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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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Pubblicato in:Biochim Biophys Acta
Autori principali: Colpan, Mert, Tolkatchev, Dmitri, Grover, Samantha, Helms, Gregory L., Cort, John R., Moroz, Natalia, Kostyukova, Alla
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Accesso online: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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