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Bodensteiner, J. B. and Engel, A. G (1978). Intracellular calcium accumulation in Duchenne dystrophy and other myopathies: A study of 567, 000 muscle fibers in 114 biopsies. Neurology 28, 439-446.[Abstract/Free Full Text]

Brinkmeier, H., Mutz, J. V., Seewald, M. J., Melzner, I. and Rudel, R (1993). Specific modifications of the membrane fatty acid composition of human myotubes and their effect on muscular sodium channels. Biochim. Biophys. Acta 1145, 8-14.[Medline]

Bulfield, G., Siller, W. G., Wight, P. A. L. and Moore, K. J (1984). X chromosome-linked muscular dystrophy (mdx) in the mouse. Proc. Nat. Acad. Sci. USA 81, 1189-1192.[Abstract/Free Full Text]

Duncan, C. J (1978). Role of intracellular calcium in promoting muscle damage: a strategy for controling the dystrophic conditions. Experientia 34, 1531-1535.[Medline]

Fong, P, Turner, P. R., Denetclaw, W. F. and Steinhardt, R. A (1990). Increased acticity of calcium leak channels in myotubes of Duchenne human and MDX mouse origin. Science 250, 673-676.[Abstract/Free Full Text]

Franco, A. Jr and Lansman, J. B (1990). Calcium entry through stretch-inactivated ion channels in mdx myotubes. Nature 344, 670-673.[Medline]

Gailly, P., Boland, B., Himpen, B., Casteels, R. and Gillis, J. M (1993). Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice. Cell Calcium 14, 474-483.

Head, S. I (1993). Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice. J. Physiol 469, 11-19.

Hoffman, E. P., Hudecki, M. S., Rosenberg, P. A., Pollina, C. M. and Kunkel, L. M (1988). Cell and fiber-type distribution of dystrophin. Neuron 2, 1019-1029.

Ho-Kim M.-A., Bedard A., Vincent M. and Rogers, P. A (1991). Dystrophin: A sensitive and reliable immunochemical assay in tissue and cell culture homogenates. Biochem. Biophys. Res. Commun 181, 1164-1172.[Medline]

Hugnot, J.-P., Gilgenkrantz, H., Chafey, P., Lambert, M., Eveno, E., Kaplan, J.-C. and Kahn, A (1993). Expression of the dystrophin gene in cultured fibroblasts. Biochem. Biophys. Res. Commun 192, 69-74.[Medline]

Hutter, O. F., Burton, F. L. and Bovell, D. L (1991). Mechanical properties of normal and mdx mouse sarcolemma: bearing on function of dystrophin. J. Muscle Res. Cell Motil 12, 585-589.[Medline]

Hutter, O. F (1992). The membrane hypothesis of Duchenne muscular dystrophy: Quest for functional evidence. J. Inher. Metab. Dis 15, 565-577.[Medline]

Ibraghimov-Beskrovnaya, O., Ervasti, J. M., Leveille, C. J., Slaughter, C. A., Sernett, S. W. and Campbell, K. P (1992). Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 355, 699-702.

Jockusch, H., Friedrich, G. and Zippel, M (1990). Serum parvalbumin, an indicator of muscle disease in murine dystrophy and myotonia. Muscle & Nerve 13, 551-555.[Medline]

Jockusch, H., Menke, A. and Heimann, P (1993). Stress models to test for the biological role of dystrophin in muscle cells. J. Muscle Res. Cell Motil 13, 237-238.

K\212mper, A. and Rodemann, H. P (1992). Alterations of protein degradation and 2-D protein pattern in muscle cells of MDX and DMD origin. Biochem. Biophys. Res. Commun 189, 1484-1490.[Medline]

Karpati, G. and Carpenter, S (1986). Small-caliber skeletal muscle fibers do not suffer deleterious consequences of dystrophic gene expression. Am. J. Med. Genet 25, 653-658.[Medline]

Koenig, M. and Kunkel, L. M (1990). Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility. J. Biol. Chem 265, 4560-4566.[Abstract/Free Full Text]

Levine, B. A., Moir, A. J. G., Patchell, V. B. and Perry, S. V (1990). The interactin of actin with dystrophin. FEBS Lett 263, 159-162.[Medline]

Liu, S. C., Derich, L. H., Agre, P. and Palek, J (1990). Alterations of the erythrocyte membrane skeletal ultrasturcture in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis. Blood 76, 198-205.[Abstract/Free Full Text]

Menke, A. and Jockusch, H (1991). Decreased osmotic stability of dystrophin-les muscle cells from the mdx mouse. Nature 349, 69-71.[Medline]

Pennington, R. J. T (1980). Clinical biochemistry of muscular dystrophy. B. Med. Bull 36, 123-126.[Free Full Text]

Petrof, B. J., Shrager, J. B., Stedman, H. H., Kelly, A. M. and Sweeney, H. L (1993). Dystrophin protects the sarcolemma from stresses developed during muscle contraction. Proc. Nat. Acad. Sci. USA 90, 3710-3714.[Abstract/Free Full Text]

Pressmar, J., Brinkmeier, H., Seewald, M. J., Naumann, T. and Rudel, R (1994). Intracellular Ca2+concentrations are not elevated in resting cultured muscle from Duchenne (DMD) patients and in MDX mouse muscle fibres. Pflugers Arch 426, 499-505.[Medline]

Rivet-Bastide, M., Imbert, N., Cognard, C., Duport, G., Rideau, Y. and Raymond, G (1993). Changes in cytosolic resting ionized calcium level and in calcium transients during in vitro development of normal and Duchenne muscular dystrophy cultured skeletal muscle measured by laser cytofluorimetry using Indo-1. Cell Calcium 14, 563-571.[Medline]

Rowland, L. P (1976). Pathogenesis of muscular dystrophies. Arch. Neurol 33, 315-321.[Abstract/Free Full Text]

Salviati, G., Betto, R., Ceoldo, S., Biasia, E, Bonilla, E., Miranda, A. F. and Dimauro, S (1989). Cell fractionation studies indicate that dystrophin is a protein of surface membranes of skeletal muscle. Biochem. J 258, 837-841.[Medline]

Savitz, D., Sidel, V. W. and Solomon, A. K (1964). Osmotic properties of human red cells. J. Gen. Physiol 48, 79-94.[Abstract/Free Full Text]

Sicinski, P., Geng, Y., Ryder-Cook, A. S., Barnard, E. A., Darlison, M. G. and Barnard, P. J (1989). The molecular basis of muscular dystrophy in the mdx mouse. Science 244, 1578-1580.[Abstract/Free Full Text]

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. and Kelly, A. M (1991). The mdx diaphragma reproduces the degenerative changes of Duchenne muscular dystrophy. Nature 352, 536-539.[Medline]

Svoboda, K., Schmidt, C. F., Branton, D. and Block, S. M (1992). Conformation and elasticity of the isolated red blood cell membrane skeleton. Biophys. J 63, 784-793.[Medline]

Turner, P. R., Westwood, T., Regen, C. M. and Steinhardt, R. A (1988). Increased protein degradation results rom elevated free calcium levels found in muscle from mdx mice. Nature 335, 735-738.[Medline]

Watkins, S. C., Hoffman, E. P., Slayter, H. S. and Kunkel, L. M (1987). Immunoelectron microscopic localization of dystrophin in myofibres. Nature 333, 863-866.


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