Mending a Broken Heart: The Role of Sarcospan in Duchenne Muscular Dystrophy-Associated Cardiomyopathy
- PMID: 26702081
- PMCID: PMC4845299
- DOI: 10.1161/JAHA.115.002928
Mending a Broken Heart: The Role of Sarcospan in Duchenne Muscular Dystrophy-Associated Cardiomyopathy
Keywords: Duchenne muscular dystrophy cardiomyopathy; Editorials; cytoskeletal dynamics; muscle disease.
Comment on
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Sarcospan Regulates Cardiac Isoproterenol Response and Prevents Duchenne Muscular Dystrophy-Associated Cardiomyopathy.J Am Heart Assoc. 2015 Dec 23;4(12):e002481. doi: 10.1161/JAHA.115.002481. J Am Heart Assoc. 2015. PMID: 26702077 Free PMC article.
References
-
- Constantin B. Dystrophin complex functions as a scaffold for signaling proteins. Biochim Biophys Acta. 2013;1838:635–642. - PubMed
-
- Ervasti J, Campbell K. Membrane organization of the dystrophin‐glycoprotein complex. Cell. 1991;66:1121–1131. - PubMed
-
- Ervasti JM. Dystrophin, its interactions with other proteins, and implications for muscular dystrophy. Biochim Biophys Acta. 2006;1772:108–117. - PubMed
-
- Menke A, Jockusch A. Decreased osmotic stability of dystrophin‐less muscle cells from mdx mouse. Nature. 1991;349:69–71. - PubMed
-
- Menke A, Jockusch H. Extent of shock‐induced membrane leakage in human and mouse myotubes depends on dystrophin. J Cell Sci. 1995;108:727–733. - PubMed
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