., Ong Choon-Nam, Codogno Patrice, Shen Han-Ming, Dual Role of 3-Methyladenine in Modulation of Autophagy via Different Temporal Patterns of Inhibition on Class I and III Phosphoinositide 3-Kinase, 10.1074/jbc.m109.080796
- Bampton Edward T. W., Goemans Christoph G., Niranjan Dhevahi, Mizushima Noboru, Tolkovsky Aviva M., The Dynamics of Autophagy Visualised in Live Cells: from Autophagosome Formation to Fusion with Endo/lysosomes, 10.4161/auto.1.1.1495
- Tormo Damià, Chęcińska Agnieszka, Alonso-Curbelo Direna, Pérez-Guijarro Eva, Cañón Estela, Riveiro-Falkenbach Erica, Calvo Tonantzin G., Larribere Lionel, Megías Diego, Mulero Francisca, Piris Miguel A., Dash Rupesh, Barral Paola M., Rodríguez-Peralto José L., Ortiz-Romero Pablo, Tüting Thomas, Fisher Paul B., Soengas María S., Targeted Activation of Innate Immunity for Therapeutic Induction of Autophagy and Apoptosis in Melanoma Cells, 10.1016/j.ccr.2009.07.004
- Lee Heung Kyu, Mattei Lisa M., Steinberg Benjamin E., Alberts Philipp, Lee Yun Hee, Chervonsky Alexander, Mizushima Noboru, Grinstein Sergio, Iwasaki Akiko, In Vivo Requirement for Atg5 in Antigen Presentation by Dendritic Cells, 10.1016/j.immuni.2009.12.006
- Tamura Naoki, Oku Masahide, Sakai Yasuyoshi, Atg8 regulates vacuolar membrane dynamics in a lipidation-independent manner in Pichia pastoris , 10.1242/jcs.070045
- Stromhaug P. E., Atg21 Is a Phosphoinositide Binding Protein Required for Efficient Lipidation and Localization of Atg8 during Uptake of Aminopeptidase I by Selective Autophagy, 10.1091/mbc.e04-02-0147
- Baens Mathijs, Noels Heidi, Broeckx Vicky, Hagens Sofie, Fevery Sabine, Billiau An D., Vankelecom Hugo, Marynen Peter, The Dark Side of EGFP: Defective Polyubiquitination, 10.1371/journal.pone.0000054
- Calì Tito, Galli Carmela, Olivari Silvia, Molinari Maurizio, Segregation and rapid turnover of EDEM1 by an autophagy-like mechanism modulates standard ERAD and folding activities, 10.1016/j.bbrc.2008.04.098
- Al-Younes Hesham M., Al-Zeer Munir A., Khalil Hany, Gussmann Joscha, Karlas Alexander, Machuy Nikolaus, Brinkmann Volker, Braun Peter R., Meyer Thomas F., Autophagy-independent function of MAP-LC3 during intracellular propagation ofChlamydia trachomatis, 10.4161/auto.7.8.15597
- Shroff H., Galbraith C. G., Galbraith J. A., White H., Gillette J., Olenych S., Davidson M. W., Betzig E., Dual-color superresolution imaging of genetically expressed probes within individual adhesion complexes, 10.1073/pnas.0710517105
- Nicklin Paul, Bergman Philip, Zhang Bailin, Triantafellow Ellen, Wang Henry, Nyfeler Beat, Yang Haidi, Hild Marc, Kung Charles, Wilson Christopher, Myer Vic E., MacKeigan Jeffrey P., Porter Jeffrey A., Wang Y. Karen, Cantley Lewis C., Finan Peter M., Murphy Leon O., Bidirectional Transport of Amino Acids Regulates mTOR and Autophagy, 10.1016/j.cell.2008.11.044
- Cherra Salvatore J., Kulich Scott M., Uechi Guy, Balasubramani Manimalha, Mountzouris John, Day Billy W., Chu Charleen T., Regulation of the autophagy protein LC3 by phosphorylation, 10.1083/jcb.201002108
- Sarkar Sovan, Korolchuk Viktor I., Renna Maurizio, Imarisio Sara, Fleming Angeleen, Williams Andrea, Garcia-Arencibia Moises, Rose Claudia, Luo Shouqing, Underwood Benjamin R., Kroemer Guido, O'Kane Cahir J., Rubinsztein David C., Complex Inhibitory Effects of Nitric Oxide on Autophagy, 10.1016/j.molcel.2011.04.029
- Rosado Carlos, Mijaljica Dalibor, Hatzinisiriou Irene, Prescott Mark, Devenish Rodney J., Rosella: A fluorescent pH-biosensor for reporting vacuolar turnover of cytosol and organelles in yeast, 10.4161/auto.5331
- Mijaljica D, Rosado CJ, Devenish RJ, Prescott M. Biosensors for monitoring autophagy In: Serra PA, ed. Biosensors-Emerging Materials and Applications. Croatia: InTech, 2011:383-400.
- Chudakov D. M., Matz M. V., Lukyanov S., Lukyanov K. A., Fluorescent Proteins and Their Applications in Imaging Living Cells and Tissues, 10.1152/physrev.00038.2009
- Zhou Cuihong, Zhong Wu, Zhou Jun, Sheng Fugeng, Fang Ziyuan, Wei Yue, Chen Yingyu, Deng Xiaoyan, Xia Bin, Lin Jian, Monitoring autophagic flux by an improved tandem fluorescent-tagged LC3 (mTagRFP-mWasabi-LC3) reveals that high-dose rapamycin impairs autophagic flux in cancer cells, 10.4161/auto.20284
- Zhou Jun, Lin Jian, Zhou Cuihong, Deng Xiaoyan, Xia Bin, Cytotoxicity of red fluorescent protein DsRed is associated with the suppression of Bcl-xL translation, 10.1016/j.febslet.2011.02.013
- Loos B., Genade S., Ellis B., Lochner A., Engelbrecht A.-M., At the core of survival: Autophagy delays the onset of both apoptotic and necrotic cell death in a model of ischemic cell injury, 10.1016/j.yexcr.2011.03.011
- Shvets Elena, Fass Ephraim, Elazar Zvulun, Utilizing flow cytometry to monitor autophagy in living mammalian cells, 10.4161/auto.5939
- Hundeshagen Phillip, Hamacher-Brady Anne, Eils Roland, Brady Nathan R, Concurrent detection of autolysosome formation and lysosomal degradation by flow cytometry in a high-content screen for inducers of autophagy, 10.1186/1741-7007-9-38
- de la Calle Claire, Joubert Pierre-Emmanuel, Law Helen K.W., Hasan Milena, Albert Matthew, Simultaneous assessment of autophagy and apoptosis using multispectral imaging cytometry, 10.4161/auto.7.9.16252
- Gannagé Monique, Dormann Dorothee, Albrecht Randy, Dengjel Jörn, Torossi Tania, Rämer Patrick C., Lee Monica, Strowig Till, Arrey Frida, Conenello Gina, Pypaert Marc, Andersen Jens, García-Sastre Adolfo, Münz Christian, Matrix Protein 2 of Influenza A Virus Blocks Autophagosome Fusion with Lysosomes, 10.1016/j.chom.2009.09.005
- Kaminskyy Vitaliy, Abdi Azadeh, Zhivotovsky Boris, A quantitative assay for the monitoring of autophagosome accumulation in different phases of the cell cycle, 10.4161/auto.7.1.13893
- Kirkin Vladimir, Lamark Trond, Sou Yu-Shin, Bjørkøy Geir, Nunn Jennifer L., Bruun Jack-Ansgar, Shvets Elena, McEwan David G., Clausen Terje H., Wild Philipp, Bilusic Ivana, Theurillat Jean-Philippe, Øvervatn Aud, Ishii Tetsuro, Elazar Zvulun, Komatsu Masaaki, Dikic Ivan, Johansen Terje, A Role for NBR1 in Autophagosomal Degradation of Ubiquitinated Substrates, 10.1016/j.molcel.2009.01.020
- Larsen Kenneth Bowitz, Lamark Trond, Øvervatn Aud, Harneshaug Ingvill, Johansen Terje, Bjørkøy Geir, A reporter cell system to monitor autophagy based on p62/SQSTM1, 10.4161/auto.6.6.12510
- Huang Jia-Jia, Li Hao-Ran, Huang Ying, Jiang Wen-Qi, Xu Rui-Hua, Huang Hui-Qiang, Lv Yue, Xia Zhong-Jun, Zhu Xiao-Feng, Lin Tong-Yu, Li Zhi-Ming, Beclin 1 expression: A predictor of prognosis in patients with extranodal natural killer T-cell lymphoma, nasal type, 10.4161/auto.6.6.12784
- Sivridis Efthimios, Koukourakis Michael I., Zois Christos E., Ledaki Ioanna, Ferguson David J.P., Harris Adrian L., Gatter Kevin C., Giatromanolaki Alexandra, LC3A-Positive Light Microscopy Detected Patterns of Autophagy and Prognosis in Operable Breast Carcinomas, 10.2353/ajpath.2010.090049
- Sivridis Efthimios, Giatromanolaki Alexandra, Liberis Vasilios, Koukourakis Michael I., Autophagy in endometrial carcinomas and prognostic relevance of 'stone-like' structures (SLS): What is destined for the atypical endometrial hyperplasia?, 10.4161/auto.7.1.13947
- Giatromanolaki Alexandra, Koukourakis Michael I., Koutsopoulos Anastasios, Chloropoulou Pelagia, Liberis Vasileios, Sivridis Efthimios, High Beclin 1 expression defines a poor prognosis in endometrial adenocarcinomas, 10.1016/j.ygyno.2011.06.023
- Chen Yongshun, Lu You, Lu Changli, Zhang Lei, Beclin-1 Expression is a Predictor of Clinical Outcome in Patients with Esophageal Squamous Cell Carcinoma and Correlated to Hypoxia-Inducible Factor (HIF)-1α Expression, 10.1007/s12253-008-9143-8
- Wan Xiang-Bo, Fan Xin-Juan, Chen Ming-Yuan, Xiang Jin, Huang Pei-Yu, Guo Ling, Wu Xiang-Yuan, Xu Jie, Long Zi-Jie, Zhao Yan, Zhou Wei-Hua, Mai Hai-Qiang, Liu Quentin, Hong Ming-Huang, Elevated Beclin 1 expression is correlated with HIF-1α in predicting poor prognosis of nasopharyngeal carcinoma, 10.4161/auto.6.3.11303
- Shi Ying-Hong, Ding Zhen-Bin, Zhou Jian, Qiu Shuang-Jian, Fan Jia, Prognostic significance of Beclin 1-dependent apoptotic activity in hepatocellular carcinoma, 10.4161/auto.5.3.7658
- Ding Z.-B., Shi Y.-H., Zhou J., Qiu S.-J., Xu Y., Dai Z., Shi G.-M., Wang X.-Y., Ke A.-W., Wu B., Fan J., Association of Autophagy Defect with a Malignant Phenotype and Poor Prognosis of Hepatocellular Carcinoma, 10.1158/0008-5472.can-08-1573
- Pirtoli Luigi, Cevenini Gabriele, Tini Paolo, Vannini Marta, Oliveri Giuseppe, Marsili Stefania, Mourmouras Vasileios, Rubino Giovanni, Miracco Clelia, The prognostic role of Beclin 1 protein expression in high-grade gliomas, 10.4161/auto.5.7.9227
- Karpathiou Georgia, Sivridis Efthimios, Koukourakis Michael I., Mikroulis Dimitrios, Bouros Demosthenes, Froudarakis Marios E., Giatromanolaki Alexandra, Light-Chain 3A Autophagic Activity and Prognostic Significance in Non-small Cell Lung Carcinomas, 10.1378/chest.10-1831
- Fujii Satoshi, Ochiai Atsushi, Enhancer of zeste homolog 2 downregulates E-cadherin by mediating histone H3 methylation in gastric cancer cells, 10.1111/j.1349-7006.2008.00743.x
- Li Bao-Xiu, Li Chun-Yan, Peng Rui-Qing, Wu Xiao-Jun, Wang Hai-Ying, Wan De-Sen, Zhu Xiao-Feng, Zhang Xiao-Shi, The expression ofbeclin 1is associated with favorable prognosis in stage IIIB colon cancers, 10.4161/auto.5.3.7491
- Koukourakis M I, Giatromanolaki A, Sivridis E, Pitiakoudis M, Gatter K C, Harris A L, Beclin 1 over- and underexpression in colorectal cancer: distinct patterns relate to prognosis and tumour hypoxia, 10.1038/sj.bjc.6605904
- Giatromanolaki A., Koukourakis M. I., Harris A. L., Polychronidis A., Gatter K. C., Sivridis E., Prognostic relevance of light chain 3 (LC3A) autophagy patterns in colorectal adenocarcinomas, 10.1136/jcp.2010.079525
- Sivridis Efthimios, Koukourakis Michael I., Mendrinos Savvas E., Karpouzis Antonios, Fiska Aliki, Kouskoukis Constantinos, Giatromanolaki Alexandra, Beclin-1 and LC3A expression in cutaneous malignant melanomas : a biphasic survival pattern for beclin-1, 10.1097/cmr.0b013e328346612c
- Giatromanolaki Alexandra N, St Charitoudis Georgios, Bechrakis Nikolaos E, Kozobolis Vassilios P, Koukourakis Michael I, Foerster Michael H, Sivridis Efthimios L, Autophagy patterns and prognosis in uveal melanomas, 10.1038/modpathol.2011.63
- McShane Lisa M., Altman Douglas G., Sauerbrei Willi, Taube Sheila E., Gion Massimo, Clark Gary M., Reporting Recommendations for Tumor Marker Prognostic Studies (REMARK), 10.1093/jnci/dji237
- Kuwahara Y, Oikawa T, Ochiai Y, Roudkenar M H, Fukumoto M, Shimura T, Ohtake Y, Ohkubo Y, Mori S, Uchiyama Y, Fukumoto M, Enhancement of autophagy is a potential modality for tumors refractory to radiotherapy, 10.1038/cddis.2011.56
- Hou Yu-Jie, Dong Li-Wei, Tan Ye-Xiong, Yang Guang-Zhen, Pan Yu-Fei, Li Zhong, Tang Liang, Wang Min, Wang Qing, Wang Hong-Yang, Inhibition of active autophagy induces apoptosis and increases chemosensitivity in cholangiocarcinoma, 10.1038/labinvest.2011.97
- O’Donovan Tracey R., O’Sullivan Gerald C., McKenna Sharon L., Induction of autophagy by drug-resistant esophageal cancer cells promotes their survival and recovery following treatment with chemotherapeutics, 10.4161/auto.7.5.15066
- Yoshimura Kentaro, Shibata Masahiro, Koike Masato, Gotoh Kunihito, Fukaya Masahiro, Watanabe Masahiko, Uchiyama Yasuo, Effects of RNA Interference of Atg4B on the Limited Proteolysis of LC3 in PC12 Cells and Expression of Atg4B in Various Rat Tissues, 10.4161/auto.2744
- Tamura Hirosumi, Shibata Masahiro, Koike Masato, Sasaki Mitsuho, Uchiyama Yasuo, Atg9A Protein, an Autophagy-related Membrane Protein, Is Localized in the Neurons of Mouse Brains, 10.1369/jhc.2010.955690
- Cui Jing, Bai Xue-Yuan, Shi Suozhu, Cui Shaoyuan, Hong Quan, Cai Guangyan, Chen Xiangmei, Age-related changes in the function of autophagy in rat kidneys, 10.1007/s11357-011-9237-1
- Mellén M A, de la Rosa E J, Boya P, The autophagic machinery is necessary for removal of cell corpses from the developing retinal neuroepithelium, 10.1038/cdd.2008.40
- Mellén María A., de la Rosa Enrique J., Boya Patricia, Autophagy is not universally required for phosphatidyl-serine exposure and apoptotic cell engulfment during neural development, 10.4161/auto.5.7.9292
- Shibata Masahiro, Yoshimura Kentaro, Furuya Norihiko, Koike Masato, Ueno Takashi, Komatsu Masaaki, Arai Hiroyuki, Tanaka Keiji, Kominami Eiki, Uchiyama Yasuo, The MAP1-LC3 conjugation system is involved in lipid droplet formation, 10.1016/j.bbrc.2009.03.039
- Komatsu Masaaki, Waguri Satoshi, Koike Masato, Sou Yu-shin, Ueno Takashi, Hara Taichi, Mizushima Noboru, Iwata Jun-ichi, Ezaki Junji, Murata Shigeo, Hamazaki Jun, Nishito Yasumasa, Iemura Shun-ichiro, Natsume Tohru, Yanagawa Toru, Uwayama Junya, Warabi Eiji, Yoshida Hiroshi, Ishii Tetsuro, Kobayashi Akira, Yamamoto Masayuki, Yue Zhenyu, Uchiyama Yasuo, Kominami Eiki, Tanaka Keiji, Homeostatic Levels of p62 Control Cytoplasmic Inclusion Body Formation in Autophagy-Deficient Mice, 10.1016/j.cell.2007.10.035
- Germain Marc, Nguyen Angela P, Le Grand J Nicole, Arbour Nicole, Vanderluit Jacqueline L, Park David S, Opferman Joseph T, Slack Ruth S, MCL-1 is a stress sensor that regulates autophagy in a developmentally regulated manner : Regulation of autophagy by MCL-1, 10.1038/emboj.2010.327
- Komatsu M., Wang Q. J., Holstein G. R., Friedrich V. L., Iwata J.-i., Kominami E., Chait B. T., Tanaka K., Yue Z., Essential role for autophagy protein Atg7 in the maintenance of axonal homeostasis and the prevention of axonal degeneration, 10.1073/pnas.0701311104
- Wang Q. J., Ding Y., Kohtz S., Mizushima N., Cristea I. M., Rout M. P., Chait B. T., Zhong Y., Heintz N., Yue Z., Induction of Autophagy in Axonal Dystrophy and Degeneration, 10.1523/jneurosci.2261-06.2006
- Nezis Ioannis P., Simonsen Anne, Sagona Antonia P., Finley Kim, Gaumer Sébastien, Contamine Didier, Rusten Tor Erik, Stenmark Harald, Brech Andreas, Ref(2)P, theDrosophila melanogasterhomologue of mammalian p62, is required for the formation of protein aggregates in adult brain, 10.1083/jcb.200711108
- Bartlett Bryan J., Isakson Pauline, Lewerenz Jan, Sanchez Heriberto, Kotzebue Roxanne W., Cumming Robert C., Harris Greg L., Nezis Ioannis P., Schubert David R., Simonsen Anne, Finley Kim D., p62, Ref(2)P and ubiquitinated proteins are conserved markers of neuronal aging, aggregate formation and progressive autophagic defects, 10.4161/auto.7.6.14943
- Lee Ju-Hyun, Yu W. Haung, Kumar Asok, Lee Sooyeon, Mohan Panaiyur S., Peterhoff Corrinne M., Wolfe Devin M., Martinez-Vicente Marta, Massey Ashish C., Sovak Guy, Uchiyama Yasuo, Westaway David, Cuervo Ana Maria, Nixon Ralph A., Lysosomal Proteolysis and Autophagy Require Presenilin 1 and Are Disrupted by Alzheimer-Related PS1 Mutations, 10.1016/j.cell.2010.05.008
- Masiero Eva, Agatea Lisa, Mammucari Cristina, Blaauw Bert, Loro Emanuele, Komatsu Masaaki, Metzger Daniel, Reggiani Carlo, Schiaffino Stefano, Sandri Marco, Autophagy Is Required to Maintain Muscle Mass, 10.1016/j.cmet.2009.10.008
- Moscat Jorge, Diaz-Meco Maria T., p62 at the Crossroads of Autophagy, Apoptosis, and Cancer, 10.1016/j.cell.2009.05.023
- Duran Angeles, Amanchy Ramars, Linares Juan F., Joshi Jayashree, Abu-Baker Shadi, Porollo Aleksey, Hansen Malene, Moscat Jorge, Diaz-Meco Maria T., p62 Is a Key Regulator of Nutrient Sensing in the mTORC1 Pathway, 10.1016/j.molcel.2011.06.038
- Komatsu M, Nat Cell Biol, 12, 213 (2010)
- Jain Ashish, Lamark Trond, Sjøttem Eva, Bowitz Larsen Kenneth, Atesoh Awuh Jane, Øvervatn Aud, McMahon Michael, Hayes John D., Johansen Terje, p62/SQSTM1Is a Target Gene for Transcription Factor NRF2 and Creates a Positive Feedback Loop by Inducing Antioxidant Response Element-driven Gene Transcription, 10.1074/jbc.m110.118976
- Bardag-Gorce Fawzia, Francis Tricia, Nan Li, Li Jun, He Lue Yan, French Barbara A., French Samuel W., Modifications in P62 occur due to proteasome inhibition in alcoholic liver disease, 10.1016/j.lfs.2005.04.020
- Myeku Natura, Figueiredo-Pereira Maria E., Dynamics of the Degradation of Ubiquitinated Proteins by Proteasomes and Autophagy : ASSOCIATION WITH SEQUESTOSOME 1/p62, 10.1074/jbc.m110.149252
- Norman Joanna M., Cohen Gerald M., Bampton Edward T.W., The in vitro cleavage of the hAtg proteins by cell death proteases, 10.4161/auto.6.8.13337
- Lelouard Hugues, Schmidt Enrico K., Camosseto Voahirana, Clavarino Giovanna, Ceppi Maurizio, Hsu Hsiang-Ting, Pierre Philippe, Regulation of translation is required for dendritic cell function and survival during activation, 10.1083/jcb.200707166
- Schmidt Enrico K, Clavarino Giovanna, Ceppi Maurizio, Pierre Philippe, SUnSET, a nonradioactive method to monitor protein synthesis, 10.1038/nmeth.1314
- Nakaso Kazuhiro, Yoshimoto Yuko, Nakano Toshiya, Takeshima Takao, Fukuhara Yoko, Yasui Kenichi, Araga Shigeru, Yanagawa Toru, Ishii Tetsuro, Nakashima Kenji, Transcriptional activation of p62/A170/ZIP during the formation of the aggregates: possible mechanisms and the role in Lewy body formation in Parkinson's disease, 10.1016/j.brainres.2004.03.029
- Zheng Q., Su H., Ranek M. J., Wang X., Autophagy and p62 in Cardiac Proteinopathy, 10.1161/circresaha.111.244707
- Colosetti Pascal, Puissant Alexandre, Robert Guillaume, Luciano Fréderic, Jacquel Arnaud, Gounon Pierre, Cassuto Jill-Patrice, Auberger Patrick, Autophagy is an important event for megakaryocytic differentiation of the chronic myelogenous leukemia K562 cell line, 10.4161/auto.5.8.9889
- Toepfer Nicholas, Childress Chandra, Parikh Ankur, Rukstalis Daniel, Yang Wannian, Atorvastatin induces autophagy in prostate cancer PC3 cells through activation ofLC3transcription, 10.4161/cbt.12.8.15978
- BenYounès Amena, Tajeddine Nicolas, Tailler Maximilien, Malik Shoaib Ahmad, Shen Shensi, Métivier Didier, Kepp Oliver, Vitale Ilio, Maiuri Maria Chiara, Kroemer Guido, A fluorescence-microscopic and cytofluorometric system for monitoring the turnover of the autophagic substrate p62/SQSTM1, 10.4161/auto.7.8.15538
- Bjørkøy Geir, Lamark Trond, Pankiv Serhiy, Øvervatn Aud, Brech Andreas, Johansen Terje, Chapter 12 Monitoring Autophagic Degradation of p62/SQSTM1, Methods in Enzymology (2009) ISBN:9780123745477 p.181-197, 10.1016/s0076-6879(08)03612-4
- Lim Junghyun, Kim Hyun-Wook, Youdim Moussa B.H., Rhyu Im Joo, Choe Kwang-Min, Oh Young J., Binding preference of p62 towards LC3-ll during dopaminergic neurotoxin-induced impairment of autophagic flux, 10.4161/auto.7.1.13909
- Waguri Satoshi, Komatsu Masaaki, Chapter 9 Biochemical and Morphological Detection of Inclusion Bodies in Autophagy‐Deficient Mice, Autophagy in Disease and Clinical Applications, Part C (2009) ISBN:9780123749369 p.181-196, 10.1016/s0076-6879(08)04009-3
- Hocking L. J., Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease, 10.1093/hmg/11.22.2735
- Mizushima Noboru, Levine Beth, Autophagy in mammalian development and differentiation, 10.1038/ncb0910-823
- Maloverjan Alla, Piirsoo Marko, Michelson Piret, Kogerman Priit, Østerlund Torben, Identification of a novel serine/threonine kinase ULK3 as a positive regulator of Hedgehog pathway, 10.1016/j.yexcr.2009.10.018
- Young A. R.J., Narita M., Ferreira M., Kirschner K., Sadaie M., Darot J. F.J., Tavare S., Arakawa S., Shimizu S., Watt F. M., Narita M., Autophagy mediates the mitotic senescence transition, 10.1101/gad.519709
- Chan Edmond Y., Tooze Sharon A., Evolution of Atg1 function and regulation, 10.4161/auto.8709
- Chan Edmond Y. W., Kir Serkan, Tooze Sharon A., siRNA Screening of the Kinome Identifies ULK1 as a Multidomain Modulator of Autophagy, 10.1074/jbc.m703663200
- Hardie D. G., AMP-activated protein kinase--an energy sensor that regulates all aspects of cell function, 10.1101/gad.17420111
- Carling David, Mayer Faith V, Sanders Matthew J, Gamblin Steven J, AMP-activated protein kinase: nature's energy sensor, 10.1038/nchembio.610
- SAMARI Hamid R., MØLLER Michael T. N., HOLDEN Lise, ASMYHR Tonje, SEGLEN Per O., Stimulation of hepatocytic AMP-activated protein kinase by okadaic acid and other autophagy-suppressive toxins, 10.1042/bj20040609
- Behrends Christian, Sowa Mathew E., Gygi Steven P., Harper J. Wade, Network organization of the human autophagy system, 10.1038/nature09204
- Chiacchiera F, Matrone A, Ferrari E, Ingravallo G, Lo Sasso G, Murzilli S, Petruzzelli M, Salvatore L, Moschetta A, Simone C, p38α blockade inhibits colorectal cancer growth in vivo by inducing a switch from HIF1α- to FoxO-dependent transcription, 10.1038/cdd.2009.36
- KOVACS A, SEGLEN P, Inhibition of hepatocytic protein degradation by methylaminopurines and inhibitors of protein synthesis, 10.1016/0304-4165(81)90189-6
- Liu Hui-Yu, Han Jianmin, Cao Sophia Y., Hong Tao, Zhuo Degen, Shi Jianbo, Liu Zhenqi, Cao Wenhong, Hepatic Autophagy Is Suppressed in the Presence of Insulin Resistance and Hyperinsulinemia : INHIBITION OF FoxO1-DEPENDENT EXPRESSION OF KEY AUTOPHAGY GENES BY INSULIN, 10.1074/jbc.m109.033936
- Mammucari Cristina, Milan Giulia, Romanello Vanina, Masiero Eva, Rudolf Ruediger, Del Piccolo Paola, Burden Steven J., Di Lisi Raffaella, Sandri Claudia, Zhao Jinghui, Goldberg Alfred L., Schiaffino Stefano, Sandri Marco, FoxO3 Controls Autophagy in Skeletal Muscle In Vivo, 10.1016/j.cmet.2007.11.001
- Mihaylova Maria M., Vasquez Debbie S., Ravnskjaer Kim, Denechaud Pierre-Damien, Yu Ruth T., Alvarez Jacqueline G., Downes Michael, Evans Ronald M., Montminy Marc, Shaw Reuben J., Class IIa Histone Deacetylases Are Hormone-Activated Regulators of FOXO and Mammalian Glucose Homeostasis, 10.1016/j.cell.2011.03.043
- Pfisterer S. G., Mauthe M., Codogno P., Proikas-Cezanne T., Ca2+/Calmodulin-Dependent Kinase (CaMK) Signaling via CaMKI and AMP-Activated Protein Kinase Contributes to the Regulation of WIPI-1 at the Onset of Autophagy, 10.1124/mol.111.071761
- Rodgers Joseph T., Lerin Carles, Gerhart-Hines Zachary, Puigserver Pere, Metabolic adaptations through the PGC-1α and SIRT1 pathways, 10.1016/j.febslet.2007.11.034
- Samari Hamid R., Seglen Per O., Inhibition of Hepatocytic Autophagy by Adenosine, Aminoimidazole-4-carboxamide Riboside, andN6-Mercaptopurine Riboside : EVIDENCE FOR INVOLVEMENT OF AMP-ACTIVATED PROTEIN KINASE, 10.1074/jbc.273.37.23758
- Sanchez Anthony MJ, Csibi Alfredo, Raibon Audrey, Cornille Karen, Gay Stéphanie, Bernardi Henri, Candau Robin, AMPK promotes skeletal muscle autophagy through activation of forkhead FoxO3a and interaction with Ulk1, 10.1002/jcb.23399
- Inoki Ken, Zhu Tianqing, Guan Kun-Liang, TSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival, 10.1016/s0092-8674(03)00929-2
- Gwinn Dana M., Shackelford David B., Egan Daniel F., Mihaylova Maria M., Mery Annabelle, Vasquez Debbie S., Turk Benjamin E., Shaw Reuben J., AMPK Phosphorylation of Raptor Mediates a Metabolic Checkpoint, 10.1016/j.molcel.2008.03.003
- Egan Dan, Kim Joungmok, Shaw Reuben J., Guan Kun-Liang, The autophagy initiating kinase ULK1 is regulated via opposing phosphorylation by AMPK and mTOR, 10.4161/auto.7.6.15123
- Egan D. F., Shackelford D. B., Mihaylova M. M., Gelino S., Kohnz R. A., Mair W., Vasquez D. S., Joshi A., Gwinn D. M., Taylor R., Asara J. M., Fitzpatrick J., Dillin A., Viollet B., Kundu M., Hansen M., Shaw R. J., Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy, 10.1126/science.1196371
- Kim Joungmok, Kundu Mondira, Viollet Benoit, Guan Kun-Liang, AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1, 10.1038/ncb2152
- Zhou Gaochao, Myers Robert, Li Ying, Chen Yuli, Shen Xiaolan, Fenyk-Melody Judy, Wu Margaret, Ventre John, Doebber Thomas, Fujii Nobuharu, Musi Nicolas, Hirshman Michael F., Goodyear Laurie J., Moller David E., Role of AMP-activated protein kinase in mechanism of metformin action, 10.1172/jci13505
- Emerling Brooke M., Viollet Benoit, Tormos Kathryn V., Chandel Navdeep S., Compound C inhibits hypoxic activation of HIF-1 independent of AMPK, 10.1016/j.febslet.2007.11.038
- Vucicevic Ljubica, Misirkic Maja, Kristina Janjetovic, Vilimanovich Urosh, Sudar Emina, Isenovic Esma, Prica Marko, Harhaji-Trajkovic Ljubica, Kravic-Stevovic Tamara, Vladimir Bumbasirevic, Trajkovic Vladimir, Compound C induces protective autophagy in cancer cells through AMPK inhibition-independent blockade of Akt/mTOR pathway, 10.4161/auto.7.1.13883
- Meley Daniel, Bauvy Chantal, Houben-Weerts Judith H. P. M., Dubbelhuis Peter F., Helmond Mariette T. J., Codogno Patrice, Meijer Alfred J., AMP-activated Protein Kinase and the Regulation of Autophagic Proteolysis, 10.1074/jbc.m605488200
- Grotemeier Antje, Alers Sebastian, Pfisterer Simon G., Paasch Florian, Daubrawa Merle, Dieterle Alexandra, Viollet Benoit, Wesselborg Sebastian, Proikas-Cezanne Tassula, Stork Björn, AMPK-independent induction of autophagy by cytosolic Ca2+ increase, 10.1016/j.cellsig.2010.01.015
- Williams Tyisha, Forsberg Lawrence J., Viollet Benoit, Brenman Jay E., Basal autophagy induction without AMP-activated protein kinase under low glucose conditions, 10.4161/auto.5.8.10090
- Shang L., Chen S., Du F., Li S., Zhao L., Wang X., Nutrient starvation elicits an acute autophagic response mediated by Ulk1 dephosphorylation and its subsequent dissociation from AMPK, 10.1073/pnas.1100844108
- Zoncu R., Bar-Peled L., Efeyan A., Wang S., Sancak Y., Sabatini D. M., mTORC1 Senses Lysosomal Amino Acids Through an Inside-Out Mechanism That Requires the Vacuolar H+-ATPase, 10.1126/science.1207056
- Di Bartolomeo Sabrina, Corazzari Marco, Nazio Francesca, Oliverio Serafina, Lisi Gaia, Antonioli Manuela, Pagliarini Vittoria, Matteoni Silvia, Fuoco Claudia, Giunta Luigi, D'Amelio Marcello, Nardacci Roberta, Romagnoli Alessandra, Piacentini Mauro, Cecconi Francesco, Fimia Gian Maria, The dynamic interaction of AMBRA1 with the dynein motor complex regulates mammalian autophagy, 10.1083/jcb.201002100
- Tang Hong-Wen, Wang Yu-Bao, Wang Shiu-Lan, Wu Mei-Hsuan, Lin Shu-Yu, Chen Guang-Chao, Atg1-mediated myosin II activation regulates autophagosome formation during starvation-induced autophagy : Atg1 regulates myosin II activation in autophagy, 10.1038/emboj.2010.338
- Jung C. H., Jun C. B., Ro S.-H., Kim Y.-M., Otto N. M., Cao J., Kundu M., Kim D.-H., ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery, 10.1091/mbc.e08-12-1249
- Chang Y.-Y., Neufeld T. P., An Atg1/Atg13 Complex with Multiple Roles in TOR-mediated Autophagy Regulation, 10.1091/mbc.e08-12-1250
- Hosokawa N., Hara T., Kaizuka T., Kishi C., Takamura A., Miura Y., Iemura S.-i., Natsume T., Takehana K., Yamada N., Guan J.-L., Oshiro N., Mizushima N., Nutrient-dependent mTORC1 Association with the ULK1-Atg13-FIP200 Complex Required for Autophagy, 10.1091/mbc.e08-12-1248
- Chan E. Y. W., Longatti A., McKnight N. C., Tooze S. A., Kinase-Inactivated ULK Proteins Inhibit Autophagy via Their Conserved C-Terminal Domains Using an Atg13-Independent Mechanism, 10.1128/mcb.01082-08
- Jung Chang Hwa, Seo Minchul, Otto Neil Michael, Kim Do-Hyung, ULK1 inhibits the kinase activity of mTORC1 and cell proliferation, 10.4161/auto.7.10.16660
- Löffler Antje S., Alers Sebastian, Dieterle Alexandra M., Keppeler Hildegard, Franz-Wachtel Mirita, Kundu Mondira, Campbell David G., Wesselborg Sebastian, Alessi Dario R., Stork Björn, Ulk1-mediated phosphorylation of AMPK constitutes a negative regulatory feedback loop, 10.4161/auto.7.7.15451
- Erlich S., Alexandrovich A., Shohami E., Pinkas-Kramarski R., Rapamycin is a neuroprotective treatment for traumatic brain injury, 10.1016/j.nbd.2006.12.003
- Lavieu Grégory, Scarlatti Francesca, Sala Giusy, Carpentier Stéphane, Levade Thierry, Ghidoni Riccardo, Botti Joëlle, Codogno Patrice, Regulation of Autophagy by Sphingosine Kinase 1 and Its Role in Cell Survival during Nutrient Starvation, 10.1074/jbc.m506182200
- Brunn G. J., Phosphorylation of the Translational Repressor PHAS-I by the Mammalian Target of Rapamycin, 10.1126/science.277.5322.99
- Yip Calvin K., Murata Kazuyoshi, Walz Thomas, Sabatini David M., Kang Seong A., Structure of the Human mTOR Complex I and Its Implications for Rapamycin Inhibition, 10.1016/j.molcel.2010.05.017
- Cheong H., Nair U., Geng J., Klionsky D. J., The Atg1 Kinase Complex Is Involved in the Regulation of Protein Recruitment to Initiate Sequestering Vesicle Formation for Nonspecific Autophagy in Saccharomyces cerevisiae, 10.1091/mbc.e07-08-0826
- Kabeya Y., Atg17 Functions in Cooperation with Atg1 and Atg13 in Yeast Autophagy, 10.1091/mbc.e04-08-0669
- Kamada Yoshiaki, Funakoshi Tomoko, Shintani Takahiro, Nagano Kazuya, Ohsumi Mariko, Ohsumi Yoshinori, Tor-Mediated Induction of Autophagy via an Apg1 Protein Kinase Complex, 10.1083/jcb.150.6.1507
- Scott Sidney V., Nice Daniel C., Nau Johnathan J., Weisman Lois S., Kamada Yoshiaki, Keizer-Gunnink Ineke, Funakoshi Tomoko, Veenhuis Marten, Ohsumi Yoshinori, Klionsky Daniel J., Apg13p and Vac8p Are Part of a Complex of Phosphoproteins That Are Required for Cytoplasm to Vacuole Targeting, 10.1074/jbc.m002813200
- Mao Kai, Wang Ke, Zhao Mantong, Xu Tao, Klionsky Daniel J., Two MAPK-signaling pathways are required for mitophagy inSaccharomyces cerevisiae, 10.1083/jcb.201102092
- Yeh Y.-Y., Wrasman K., Herman P. K., Autophosphorylation Within the Atg1 Activation Loop Is Required for Both Kinase Activity and the Induction of Autophagy in Saccharomyces cerevisiae, 10.1534/genetics.110.116566
- Singh Kamini, Matsuyama Shigemi, Drazba Judith A., Almasan Alexandru, Autophagy-dependent senescence in response to DNA damage and chronic apoptotic stress, 10.4161/auto.8.2.18600
- Djavaheri-Mergny Mojgan, Amelotti Manuela, Mathieu Julie, Besançon Françoise, Bauvy Chantal, Souquère Sylvie, Pierron Gérard, Codogno Patrice, NF-κB Activation Represses Tumor Necrosis Factor-α-induced Autophagy, 10.1074/jbc.m602097200
- Liu Zhihua, Lenardo Michael J., Reactive Oxygen Species Regulate Autophagy through Redox-Sensitive Proteases, 10.1016/j.devcel.2007.03.016
- Scarlatti Francesca, Bauvy Chantal, Ventruti Annamaria, Sala Giusy, Cluzeaud Françoise, Vandewalle Alain, Ghidoni Riccardo, Codogno Patrice, Ceramide-mediated Macroautophagy Involves Inhibition of Protein Kinase B and Up-regulation of Beclin 1, 10.1074/jbc.m313561200
- Scherz-Shouval Ruth, Shvets Elena, Fass Ephraim, Shorer Hagai, Gil Lidor, Elazar Zvulun, Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4, 10.1038/sj.emboj.7601623
- Zeng X., Kinsella T. J., Mammalian Target of Rapamycin and S6 Kinase 1 Positively Regulate 6-thioguanine-Induced Autophagy, 10.1158/0008-5472.can-07-6163
- Yu Li, McPhee Christina K., Zheng Lixin, Mardones Gonzalo A., Rong Yueguang, Peng Junya, Mi Na, Zhao Ying, Liu Zhihua, Wan Fengyi, Hailey Dale W., Oorschot Viola, Klumperman Judith, Baehrecke Eric H., Lenardo Michael J., Termination of autophagy and reformation of lysosomes regulated by mTOR, 10.1038/nature09076
- Mochizuki Hiroaki, Toda Hirofumi, Ando Mai, Kurusu Mitsuhiko, Tomoda Toshifumi, Furukubo-Tokunaga Katsuo, Unc-51/ATG1 Controls Axonal and Dendritic Development via Kinesin-Mediated Vesicle Transport in the Drosophila Brain, 10.1371/journal.pone.0019632
- Wairkar Y. P., Toda H., Mochizuki H., Furukubo-Tokunaga K., Tomoda T., DiAntonio A., Unc-51 Controls Active Zone Density and Protein Composition by Downregulating ERK Signaling, 10.1523/jneurosci.3848-08.2009
- Loh S H Y, Francescut L, Lingor P, Bähr M, Nicotera P, Identification of new kinase clusters required for neurite outgrowth and retraction by a loss-of-function RNA interference screen, 10.1038/sj.cdd.4402258
- Zhou X., Babu J. R., da Silva S., Shu Q., Graef I. A., Oliver T., Tomoda T., Tani T., Wooten M. W., Wang F., Unc-51-like kinase 1/2-mediated endocytic processes regulate filopodia extension and branching of sensory axons, 10.1073/pnas.0701402104
- Tomoda T., Role of Unc51.1 and its binding partners in CNS axon outgrowth, 10.1101/gad.1151204
- Okazaki Noriko, Yan Jin, Yuasa Shigeki, Ueno Takashi, Kominami Eiki, Masuho Yasuhiko, Koga Hisashi, Muramatsu Masa-aki, Interaction of the Unc-51-like kinase and microtubule-associated protein light chain 3 related proteins in the brain: possible role of vesicular transport in axonal elongation, 10.1016/s0169-328x(00)00218-7
- Young A. R. J., Starvation and ULK1-dependent cycling of mammalian Atg9 between the TGN and endosomes, 10.1242/jcs.03172
- Reggiori Fulvio, Shintani Takahiro, Chong Huira, Nair Usha, Klionsky Daniel J., Atg9 Cycles Between Mitochondria and the Pre-Autophagosomal Structure in Yeasts, 10.4161/auto.1.2.1840
- Mari Muriel, Griffith Janice, Rieter Ester, Krishnappa Lakshmi, Klionsky Daniel J., Reggiori Fulvio, An Atg9-containing compartment that functions in the early steps of autophagosome biogenesis, 10.1083/jcb.200912089
- Reggiori Fulvio, Tucker Katherine A., Stromhaug Per E., Klionsky Daniel J., The Atg1-Atg13 Complex Regulates Atg9 and Atg23 Retrieval Transport from the Pre-Autophagosomal Structure, 10.1016/s1534-5807(03)00402-7
- Mizushima N., Mouse Apg16L, a novel WD-repeat protein, targets to the autophagic isolation membrane with the Apg12-Apg5 conjugate, 10.1242/jcs.00381
- Mizushima Noboru, Yamamoto Akitsugu, Hatano Masahiko, Kobayashi Yoshinori, Kabeya Yukiko, Suzuki Kuninori, Tokuhisa Takeshi, Ohsumi Yoshinori, Yoshimori Tamotsu, Dissection of Autophagosome Formation Using Apg5-Deficient Mouse Embryonic Stem Cells, 10.1083/jcb.152.4.657
- Thompson A. R., Autophagic Nutrient Recycling in Arabidopsis Directed by the ATG8 and ATG12 Conjugation Pathways, 10.1104/pp.105.060673
- Yousefi Shida, Perozzo Remo, Schmid Inès, Ziemiecki Andrew, Schaffner Thomas, Scapozza Leonardo, Brunner Thomas, Simon Hans-Uwe, Calpain-mediated cleavage of Atg5 switches autophagy to apoptosis, 10.1038/ncb1482
- Kihara Akio, Noda Takeshi, Ishihara Naotada, Ohsumi Yoshinori, Two Distinct Vps34 Phosphatidylinositol 3–Kinase Complexes Function in Autophagy and Carboxypeptidase Y Sorting inSaccharomyces cerevisiae, 10.1083/jcb.152.3.519
- Matsunaga Kohichi, Saitoh Tatsuya, Tabata Keisuke, Omori Hiroko, Satoh Takashi, Kurotori Naoki, Maejima Ikuko, Shirahama-Noda Kanae, Ichimura Tohru, Isobe Toshiaki, Akira Shizuo, Noda Takeshi, Yoshimori Tamotsu, Two Beclin 1-binding proteins, Atg14L and Rubicon, reciprocally regulate autophagy at different stages, 10.1038/ncb1846
- Zhong Yun, Wang Qing Jun, Li Xianting, Yan Ying, Backer Jonathan M., Chait Brian T., Heintz Nathaniel, Yue Zhenyu, Distinct regulation of autophagic activity by Atg14L and Rubicon associated with Beclin 1–phosphatidylinositol-3-kinase complex, 10.1038/ncb1854
- Sun Q., Fan W., Chen K., Ding X., Chen S., Zhong Q., Identification of Barkor as a mammalian autophagy-specific factor for Beclin 1 and class III phosphatidylinositol 3-kinase, 10.1073/pnas.0810452105
- Itakura E., Kishi C., Inoue K., Mizushima N., Beclin 1 Forms Two Distinct Phosphatidylinositol 3-Kinase Complexes with Mammalian Atg14 and UVRAG, 10.1091/mbc.e08-01-0080
- Fan W., Nassiri A., Zhong Q., Autophagosome targeting and membrane curvature sensing by Barkor/Atg14(L), 10.1073/pnas.1016472108
- Matsunaga Kohichi, Morita Eiji, Saitoh Tatsuya, Akira Shizuo, Ktistakis Nicholas T., Izumi Tetsuro, Noda Takeshi, Yoshimori Tamotsu, Autophagy requires endoplasmic reticulum targeting of the PI3-kinase complex via Atg14L, 10.1083/jcb.200911141
- Ravikumar Brinda, Moreau Kevin, Jahreiss Luca, Puri Claudia, Rubinsztein David C., Plasma membrane contributes to the formation of pre-autophagosomal structures, 10.1038/ncb2078
- Guan J., Stromhaug P. E., George M. D., Habibzadegah-Tari P., Bevan A., Dunn W. A., Klionsky D. J., Cvt18/Gsa12 Is Required for Cytoplasm-to-Vacuole Transport, Pexophagy, and Autophagy in Saccharomyces cerevisiae and Pichia pastoris, 10.1091/mbc.12.12.3821
- Barth Henning, Meiling-Wesse Khuyen, Epple Ulrike D, Thumm Michael, Autophagy and the cytoplasm to vacuole targeting pathway both require Aut10p, 10.1016/s0014-5793(01)03016-2
- Proikas-Cezanne Tassula, Waddell Scott, Gaugel Anja, Frickey Tancred, Lupas Andrei, Nordheim Alfred, WIPI-1α (WIPI49), a member of the novel 7-bladed WIPI protein family, is aberrantly expressed in human cancer and is linked to starvation-induced autophagy, 10.1038/sj.onc.1208331
- Monastyrska Iryna, Klionsky Daniel J., Autophagy in organelle homeostasis: Peroxisome turnover, 10.1016/j.mam.2006.08.004
- Nair Usha, Klionsky Daniel J., Molecular Mechanisms and Regulation of Specific and Nonspecific Autophagy Pathways in Yeast, 10.1074/jbc.r500016200
- Tallóczy Zsolt, Virgin, IV Herbert, Levine Beth, PKR-Dependent Xenophagic Degradation of Herpes Simplex Virus Type 1, 10.4161/auto.2176
- Polson Hannah E.J., de Lartigue Jane, Rigden Daniel J., Reedijk Marco, Urbé Sylvie, Clague Michael J., Tooze Sharon A., Mammalian Atg18 (WIPI2) localizes to omegasome-anchored phagophores and positively regulates LC3 lipidation, 10.4161/auto.6.4.11863
- Proikas-Cezanne Tassula, Ruckerbauer Sabine, Stierhof York-Dieter, Berg Carolin, Nordheim Alfred, Human WIPI-1 puncta-formation: A novel assay to assess mammalian autophagy, 10.1016/j.febslet.2007.06.040
- Itakura Eisuke, Mizushima Noboru, Characterization of autophagosome formation site by a hierarchical analysis of mammalian Atg proteins, 10.4161/auto.6.6.12709
- Mauthe Mario, Jacob Anke, Freiberger Sandra, Hentschel Katharina, Stierhof York-Dieter, Codogno Patrice, Proikas-Cezanne Tassula, Resveratrol-mediated autophagy requires WIPI-1-regulated LC3 lipidation in the absence of induced phagophore formation, 10.4161/auto.7.12.17802
- Lu Qun, Yang Peiguo, Huang Xinxin, Hu Wanqiu, Guo Bin, Wu Fan, Lin Long, Kovács Attila L., Yu Li, Zhang Hong, The WD40 Repeat PtdIns(3)P-Binding Protein EPG-6 Regulates Progression of Omegasomes to Autophagosomes, 10.1016/j.devcel.2011.06.024
- Yang Zhifen, Klionsky Daniel J, Mammalian autophagy: core molecular machinery and signaling regulation, 10.1016/j.ceb.2009.11.014
- Cao Yang, Klionsky Daniel J, Physiological functions of Atg6/Beclin 1: a unique autophagy-related protein, 10.1038/cr.2007.78
- Pattingre Sophie, Tassa Amina, Qu Xueping, Garuti Rita, Liang Xiao Huan, Mizushima Noboru, Packer Milton, Schneider Michael D., Levine Beth, Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy, 10.1016/j.cell.2005.07.002
- Zalckvar Einat, Berissi Hanna, Mizrachy Liat, Idelchuk Yulia, Koren Itay, Eisenstein Miriam, Sabanay Helena, Pinkas-Kramarski Ronit, Kimchi Adi, DAP-kinase-mediated phosphorylation on the BH3 domain of beclin 1 promotes dissociation of beclin 1 from Bcl-XL and induction of autophagy, 10.1038/embor.2008.246
- Wei Yongjie, Sinha Sangita C., Levine Beth, Dual Role of JNK1-mediated phosphorylation of Bcl-2 in autophagy and apoptosis regulation, 10.4161/auto.6788
- Wei Yongjie, Pattingre Sophie, Sinha Sangita, Bassik Michael, Levine Beth, JNK1-Mediated Phosphorylation of Bcl-2 Regulates Starvation-Induced Autophagy, 10.1016/j.molcel.2008.06.001
- Lossi Laura, Gambino Graziana, Ferrini Francesco, Alasia Silvia, Merighi Adalberto, Posttranslational regulation of BCL2 levels in cerebellar granule cells: A mechanism of neuronal survival, 10.1002/dneu.20744
- Lossi Laura, Gambino Graziana, Salio Chiara, Merighi Adalberto, Autophagy Regulates the Post-Translational Cleavage of BCL-2 and Promotes Neuronal Survival, 10.1100/tsw.2010.82
- Scarlatti F, Maffei R, Beau I, Codogno P, Ghidoni R, Role of non-canonical Beclin 1-independent autophagy in cell death induced by resveratrol in human breast cancer cells, 10.1038/cdd.2008.51
- Kang R, Zeh H J, Lotze M T, Tang D, The Beclin 1 network regulates autophagy and apoptosis, 10.1038/cdd.2010.191
- Kihara Akio, Kabeya Yukiko, Ohsumi Yoshinori, Yoshimori Tamotsu, Beclin-phosphatidylinositol 3-kinase complex functions at thetrans-Golgi network, 10.1093/embo-reports/kve061
- Amritraj Asha, Peake Kyle, Kodam Anitha, Salio Chiara, Merighi Adalberto, Vance Jean E., Kar Satyabrata, Increased Activity and Altered Subcellular Distribution of Lysosomal Enzymes Determine Neuronal Vulnerability in Niemann-Pick Type C1-Deficient Mice, 10.2353/ajpath.2009.081096
- Castino Roberta, Bellio Natascia, Follo Carlo, Murphy David, Isidoro Ciro, Inhibition of PI3k Class III–Dependent Autophagy Prevents Apoptosis and Necrosis by Oxidative Stress in Dopaminergic Neuroblastoma Cells, 10.1093/toxsci/kfq170
- Yue Zhenyu, Horton Antony, Bravin Monica, DeJager Philip L., Selimi Fekrije, Heintz Nathaniel, A Novel Protein Complex Linking the δ2 Glutamate Receptor and Autophagy, 10.1016/s0896-6273(02)00861-9
- Axe Elizabeth L., Walker Simon A., Manifava Maria, Chandra Priya, Roderick H. Llewelyn, Habermann Anja, Griffiths Gareth, Ktistakis Nicholas T., Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum, 10.1083/jcb.200803137
- Crighton Diane, Wilkinson Simon, O'Prey Jim, Syed Nelofer, Smith Paul, Harrison Paul R., Gasco Milena, Garrone Ornella, Crook Tim, Ryan Kevin M., DRAM, a p53-Induced Modulator of Autophagy, Is Critical for Apoptosis, 10.1016/j.cell.2006.05.034
- Valbuena Alberto, Castro-Obregón Susana, Lazo Pedro A., Downregulation of VRK1 by p53 in Response to DNA Damage Is Mediated by the Autophagic Pathway, 10.1371/journal.pone.0017320
- Lorin Séverine, Pierron Gérard, Ryan Kevin M., Codogno Patrice, Djavaheri-Mergny Mojgan, Evidence for the interplay between JNK and p53-DRAM signaling pathways in the regulation of autophagy, 10.4161/auto.6.1.10537
- Nara Atsuki, Mizushima Noboru, Yamamoto Akitsugu, Kabeya Yukiko, Ohsumi Yoshinori, Yoshimori Tamotsu, SKD1 AAA ATPase-Dependent Endosomal Transport is Involved in Autolysosome Formation, 10.1247/csf.27.29
- Kirisako Takayoshi, Baba Misuzu, Ishihara Naotada, Miyazawa Kouichi, Ohsumi Mariko, Yoshimori Tamotsu, Noda Takeshi, Ohsumi Yoshinori, Formation Process of Autophagosome Is Traced with Apg8/Aut7p in Yeast, 10.1083/jcb.147.2.435
- Kouroku Y, Fujita E, Tanida I, Ueno T, Isoai A, Kumagai H, Ogawa S, Kaufman R J, Kominami E, Momoi T, ER stress (PERK/eIF2α phosphorylation) mediates the polyglutamine-induced LC3 conversion, an essential step for autophagy formation, 10.1038/sj.cdd.4401984
- Moussay Etienne, Kaoma Tony, Baginska Joanna, Muller Arnaud, Van Moer Kris, Nicot Nathalie, Nazarov Petr V., Vallar Laurent, Chouaib Salem, Berchem Guy, Janji Bassam, The acquisition of resistance to TNFα in breast cancer cells is associated with constitutive activation of autophagy as revealed by a transcriptome analysis using a custom microarray, 10.4161/auto.7.7.15454
- Mitroulis Ioannis, Kourtzelis Ioannis, Kambas Konstantinos, Rafail Stavros, Chrysanthopoulou Akrivi, Speletas Matthaios, Ritis Konstantinos, Regulation of the autophagic machinery in human neutrophils, 10.1002/eji.200940025
- Rodríguez-Muela N, Germain F, Mariño G, Fitze P S, Boya P, Autophagy promotes survival of retinal ganglion cells after optic nerve axotomy in mice, 10.1038/cdd.2011.88
- Vázquez Patricia, Arroba Ana I., Cecconi Francesco, de la Rosa Enrique J., Boya Patricia, De Pablo Flora, Atg5 and Ambra1 differentially modulate neurogenesis in neural stem cells, 10.4161/auto.8.2.18535
- Rouschop Kasper M.A., van den Beucken Twan, Dubois Ludwig, Niessen Hanneke, Bussink Johan, Savelkouls Kim, Keulers Tom, Mujcic Hilda, Landuyt Willy, Voncken Jan Willem, Lambin Philippe, van der Kogel Albert J., Koritzinsky Marianne, Wouters Bradly G., The unfolded protein response protects human tumor cells during hypoxia through regulation of the autophagy genes MAP1LC3B and ATG5, 10.1172/jci40027
- Gorski Sharon M., Chittaranjan Suganthi, Pleasance Erin D., Freeman J.D., Anderson Carrie L., Varhol Richard J., Coughlin Shaun M., Zuyderduyn Scott D., Jones Steven J.M., Marra Marco A., A SAGE Approach to Discovery of Genes Involved in Autophagic Cell Death, 10.1016/s0960-9822(03)00082-4
- Lee Cheng-Yu, Clough Emily A., Yellon Paula, Teslovich Tanya M., Stephan Dietrich A., Baehrecke Eric H., Genome-Wide Analyses of Steroid- and Radiation-Triggered Programmed Cell Death in Drosophila, 10.1016/s0960-9822(03)00085-x
- Denton Donna, Shravage Bhupendra V., Simin Rachel, Baehrecke Eric H., Kumar Sharad, Larval midgut destruction in Drosophila: Not dependent on caspases but suppressed by the loss of autophagy, 10.4161/auto.6.1.10601
- Franzetti Eleonora, Huang Zhi-Jun, Shi Yan-Xia, Xie Kun, Deng Xiao-Juan, Li Jian-Ping, Li Qing-Rong, Yang Wan-Ying, Zeng Wen-Nian, Casartelli Morena, Deng Hui-Min, Cappellozza Silvia, Grimaldi Annalisa, Xia Qingyou, Tettamanti Gianluca, Cao Yang, Feng Qili, Autophagy precedes apoptosis during the remodeling of silkworm larval midgut, 10.1007/s10495-011-0675-0
- Juhász G, Puskás L G, Komonyi O, Érdi B, Maróy P, Neufeld T P, Sass M, Gene expression profiling identifies FKBP39 as an inhibitor of autophagy in larval Drosophila fat body, 10.1038/sj.cdd.4402123
- Barth J M I, Szabad J, Hafen E, Köhler K, Autophagy in Drosophila ovaries is induced by starvation and is required for oogenesis, 10.1038/cdd.2010.157
- LECKER S. H., Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression, 10.1096/fj.03-0610com
- Phillips A. R., Suttangkakul A., Vierstra R. D., The ATG12-Conjugating Enzyme ATG10 Is Essential for Autophagic Vesicle Formation in Arabidopsis thaliana, 10.1534/genetics.107.086199
- Seiliez Iban, Gutierrez Joaquim, Salmerón Cristina, Skiba-Cassy Sandrine, Chauvin Charline, Dias Karine, Kaushik Sadasivam, Tesseraud Sophie, Panserat Stephane, An in vivo and in vitro assessment of autophagy-related gene expression in muscle of rainbow trout (Oncorhynchus mykiss), 10.1016/j.cbpb.2010.06.011
- Lapierre Louis R., Gelino Sara, Meléndez Alicia, Hansen Malene, Autophagy and Lipid Metabolism Coordinately Modulate Life Span in Germline-less C. elegans, 10.1016/j.cub.2011.07.042
- Sandri M., Autophagy in health and disease. 3. Involvement of autophagy in muscle atrophy, 10.1152/ajpcell.00531.2009
- Eisenberg Tobias, Knauer Heide, Schauer Alexandra, Büttner Sabrina, Ruckenstuhl Christoph, Carmona-Gutierrez Didac, Ring Julia, Schroeder Sabrina, Magnes Christoph, Antonacci Lucia, Fussi Heike, Deszcz Luiza, Hartl Regina, Schraml Elisabeth, Criollo Alfredo, Megalou Evgenia, Weiskopf Daniela, Laun Peter, Heeren Gino, Breitenbach Michael, Grubeck-Loebenstein Beatrix, Herker Eva, Fahrenkrog Birthe, Fröhlich Kai-Uwe, Sinner Frank, Tavernarakis Nektarios, Minois Nadege, Kroemer Guido, Madeo Frank, Induction of autophagy by spermidine promotes longevity, 10.1038/ncb1975
- Ropolo Alejandro, Grasso Daniel, Pardo Romina, Sacchetti Maria L., Archange Cendrine, Re Andrea Lo, Seux Mylene, Nowak Jonathan, Gonzalez Claudio D., Iovanna Juan L., Vaccaro Maria I., The Pancreatitis-induced Vacuole Membrane Protein 1 Triggers Autophagy in Mammalian Cells, 10.1074/jbc.m706956200
- Tian Ye, Li Zhipeng, Hu Wanqiu, Ren Haiyan, Tian E., Zhao Yu, Lu Qun, Huang Xinxin, Yang Peiguo, Li Xin, Wang Xiaochen, Kovács Attila L., Yu Li, Zhang Hong, C. elegans Screen Identifies Autophagy Genes Specific to Multicellular Organisms, 10.1016/j.cell.2010.04.034
- Settembre C., Di Malta C., Polito V. A., Arencibia M. G., Vetrini F., Erdin S., Erdin S. U., Huynh T., Medina D., Colella P., Sardiello M., Rubinsztein D. C., Ballabio A., TFEB Links Autophagy to Lysosomal Biogenesis, 10.1126/science.1204592
- Sardiello M., Palmieri M., di Ronza A., Medina D. L., Valenza M., Gennarino V. A., Di Malta C., Donaudy F., Embrione V., Polishchuk R. S., Banfi S., Parenti G., Cattaneo E., Ballabio A., A Gene Network Regulating Lysosomal Biogenesis and Function, 10.1126/science.1174447
- Palmieri Michela, Impey Soren, Kang Hyojin, di Ronza Alberto, Pelz Carl, Sardiello Marco, Ballabio Andrea, Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways, 10.1093/hmg/ddr306
- Kang Y.-A., Sanalkumar R., O'Geen H., Linnemann A. K., Chang C.-J., Bouhassira E. E., Farnham P. J., Keles S., Bresnick E. H., Autophagy Driven by a Master Regulator of Hematopoiesis, 10.1128/mcb.06166-11
- Ma Di, Panda Satchidananda, Lin Jiandie D, Temporal orchestration of circadian autophagy rhythm by C/EBPβ : C/EBPβ regulates circadian autophagy rhythm, 10.1038/emboj.2011.322
- Brest Patrick, Lapaquette Pierre, Souidi Mouloud, Lebrigand Kevin, Cesaro Annabelle, Vouret-Craviari Valérie, Mari Bernard, Barbry Pascal, Mosnier Jean-François, Hébuterne Xavier, Harel-Bellan Annick, Mograbi Baharia, Darfeuille-Michaud Arlette, Hofman Paul, A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn's disease, 10.1038/ng.762
- Meenhuis A., van Veelen P. A., de Looper H., van Boxtel N., van den Berge I. J., Sun S. M., Taskesen E., Stern P., de Ru A. H., van Adrichem A. J., Demmers J., Jongen-Lavrencic M., Lowenberg B., Touw I. P., Sharp P. A., Erkeland S. J., MiR-17/20/93/106 promote hematopoietic cell expansion by targeting sequestosome 1-regulated pathways in mice, 10.1182/blood-2011-02-336487
- Roccaro A. M., Sacco A., Jia X., Azab A. K., Maiso P., Ngo H. T., Azab F., Runnels J., Quang P., Ghobrial I. M., microRNA-dependent modulation of histone acetylation in Waldenstrom macroglobulinemia, 10.1182/blood-2010-01-265686
- Martinet Wim, De Meyer Guido R.Y., Andries Luc, Herman Arnold G., Kockx Mark M., In Situ Detection of Starvation-induced Autophagy, 10.1369/jhc.5a6743.2005
- Pattingre Sophie, Petiot Anne, Codogno Patrice, Analyses of Gα-Interacting Protein and Activator of G-Protein-Signaling-3 Functions in Macroautophagy, Methods in Enzymology (2004) ISBN:9780121827953 p.17-31, 10.1016/s0076-6879(04)90002-x
- Bauvy Chantal, Meijer Alfred J., Codogno Patrice, Chapter 4 Assaying of Autophagic Protein Degradation, Methods in Enzymology (2009) ISBN:9780123745477 p.47-61, 10.1016/s0076-6879(08)03604-5
- Ichimura Yoshinobu, Kumanomidou Taichi, Sou Yu-shin, Mizushima Tsunehiro, Ezaki Junji, Ueno Takashi, Kominami Eiki, Yamane Takashi, Tanaka Keiji, Komatsu Masaaki, Structural Basis for Sorting Mechanism of p62 in Selective Autophagy, 10.1074/jbc.m802182200
- Kabuta Tomohiro, Furuta Akiko, Aoki Shunsuke, Furuta Koh, Wada Keiji, Aberrant Interaction between Parkinson Disease-associated Mutant UCH-L1 and the Lysosomal Receptor for Chaperone-mediated Autophagy, 10.1074/jbc.m801918200
- Ding Wen-Xing, Ni Hong-Min, Gao Wentao, Yoshimori Tamotsu, Stolz Donna B., Ron David, Yin Xiao-Ming, Linking of Autophagy to Ubiquitin-Proteasome System Is Important for the Regulation of Endoplasmic Reticulum Stress and Cell Viability, 10.2353/ajpath.2007.070188
- Iwata Atsushi, Riley Brigit E., Johnston Jennifer A., Kopito Ron R., HDAC6 and Microtubules Are Required for Autophagic Degradation of Aggregated Huntingtin, 10.1074/jbc.m508786200
- Pandey Udai Bhan, Nie Zhiping, Batlevi Yakup, McCray Brett A., Ritson Gillian P., Nedelsky Natalia B., Schwartz Stephanie L., DiProspero Nicholas A., Knight Melanie A., Schuldiner Oren, Padmanabhan Ranjani, Hild Marc, Berry Deborah L., Garza Dan, Hubbert Charlotte C., Yao Tso-Pang, Baehrecke Eric H., Taylor J. Paul, HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS, 10.1038/nature05853
- Tomek K., Wagner R., Varga F., Singer C. F., Karlic H., Grunt T. W., Blockade of Fatty Acid Synthase Induces Ubiquitination and Degradation of Phosphoinositide-3-Kinase Signaling Proteins in Ovarian Cancer, 10.1158/1541-7786.mcr-10-0467
- Zimmermann Andrea C., Zarei Mostafa, Eiselein Sven, Dengjel Jörn, Quantitative proteomics for the analysis of spatio-temporal protein dynamics during autophagy, 10.4161/auto.6.8.12786
- Kristensen Anders Riis, Schandorff Søren, Høyer-Hansen Maria, Nielsen Maria Overbeck, Jäättelä Marja, Dengjel Jörn, Andersen Jens S., Ordered Organelle Degradation during Starvation-induced Autophagy, 10.1074/mcp.m800184-mcp200
- Furuya N., Kanazawa T., Fujimura S., Ueno T., Kominami E., Kadowaki M., Leupeptin-Induced Appearance of Partial Fragment of Betaine Homocysteine Methyltransferase during Autophagic Maturation in Rat Hepatocytes, 10.1093/oxfordjournals.jbchem.a002859
- Ueno Takashi, Ishidoh Kazumi, Mineki Reiko, Tanida Isei, Murayama Kimie, Kadowaki Motoni, Kominami Eiki, Autolysosomal Membrane-associated Betaine Homocysteine Methyltransferase : LIMITED DEGRADATION FRAGMENT OF A SEQUESTERED CYTOSOLIC ENZYME MONITORING AUTOPHAGY, 10.1074/jbc.274.21.15222
- Øverbye Anders, Sætre Frank, Hagen Linda Korseberg, Johansen Harald Thidemann, Seglen Per O., Autophagic activity measured in whole rat hepatocytes as the accumulation of a novel BHMT fragment (p10), generated in amphisomes by the asparaginyl proteinase, legumain, 10.4161/auto.7.9.16436
- Seglen Per O., Øverbye Anders, Sætre Frank, Chapter 5 Sequestration Assays for Mammalian Autophagy, Methods in Enzymology (2009) ISBN:9780123745477 p.63-83, 10.1016/s0076-6879(08)03605-7
- Mercer Carol A., Kaliappan Alagammai, Dennis Patrick B., Macroautophagy-dependent, intralysosomal cleavage of a betaine homocysteine methyltransferase fusion protein requires stable multimerization, 10.4161/auto.5275
- Nimmerjahn Falk, Milosevic Slavoljub, Behrends Uta, Jaffee Elizabeth M., Pardoll Drew M., Bornkamm Georg W., Mautner Josef, Major histocompatibility complex class II-restricted presentation of a cytosolic antigen by autophagy, 10.1002/eji.200323730
- Taylor G. S., Long H. M., Haigh T. A., Larsen M., Brooks J., Rickinson A. B., A Role for Intercellular Antigen Transfer in the Recognition of EBV-Transformed B Cell Lines by EBV Nuclear Antigen-Specific CD4+ T Cells, 10.4049/jimmunol.177.6.3746
- Klionsky DJ, EMBO J, 8, 2241 (1989)
- Venerando R, Am J Physiol, 266, C455 (1994)
- Häussinger D, Hallbrucker C, vom Dahl S, Lang F, Gerok W, Cell swelling inhibits proteolysis in perfused rat liver, 10.1042/bj2720239
- vom Dahl S, Häussinger D, Cell hydration and proteolysis control in liver, 10.1042/bj3120988
- Cuervo A. M., Impaired Degradation of Mutant -Synuclein by Chaperone-Mediated Autophagy, 10.1126/science.1101738
- Reggiori F., The Actin Cytoskeleton Is Required for Selective Types of Autophagy, but Not Nonspecific Autophagy, in the Yeast Saccharomyces cerevisiae, 10.1091/mbc.e05-07-0629
- Manjithaya Ravi, Jain Shveta, Farré Jean-Claude, Subramani Suresh, A yeast MAPK cascade regulates pexophagy but not other autophagy pathways, 10.1083/jcb.200909154
- Journo Dikla, Mor Angelika, Abeliovich Hagai, Aup1-mediated Regulation of Rtg3 during Mitophagy, 10.1074/jbc.m109.048140
- Kanki Tomotake, Klionsky Daniel J., Mitophagy in Yeast Occurs through a Selective Mechanism, 10.1074/jbc.m802403200
- Kanki T., Wang K., Baba M., Bartholomew C. R., Lynch-Day M. A., Du Z., Geng J., Mao K., Yang Z., Yen W.-L., Klionsky D. J., A Genomic Screen for Yeast Mutants Defective in Selective Mitochondria Autophagy, 10.1091/mbc.e09-03-0225
- Kanki Tomotake, Wang Ke, Cao Yang, Baba Misuzu, Klionsky Daniel J., Atg32 Is a Mitochondrial Protein that Confers Selectivity during Mitophagy, 10.1016/j.devcel.2009.06.014
- Okamoto Koji, Kondo-Okamoto Noriko, Ohsumi Yoshinori, Mitochondria-Anchored Receptor Atg32 Mediates Degradation of Mitochondria via Selective Autophagy, 10.1016/j.devcel.2009.06.013
- Sakai Yasuyoshi, Koller Antonius, Rangell Linda K., Keller Gilbert A., Subramani Suresh, Peroxisome Degradation by Microautophagy inPichia pastoris: Identification of Specific Steps and Morphological Intermediates, 10.1083/jcb.141.3.625
- NAZARKO T, NICAUD J, SIBIRNY A, Observation of the peroxisome?vacuole dynamics by fluorescence microscopy with a single filter set, 10.1016/j.cellbi.2004.11.014
- Roetzer Andreas, Gratz Nina, Kovarik Pavel, Schüller Christoph, Autophagy supportsCandida glabratasurvival during phagocytosis, 10.1111/j.1462-5822.2009.01391.x
- Bormann Christiane, Sahm Hermann, Degradation of microbodies in relation of activities of alcohol oxidase and catalase inCandida boidinii, 10.1007/bf00689353
- Stasyk Oleh V., Nazarko Taras Y., Sibirny Andriy A., Chapter 16 Methods of Plate Pexophagy Monitoring and Positive Selection for ATG Gene Cloning in Yeasts, Methods in Enzymology (2008) ISBN:9780123745484 p.229-239, 10.1016/s0076-6879(08)03216-3
- Hutchins MU, J Cell Sci, 112, 4079 (1999)
- Mukaiyama Hiroyuki, Oku Masahide, Baba Misuzu, Samizo Takeshi, Hammond Adam T., Glick Benjamin S., Kato Nobuo, Sakai Yasuyoshi, Paz2 and 13 other PAZ gene products regulate vacuolar engulfment of peroxisomes during micropexophagy, 10.1046/j.1356-9597.2001.00499.x
- Tuttle DL, J Cell Sci, 108, 25 (1995)
- Nazarko Taras Y., Huang Ju, Nicaud Jean-Marc, Klionsky Daniel J., Sibirny Andrei A., Early Secretory Pathway GeneTRS85is Required for Selective Macroautophagy of Peroxisomes inYarrowia lipolytica, 10.4161/auto.1.1.1512
- Veenhuis Marten, Douma Anneke, Harder Wim, Osumi Masako, Degradation and turnover of peroxisomes in the yeast Hansenula polymorpha induced by selective inactivation of peroxisomal enzymes, 10.1007/bf00407757
- Monosov E Z, Wenzel T J, Lüers G H, Heyman J A, Subramani S, Labeling of peroxisomes with green fluorescent protein in living P. pastoris cells., 10.1177/44.6.8666743
- Wiemer Erik A.C., Wenzel Thibaut, Deerinck Thomas J., Ellisman Mark H., Subramani Suresh, Visualization of the Peroxisomal Compartment in Living Mammalian Cells: Dynamic Behavior and Association with Microtubules, 10.1083/jcb.136.1.71
- Monastyrska Iryna, van der Heide Meis, Krikken Arjen M., Kiel Jan A.K.W., van der Klei Ida J., Veenhuis Marten, Atg8 is Essential for Macropexophagy in Hansenula polymorpha, 10.1111/j.1600-0854.2004.00252.x
- Devenish Rodney J., Prescott Mark, Turcic Kristina, Mijaljica Dalibor, Chapter 9 Monitoring Organelle Turnover in Yeast Using Fluorescent Protein Tags, Methods in Enzymology (2008) ISBN:9780123745484 p.109-131, 10.1016/s0076-6879(08)03209-6
- Farré Jean-Claude, Manjithaya Ravi, Mathewson Richard D., Subramani Suresh, PpAtg30 Tags Peroxisomes for Turnover by Selective Autophagy, 10.1016/j.devcel.2007.12.011
- Kanki Tomotake, Klionsky Daniel J., The molecular mechanism of mitochondria autophagy in yeast, 10.1111/j.1365-2958.2009.07035.x
- Tal Ruth, Winter Gal, Ecker Nitai, Klionsky Daniel J., Abeliovich Hagai, Aup1p, a Yeast Mitochondrial Protein Phosphatase Homolog, Is Required for Efficient Stationary Phase Mitophagy and Cell Survival, 10.1074/jbc.m605940200
- Abeliovich Hagai, Stationary-Phase Mitophagy in RespiringSaccharomyces cerevisiae, 10.1089/ars.2010.3807
- Aksam Eda Bener, Koek Anne, Jourdan Stefanie, Veenhuis Marten, van der Klei Ida J., A Peroxisomal Lon Protease and Peroxisome Degradation by Autophagy Play Key Roles in Vitality ofHansenula polymorphaCells, 10.4161/auto.3534
- Roberts P., Piecemeal Microautophagy of Nucleus in Saccharomyces cerevisiae, 10.1091/mbc.e02-08-0483
- Krick R., Muehe Y., Prick T., Bremer S., Schlotterhose P., Eskelinen E.- L., Millen J., Goldfarb D. S., Thumm M., Piecemeal Microautophagy of the Nucleus Requires the Core Macroautophagy Genes, 10.1091/mbc.e08-04-0363
- Farré Jean-Claude, Krick Roswitha, Subramani Suresh, Thumm Michael, Turnover of organelles by autophagy in yeast, 10.1016/j.ceb.2009.04.015
- Kvam Erik, Goldfarb David S., Structure and function of nucleus-vacuole junctions: outer-nuclear-membrane targeting of Nvj1p and a role in tryptophan uptake, 10.1242/jcs.03093
- Millen Jonathan I., Krick Roswitha, Prick Tanja, Thumm Michael, Goldfarb David S., Measuring piecemeal microautophagy of the nucleus inSaccharomyces cerevisiae, 10.4161/auto.5.1.7181
- Bernales Sebastián, McDonald Kent L, Walter Peter, Autophagy Counterbalances Endoplasmic Reticulum Expansion during the Unfolded Protein Response, 10.1371/journal.pbio.0040423
- Yorimitsu Tomohiro, Nair Usha, Yang Zhifen, Klionsky Daniel J., Endoplasmic Reticulum Stress Triggers Autophagy, 10.1074/jbc.m607007200
- Klionsky Daniel J., Cuervo Ana Maria, Dunn, Jr. William A., Levine Beth, van der Klei Ida J., Seglen Per O., How Shall I Eat Thee?, 10.4161/auto.4377
- Fujita Eriko, Kouroku Yoriko, Isoai Atsushi, Kumagai Hiromichi, Misutani Akifumi, Matsuda Chie, Hayashi Yukiko K., Momoi Takashi, Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II), 10.1093/hmg/ddm002
- Kraft Claudine, Deplazes Anna, Sohrmann Marc, Peter Matthias, Mature ribosomes are selectively degraded upon starvation by an autophagy pathway requiring the Ubp3p/Bre5p ubiquitin protease, 10.1038/ncb1723
- Yorimitsu T., Atg11 Links Cargo to the Vesicle-forming Machinery in the Cytoplasm to Vacuole Targeting Pathway, 10.1091/mbc.e04-11-1035
- Shintani Takahiro, Huang Wei-Pang, Stromhaug Per E., Klionsky Daniel J., Mechanism of Cargo Selection in the Cytoplasm to Vacuole Targeting Pathway, 10.1016/s1534-5807(02)00373-8
- Abeliovich H., Cytoplasm to vacuole trafficking of aminopeptidase I requires a t-SNARE-Sec1p complex composed of Tlg2p and Vps45p, 10.1093/emboj/18.21.6005
- Brown C.R., Chiang Hui-Ling, A selective autophagy pathway that degrades gluconeogenic enzymes during catabolite inactivation, 10.4161/cib.7711
- Schüle Thomas, Rose Matthias, Entian Karl-Dieter, Thumm Michael, Wolf Dieter H., Ubc8p functions in catabolite degradation of fructose-1,6-bisphosphatase in yeast, 10.1093/emboj/19.10.2161
- Schork Stefan M., Thumm Michael, Wolf Dieter H., Catabolite Inactivation of Fructose-1,6-bisphosphatase ofSaccharomyces cerevisiae : DEGRADATION OCCURS VIA THE UBIQUITIN PATHWAY, 10.1074/jbc.270.44.26446
- Regelmann J., Catabolite Degradation of Fructose-1,6-bisphosphatase in the Yeast Saccharomyces cerevisiae: A Genome-wide Screen Identifies Eight Novel GID Genes and Indicates the Existence of Two Degradation Pathways, 10.1091/mbc.e02-08-0456
- Hung Guo-Chiuan, Brown C. Randell, Wolfe Allison B., Liu Jingjing, Chiang Hui-Ling, Degradation of the Gluconeogenic Enzymes Fructose-1,6-bisphosphatase and Malate Dehydrogenase Is Mediated by Distinct Proteolytic Pathways and Signaling Events, 10.1074/jbc.m404544200
- Chiang Hui-Ling, Schekman Randy, Hamamoto Susan, Selective Uptake of Cytosolic, Peroxisomal, and Plasma Membrane Proteins into the Yeast Lysosome for Degradation, 10.1074/jbc.271.17.9934
- Huang Pei-Hsin, Chiang Hui-Ling, Identification of Novel Vesicles in the Cytosol to Vacuole Protein Degradation Pathway, 10.1083/jcb.136.4.803
- Alibhoy Abbas A., Giardina Bennett J., Dunton Danielle D., Chiang Hui-Ling, Vid30 is required for the association of Vid vesicles and actin patches in the vacuole import and degradation pathway, 10.4161/auto.8.1.18104
- Brown C. Randell, Wolfe Allison B., Cui Dongying, Chiang Hui-Ling, The Vacuolar Import and Degradation Pathway Merges with the Endocytic Pathway to Deliver Fructose-1,6-bisphosphatase to the Vacuole for Degradation, 10.1074/jbc.m709922200
- Chiang Meng-Chieh, Chiang Hui-Ling, Vid24p, a Novel Protein Localized to the Fructose-1,6-bisphosphatase–containing Vesicles, Regulates Targeting of Fructose-1,6-bisphosphatase from the Vesicles to the Vacuole for Degradation, 10.1083/jcb.140.6.1347
- Brown C. Randell, Dunton Danielle, Chiang Hui-Ling, The Vacuole Import and Degradation Pathway Utilizes Early Steps of Endocytosis and Actin Polymerization to Deliver Cargo Proteins to the Vacuole for Degradation, 10.1074/jbc.m109.028241
- Vida T. A., A new vital stain for visualizing vacuolar membrane dynamics and endocytosis in yeast, 10.1083/jcb.128.5.779
- Brown C. Randell, Hung Guo-Chiuan, Dunton Danielle, Chiang Hui-Ling, The TOR Complex 1 Is Distributed in Endosomes and in Retrograde Vesicles That Form from the Vacuole Membrane and Plays an Important Role in the Vacuole Import and Degradation Pathway, 10.1074/jbc.m109.075143
- Geisler Sven, Holmström Kira M., Treis Angela, Skujat Diana, Weber Stephanie S., Fiesel Fabienne C., Kahle Philipp J., Springer Wolfdieter, The PINK1/Parkin-mediated mitophagy is compromised by PD-associated mutations, 10.4161/auto.6.7.13286
- Geisler Sven, Holmström Kira M., Skujat Diana, Fiesel Fabienne C., Rothfuss Oliver C., Kahle Philipp J., Springer Wolfdieter, PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1, 10.1038/ncb2012
- Boya P., Gonzalez-Polo R.-A., Casares N., Perfettini J.-L., Dessen P., Larochette N., Metivier D., Meley D., Souquere S., Yoshimori T., Pierron G., Codogno P., Kroemer G., Inhibition of Macroautophagy Triggers Apoptosis, 10.1128/mcb.25.3.1025-1040.2005
- Katayama Hiroyuki, Kogure Takako, Mizushima Noboru, Yoshimori Tamotsu, Miyawaki Atsushi, A Sensitive and Quantitative Technique for Detecting Autophagic Events Based on Lysosomal Delivery, 10.1016/j.chembiol.2011.05.013
- Yang Jin-Yi, Yang Wei Yuan, Spatiotemporally controlled initiation of Parkin-mediated mitophagy within single cells, 10.4161/auto.7.10.16626
- Luiken J.J.F.P., van den Berg M., Heikoop J.C., Meijer A.J., Autophagic degradation of peroxisomes in isolated rat hepatocytes, 10.1016/0014-5793(92)80596-9
- Yokota S, Eur J Cell Biol, 61, 67 (1993)
- Huybrechts Sofie J., Van Veldhoven Paul P., Brees Chantal, Mannaerts Guy P., Los Georgyi V., Fransen Marc, Peroxisome Dynamics in Cultured Mammalian Cells, 10.1111/j.1600-0854.2009.00970.x
- Lee Joo-Yong, Nagano Yoshito, Taylor J. Paul, Lim Kah Leong, Yao Tso-Pang, Disease-causing mutations in Parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy, 10.1083/jcb.201001039
- Chan Nickie C., Salazar Anna M., Pham Anh H., Sweredoski Michael J., Kolawa Natalie J., Graham Robert L.J., Hess Sonja, Chan David C., Broad activation of the ubiquitin–proteasome system by Parkin is critical for mitophagy, 10.1093/hmg/ddr048
- Tanaka Atsushi, Cleland Megan M., Xu Shan, Narendra Derek P., Suen Der-Fen, Karbowski Mariusz, Youle Richard J., Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin, 10.1083/jcb.201007013
- Yoshii Saori R., Kishi Chieko, Ishihara Naotada, Mizushima Noboru, Parkin Mediates Proteasome-dependent Protein Degradation and Rupture of the Outer Mitochondrial Membrane, 10.1074/jbc.m110.209338
- Okatsu K, Genes Cells, 15, 887 (2010)
- Lyamzaev Konstantin G., Nepryakhina Olga K., Saprunova Valeria B., Bakeeva Lora E., Pletjushkina Olga Yu., Chernyak Boris V., Skulachev Vladimir P., Novel mechanism of elimination of malfunctioning mitochondria (mitoptosis): Formation of mitoptotic bodies and extrusion of mitochondrial material from the cell, 10.1016/j.bbabio.2008.03.027
- Hara-Kuge Sayuri, Fujiki Yukio, The peroxin Pex14p is involved in LC3-dependent degradation of mammalian peroxisomes, 10.1016/j.yexcr.2008.09.015
- Ezaki Junji, Kominami Eiki, Ueno Takashi, Peroxisome degradation in mammals, 10.1002/iub.537
- Øverbye Anders, Brinchmann Monica Fengsrud, Seglen Per O., Proteomic Analysis of Membrane-Associated Proteins from Rat Liver Autophagosomes, 10.4161/auto.3910
- Ju Jeong-Sun, Miller Sara E., Jackson Erin, Cadwell Ken, Piwnica-Worms David, Weihl Conrad C., Quantitation of selective autophagic protein aggregate degradation in vitro and in vivo using luciferase reporters, 10.4161/auto.5.4.7761
- Fuentealba Rodrigo A., Marasa Jayne, Diamond Marc I., Piwnica-Worms David, Weihl Conrad C., An aggregation sensing reporter identifies leflunomide and teriflunomide as polyglutamine aggregate inhibitors, 10.1093/hmg/ddr500
- Webster Paul, Cytoplasmic Bacteria and the Autophagic Pathway, 10.4161/auto.2826
- Dubuisson Jean-Francois, Swanson Michele S., Mouse infection by Legionella, a Model to Analyze Autophagy, 10.4161/auto.2831
- Jordan Tristan X., Randall Glenn, Manipulation or capitulation: virus interactions with autophagy, 10.1016/j.micinf.2011.09.007
- Knodler Leigh A., Celli Jean, Eating the strangers within: host control of intracellular bacteria via xenophagy : Mechanisms of antibacterial autophagy, 10.1111/j.1462-5822.2011.01632.x
- Levine Beth, Mizushima Noboru, Virgin Herbert W., Autophagy in immunity and inflammation, 10.1038/nature09782
- Deretic Vojo, Autophagy in immunity and cell-autonomous defense against intracellular microbes : Autophagy in immunity, 10.1111/j.1600-065x.2010.00995.x
- Kageyama S., Omori H., Saitoh T., Sone T., Guan J.-L., Akira S., Imamoto F., Noda T., Yoshimori T., The LC3 recruitment mechanism is separate from Atg9L1-dependent membrane formation in the autophagic response against Salmonella, 10.1091/mbc.e10-11-0893
- Zheng Y. T., Shahnazari S., Brech A., Lamark T., Johansen T., Brumell J. H., The Adaptor Protein p62/SQSTM1 Targets Invading Bacteria to the Autophagy Pathway, 10.4049/jimmunol.0900441
- Thurston Teresa L M, Ryzhakov Grigory, Bloor Stuart, von Muhlinen Natalia, Randow Felix, The TBK1 adaptor and autophagy receptor NDP52 restricts the proliferation of ubiquitin-coated bacteria, 10.1038/ni.1800
- Wild P., Farhan H., McEwan D. G., Wagner S., Rogov V. V., Brady N. R., Richter B., Korac J., Waidmann O., Choudhary C., Dotsch V., Bumann D., Dikic I., Phosphorylation of the Autophagy Receptor Optineurin Restricts Salmonella Growth, 10.1126/science.1205405
- Huang J., Canadien V., Lam G. Y., Steinberg B. E., Dinauer M. C., Magalhaes M. A. O., Glogauer M., Grinstein S., Brumell J. H., Activation of antibacterial autophagy by NADPH oxidases, 10.1073/pnas.0811045106
- Rich Kathryn A., Burkett Chelsea, Webster Paul, Cytoplasmic bacteria can be targets for autophagy, 10.1046/j.1462-5822.2003.00292.x
- Shahnazari Shahab, Brumell John H, Mechanisms and consequences of bacterial targeting by the autophagy pathway, 10.1016/j.mib.2010.11.001
- McLean Jeffrey E., Wudzinska Aleksandra, Datan Emmanuel, Quaglino Daniela, Zakeri Zahra, Flavivirus NS4A-induced Autophagy Protects Cells against Death and Enhances Virus Replication, 10.1074/jbc.m110.192500
- Mao Yi, Da Liang, Tang Hong, Yang Jiali, Lei Yinrui, Tiollais Pierre, Li Tsaiping, Zhao Mujun, Hepatitis B virus X protein reduces starvation-induced cell death through activation of autophagy and inhibition of mitochondrial apoptotic pathway, 10.1016/j.bbrc.2011.10.013
- Orvedahl Anthony, Alexander Diane, Tallóczy Zsolt, Sun Qihua, Wei Yongjie, Zhang Wei, Burns Dennis, Leib David A., Levine Beth, HSV-1 ICP34.5 Confers Neurovirulence by Targeting the Beclin 1 Autophagy Protein, 10.1016/j.chom.2006.12.001
- Alexander D. E., Ward S. L., Mizushima N., Levine B., Leib D. A., Analysis of the Role of Autophagy in Replication of Herpes Simplex Virus in Cell Culture, 10.1128/jvi.01356-07
- Leib D. A., Alexander D. E., Cox D., Yin J., Ferguson T. A., Interaction of ICP34.5 with Beclin 1 Modulates Herpes Simplex Virus Type 1 Pathogenesis through Control of CD4+ T-Cell Responses, 10.1128/jvi.01676-09
- Zhang Haiyan, Monken Claude E., Lenard John, Mizushima Noboru, Lattime Edmund C., Jin Shengkan, Cellular Autophagy Machinery is not Required for Vaccinia Virus Replication and Maturation, 10.4161/auto.2.2.2297
- Heaton Nicholas S., Randall Glenn, Dengue Virus and Autophagy, 10.3390/v3081332
- Dreux M., Gastaminza P., Wieland S. F., Chisari F. V., The autophagy machinery is required to initiate hepatitis C virus replication, 10.1073/pnas.0907344106
- Collins Cathleen A., De Mazière Ann, van Dijk Suzanne, Carlsson Fredric, Klumperman Judith, Brown Eric J., Atg5-Independent Sequestration of Ubiquitinated Mycobacteria, 10.1371/journal.ppat.1000430
- Moreau Kevin, Lacas-Gervais Sandra, Fujita Naonobu, Sebbane Florent, Yoshimori Tamotsu, Simonet Michel, Lafont Frank, Autophagosomes can support Yersinia pseudotuberculosis replication in macrophages : Y. pseudotuberculosis intracellular traffic, 10.1111/j.1462-5822.2010.01456.x
- Singh Rajat, Kaushik Susmita, Wang Yongjun, Xiang Youqing, Novak Inna, Komatsu Masaaki, Tanaka Keiji, Cuervo Ana Maria, Czaja Mark J., Autophagy regulates lipid metabolism, 10.1038/nature07976
- Grasso Daniel, Ropolo Alejandro, Lo Ré Andrea, Boggio Verónica, Molejón María I., Iovanna Juan L., Gonzalez Claudio D., Urrutia Raúl, Vaccaro María I., Zymophagy, a Novel Selective Autophagy Pathway Mediated by VMP1-USP9x-p62, Prevents Pancreatic Cell Death, 10.1074/jbc.m110.197301
- Al Rawi Sara, Louvet-Vallée Sophie, Djeddi Abderazak, Sachse Martin, Culetto Emmanuel, Hajjar Connie, Boyd Lynn, Legouis Renaud, Galy Vincent, Allophagy : A macroautophagic process degrading spermatozoid-inherited organelles, 10.4161/auto.19242
- Sato Miyuki, Sato Ken, Maternal inheritance of mitochondrial DNA : Degradation of paternal mitochondria by allogeneic organelle autophagy, allophagy, 10.4161/auto.19243
- Al Rawi S., Louvet-Vallee S., Djeddi A., Sachse M., Culetto E., Hajjar C., Boyd L., Legouis R., Galy V., Postfertilization Autophagy of Sperm Organelles Prevents Paternal Mitochondrial DNA Transmission, 10.1126/science.1211878
- Sato M., Sato K., Degradation of Paternal Mitochondria by Fertilization-Triggered Autophagy in C. elegans Embryos, 10.1126/science.1210333
- Seglen Per O., Gordon Paul B., Tolleshaug Helge, Høyvik Henrik, Use of [3H]raffinose as a specific probe of autophagic sequestration, 10.1016/0014-4827(86)90446-5
- Kopitz J., Nonselective autophagy of cytosolic enzymes by isolated rat hepatocytes, 10.1083/jcb.111.3.941
- Nair Usha, Thumm Michael, Klionsky Daniel J, Krick Roswitha, GFP-Atg8 protease protection as a tool to monitor autophagosome biogenesis, 10.4161/auto.7.12.18424
- Plomp PJ, J Biol Chem, 264, 6699 (1989)
- Hoyvik H., Inhibition of autophagic-lysosomal delivery and autophagic lactolysis by asparagine, 10.1083/jcb.113.6.1305
- Rodriguez-Enriquez Sara, Kim Insil, Currin Robert T., Lemasters John J., Tracker Dyes to Probe Mitochondrial Autophagy (Mitophagy) in Rat Hepatocytes, 10.4161/auto.2229
- Lorenz Holger, Hailey Dale W, Lippincott-Schwartz Jennifer, Fluorescence protease protection of GFP chimeras to reveal protein topology and subcellular localization, 10.1038/nmeth857
- Dagda Ruben K., Zhu Jianhui, Kulich Scott M., Chu Charleen T., Mitochondrially localized ERK2 regulates mitophagy and autophagic cell stress, 10.4161/auto.6458
- McNeil P. L., A method for incorporating macromolecules into adherent cells, 10.1083/jcb.98.4.1556
- Kim John, Huang Wei-Pang, Stromhaug Per E., Klionsky Daniel J., Convergence of Multiple Autophagy and Cytoplasm to Vacuole Targeting Components to a Perivacuolar Membrane Compartment Prior tode NovoVesicle Formation, 10.1074/jbc.m109134200
- Kovács Attila L., László Lajos, Kovács János, Effect of amino acids and cycloheximide on changes caused by vinblastine, leupeptin and methylamine in the autophagic/lysosomal system of mouse hepatocytes in vivo, 10.1016/0014-4827(85)90154-5
- Swanson Michele S., Byrne Brenda G., Dubuisson Jean‐Francois, Chapter 23 Kinetic Analysis of Autophagosome Formation and Turnover in Primary Mouse Macrophages, Methods in Enzymology (2009) ISBN:9780123745477 p.383-402, 10.1016/s0076-6879(08)03623-9
- BEUGNET Anne, TEE Andrew R., TAYLOR Peter M., PROUD Christopher G., Regulation of targets of mTOR (mammalian target of rapamycin) signalling by intracellular amino acid availability, 10.1042/bj20021266
- Urban Jörg, Soulard Alexandre, Huber Alexandre, Lippman Soyeon, Mukhopadhyay Debdyuti, Deloche Olivier, Wanke Valeria, Anrather Dorothea, Ammerer Gustav, Riezman Howard, Broach James R., De Virgilio Claudio, Hall Michael N., Loewith Robbie, Sch9 Is a Major Target of TORC1 in Saccharomyces cerevisiae, 10.1016/j.molcel.2007.04.020
- Jomain-Baum M, J Biol Chem, 248, 1536 (1973)
- Garber AJ, J Biol Chem, 248, 1530 (1973)
- Mora R, Glia, 58, 1364 (2010)
- Bright Nicholas A., Lindsay Margaret R., Stewart Abigail, Luzio J. Paul, The Relationship Between Lumenal and Limiting Membranes in Swollen Late Endocytic Compartments Formed After Wortmannin Treatment or Sucrose Accumulation, 10.1034/j.1600-0854.2001.20906.x
- Deter R. L., QUANTITATIVE CHARACTERIZATION OF DENSE BODY, AUTOPHAGIC VACUOLE, AND ACID PHOSPHATASE-BEARING PARTICLE POPULATIONS DURING THE EARLY PHASES OF GLUCAGON-INDUCED AUTOPHAGY IN RAT LIVER, 10.1083/jcb.48.3.473
- Deter R.L., Analog modeling of glucagon-induced autophagy in rat liver, 10.1016/0014-4827(75)90538-8
- Deter R.L., Analog modeling of glucagon-induced autophagy in rat liver, 10.1016/0014-4827(75)90539-x
- Deter R. L., PARTICIPATION OF LYSOSOMES IN CELLULAR AUTOPHAGY INDUCED IN RAT LIVER BY GLUCAGON, 10.1083/jcb.35.2.c11
- Deter R. L., INFLUENCE OF GLUCAGON, AN INDUCER OF CELLULAR AUTOPHAGY, ON SOME PHYSICAL PROPERTIES OF RAT LIVER LYSOSOMES, 10.1083/jcb.33.2.437
- STRØMHAUG Per Eivind, BERG Trond Olav, FENGSRUD Monica, SEGLEN Per O., Purification and characterization of autophagosomes from rat hepatocytes, 10.1042/bj3350217
- Deter RL. Electron microscopic evaluation of subcellular fractions obtained by ultracentrifugation. In: Hayat MA, ed. Principles and Techniques of Electron Microscopy. New York: Van Nostrand Reinhold Co., 1973:199-235.
- Marzella L., Isolation of autophagic vacuoles from rat liver: morphological and biochemical characterization, 10.1083/jcb.93.1.144
- Wattiaux R., Isolation of rat liver lysosomes by isopycnic centrifugation in a metrizamide gradient, 10.1083/jcb.78.2.349
- Rodríguez-Navarro Jose A., Rodríguez Laura, Casarejos María J., Solano Rosa M., Gómez Ana, Perucho Juan, Cuervo Ana María, García de Yébenes Justo, Mena María A., Trehalose ameliorates dopaminergic and tau pathology in parkin deleted/tau overexpressing mice through autophagy activation, 10.1016/j.nbd.2010.05.014
- Weibel ER, Bolender RP. Stereological techniques for electron microscopic morphometry. In: Hayat MA, ed. Principles and Techniques of Electron Microscopy. New York: Van Nostrand Reinhold Co., 1973:237-96.
- Baudhuin P., ELECTRON MICROSCOPIC EXAMINATION OF SUBCELLULAR FRACTIONS: I. The Preparation of Representative Samples from Suspensions of Particles, 10.1083/jcb.32.1.181
- Baudhuin P., ELECTRON MICROSCOPIC EXAMINATION OF SUBCELLULAR FRACTIONS: II. Quantitative Analysis of the Mitochondrial Population Isolated from Rat Liver, 10.1083/jcb.35.3.631
- Storrie Brian, Amadden Edward, [16] Isolation of subcellular organelles, Methods in Enzymology (1990) ISBN:9780121820831 p.203-225, 10.1016/0076-6879(90)82018-w
- Balch William E., Rothman James E., Characterization of protein transport between successive compartments of the Golgi apparatus: Asymmetric properties of donor and acceptor activities in a cell-free system, 10.1016/0003-9861(85)90046-3
- Graham JM. Isolation of lysosomes from tissues and cells by differential and density gradient centrifugation. In: Bonifacino JS, Dasso M, Harfod JB, Lippincott-Schwartz J and Yamada KM, eds. Current Protocols in Cell Biology: John Wiley & Sons, Inc., 2000:Unit 3.6.
- Cuervo Ana Maria, Dice J. Fred, Knecht Erwin, A Population of Rat Liver Lysosomes Responsible for the Selective Uptake and Degradation of Cytosolic Proteins, 10.1074/jbc.272.9.5606
- Iwai-Kanai Eri, Yuan Hua, Huang Chengqun, Sayen M. Richard, Perry-Garza Cynthia N., Kim Lucy, Gottlieb Roberta A., A method to measure cardiac autophagic flux in vivo, 10.4161/auto.5603
- Zhu Hongxin, Tannous Paul, Johnstone Janet L., Kong Yongli, Shelton John M., Richardson James A., Le Vien, Levine Beth, Rothermel Beverly A., Hill Joseph A., Cardiac autophagy is a maladaptive response to hemodynamic stress, 10.1172/jci27523
- Ding Wen–Xing, Li Min, Chen Xiaoyun, Ni Hong–Min, Lin Chih–Wen, Gao Wentao, Lu Binfeng, Stolz Donna B., Clemens Dahn L., Yin Xiao–Ming, Autophagy Reduces Acute Ethanol-Induced Hepatotoxicity and Steatosis in Mice, 10.1053/j.gastro.2010.07.041
- Chiarelli Roberto, Agnello Maria, Roccheri Maria Carmela, Sea urchin embryos as a model system for studying autophagy induced by cadmium stress, 10.4161/auto.7.9.16450
- MORICI GIOVANNI, AGNELLO MARIA, SPAGNOLO FILIPPO, ROCCHERI MARIA CARMELA, LIEGRO CARLO MARIA DI, RINALDI ANNA MARIA, Confocal microscopy study of the distribution, content and activity of mitochondria during Paracentrotus lividus development, 10.1111/j.1365-2818.2007.01860.x
- Martinet Wim, Meyer Guido R.Y. De, Andries Luc, Herman Arnold G., Kockx Mark M., Detection of Autophagy in Tissue by Standard Immunohistochemistry: Possibilities and Limitations, 10.4161/auto.2217
- Holt Sarah V., Wyspianska Beata, Randall Kevin J., James Dominic, Foster John R., Wilkinson Robert W., The Development of an Immunohistochemical Method to Detect the Autophagy-Associated Protein LC3-II in Human Tumor Xenografts, 10.1177/0192623310396903
- Kimura Shunsuke, Fujita Naonobu, Noda Takeshi, Yoshimori Tamotsu, Chapter 1 Monitoring Autophagy in Mammalian Cultured Cells through the Dynamics of LC3, Methods in Enzymology (2009) ISBN:9780123745477 p.1-12, 10.1016/s0076-6879(08)03601-x
- Dehay B., Bove J., Rodriguez-Muela N., Perier C., Recasens A., Boya P., Vila M., Pathogenic Lysosomal Depletion in Parkinson's Disease, 10.1523/jneurosci.1920-10.2010
- Ouimet Mireille, Franklin Vivian, Mak Esther, Liao Xianghai, Tabas Ira, Marcel Yves L., Autophagy Regulates Cholesterol Efflux from Macrophage Foam Cells via Lysosomal Acid Lipase, 10.1016/j.cmet.2011.03.023
- Gomes Ligia C., Benedetto Giulietta Di, Scorrano Luca, During autophagy mitochondria elongate, are spared from degradation and sustain cell viability, 10.1038/ncb2220
- Grumati Paolo, Coletto Luisa, Sabatelli Patrizia, Cescon Matilde, Angelin Alessia, Bertaggia Enrico, Blaauw Bert, Urciuolo Anna, Tiepolo Tania, Merlini Luciano, Maraldi Nadir M, Bernardi Paolo, Sandri Marco, Bonaldo Paolo, Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration, 10.1038/nm.2247
- Haspel Jeffrey, Shaik Rahamthulla S., Ifedigbo Emeka, Nakahira Kiichi, Dolinay Tamas, Englert Joshua A., Choi Augustine M.K., Characterization of macroautophagic flux in vivo using a leupeptin-based assay, 10.4161/auto.7.6.15100
- UCHIYAMA Yasuo, Autophagic Cell Death and Its Execution by Lysosomal Cathepsins., 10.1679/aohc.64.233
- Biolo G, Am J Physiol, 268, E75 (1995)
- Svanberg Elisabeth, Moller-Loswick Ann-Charlotte, Matthews Dwight E, Korner Ulla, Andersson Marianne, Lundholm Kent, The role of glucose, long-chain triglycerides and amino acids for promotion of amino acid balance across peripheral tissues in man, 10.1046/j.1365-2281.1999.00183.x
- Volpi E, Ferrando A A, Yeckel C W, Tipton K D, Wolfe R R, Exogenous amino acids stimulate net muscle protein synthesis in the elderly., 10.1172/jci939
- Denne SC, Am J Physiol, 261, E809 (1991)
- Fukagawa NK, Am J Physiol, 256, E288 (1989)
- Gelfand R A, Barrett E J, Effect of physiologic hyperinsulinemia on skeletal muscle protein synthesis and breakdown in man., 10.1172/jci113033
- Mortimore G E, Poso A R, Intracellular Protein Catabolism and its Control During Nutrient Deprivation and Supply, 10.1146/annurev.nu.07.070187.002543
- Pozefsky Thomas, Felig Philip, Tobin Jordan D., Soeldner J. Stuart, Cahill George F., Amino acid balance across tissues of the forearm in postabsorptive man. Effects of insulin at two dose levels, 10.1172/jci106193
- Weber S. M., Levitz S. M., Chloroquine Interferes with Lipopolysaccharide-Induced TNF- Gene Expression by a Nonlysosomotropic Mechanism, 10.4049/jimmunol.165.3.1534
- Paludan C., Endogenous MHC Class II Processing of a Viral Nuclear Antigen After Autophagy, 10.1126/science.1104904
- Chotechuang Nattida, Azzout-Marniche Dalila, Bos Cécile, Chaumontet Catherine, Gaudichon Claire, Tomé Daniel, Down-regulation of the ubiquitin–proteasome proteolysis system by amino acids and insulin involves the adenosine monophosphate-activated protein kinase and mammalian target of rapamycin pathways in rat hepatocytes, 10.1007/s00726-010-0765-2
- Bedford Lynn, Lowe James, Dick Lawrence R., Mayer R. John, Brownell James E., Ubiquitin-like protein conjugation and the ubiquitin–proteasome system as drug targets, 10.1038/nrd3321
- Akagi Yoshitaka, Isaka Yoshitaka, Akagi Akiko, Ikawa Masahito, Takenaka Masaru, Moriyama Toshiki, Yamauchi Atsushi, Horio Masaru, Ueda Naohiko, Okabe Masaru, Imai Enyu, Transcriptional activation of a hybrid promoter composed of cytomegalovirus enhancer and β-actin/β-globin gene in glomerular epithelial cells in vivo, 10.1038/ki.1997.172
- Kimura T., Takabatake Y., Takahashi A., Kaimori J.-y., Matsui I., Namba T., Kitamura H., Niimura F., Matsusaka T., Soga T., Rakugi H., Isaka Y., Autophagy Protects the Proximal Tubule from Degeneration and Acute Ischemic Injury, 10.1681/asn.2010070705
- Hartleben Björn, Gödel Markus, Meyer-Schwesinger Catherine, Liu Shuya, Ulrich Theresa, Köbler Sven, Wiech Thorsten, Grahammer Florian, Arnold Sebastian J., Lindenmeyer Maja T., Cohen Clemens D., Pavenstädt Hermann, Kerjaschki Dontscho, Mizushima Noboru, Shaw Andrey S., Walz Gerd, Huber Tobias B., Autophagy influences glomerular disease susceptibility and maintains podocyte homeostasis in aging mice, 10.1172/jci39492
- Berry Deborah L., Baehrecke Eric H., Growth Arrest and Autophagy Are Required for Salivary Gland Cell Degradation in Drosophila, 10.1016/j.cell.2007.10.048
- Aits Sonja, Gustafsson Lotta, Hallgren Oskar, Brest Patrick, Gustafsson Mattias, Trulsson Maria, Mossberg Ann-Kristin, Simon Hans-Uwe, Mograbi Baharia, Svanborg Catharina, HAMLET (human α-lactalbumin made lethal to tumor cells) triggers autophagic tumor cell death, 10.1002/ijc.24076
- Koike Masato, Shibata Masahiro, Tadakoshi Masao, Gotoh Kunihito, Komatsu Masaaki, Waguri Satoshi, Kawahara Nobutaka, Kuida Keisuke, Nagata Shigekazu, Kominami Eiki, Tanaka Keiji, Uchiyama Yasuo, Inhibition of Autophagy Prevents Hippocampal Pyramidal Neuron Death after Hypoxic-Ischemic Injury, 10.2353/ajpath.2008.070876
- Hou Y.C. Claire, Hannigan Adrienne M., Gorski Sharon M., An executioner caspase regulates autophagy, 10.4161/auto.5.4.8061
- Nezis Ioannis P., Shravage Bhupendra V., Sagona Antonia P., Lamark Trond, Bjørkøy Geir, Johansen Terje, Rusten Tor Erik, Brech Andreas, Baehrecke Eric H., Stenmark Harald, Autophagic degradation of dBruce controls DNA fragmentation in nurse cells during lateDrosophila melanogasteroogenesis, 10.1083/jcb.201002035
- Piras Antonio, Gianetto Daniele, Conte Daniele, Bosone Alex, Vercelli Alessandro, Activation of Autophagy in a Rat Model of Retinal Ischemia following High Intraocular Pressure, 10.1371/journal.pone.0022514
- Schwarze Per E., Seglen Per O., Reduced autophagic activity, improved protein balance and enhanced in vitro survival of hepatocytes isolated from carcinogen-treated rats, 10.1016/0014-4827(85)90148-x
- Russo R, Berliocchi L, Adornetto A, Varano G P, Cavaliere F, Nucci C, Rotiroti D, Morrone L A, Bagetta G, Corasaniti M T, Calpain-mediated cleavage of Beclin-1 and autophagy deregulation following retinal ischemic injury in vivo, 10.1038/cddis.2011.29
- Denton D, Nicolson S, Kumar S, Cell death by autophagy: facts and apparent artefacts, 10.1038/cdd.2011.146
- Beaulaton Jacques, Lockshin Richard A., Ultrastructural study of the normal degeneration of the intersegmental muscles ofAntheraea polyphemus andManduca sexta (Insecta, lepidoptera) with particular reference to cellular autophagy, 10.1002/jmor.1051540104
- Clarke PeterG.H., Developmental cell death: morphological diversity and multiple mechanisms, 10.1007/bf00174615
- Galluzzi L, Vitale I, Abrams J M, Alnemri E S, Baehrecke E H, Blagosklonny M V, Dawson T M, Dawson V L, El-Deiry W S, Fulda S, Gottlieb E, Green D R, Hengartner M O, Kepp O, Knight R A, Kumar S, Lipton S A, Lu X, Madeo F, Malorni W, Mehlen P, Nuñez G, Peter M E, Piacentini M, Rubinsztein D C, Shi Y, Simon H-U, Vandenabeele P, White E, Yuan J, Zhivotovsky B, Melino G, Kroemer G, Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012, 10.1038/cdd.2011.96
- Kroemer Guido, Levine Beth, Autophagic cell death: the story of a misnomer, 10.1038/nrm2529
- van Doorn W G, Beers E P, Dangl J L, Franklin-Tong V E, Gallois P, Hara-Nishimura I, Jones A M, Kawai-Yamada M, Lam E, Mundy J, Mur L A J, Petersen M, Smertenko A, Taliansky M, Van Breusegem F, Wolpert T, Woltering E, Zhivotovsky B, Bozhkov P V, Morphological classification of plant cell deaths, 10.1038/cdd.2011.36
- Giusti Corinne, Tresse Emilie, Luciani Marie-Françoise, Golstein Pierre, Autophagic cell death: Analysis in Dictyostelium, 10.1016/j.bbamcr.2008.12.005
- Luciani Marie-Françoise, Giusti Corinne, Harms Birthe, Oshima Yoshiteru, Kikuchi Haruhisa, Kubohara Yuzuru, Golstein Pierre, Atg1 allows second-signaled autophagic cell death in Dictyostelium, 10.4161/auto.7.5.14957
- Uchikawa Toru, Yamamoto Akitsugu, Inouye Kei, Origin and function of the stalk-cell vacuole in Dictyostelium, 10.1016/j.ydbio.2011.01.014
- Galluzzi L, Aaronson S A, Abrams J, Alnemri E S, Andrews D W, Baehrecke E H, Bazan N G, Blagosklonny M V, Blomgren K, Borner C, Bredesen D E, Brenner C, Castedo M, Cidlowski J A, Ciechanover A, Cohen G M, De Laurenzi V, De Maria R, Deshmukh M, Dynlacht B D, El-Deiry W S, Flavell R A, Fulda S, Garrido C, Golstein P, Gougeon M-L, Green D R, Gronemeyer H, Hajnóczky G, Hardwick J M, Hengartner M O, Ichijo H, Jäättelä M, Kepp O, Kimchi A, Klionsky D J, Knight R A, Kornbluth S, Kumar S, Levine B, Lipton S A, Lugli E, Madeo F, Malorni W, Marine J-CW, Martin S J, Medema J P, Mehlen P, Melino G, Moll U M, Morselli E, Nagata S, Nicholson D W, Nicotera P, Nuñez G, Oren M, Penninger J, Pervaiz S, Peter M E, Piacentini M, Prehn J H M, Puthalakath H, Rabinovich G A, Rizzuto R, Rodrigues C M P, Rubinsztein D C, Rudel T, Scorrano L, Simon H-U, Steller H, Tschopp J, Tsujimoto Y, Vandenabeele P, Vitale I, Vousden K H, Youle R J, Yuan J, Zhivotovsky B, Kroemer G, Guidelines for the use and interpretation of assays for monitoring cell death in higher eukaryotes, 10.1038/cdd.2009.44
- Guimarães Cinthya A., Benchimol Marlene, Amarante-Mendes Gustavo P., Linden Rafael, Alternative Programs of Cell Death in Developing Retinal Tissue, 10.1074/jbc.m306547200
- Lossi Laura, Gambino Graziana, Mioletti Silvia, Merighi Adalberto, In vivo analysis reveals different apoptotic pathways in pre- and postmigratory cerebellar granule cells of rabbit, 10.1002/neu.20032
- Lossi Laura, Alasia Silvia, Salio Chiara, Merighi Adalberto, Cell death and proliferation in acute slices and organotypic cultures of mammalian CNS, 10.1016/j.pneurobio.2009.01.002
- Thorburn Andrew, I think autophagy controls the death of my cells: What do I do to get my paper published?, 10.4161/auto.7.5.14797
- Kaushik S., Bandyopadhyay U., Sridhar S., Kiffin R., Martinez-Vicente M., Kon M., Orenstein S. J., Wong E., Cuervo A. M., Chaperone-mediated autophagy at a glance, 10.1242/jcs.073874
- Arias Esperanza, Cuervo Ana Maria, Chaperone-mediated autophagy in protein quality control, 10.1016/j.ceb.2010.10.009
- Kaushik Susmita, Cuervo Ana Maria, Chapter 19 Methods to Monitor Chaperone‐Mediated Autophagy, Methods in Enzymology (2009) ISBN:9780123745477 p.297-324, 10.1016/s0076-6879(08)03619-7
- Fred Dice J., Peptide sequences that target cytosolic proteins for lysosomal proteolysis, 10.1016/0968-0004(90)90019-8
- Cuervo A. M., Dice J. F., A Receptor for the Selective Uptake and Degradation of Proteins by Lysosomes, 10.1126/science.273.5274.501
- Cuervo AM, J Cell Sci, 113, 4441 (2000)
- Finn Patrick F., Mesires Nicholas T., Vine Michaela, Dice J. Fred, Effects of Small Molecules on Chaperone-Mediated Autophagy, 10.4161/auto.1.3.2000
- Bandyopadhyay U., Kaushik S., Varticovski L., Cuervo A. M., The Chaperone-Mediated Autophagy Receptor Organizes in Dynamic Protein Complexes at the Lysosomal Membrane, 10.1128/mcb.02070-07
- Aniento F., Cytoplasmic dynein-dependent vesicular transport from early to late endosomes [published erratum appears in J Cell Biol 1994 Feb;124(3):397], 10.1083/jcb.123.6.1373
- Salvador N, J Biol Chem, 275, 27447 (2000)
- Koga Hiroshi, Martinez-Vicente Marta, Macian Fernando, Verkhusha Vladislav V., Cuervo Ana Maria, A photoconvertible fluorescent reporter to track chaperone-mediated autophagy, 10.1038/ncomms1393
- Sahu Ranjit, Kaushik Susmita, Clement Cristina C., Cannizzo Elvira S., Scharf Brian, Follenzi Antonia, Potolicchio Ilaria, Nieves Edward, Cuervo Ana Maria, Santambrogio Laura, Microautophagy of Cytosolic Proteins by Late Endosomes, 10.1016/j.devcel.2010.12.003
- Arndt Verena, Dick Nikolaus, Tawo Riga, Dreiseidler Michael, Wenzel Daniela, Hesse Michael, Fürst Dieter O., Saftig Paul, Saint Robert, Fleischmann Bernd K., Hoch Michael, Höhfeld Jörg, Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance, 10.1016/j.cub.2009.11.022
- Niemann Axel, Baltes Jennifer, Elsässer Hans-Peter, Fluorescence Properties and Staining Behavior of Monodansylpentane, a Structural Homologue of the Lysosomotropic Agent Monodansylcadaverine, 10.1177/002215540104900205
- Paglin S, Cancer Res, 61, 439 (2001)
- Florez-McClure M. L., The p75 Neurotrophin Receptor Can Induce Autophagy and Death of Cerebellar Purkinje Neurons, 10.1523/jneurosci.5744-03.2004
- Moriyasu Yuji, Hattori Masaki, Jauh Guang-Yuh, Rogers John C., Alpha Tonoplast Intrinsic Protein is Specifically Associated with Vacuole Membrane Involved in an Autophagic Process, 10.1093/pcp/pcg100
- Biederbick A, Eur J Cell Biol, 66, 3 (1995)
- Høyer-Hansen M, Bastholm L, Mathiasen I S, Elling F, Jäättelä M, Vitamin D analog EB1089 triggers dramatic lysosomal changes and Beclin 1-mediated autophagic cell death, 10.1038/sj.cdd.4401651
- Munafó DB, J Cell Sci, 114, 3619 (2001)
- Gutierrez M. G., Rab7 is required for the normal progression of the autophagic pathway in mammalian cells, 10.1242/jcs.01114
- Freundt Eric C, Czapiga Meggan, Lenardo Michael J, Photoconversion of Lysotracker Red to a green fluorescent molecule, 10.1038/cr.2007.80
- Rubinsztein David C., Gestwicki Jason E., Murphy Leon O., Klionsky Daniel J., Potential therapeutic applications of autophagy, 10.1038/nrd2272
- Funderburk Sarah F., Wang Qing Jun, Yue Zhenyu, The Beclin 1–VPS34 complex – at the crossroads of autophagy and beyond, 10.1016/j.tcb.2010.03.002
- Levine Beth, Sinha Sangita C., Kroemer Guido, Bcl-2 family members: Dual regulators of apoptosis and autophagy, 10.4161/auto.6260
- Simonsen Anne, Tooze Sharon A., Coordination of membrane events during autophagy by multiple class III PI3-kinase complexes, 10.1083/jcb.200907014
- Pyo Jong-Ok, Jang Mi-Hee, Kwon Yun-Kyung, Lee Ho-June, Jun Joon-IL, Woo Ha-Na, Cho Dong-Hyung, Choi BoYoun, Lee Heuiran, Kim Joo-Hang, Mizushima Noboru, Oshumi Yoshinori, Jung Yong-Keun, Essential Roles of Atg5 and FADD in Autophagic Cell Death : DISSECTION OF AUTOPHAGIC CELL DEATH INTO VACUOLE FORMATION AND CELL DEATH, 10.1074/jbc.m413934200
- Petiot A., Ogier-Denis E., Blommaart E. F. C., Meijer A. J., Codogno P., Distinct Classes of Phosphatidylinositol 3'-Kinases Are Involved in Signaling Pathways That Control Macroautophagy in HT-29 Cells, 10.1074/jbc.275.2.992
- Harris James, Hartman Michelle, Roche Caitrionna, Zeng Shijuan G., O'Shea Amy, Sharp Fiona A., Lambe Eimear M., Creagh Emma M., Golenbock Douglas T., Tschopp Jurg, Kornfeld Hardy, Fitzgerald Katherine A., Lavelle Ed C., Autophagy Controls IL-1β Secretion by Targeting Pro-IL-1β for Degradation, 10.1074/jbc.m110.202911
- Crişan Tania O., Plantinga Theo S., van de Veerdonk Frank L., Farcaş Marius F., Stoffels Monique, Kullberg Bart-Jan, van der Meer Jos W. M., Joosten Leo A. B., Netea Mihai G., Inflammasome-Independent Modulation of Cytokine Response by Autophagy in Human Cells, 10.1371/journal.pone.0018666
- Kleinnijenhuis Johanneke, Oosting Marije, Plantinga Theo S., van der Meer Jos W.M., Joosten Leo A.B., Crevel Reinout V., Netea Mihai G., Autophagy modulates the Mycobacterium tuberculosis-induced cytokine response : Autophagy and Mycobacterium tuberculosis, 10.1111/j.1365-2567.2011.03494.x
- Cantino D, Boll Soc Ital Biol Sper, 55, 1884 (1979)
- Kovács János, Morphometric study of the effect of leupeptin, vinblastine, estron acetate and cycloheximide on the autophagic vacuole-lysosomal compartments in mouse seminal vesicle cells, 10.1007/bf02890372
- Papadopoulos T, Lab Invest, 54, 100 (1986)
- Rumpelt H. J., Albring M., Thoenes W., Prevention of D-galactosamine-induced hepatocellular autophagocytosis by cycloheximide, 10.1007/bf02894074
- Rumpelt HJ, Am J Pathol, 91, 49 (1978)
- Kovács Attila L., Kovács János, Autophagocytosis in mouse seminal vesicle cells in vitro : Temperature dependence and effects of vinblastine and inhibitors of protein synthesis, 10.1007/bf02889018
- Rodemann H. Peter, Dittmann Klaus, Toulany Mahmoud, Radiation-induced EGFR-signaling and control of DNA-damage repair, 10.1080/09553000701769970
- Chaachouay Hassan, Ohneseit Petra, Toulany Mahmoud, Kehlbach Rainer, Multhoff Gabriele, Rodemann H. Peter, Autophagy contributes to resistance of tumor cells to ionizing radiation, 10.1016/j.radonc.2011.06.002
- Apel A., Herr I., Schwarz H., Rodemann H. P., Mayer A., Blocked Autophagy Sensitizes Resistant Carcinoma Cells to Radiation Therapy, 10.1158/0008-5472.can-07-0562
- Eng C. H., Yu K., Lucas J., White E., Abraham R. T., Ammonia Derived from Glutaminolysis Is a Diffusible Regulator of Autophagy, 10.1126/scisignal.2000911
- Seglen PO, Mol Pharmacol, 18, 468 (1980)
- Cheong H., Lindsten T., Wu J., Lu C., Thompson C. B., Ammonia-induced autophagy is independent of ULK1/ULK2 kinases, 10.1073/pnas.1107969108
- Wei Pengfei, Zhang Li, Lu Yang, Man Na, Wen Longping, C60(Nd) nanoparticles enhance chemotherapeutic susceptibility of cancer cells by modulation of autophagy, 10.1088/0957-4484/21/49/495101
- Lee Do Hee, Goldberg Alfred L, Proteasome inhibitors: valuable new tools for cell biologists, 10.1016/s0962-8924(98)01346-4
- Mehdi Shujaath, Cell-penetrating inhibitors of calpain, 10.1016/0968-0004(91)90058-4
- HOLEN Ingunn, GORDON Paul B., SEGLEN Per O., Inhibition of hepatocytic autophagy by okadaic acid and other protein phosphatase inhibitors, 10.1111/j.1432-1033.1993.tb18013.x
- Sasaki K, Murata M, Yasumoto T, Mieskes G, Takai A, Affinity of okadaic acid to type-1 and type-2A protein phosphatases is markedly reduced by oxidation of its 27-hydroxyl group, 10.1042/bj2980259
- Robinson D. G., Albrecht S., Moriysu Y., The V-ATPase inhibitors concanamycin A and bafilomycin A lead to Golgi swelling in tobacco BY-2 cells, 10.1007/s00709-004-0070-6
- Wu Ya Chun, Wu William Ka Kei, Li Youming, Yu Le, Li Zhi Jie, Wong Clover Ching Man, Li Hai Tao, Sung Joseph Jao Yiu, Cho Chi Hin, Inhibition of macroautophagy by bafilomycin A1 lowers proliferation and induces apoptosis in colon cancer cells, 10.1016/j.bbrc.2009.03.051
- Yamamoto Akitsugu, Tagawa Yoshihiro, Yoshimori Tamotsu, Moriyama Yoshinori, Masaki Ryuichi, Tashiro Yutaka, Bafilomycin A1 Prevents Maturation of Autophagic Vacuoles by Inhibiting Fusion between Autophagosomes and Lysosomes in Rat Hepatoma Cell Line, H-4-II-E Cells., 10.1247/csf.23.33
- Ostenfeld Marie Stampe, Høyer-Hansen Maria, Bastholm Lone, Fehrenbacher Nicole, Olsen Ole Dines, Groth-Pedersen Line, Puustinen Pietri, Kirkegaard-Sørensen Thomas, Nylandsted Jesper, Farkas Thomas, Jäättelä Marja, Anti-cancer agent siramesine is a lysosomotropic detergent that induces cytoprotective autophagosome accumulation, 10.4161/auto.5774
- Matsuoka K., A Vacuolar-Type H+-ATPase in a Nonvacuolar Organelle Is Required for the Sorting of Soluble Vacuolar Protein Precursors in Tobacco Cells, 10.1105/tpc.9.4.533
- Arstila A.U., Nuuja I.J.M., Trump B.F., Studies on cellular autophagocytosis, 10.1016/0014-4827(74)90477-7
- Hirsimäki Y., Arstila A.U., Trump B.F., Autophagocytosis: In vitro induction by microtubule poisons, 10.1016/0014-4827(75)90630-8
- Kominami E, J Biol Chem, 258, 6093 (1983)
- Réz G, J Submicrosc Cytol Pathol, 22, 529 (1990)
- Oliva Olivia, Réz Gábor, Pálfia Zsolt, Fellinger Erzsébet, Dynamics of vinblastine-induced autophagocytosis in murine pancreatic acinar cells: Influence of cycloheximide post-treatments, 10.1016/0014-4800(92)90025-7
- von Haefen Clarissa, Mei Wei, Menk Mario, Klemz Roman, Jones Ansgar, Wernecke Klaus-Dieter, Spies Claudia D., Ethanol Changes Gene Expression of Transcription Factors and Cytokine Production of CD4+ T-Cell Subsets in PBMCs Stimulated With LPS : ETHANOL IMPAIRS T-HELPER CELL SUBSETS, 10.1111/j.1530-0277.2010.01376.x
- Krüger Ulrike, Wang Yipeng, Kumar Satish, Mandelkow Eva-Maria, Autophagic degradation of tau in primary neurons and its enhancement by trehalose, 10.1016/j.neurobiolaging.2011.11.009
- Williams Andrea, Sarkar Sovan, Cuddon Paul, Ttofi Evangelia K, Saiki Shinji, Siddiqi Farah H, Jahreiss Luca, Fleming Angeleen, Pask Dean, Goldsmith Paul, O'Kane Cahir J, Floto Rodrigo Andres, Rubinsztein David C, Novel targets for Huntington's disease in an mTOR-independent autophagy pathway, 10.1038/nchembio.79
- Palomo G. M., Cerrato T., Gargini R., Diaz-Nido J., Silencing of frataxin gene expression triggers p53-dependent apoptosis in human neuron-like cells, 10.1093/hmg/ddr187
- Feldman Morris E, Apsel Beth, Uotila Aino, Loewith Robbie, Knight Zachary A, Ruggero Davide, Shokat Kevan M, Active-Site Inhibitors of mTOR Target Rapamycin-Resistant Outputs of mTORC1 and mTORC2, 10.1371/journal.pbio.1000038
- Fleming Angeleen, Noda Takeshi, Yoshimori Tamotsu, Rubinsztein David C, Chemical modulators of autophagy as biological probes and potential therapeutics, 10.1038/nchembio.500
- Yu K., Toral-Barza L., Shi C., Zhang W.-G., Lucas J., Shor B., Kim J., Verheijen J., Curran K., Malwitz D. J., Cole D. C., Ellingboe J., Ayral-Kaloustian S., Mansour T. S., Gibbons J. J., Abraham R. T., Nowak P., Zask A., Biochemical, Cellular, and In vivo Activity of Novel ATP-Competitive and Selective Inhibitors of the Mammalian Target of Rapamycin, 10.1158/0008-5472.can-09-0299
- Chresta C. M., Davies B. R., Hickson I., Harding T., Cosulich S., Critchlow S. E., Vincent J. P., Ellston R., Jones D., Sini P., James D., Howard Z., Dudley P., Hughes G., Smith L., Maguire S., Hummersone M., Malagu K., Menear K., Jenkins R., Jacobsen M., Smith G. C.M., Guichard S., Pass M., AZD8055 Is a Potent, Selective, and Orally Bioavailable ATP-Competitive Mammalian Target of Rapamycin Kinase Inhibitor with In vitro and In vivo Antitumor Activity, 10.1158/0008-5472.can-09-1751
- Roscic Ana, Baldo Barbara, Crochemore Christophe, Marcellin David, Paganetti Paolo, Induction of autophagy with catalytic mTOR inhibitors reduces huntingtin aggregates in a neuronal cell model : Catalytic mTOR inhibitors reduces Htt aggregates, 10.1111/j.1471-4159.2011.07435.x
- Fan Q.-W., Cheng C., Hackett C., Feldman M., Houseman B. T., Nicolaides T., Haas-Kogan D., James C. D., Oakes S. A., Debnath J., Shokat K. M., Weiss W. A., Akt and Autophagy Cooperate to Promote Survival of Drug-Resistant Glioma, 10.1126/scisignal.2001017
- Sakagami Hiroshi, Kawase Masami, Wakabayashi Hidetsugu, Kurihara Teruo, Factors that Affect the Type of Cell Death Induced by Chemicals, 10.4161/auto.4594
- Doelling J. H., The APG8/12-activating Enzyme APG7 Is Required for Proper Nutrient Recycling and Senescence in Arabidopsis thaliana, 10.1074/jbc.m204630200
- Fimia GM, Nature, 447, 1121 (2007)
- Kuma Akiko, Hatano Masahiko, Matsui Makoto, Yamamoto Akitsugu, Nakaya Haruaki, Yoshimori Tamotsu, Ohsumi Yoshinori, Tokuhisa Takeshi, Mizushima Noboru, The role of autophagy during the early neonatal starvation period, 10.1038/nature03029
- Zhu Hua, Wu Hao, Liu Xiuping, Li Biao, Chen Yun, Ren Xingcong, Liu Chang-Gong, Yang Jin-Ming, Regulation of autophagy by a beclin 1-targeted microRNA, miR-30a, in cancer cells, 10.4161/auto.9064
- Hamacher-Brady A, Brady N R, Logue S E, Sayen M R, Jinno M, Kirshenbaum L A, Gottlieb R A, Gustafsson Å B, Response to myocardial ischemia/reperfusion injury involves Bnip3 and autophagy, 10.1038/sj.cdd.4401936
- Yang Ling, Li Ping, Fu Suneng, Calay Ediz S., Hotamisligil Gökhan S., Defective Hepatic Autophagy in Obesity Promotes ER Stress and Causes Insulin Resistance, 10.1016/j.cmet.2010.04.005
- Poeck Hendrik, Besch Robert, Maihoefer Cornelius, Renn Marcel, Tormo Damia, Morskaya Svetlana Shulga, Kirschnek Susanne, Gaffal Evelyn, Landsberg Jennifer, Hellmuth Johannes, Schmidt Andreas, Anz David, Bscheider Michael, Schwerd Tobias, Berking Carola, Bourquin Carole, Kalinke Ulrich, Kremmer Elisabeth, Kato Hiroki, Akira Shizuo, Meyers Rachel, Häcker Georg, Neuenhahn Michael, Busch Dirk, Ruland Jürgen, Rothenfusser Simon, Prinz Marco, Hornung Veit, Endres Stefan, Tüting Thomas, Hartmann Gunther, 5′-triphosphate-siRNA: turning gene silencing and Rig-I activation against melanoma, 10.1038/nm.1887
- Delgado Mónica A, Elmaoued Rasha A, Davis Alexander S, Kyei George, Deretic Vojo, Toll-like receptors control autophagy, 10.1038/emboj.2008.31
- Pua Heather H., Dzhagalov Ivan, Chuck Mariana, Mizushima Noboru, He You-Wen, A critical role for the autophagy gene Atg5 in T cell survival and proliferation, 10.1084/jem.20061303
- Miller Brian C., Zhao Zijiang, Stephenson Linda M., Cadwell Ken, Pua Heather H., Lee Heung Kyu, Mizushima Noboru, Iwasaki Akiko, He You-Wen, Swat Wojciech, Virgin, IV Herbert W., The autophagy geneATG5plays an essential role in B lymphocyte development, 10.4161/auto.5474
- Lee Jong-Soo, Li Qinglin, Lee June-Yong, Lee Sun-Hwa, Jeong Joseph H., Lee Hye-Ra, Chang Heesoon, Zhou Fu-Chun, Gao Shou-Jiang, Liang Chengyu, Jung Jae U., FLIP-mediated autophagy regulation in cell death control, 10.1038/ncb1980
- Kyei George B., Dinkins Christina, Davis Alexander S., Roberts Esteban, Singh Sudha B., Dong Chunsheng, Wu Li, Kominami Eiki, Ueno Takashi, Yamamoto Akitsugu, Federico Maurizio, Panganiban Antonito, Vergne Isabelle, Deretic Vojo, Autophagy pathway intersects with HIV-1 biosynthesis and regulates viral yields in macrophages, 10.1083/jcb.200903070
- Kimball Scot R., Siegfried Brett A., Jefferson Leonard S., Glucagon Represses Signaling through the Mammalian Target of Rapamycin in Rat Liver by Activating AMP-activated Protein Kinase, 10.1074/jbc.m410755200
- Blommaart Edward F. C., Luiken Joost J. F. P., Blommaart Pietjan J. E., van Woerkom George M., Meijer Alfred J., Phosphorylation of Ribosomal Protein S6 Is Inhibitory for Autophagy in Isolated Rat Hepatocytes, 10.1074/jbc.270.5.2320
- Klionsky Daniel J., Meijer Alfred J., Codogno Patrice, Neufeld Thomas P., Scott Ryan C., Autophagy and p70S6 Kinase, 10.4161/auto.1.1.1536
- Noda Takeshi, Ohsumi Yoshinori, Tor, a Phosphatidylinositol Kinase Homologue, Controls Autophagy in Yeast, 10.1074/jbc.273.7.3963
- Sarkar Sovan, Floto R. Andres, Berger Zdenek, Imarisio Sara, Cordenier Axelle, Pasco Matthieu, Cook Lynnette J., Rubinsztein David C., Lithium induces autophagy by inhibiting inositol monophosphatase, 10.1083/jcb.200504035
- Høyer-Hansen Maria, Bastholm Lone, Szyniarowski Piotr, Campanella Michelangelo, Szabadkai György, Farkas Thomas, Bianchi Katiuscia, Fehrenbacher Nicole, Elling Folmer, Rizzuto Rosario, Mathiasen Ida Stenfeldt, Jäättelä Marja, Control of Macroautophagy by Calcium, Calmodulin-Dependent Kinase Kinase-β, and Bcl-2, 10.1016/j.molcel.2006.12.009
- Furuya N, Liang XH, Levine B. Autophagy and cancer. In: Klionsky DJ, ed. Autophagy. Georgetown, TX: Landes Bioscience, 2004:241-55.
- de Medina Philippe, Paillasse Michael R., Ségala Gregory, Khallouki Farid, Brillouet Severine, Dalenc Florence, Courbon Frederic, Record Michel, Poirot Marc, Silvente-Poirot Sandrine, Importance of cholesterol and oxysterols metabolism in the pharmacology of tamoxifen and other AEBS ligands, 10.1016/j.chemphyslip.2011.05.005
- de Medina P, Payré B, Boubekeur N, Bertrand-Michel J, Tercé F, Silvente-Poirot S, Poirot M, Ligands of the antiestrogen-binding site induce active cell death and autophagy in human breast cancer cells through the modulation of cholesterol metabolism, 10.1038/cdd.2009.62
- Sarkar Sovan, Perlstein Ethan O, Imarisio Sara, Pineau Sandra, Cordenier Axelle, Maglathlin Rebecca L, Webster John A, Lewis Timothy A, O'Kane Cahir J, Schreiber Stuart L, Rubinsztein David C, Small molecules enhance autophagy and reduce toxicity in Huntington's disease models, 10.1038/nchembio883
- Zhang L., Yu J., Pan H., Hu P., Hao Y., Cai W., Zhu H., Yu A. D., Xie X., Ma D., Yuan J., Small molecule regulators of autophagy identified by an image-based high-throughput screen, 10.1073/pnas.0709695104
- Cárdenas César, Miller Russell A., Smith Ian, Bui Thi, Molgó Jordi, Müller Marioly, Vais Horia, Cheung King-Ho, Yang Jun, Parker Ian, Thompson Craig B., Birnbaum Morris J., Hallows Kenneth R., Foskett J. Kevin, Essential Regulation of Cell Bioenergetics by Constitutive InsP3 Receptor Ca2+ Transfer to Mitochondria, 10.1016/j.cell.2010.06.007
- Vicencio J M, Ortiz C, Criollo A, Jones A W E, Kepp O, Galluzzi L, Joza N, Vitale I, Morselli E, Tailler M, Castedo M, Maiuri M C, Molgó J, Szabadkai G, Lavandero S, Kroemer G, The inositol 1,4,5-trisphosphate receptor regulates autophagy through its interaction with Beclin 1, 10.1038/cdd.2009.34
- Dayan Frédéric, Bilton Rebecca L., Laferrière Julie, Trottier Eric, Roux Danièle, Pouyssegur Jacques, Mazure Nathalie. M., Activation of HIF-1α in exponentially growing cells via hypoxic stimulation is independent of the Akt/mTOR pathway, 10.1002/jcp.21584
- Bellot G., Garcia-Medina R., Gounon P., Chiche J., Roux D., Pouyssegur J., Mazure N. M., Hypoxia-Induced Autophagy Is Mediated through Hypoxia-Inducible Factor Induction of BNIP3 and BNIP3L via Their BH3 Domains, 10.1128/mcb.00166-09
- Yamashita Shun-ichi, Yurimoto Hiroya, Murakami Dai, Yoshikawa Mari, Oku Masahide, Sakai Yasuyoshi, Lag-phase autophagy in the methylotrophic yeastPichia pastoris, 10.1111/j.1365-2443.2009.01316.x
- van Zutphen Tim, Baerends Richard JS, Susanna Kim A, de Jong Anne, Kuipers Oscar P, Veenhuis Marten, van der Klei Ida J, Adaptation of Hansenula polymorpha to methanol: a transcriptome analysis, 10.1186/1471-2164-11-1
- Inoue Yuko, Suzuki Takao, Hattori Masaki, Yoshimoto Kohki, Ohsumi Yoshinori, Moriyasu Yuji, AtATG Genes, Homologs of Yeast Autophagy Genes, are Involved in Constitutive Autophagy in Arabidopsis Root Tip Cells , 10.1093/pcp/pcl031
- Yano Kanako, Suzuki Takao, Moriyasu Yuji, Constitutive Autophagy in Plant Root Cells, 10.4161/auto.4158
- Gordon PB, Biochem Soc Symp, 55, 129 (1989)
- Poli A, J Cell Sci, 48, 1 (1981)
- Schliess Freimut, Reissmann Regina, Reinehr Roland, vom Dahl Stephan, Häussinger Dieter, Involvement of Integrins and Src in Insulin Signaling toward Autophagic Proteolysis in Rat Liver, 10.1074/jbc.m313901200
- vom DAHL Stephan, DOMBROWSKI Frank, SCHMITT Marcus, SCHLIESS Freimut, PFEIFER Ulrich, HÄUSSINGER Dieter, Cell hydration controls autophagosome formation in rat liver in a microtubule-dependent way downstream from p38MAPK activation, 10.1042/0264-6021:3540031
- vom Dahl S, Stoll B, Gerok W, Häussinger D, Inhibition of proteolysis by cell swelling in the liver requires intact microtubular structures, 10.1042/bj3080529
- Kovacs Attila Lajos, Zhang Hong, Role of autophagy inCaenorhabditis elegans, 10.1016/j.febslet.2010.02.002
- Zhang Yuxia, Yan Libo, Zhou Zhi, Yang Peiguo, Tian E., Zhang Kai, Zhao Yu, Li Zhipeng, Song Bing, Han Jinghua, Miao Long, Zhang Hong, SEPA-1 Mediates the Specific Recognition and Degradation of P Granule Components by Autophagy in C. elegans, 10.1016/j.cell.2008.12.022
- Morselli E, Maiuri M C, Markaki M, Megalou E, Pasparaki A, Palikaras K, Criollo A, Galluzzi L, Malik S A, Vitale I, Michaud M, Madeo F, Tavernarakis N, Kroemer G, Caloric restriction and resveratrol promote longevity through the Sirtuin-1-dependent induction of autophagy, 10.1038/cddis.2009.8
- Gosai Sager J., Kwak Joon Hyeok, Luke Cliff J., Long Olivia S., King Dale E., Kovatch Kevin J., Johnston Paul A., Shun Tong Ying, Lazo John S., Perlmutter David H., Silverman Gary A., Pak Stephen C., Automated High-Content Live Animal Drug Screening Using C. elegans Expressing the Aggregation Prone Serpin α1-antitrypsin Z, 10.1371/journal.pone.0015460
- Alberti Adriana, Michelet Xavier, Djeddi Abderazak, Legouis Renaud, The autophagosomal protein LGG-2 acts synergistically with LGG-1 in dauer formation and longevity in C. elegans, 10.4161/auto.6.5.12252
- Kang C., You Y.-j., Avery L., Dual roles of autophagy in the survival of Caenorhabditis elegans during starvation, 10.1101/gad.1573107
- Willig Katrin I, Kellner Robert R, Medda Rebecca, Hein Birka, Jakobs Stefan, Hell Stefan W, Nanoscale resolution in GFP-based microscopy, 10.1038/nmeth922
- Huang Bo, Bates Mark, Zhuang Xiaowei, Super-Resolution Fluorescence Microscopy, 10.1146/annurev.biochem.77.061906.092014
- Alers Sebastian, Löffler Antje S., Paasch Florian, Dieterle Alexandra M., Keppeler Hildegard, Lauber Kirsten, Campbell David G, Fehrenbacher Birgit, Schaller Martin, Wesselborg Sebastian, Stork Björn, Atg13 and FIP200 act independently of Ulk1 and Ulk2 in autophagy induction, 10.4161/auto.7.12.18027
- Brown William R. A., Hubbard Simon J., Tickle Cheryll, Wilson Stuart A., The chicken as a model for large-scale analysis of vertebrate gene function, 10.1038/nrg998
- Baba Timothy W., Giroir Brett P., Humphries Eric H., Cell lines derived from avian lymphomas exhibit two distinct phenotypes, 10.1016/0042-6822(85)90312-5
- Shelly Spencer, Lukinova Nina, Bambina Shelly, Berman Allison, Cherry Sara, Autophagy Is an Essential Component of Drosophila Immunity against Vesicular Stomatitis Virus, 10.1016/j.immuni.2009.02.009
- Hou Ying-Chen Claire, Chittaranjan Suganthi, Barbosa Sharon González, McCall Kimberly, Gorski Sharon M., Effector caspase Dcp-1 and IAP protein Bruce regulate starvation-induced autophagy duringDrosophila melanogasteroogenesis, 10.1083/jcb.200712091
- Fouillet Antoine, Levet Clemence, Virgone Angelique, Robin Marion, Dourlen Pierre, Rieusset Jennifer, Belaidi Elise, Ovize Michel, Touret Monique, Nataf Serge, Mollereau Bertrand, ER stress inhibits neuronal death by promoting autophagy, 10.4161/auto.19716
- Josefsen Lone, Droce Aida, Sondergaard Teis Esben, Sørensen Jens Laurids, Bormann Jörg, Schäfer Wilhelm, Giese Henriette, Olsson Stefan, Autophagy provides nutrients for nonassimilating fungal structures and is necessary for plant colonization but not for infection in the necrotrophic plant pathogen Fusarium graminearum, 10.4161/auto.18705
- NADAL MARINA, GOLD SCOTT E., The autophagy genes atg8 and atg1 affect morphogenesis and pathogenicity in Ustilago maydis : Autophagy in U. maydis, the corn smut pathogen, 10.1111/j.1364-3703.2010.00620.x
- POLLACK J, HARRIS S, MARTEN M, Autophagy in filamentous fungi, 10.1016/j.fgb.2008.10.010
- Richie D. L., Fuller K. K., Fortwendel J., Miley M. D., McCarthy J. W., Feldmesser M., Rhodes J. C., Askew D. S., Unexpected Link between Metal Ion Deficiency and Autophagy in Aspergillus fumigatus, 10.1128/ec.00224-07
- Pinan-Lucarre B., Balguerie A., Clave C., Accelerated Cell Death in Podospora Autophagy Mutants, 10.1128/ec.4.11.1765-1774.2005
- Asakura M., Ninomiya S., Sugimoto M., Oku M., Yamashita S.-i., Okuno T., Sakai Y., Takano Y., Atg26-Mediated Pexophagy Is Required for Host Invasion by the Plant Pathogenic Fungus Colletotrichum orbiculare, 10.1105/tpc.108.060996
- Liu X.-H., Lu J.-P., Zhang L., Dong B., Min H., Lin F.-C., Involvement of a Magnaporthe grisea Serine/Threonine Kinase Gene, MgATG1, in Appressorium Turgor and Pathogenesis, 10.1128/ec.00011-07
- Nguyen Long Nam, Bormann Jörg, Le Giang Thi Thu, Stärkel Cornelia, Olsson Stefan, Nosanchuk Joshua D., Giese Henriette, Schäfer Wilhelm, Autophagy-related lipase FgATG15 of Fusarium graminearum is important for lipid turnover and plant infection, 10.1016/j.fgb.2010.11.004
- Deng Yi Zhen, Ramos‐Pamplona Marilou, Naqvi Naweed I., Chapter 20 Methods for Functional Analysis of Macroautophagy in Filamentous Fungi, Methods in Enzymology (2008) ISBN:9780123745484 p.295-310, 10.1016/s0076-6879(08)03220-5
- Berger B, Sociobiology, 45, 261 (2005)
- Silva-Zacarin E C M, Tomaino G A, Brocheto-Braga M R, Taboga S R, Silva de Moraes R L M, Programmed cell death in the larval salivary glands of Apis mellifera (Hymenoptera, Apidae), 10.1007/s12038-007-0031-2
- GREGORC A, PROGRAMMED CELL DEATH IN THE HONEY-BEE (APIS MELLIFERAL.) LARVAE MIDGUT, 10.1006/cbir.1997.0127
- Navajas M, Migeon A, Alaux C, Martin-Magniette ML, Robinson GE, Evans JD, Cros-Arteil S, Crauser D, Le Conte Y, Differential gene expression of the honey bee Apis mellifera associated with Varroa destructor infection, 10.1186/1471-2164-9-301
- Spruessel A, Biotechniques, 36, 1030 (2004)
- Espina Virginia, Edmiston Kirsten H., Heiby Michael, Pierobon Mariaelena, Sciro Manuela, Merritt Barbara, Banks Stacey, Deng Jianghong, VanMeter Amy J., Geho David H., Pastore Lucia, Sennesh Joel, Petricoin Emanuel F., Liotta Lance A., A Portrait of Tissue Phosphoprotein Stability in the Clinical Tissue Procurement Process, 10.1074/mcp.m700596-mcp200
- Barth Sandra, Glick Danielle, Macleod Kay F, Autophagy: assays and artifacts, 10.1002/path.2694
- Nixon Ralph A., Wegiel Jerzy, Kumar Asok, Yu Wai Haung, Peterhoff Corrinne, Cataldo Anne, Cuervo Ana Maria, Extensive Involvement of Autophagy in Alzheimer Disease: An Immuno-Electron Microscopy Study, 10.1093/jnen/64.2.113
- Vanhorebeek Ilse, Gunst Jan, Derde Sarah, Derese Inge, Boussemaere Magaly, Güiza Fabian, Martinet Wim, Timmermans Jean-Pierre, D'Hoore André, Wouters Pieter J., Van den Berghe Greet, Insufficient Activation of Autophagy Allows Cellular Damage to Accumulate in Critically Ill Patients, 10.1210/jc.2010-2563
- Nyman Elin, Brännmark Cecilia, Palmér Robert, Brugård Jan, Nyström Fredrik H., Strålfors Peter, Cedersund Gunnar, A Hierarchical Whole-body Modeling Approach Elucidates the Link betweenin VitroInsulin Signaling andin VivoGlucose Homeostasis, 10.1074/jbc.m110.188987
- Buzgariu Wanda, Chera Simona, Galliot Brigitte, Chapter Twenty‐Six Methods to Investigate Autophagy During Starvation and Regeneration in Hydra, Methods in Enzymology (2008) ISBN:9780123745484 p.409-437, 10.1016/s0076-6879(08)03226-6
- Chera Simona, Buzgariu Wanda, Ghila Luiza, Galliot Brigitte, Autophagy in Hydra: A response to starvation and stress in early animal evolution, 10.1016/j.bbamcr.2009.03.010
- Chera S., Silencing of the hydra serine protease inhibitor Kazal1 gene mimics the human SPINK1 pancreatic phenotype, 10.1242/jcs.02807
- Galliot Brigitte, Autophagy and Self-Preservation: A Step Ahead from Cell Plasticity?, 10.4161/auto.2706
- Galliot Brigitte, Miljkovic-Licina Marijana, de Rosa Renaud, Chera Simona, Hydra, a niche for cell and developmental plasticity, 10.1016/j.semcdb.2006.05.005
- Sala-Mercado J. A., Wider J., Reddy Undyala V. V., Jahania S., Yoo W., Mentzer R. M., Gottlieb R. A., Przyklenk K., Profound Cardioprotection With Chloramphenicol Succinate in the Swine Model of Myocardial Ischemia-Reperfusion Injury, 10.1161/circulationaha.109.928242
- Sobolewska Agnieszka, Motyl Tomasz, Gajewska Malgorzata, Role and regulation of autophagy in the development of acinar structures formed by bovine BME-UV1 mammary epithelial cells, 10.1016/j.ejcb.2011.06.007
- Motyl Tomasz, Gajewska Malgorzata, Zarzynska Joanna, Sobolewska Agnieszka, Gajkowska Barbara, Regulation of Autophagy in Bovine Mammary Epithelial Cells, 10.4161/auto.4491
- Sobolewska Agnieszka, Gajewska Malgorzata, Zarzyńska Joanna, Gajkowska Barbara, Motyl Tomasz, IGF-I, EGF, and sex steroids regulate autophagy in bovine mammary epithelial cells via the mTOR pathway, 10.1016/j.ejcb.2008.09.004
- Facey Caroline O. B., Lockshin Richard A., The execution phase of autophagy associated PCD during insect metamorphosis, 10.1007/s10495-010-0499-3
- Malagoli Davide, Abdalla Fabio C., Cao Yang, Feng Qili, Fujisaki Kozo, Gregorc Ales, Matsuo Tomohide, Nezis Ioannis P., Papassideri Issidora S., Sass Miklós, Silva-Zacarin Elaine C.M., Tettamanti Gianluca, Umemiya-Shirafuji Rika, Autophagy and its physiological relevance in arthropods: Current knowledge and perspectives, 10.4161/auto.6.5.11962
- Mpakou Vicky E., Nezis Ioannis P., Stravopodis Dimitrios J., Margaritis Lukas H., Papassideri Issidora S., Programmed cell death of the ovarian nurse cells during oogenesis of the silkmoth Bombyx mori, 10.1111/j.1440-169x.2006.00878.x
- Mpakou Vicky E., Nezis Ioannis P., Stravopodis Dimitrios J., Margaritis Lukas H., Papassideri Issidora S., Different modes of programmed cell death during oogenesis of the silkmothBombyx mori, 10.4161/auto.5205
- Sumithra Purushothaman, Britto Cathrin P., Krishnan Muthukalingan, Modes of cell death in the pupal perivisceral fat body tissue of the silkworm Bombyx mori L., 10.1007/s00441-009-0898-3
- Tettamanti Gianluca, Grimaldi Annalisa, Casartelli Morena, Ambrosetti Elena, Ponti Benedetta, Congiu Terenzio, Ferrarese Roberto, Rivas-Pena Maria Luisa, Pennacchio Francesco, Eguileor Magda de, Programmed cell death and stem cell differentiation are responsible for midgut replacement in Heliothis virescens during prepupal instar, 10.1007/s00441-007-0449-8
- Goncu Ebru, Parlak Osman, Some autophagic and apoptotic features of programmed cell death in the anterior silk glands of the silkworm,Bombyx mori, 10.4161/auto.6953
- Zhou S., Zhou Q., Liu Y., Wang S., Wen D., He Q., Wang W., Bendena W. G., Li S., TwoTorgenes in the silkwormBombyx mori : Two silkwormTorgenes, 10.1111/j.1365-2583.2010.01026.x
- Zhang Xuan, Hu Zhan-Ying, Li Wei-Fang, Li Qing-Rong, Deng Xiao-Juan, Yang Wan-Ying, Cao Yang, Zhou Cong-Zhao, Systematic cloning and analysis of autophagy-related genes from the silkworm Bombyx mori, 10.1186/1471-2199-10-50
- Li Qingrong, Deng Xiaojuan, Huang Zhijun, Zheng Sichun, Tettamanti Gianluca, Cao Yang, Feng Qili, Expression of autophagy-related genes in the anterior silk gland of the silkworm (Bombyx mori) during metamorphosis, 10.1139/z11-075
- Thomé Ralph G., Santos Helio B., Arantes Fabio P., Domingos Fabrício F.T., Bazzoli Nilo, Rizzo Elizete, Dual roles for autophagy during follicular atresia in fish ovary, 10.4161/auto.5.1.7302
- Santos H.B., Thomé R.G., Arantes F.P., Sato Y., Bazzoli N., Rizzo E., Ovarian follicular atresia is mediated by heterophagy, autophagy, and apoptosis in Prochilodus argenteus and Leporinus taeniatus (Teleostei: Characiformes), 10.1016/j.theriogenology.2008.06.091
- Santos H. B., Sato Y., Moro L., Bazzoli N., Rizzo E., Relationship among follicular apoptosis, integrin β1 and collagen type IV during early ovarian regression in the teleost Prochilodus argenteus after induced spawning, 10.1007/s00441-007-0540-1
- Santos H. B., Rizzo E., Bazzoli N., Sato Y., Moro L., Ovarian regression and apoptosis in the South American teleost Leporinus taeniatus Lutken (Characiformes, Anostomidae) from the Sao Francisco Basin, 10.1111/j.1095-8649.2005.00854.x
- Couve E., Schmachtenberg O., Autophagic Activity and Aging in Human Odontoblasts, 10.1177/0022034510393347
- González‐Estévez Cristina, Chapter Twenty‐Seven Autophagy in Freshwater Planarians, Methods in Enzymology (2008) ISBN:9780123745484 p.439-465, 10.1016/s0076-6879(08)03227-8
- Gonzalez-Estevez C., Felix D. A., Aboobaker A. A., Salo E., Gtdap-1 promotes autophagy and is required for planarian remodeling during regeneration and starvation, 10.1073/pnas.0703588104
- Toyooka Kiminori, Moriyasu Yuji, Goto Yumi, Takeuchi Masaki, Fukuda Hiroo, Matsuoka Ken, Protein Aggregates are Transported to Vacuoles by Macroautophagic Mechanism in Nutrient-Starved Plant Cells, 10.4161/auto.2.2.2366
- Svenning Steingrim, Lamark Trond, Krause Kirsten, Johansen Terje, Plant NBR1 is a selective autophagy substrate and a functional hybrid of the mammalian autophagic adapters NBR1 and p62/SQSTM1, 10.4161/auto.7.9.16389
- Zientara-Rytter Katarzyna, Łukomska Jolanta, Moniuszko Grzegorz, Gwozdecki Rafał, Surowiecki Przemysław, Lewandowska Małgorzata, Liszewska Frantz, Wawrzyńska Anna, Sirko Agnieszka, Identification and functional analysis of Joka2, a tobacco member of the family of selective autophagy cargo receptors, 10.4161/auto.7.10.16617
- Takeshige K., Autophagy in yeast demonstrated with proteinase-deficient mutants and conditions for its induction, 10.1083/jcb.119.2.301
- Moriyasu Y., Ohsumi Y., Autophagy in Tobacco Suspension-Cultured Cells in Response to Sucrose Starvation, 10.1104/pp.111.4.1233
- Calvo-Garrido Javier, Carilla-Latorre Sergio, Kubohara Yuzuru, Santos-Rodrigo Natalia, Mesquita Ana, Soldati Thierry, Golstein Pierre, Escalante Ricardo, Autophagy in Dictyostelium: Genes and pathways, cell death and infection, 10.4161/auto.6.6.12513
- Tung Sze Man, Ünal Can, Ley Alexandra, Peña Cohue, Tunggal Budi, Noegel Angelika A., Krut Oleg, Steinert Michael, Eichinger Ludwig, Loss of Dictyostelium ATG9 results in a pleiotropic phenotype affecting growth, development, phagocytosis and clearance and replication of Legionella pneumophila : Autophagy in growth, development, phagocytosis and infection, 10.1111/j.1462-5822.2010.01432.x
- Bozzaro Salvatore, Eichinger Ludwig, The Professional Phagocyte Dictyostelium discoideum as a Model Host for Bacterial Pathogens, 10.2174/138945011795677782
- Duszenko Michael, Ginger Michael L., Brennand Ana, Gualdrón-López Melisa, Colombo María Isabel, Coombs Graham H., Coppens Isabelle, Jayabalasingham Bamini, Langsley Gordon, Lisboa de Castro Solange, Menna-Barreto Rubem, Mottram Jeremy C., Navarro Miguel, Rigden Daniel J., Romano Patricia S., Stoka Veronika, Turk Boris, Michels Paul A.M., Autophagy in protists, 10.4161/auto.7.2.13310
- Barquilla A., Crespo J. L., Navarro M., Rapamycin inhibits trypanosome cell growth by preventing TOR complex 2 formation, 10.1073/pnas.0802668105
- Morais Pedro, Lamas Jesús, Sanmartín Manuel L., Orallo Francisco, Leiro José, Resveratrol Induces Mitochondrial Alterations, Autophagy and a Cryptobiosis-like State in Scuticociliates, 10.1016/j.protis.2009.04.004
- Yakisich J S, Kapler G M, The effect of phosphoinositide 3-kinase inhibitors on programmed nuclear degradation in Tetrahymena and fate of surviving nuclei, 10.1038/sj.cdd.4401473
- Akematsu Takahiko, Pearlman Ronald E., Endoh Hiroshi, Gigantic macroautophagy in programmed nuclear death ofTetrahymena thermophila, 10.4161/auto.6.7.13287
- Thorgaard Gary H., Bailey George S., Williams David, Buhler Donald R., Kaattari Stephen L., Ristow Sandra S., Hansen John D., Winton James R., Bartholomew Jerri L., Nagler James J., Walsh Patrick J., Vijayan Matt M., Devlin Robert H., Hardy Ronald W., Overturf Kenneth E., Young William P., Robison Barrie D., Rexroad Caird, Palti Yniv, Status and opportunities for genomics research with rainbow trout, 10.1016/s1096-4959(02)00167-7
- Govoroun Marina, Le Gac Florence, Guiguen Yann, 10.1186/1471-2164-7-196
- Rexroad III C.E., Lee Y., Keele J.W., Karamycheva S., Brown G., Koop B., Gahr S.A., Palti Y., Quackenbush J., Sequence analysis of a rainbow trout cDNA library and creation of a gene index, 10.1159/000075773
- Rise M. L., Development and Application of a Salmonid EST Database and cDNA Microarray: Data Mining and Interspecific Hybridization Characteristics, 10.1101/gr.1687304
- Salem Mohamed, Rexroad III Caird E, Wang Jiannan, Thorgaard Gary H, Yao Jianbo, Characterization of the rainbow trout transcriptome using Sanger and 454-pyrosequencing approaches, 10.1186/1471-2164-11-564
- Polakof Sergio, Panserat Stéphane, Craig Paul M., Martyres David J., Plagnes-Juan Elisabeth, Savari Sharareh, Aris-Brosou Stéphane, Moon Thomas W., The Metabolic Consequences of Hepatic AMP-Kinase Phosphorylation in Rainbow Trout, 10.1371/journal.pone.0020228
- Seiliez I., Gabillard J.-C., Skiba-Cassy S., Garcia-Serrana D., Gutierrez J., Kaushik S., Panserat S., Tesseraud S., An in vivo and in vitro assessment of TOR signaling cascade in rainbow trout (Oncorhynchus mykiss), 10.1152/ajpregu.00146.2008
- Seiliez Iban, Gabillard Jean-Charles, Riflade Marine, Sadoul Bastien, Dias Karine, Avérous Julien, Tesseraud Sophie, Skiba Sandrine, Panserat Stéphane, Amino acids downregulate the expression of several autophagy-related genes in rainbow trout myoblasts, 10.4161/auto.18863
- Umemiya Rika, Matsuo Tomohide, Hatta Takeshi, Sakakibara Shin-ichi, Boldbaatar Damdinsuren, Fujisaki Kozo, Cloning and characterization of an autophagy-related gene, ATG12, from the three-host tick Haemaphysalis longicornis, 10.1016/j.ibmb.2007.05.006
- Kawano Suguru, Umemiya-Shirafuji Rika, Boldbaatar Damdinsuren, Matsuoka Kenji, Tanaka Tetsuya, Fujisaki Kozo, Cloning and characterization of the autophagy-related gene 6 from the hard tick, Haemaphysalis longicornis, 10.1007/s00436-011-2429-x
- Umemiya-Shirafuji Rika, Matsuo Tomohide, Liao Min, Boldbaatar Damdinsuren, Battur Banzragch, Suzuki Hiroshi I., Fujisaki Kozo, Increased expression of ATG genes during nonfeeding periods in the tickHaemaphysalis longicornis, 10.4161/auto.6.4.11668
- Piggott N, Genes Genomes Genetics, 1, 353 (2011)
- Cebollero E., Gonzalez R., Induction of Autophagy by Second-Fermentation Yeasts during Elaboration of Sparkling Wines, 10.1128/aem.02920-05
- Marks Virginia D., Ho Sui Shannan J., Erasmus Daniel, van der Merwe George K., Brumm Jochen, Wasserman Wyeth W., Bryan Jennifer, van Vuuren Hennie J. J., Dynamics of the yeast transcriptome during wine fermentation reveals a novel fermentation stress response, 10.1111/j.1567-1364.2007.00338.x
- Mendes-Ferreira A., Sampaio-Marques B., Barbosa C., Rodrigues F., Costa V., Mendes-Faia A., Ludovico P., Leao C., Accumulation of Non-Superoxide Anion Reactive Oxygen Species Mediates Nitrogen-Limited Alcoholic Fermentation by Saccharomyces cerevisiae, 10.1128/aem.01535-10
- Rossignol Tristan, Dulau Laurent, Julien Anne, Blondin Bruno, Genome-wide monitoring of wine yeast gene expression during alcoholic fermentation, 10.1002/yea.1046
- Teixeira M. C., Raposo L. R., Mira N. P., Lourenco A. B., Sa-Correia I., Genome-Wide Identification of Saccharomyces cerevisiae Genes Required for Maximal Tolerance to Ethanol, 10.1128/aem.00845-09
- Yoshikawa Katsunori, Tanaka Tadamasa, Furusawa Chikara, Nagahisa Keisuke, Hirasawa Takashi, Shimizu Hiroshi, Comprehensive phenotypic analysis for identification of genes affecting growth under ethanol stress inSaccharomyces cerevisiae, 10.1111/j.1567-1364.2008.00456.x
- Hazan R., Levine A., Abeliovich H., Benzoic Acid, a Weak Organic Acid Food Preservative, Exerts Specific Effects on Intracellular Membrane Trafficking Pathways in Saccharomyces cerevisiae, 10.1128/aem.70.8.4449-4457.2004
- Winter Gal, Hazan Reut, Bakalinsky Alan T., Abeliovich Hagai, Caffeine induces macroautophagy and confers a cytocidal effect on food spoilage yeast in combination with benzoic acid, 10.4161/auto.5127
- Singletary K., Milner J., Diet, Autophagy, and Cancer: A Review, 10.1158/1055-9965.epi-07-2917
- Su Chun-Li, Chen Fang-Nan, Won Shen-Jeu, Involvement of apoptosis and autophagy in reducing mouse hepatoma ML-1 cell growth in inbred BALB/c mice by bacterial fermented soybean products, 10.1016/j.fct.2010.08.017
- Abeliovich Hagai, Gonzalez Ramon, Autophagy in food biotechnology, 10.4161/auto.5.7.9213
- He Congcong, Bartholomew Clinton R., Zhou Weibin, Klionsky Daniel J., Assaying autophagic activity in transgenic GFP-Lc3 and GFP-Gabarap zebrafish embryos, 10.4161/auto.5.4.7768
- Komoike Yuta, Shimojima Keiko, Liang Jao-Shwann, Fujii Hiroshi, Maegaki Yoshihiro, Osawa Makiko, Fujii Sakiko, Higashinakagawa Toru, Yamamoto Toshiyuki, A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish, 10.1038/jhg.2010.1
- Dowling J.J., Low S.E., Busta A.S., Feldman E.L., Zebrafish MTMR14 is required for excitation–contraction coupling, developmental motor function and the regulation of autophagy, 10.1093/hmg/ddq153
- Makky Khadijah, Tekiela Jackie, Mayer Alan N., Target of rapamycin (TOR) signaling controls epithelial morphogenesis in the vertebrate intestine, 10.1016/j.ydbio.2006.11.030
- Klionsky Daniel J, Baehrecke Eric H., Brumell John H., Chu Charleen T., Codogno Patrice, Cuervo Ana Maria, Debnath Jayanta, Deretic Vojo, Elazar Zvulun, Eskelinen Eeva-Liisa, Finkbeiner Steven, Fueyo-Margareto Juan, Gewirtz David A., Jäättelä Marja, Kroemer Guido, Levine Beth, Melia Thomas J., Mizushima Noboru, Rubinsztein David C., Simonsen Anne, Thorburn Andrew, Thumm Michael, Tooze Sharon A., A comprehensive glossary of autophagy-related molecules and processes (2ndedition), 10.4161/auto.7.11.17661
- Klionsky Daniel J., Codogno Patrice, Cuervo Ana Maria, Deretic Vojo, Elazar Zvulun, Fueyo-Margareto Juan, Gewirtz David A., Kroemer Guido, Levine Beth, Mizushima Noboru, Rubinsztein David C., Thumm Michael, Tooze Sharon A., A comprehensive glossary of autophagy-related molecules and processes, 10.4161/auto.6.4.12244
Bibliographic reference | Klionsky, Daniel J ; Batoko, Henri ; Gailly, Philippe ; et. al. Guidelines for the use and interpretation of assays for monitoring autophagy.. In: Autophagy, Vol. 8, no. 4, p. 445-544 (2012) |
---|---|
Permanent URL | http://hdl.handle.net/2078.1/120154 |