Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle

Limb-girdle muscular dystrophy type 2A (LGMD2A) is a form of muscular dystrophy caused by mutations in calpain 3 (CAPN3). Several studies have implicated Ca(2+) dysregulation as an underlying event in several muscular dystrophies, including LGMD2A. In this study we used mouse and human myotube cultu...

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Detaylı Bibliyografya
Yayımlandı:Expert Rev Mol Med
Asıl Yazarlar: Toral-Ojeda, Ivan, Aldanondo, Garazi, Lasa-Elgarresta, Jaione, Lasa-Fernández, Haizpea, Fernández-Torrón, Roberto, López de Munain, Adolfo, Vallejo-Illarramendi, Ainara
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cambridge University Press 2016
Konular:
Discovery
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4836212/
https://ncbi.nlm.nih.gov/pubmed/27055500
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/erm.2016.9
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