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Efficient in vivo electroporation of the postnatal rodent forebrain.

Bibliographic reference Boutin, Camille ; Diestel, Simone ; Desoeuvre, Angélique ; Tiveron, Marie-Catherine ; Cremer, Harold. Efficient in vivo electroporation of the postnatal rodent forebrain.. In: PLoS One, Vol. 3, no.4, p. e1883 (2008)
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  1. Nakamura Harukazu, Katahira Tatsuya, Sato Tatsuya, Watanabe Yuji, Funahashi Jun-ichi, Gain- and loss-of-function in chick embryos by electroporation, 10.1016/j.mod.2004.05.013
  2. Saito Tetsuichiro, Nakatsuji Norio, Efficient Gene Transfer into the Embryonic Mouse Brain Using in Vivo Electroporation, 10.1006/dbio.2001.0439
  3. LM Mir, Adv Genet, 54, 83 (2005)
  4. Matsuda T., Cepko C. L., Electroporation and RNA interference in the rodent retina in vivo and in vitro, 10.1073/pnas.2235688100
  5. Matsuda Takahiko, Cepko Constance L., Controlled expression of transgenes introduced byin vivoelectroporation, 10.1073/pnas.0610155104
  6. Konishi Y., Cdh1-APC Controls Axonal Growth and Patterning in the Mammalian Brain, 10.1126/science.1093712
  7. A Alvarez-Buylla, J Neurosci, 22, 629 (2002)
  8. Morin Xavier, Jaouen Florence, Durbec Pascale, Control of planar divisions by the G-protein regulator LGN maintains progenitors in the chick neuroepithelium, 10.1038/nn1984
  9. Misson Jean-Paul, Edwards Michael A., Yamamoto Miyuki, Caviness Verne S., Identification of radial glial cells within the developing murine central nervous system: studies based upon a new immunohistochemical marker, 10.1016/0165-3806(88)90121-6
  10. Cremer Harold, Lange Rita, Christoph Annette, Plomann Markus, Vopper Gaby, Roes Jürgen, Brown Russell, Baldwin Stanley, Kraemer Philipp, Scheff Stephen, Barthels Dagmar, Rajewsky Klaus, Wille Wolfgang, Inactivation of the N-CAM gene in mice results in size reduction of the olfactory bulb and deficits in spatial learning, 10.1038/367455a0
  11. Lois C., Garc a-Verdugo J.-M., Alvarez-Buylla A., Chain Migration of Neuronal Precursors, 10.1126/science.271.5251.978
  12. G Chazal, J Neurosci, 20, 1446 (2000)
  13. F Doetsch, J Neurosci, 17, 5046 (1997)
  14. Diestel S., Schaefer D., Cremer H., Schmitz B., NCAM is ubiquitylated, endocytosed and recycled in neurons, 10.1242/jcs.019729
  15. Kim Ju Hee, Lee Jung-Ha, Park Jin-Yong, Park Chang-Hwan, Yun Chae-Ok, Lee Sang-Hun, Lee Yong-Sung, Son Hyeon, Retrovirally transduced NCAM140 facilitates neuronal fate choice of hippocampal progenitor cells : NCAM140 facilities neuronal differentiation, 10.1111/j.1471-4159.2005.03208.x
  16. Kippin T. E., p21 loss compromises the relative quiescence of forebrain stem cell proliferation leading to exhaustion of their proliferation capacity, 10.1101/gad.1272305
  17. Miller Victor M., Paulson Henry L., Gonzalez-Alegre Pedro, RNA Interference in Neuroscience: Progress and Challenges, 10.1007/s10571-005-8447-4
  18. Doetsch F., Garcia-Verdugo J. M., Alvarez-Buylla A., Regeneration of a germinal layer in the adult mammalian brain, 10.1073/pnas.96.20.11619
  19. Nelson Sacha B, Hempel Chris, Sugino Ken, Probing the transcriptome of neuronal cell types, 10.1016/j.conb.2006.08.006
  20. Hack Iris, Bancila Mircea, Loulier Karine, Carroll Patrick, Cremer Harold, Reelin is a detachment signal in tangential chain-migration during postnatal neurogenesis, 10.1038/nn923