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Localization of the Binding Interface between Leiomodin-2 and α-Tropomyosin

The development of some familial dilated cardiomyopathies (DCM) correlates with the presence of mutations in proteins that regulate the organization and function of thin filaments in cardiac muscle cells. Harmful effects of some mutations might be caused by disruption of yet uncharacterized protein-...

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Detalhes bibliográficos
Publicado no:Biochim Biophys Acta
Main Authors: Colpan, Mert, Tolkatchev, Dmitri, Grover, Samantha, Helms, Gregory L., Cort, John R., Moroz, Natalia, Kostyukova, Alla
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5079754/
https://ncbi.nlm.nih.gov/pubmed/26873245
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbapap.2016.02.009
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