Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice
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K. Davies | J. Gillis | N. Deconinck | J. Tinsley | F. Backer | R. Fisher | D. Kahn | S. Phelps
[1] G. Karpati. Utrophin muscles in on the action , 1997, Nature Medicine.
[2] K. Davies,et al. Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene , 1996, Nature.
[3] L. Metzinger,et al. Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress , 1996, British journal of pharmacology.
[4] M. Perricaudet,et al. Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[5] D. Blake,et al. Utrophin: A Structural and Functional Comparison to Dystrophin , 1996, Brain pathology.
[6] K. Campbell,et al. Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle. , 1995, Current opinion in neurology.
[7] J. Faulkner,et al. Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice. , 1995, Human molecular genetics.
[8] S. Winder,et al. Calcium/calmodulin‐dependent regulation of the NH2‐terminal F‐actin binding domain of utrophin , 1995, FEBS letters.
[9] R. Edwards,et al. Time course of changes in plasma membrane permeability in the dystrophin‐deficient mdx mouse , 1994, Muscle & nerve.
[10] Y. Takeshima,et al. Amino‐terminal deletion of 53% of dystrophin results in an intermediate Duchenne‐Becker muscular dystrophy phenotype , 1994, Neurology.
[11] K. Davies,et al. Utrophin: A potential replacement for dystrophin? , 1993, Neuromuscular Disorders.
[12] S. Hirai,et al. Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects , 1993, Journal of the Neurological Sciences.
[13] S. Head. Membrane potential, resting calcium and calcium transients in isolated muscle fibres from normal and dystrophic mice. , 1993, The Journal of physiology.
[14] K. Campbell,et al. Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity , 1993, Nature.
[15] J. Gillis,et al. Critical evaluation of cytosolic calcium determination in resting muscle fibres from normal and dystrophic (mdx) mice. , 1993, Cell calcium.
[16] H. Sweeney,et al. Dystrophin protects the sarcolemma from stresses developed during muscle contraction. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[17] K. Davies,et al. Localization and Quantitation of the Chromosome 6-Encoded Dystrophin-Related Protein in Normal and Pathological Human Muscle , 1993, Journal of neuropathology and experimental neurology.
[18] P. Briand,et al. Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice , 1993, Nature.
[19] K. Davies,et al. Primary structure of dystrophin-related protein , 1992, Nature.
[20] J. Ervasti,et al. Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle , 1992, Nature.
[21] W. Denetclaw,et al. Increased calcium influx in dystrophic muscle , 1991, The Journal of cell biology.
[22] J. Lansman,et al. Developmental regulation of mechanosensitive calcium channels in skeletal muscle from normal and mdx mice , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[23] J. Shrager,et al. The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy , 1991, Nature.
[24] J. Léger,et al. A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice Immunological evidence , 1991, FEBS letters.
[25] H. Jockusch,et al. Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse , 1991, Nature.
[26] S. Carpenter,et al. Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions , 1990, Journal of the Neurological Sciences.
[27] C. Carlson,et al. A noninvasive procedure to detect muscle weakness in the mdx mouse , 1990, Muscle & nerve.
[28] N. Curtin,et al. THE mdx MOUSE SKELETAL MUSCLE MYOPATHY: II. CONTRACTILE PROPERTIES , 1988, Neuropathology and applied neurobiology.
[29] H. Blau,et al. Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy , 1988, Cell.
[30] R. Tsien,et al. A new generation of Ca2+ indicators with greatly improved fluorescence properties. , 1985, The Journal of biological chemistry.
[31] J. Bodensteiner,et al. Intracellular calcium accumulation in Duchenne dystrophy and other myopathies , 1978, Neurology.
[32] Norman T. J. Bailey,et al. Statistical Methods in Biology , 1959 .