A carregar...

Single Molecule Kinetics in the Familial Hypertrophic Cardiomyopathy D166V Mutant Mouse Heart

One of the sarcomeric mutations associated with a malignant phenotype of Familial Hypertrophic Cardiomyopathy (FHC) is the D166V point mutation in the ventricular myosin regulatory light chain (RLC) encoded by the MYL2 gene. In this report we show that the rates of myosin cross-bridge attachment and...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Muthu, P., Mettikolla, P., Calander, N., Luchowski, R., Gryczynski, I., Gryczynski, Z., Szczesna-Cordary, D., Borejdo, J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2854267/
https://ncbi.nlm.nih.gov/pubmed/19914255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2009.11.004
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!