Angiogenesis as a novel therapeutic strategy for Duchenne muscular dystrophy through decreased ischemia and increased satellite cells

Duchenne muscular dystrophy (DMD) is the most common hereditary muscular dystrophy caused by mutation in dystrophin, and there is no curative therapy. Dystrophin is a protein which forms the dystrophin-associated glycoprotein complex (DGC) at the sarcolemma linking the muscle cytoskeleton to the ext...

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Detalles Bibliográficos
Autores principales: Shimizu-Motohashi, Yuko, Asakura, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927135/
https://www.ncbi.nlm.nih.gov/pubmed/24600399
http://dx.doi.org/10.3389/fphys.2014.00050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927135/
https://www.ncbi.nlm.nih.gov/pubmed/24600399
http://dx.doi.org/10.3389/fphys.2014.00050

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