Defective membrane repair in dysferlin-deficient muscular dystrophy-Reference-Cited by-同舟云学术

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Defective membrane repair in dysferlin-deficient muscular dystrophy

Published:2003-05 Issue:6936 Volume:423 Page:168-172
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Bansal Dimple,Miyake Katsuya,Vogel Steven S.,Groh Séverine,Chen Chien-Chang,Williamson Roger,McNeil Paul L.,Campbell Kevin P.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature01573.pdf

Reference27 articles.

1. Cohn, R. D. & Campbell, K. P. Molecular basis of muscular dystrophies. Muscle Nerve 23, 1456–1471 (2000)

2. Bashir, R. et al. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nature Genet. 20, 37–42 (1998)

3. Liu, J. et al. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nature Genet. 20, 31–36 (1998)

4. Achanzar, W. E. & Ward, S. A nematode gene required for sperm vesicle fusion. J. Cell Sci. 110, 1073–1081 (1997)

5. Piccolo, F., Moore, S. A., Ford, G. C. & Campbell, K. P. Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb-girdle muscular dystrophies. Ann. Neurol. 48, 902–912 (2000)

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2. Osteocyte Sptbn1 Deficiency Alters Cell Survival and Mechanotransduction Following Formation of Plasma Membrane Disruptions (PMD) from Mechanical Loading;Calcified Tissue International;2024-09-14

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5. Apolipoprotein E knockout, but not cholesteryl ester transfer protein (CETP)-associated high-density lipoprotein cholesterol (HDL-C) lowering, exacerbates muscle wasting in dysferlin-null mice;Lipids in Health and Disease;2024-08-13

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