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Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch.

Bibliographic reference Moens, Paul ; Baatsen, P H ; Maréchal, Georges. Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch.. In: Journal of muscle research and cell motility, Vol. 14, no. 4, p. 446-51 (1993)
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  1. Carpenter, S. & Karpati, G. (1979) Duchenne muscular dystrophy. Plasma membrane loss initiates muscle cell necrosis unless it is repaired. Brain 102, 147?61.
  2. Carpenter, S., Karpati, G., Zubrycka-Gaarn, E., Bulman, D. E., Ray, P. N. & Worton, R. G. (1990) Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study. Muscle Nerve 13, 376?80.
  3. Coulton, G. R., Curtin, N. A., Morgan, J. E. & Partridge, T. A. (1988) The mdx mouse skeletal muscle myopathy. I. A histological, morphometric and biochemical investigation. Neuropath. Appl. Neurobiol. 14, 299?314.
  4. Cullen, M. J., Walsh, J., Nicholson, L. V. B. & Harris, J. B. (1990) Ultrastructural localization of dystrophin in human muscle by using gold immunolabelling. Proc. R. Soc. Lond. B 240, 197?210.
  5. Dimario, J. X., Uzman, A. & Strohman, R. C. (1991) Fiber regeneration is not persistent in dystrophic (mdx) mouse skeletal muscle. Devel. Biol. 148, 314?21.
  6. Duncan, C. J. (1987) Role of calcium in triggering rapid ultrastructural damage in muscle: a study with chemically skinned fibres. J. Cell Sci. 87, 581?94.
  7. Duncan, C. J. (1989) Mechanisms that produce rapid damage to myofilaments of amphibian skeletal muscle. Muscle Nerve 12, 210?18.
  8. Duncan, C. J. & Jackson, M. J. (1987) Different mechanisms mediate, structural changes and intracellular enzyme efflux following damage to skeletal muscle. J. Cell Sci. 87, 183?8.
  9. Ervasti, J. M. & Campbell, K. P. (1991) Membrane organization of the dystrophin-glycoprotein complex. Cell 66, 1121?31.
  10. Faulkner, J. A., Jones, D. A. & Round, J. M. (1989) Injury to skeletal muscles of mice by forced lengthening during contractions. Quart. J. Exp. Physiol. 74, 661?70.
  11. Ibraghimov-Beskrovnaya, O., Ervasti, J. M., Leveille, C. J., Slaughter, C. A., Sernett, S. W. & Campbell, K. P. (1992) Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 355, 696?702.
  12. Karpati, G. & Carpenter, S. (1986) Small-caliber muscle fibres do not suffer deleterious consequences of dystrophic gene expression. Am. J. Med. Genet. 25, 653?8.
  13. Mcardle, A., Edwards, R. H. T. & Jackson, M. J. (1991) Effects of contractile activity on muscle damage in the dystrophin-deficient mdx mouse. Clin. Sci. 80, 367?71.
  14. Mccully, K. K. & Faulkner, J. A. (1985) Injury to skeletal muscle fibers of mice following lengthening contractions. J. Appl. Physiol. 59, 119?26.
  15. Mccully, K. K. & Faulkner, J. A. (1986) Characteristics of lengthening contractions associated with injury to skeletal muscle fibers. J. Appl. Physiol. 61, 293?9.
  16. Maréchal, G. & Plaghki, L. (1979) The deficit of the isometric tetanic tension redeveloped after a release of frog muscle at constant velocity. J. Gen. Physiol. 73, 453?67.
  17. Menke, A. & Jockusch, H. (1991) Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse. Nature 349, 69?71.
  18. Miike, T. (1983) Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies. Muscle Nerve 6, 545?52.
  19. Moens, P. D., Beckers-Bleukx & Maréchal, G. (1990) Maximal isometric forces of mdx muscles. In Muscle and Motility 2, Proceedings of XIXth European Conference, Brussels (edited by Maréchal, G. & Carraro, U.) pp. 299?301. Andover, UK: Intercept Ltd.
  20. Newham, D. J., Mcphail, G., Mills, K. R. & Edwards, R. H. T. (1983) Ultrastructural changes after concentric and eccentric contractions of human muscle. J. Neurol. Sci. 61, 109?22.
  21. SACCO, P., JONES, D. A., DICK, J. & VRBOVÁ, G. (1991) The susceptibility of normal and dystrophic mouse muscles to damage. J. Physiol. (Lond.) 438, 154P.
  22. Samitt, C. E. & Bonilla, E. (1990) Immunocytochemical study of dystrophin at the myotendinous junction. Muscle Nerve 13, 493?500.
  23. Shimizu, T., Matsumara, K., Sunada, Y. & Mannen, T. (1989) Dense immunostainings on both neuromuscular and myotendon junctions with anti-dystrophin monoclonal antibody. Biomed. Res. 10, 405?9.
  24. Schmalbruch, H. (1984) Regenerated muscle fibers in Duchenne muscular dystrophy: a serial section study. Neurology 34, 60?5.
  25. Stedman, H. H., Sweeney, H. L., Shrager, J. B., Maguire, H. C., Panettieri, R. A., Petrof, B., Narusawa, M., Leferovich, J. M., Sladky, J. T. & Kelly, A. M. (1991) The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy. Nature 352, 536?9.
  26. Stretton, A. O. W. & Kravitz, E. A. (1968) Neuronal geometry: determination with a technique of intracellular dye injection. Science 162, 132?4.
  27. Watkins, S. C., Hoffman, E. P., Slayter, H. S. & Kunkel, L. M. (1988) Immunoelectron microscopic localization of dystrophin in myofibres. Nature 333, 863?6.
  28. Webster, C., Silberstein, L., Hays, A. P. & Blau, H. M. (1988) Fast fibers are preferentially affected in Duchenne muscular dystrophy. Cell 52, 503?13.
  29. Weller, B., Karpati, G. & Carpenter, S. (1990) Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions. J. Neurol. Sci. 100, 9?13.