Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca2+ sensitivity-Reference-Cited by-同舟云学术

Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca2+ sensitivity

Published:2013-03-27 Issue:1 Volume:99 Page:65-73
ISSN:1755-3245
Container-title:Cardiovascular Research
language:en
Short-container-title:

Author:

Memo Massimiliano,Leung Man-Ching,Ward Douglas G.,dos Remedios Cristobal,Morimoto Sachio,Zhang Lianfeng,Ravenscroft Gianina,McNamara Elyshia,Nowak Kristen J.,Marston Steven B.,Messer Andrew E.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Link

http://academic.oup.com/cardiovascres/article-pdf/99/1/65/17393940/cvt071.pdf

Reference45 articles.

1. Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy;Mogensen;J Am Coll Cardiol,2004

2. Sarcomeric protein mutations in dilated cardiomyopathy;Chang;Heart Fail Rev,2005

3. Genetics of familial dilated cardiomyopathy;Menon;Prog Ped Cardiol,2008

4. How do mutations in contractile proteins cause the primary familial cardiomyopathies?;Marston;J Cardiovasc Transl Res,2011

5. Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes;Tardiff;Heart Fail Rev,2005

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