Dystrophin Is Required for the Normal Function of the Cardio-Protective K(ATP) Channel in Cardiomyocytes

Duchenne and Becker muscular dystrophy patients often develop a cardiomyopathy for which the pathogenesis is still unknown. We have employed the murine animal model of Duchenne muscular dystrophy (mdx), which develops a cardiomyopathy that includes some characteristics of the human disease, to study...

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Detalles Bibliográficos
Autores principales: Graciotti, Laura, Becker, Jodi, Granata, Anna Luisa, Procopio, Antonio Domenico, Tessarollo, Lino, Fulgenzi, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205025/
https://www.ncbi.nlm.nih.gov/pubmed/22066028
http://dx.doi.org/10.1371/journal.pone.0027034

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205025/
https://www.ncbi.nlm.nih.gov/pubmed/22066028
http://dx.doi.org/10.1371/journal.pone.0027034

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