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COUP-TFII regulates satellite cell function and muscular dystrophy

Duchenne muscular dystrophy (DMD) is a severe and progressive muscle-wasting disease caused by mutations in the dystrophin gene. Although dystrophin deficiency in myofiber triggers the disease’s pathological changes, the degree of satellite cell (SC) dysfunction defines disease progression. Here, we...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Clin Invest
Prif Awduron: Xie, Xin, Tsai, Sophia Y., Tsai, Ming-Jer
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Clinical Investigation 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5096817/
https://ncbi.nlm.nih.gov/pubmed/27617862
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI87414
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