Cathepsin S Contributes to the Pathogenesis of Muscular Dystrophy in Mice

Duchenne muscular dystrophy (DMD) is an X-linked recessive disease caused by mutations in the gene encoding dystrophin. Loss of dystrophin protein compromises the stability of the sarcolemma membrane surrounding each muscle cell fiber, leading to membrane ruptures and leakiness that induces myofiber...

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Foilsithe in:J Biol Chem
Main Authors: Tjondrokoesoemo, Andoria, Schips, Tobias G., Sargent, Michelle A., Vanhoutte, Davy, Kanisicak, Onur, Prasad, Vikram, Lin, Suh-Chin J., Maillet, Marjorie, Molkentin, Jeffery D.
Formáid: Artigo
Teanga:Inglês
Foilsithe: American Society for Biochemistry and Molecular Biology 2016
Ábhair:
Molecular Bases of Disease
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4858995/
https://ncbi.nlm.nih.gov/pubmed/26966179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M116.719054
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