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Myosin regulatory light chain phosphorylation enhances cardiac β-myosin in vitro motility under load

Familial hypertrophic cardiomyopathy (HCM) is characterized by left ventricular hypertrophy and myofibrillar disarray, and often results in sudden cardiac death. Two HCM mutations, N47K and R58Q, are located in the myosin regulatory light chain (RLC). The RLC mechanically stabilizes the myosin lever...

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Detalhes bibliográficos
Publicado no:Arch Biochem Biophys
Main Authors: Karabina, Anastasia, Kazmierczak, Katarzyna, Szczesna-Cordary, Danuta, Moore, Jeffrey R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4790447/
https://ncbi.nlm.nih.gov/pubmed/26116789
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.abb.2015.06.014
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