Axial stretch-dependent cation entry in dystrophic cardiomyopathy: Involvement of several TRPs channels-Reference-Cited by-同舟云学术

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Axial stretch-dependent cation entry in dystrophic cardiomyopathy: Involvement of several TRPs channels

Published:2016-04 Issue:4 Volume:59 Page:145-155
ISSN:0143-4160
Container-title:Cell Calcium
language:en
Short-container-title:Cell Calcium

Author:

Aguettaz E.,Lopez J.J.,Krzesiak A.,Lipskaia L.,Adnot S.,Hajjar R.J.,Cognard C.,Constantin B.,Sebille S.

Funder

Association Française contre les Myopathies-Telethon

NIH RO1

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Physiology

Reference71 articles.

1. X-linked dilated cardiomyopathy and the dystrophin gene;Ferlini;Neuromuscul. Disord.,1999

2. Cardiomyopathy of Duchenne muscular dystrophy: current understanding and future directions;Spurney;Muscle Nerve,2011

3. Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment;Monaco;Nature,1985

4. Ultrastructural and functional alterations of EC coupling elements in mdx cardiomyocytes: an analysis from membrane surface to depth;Lorin;Cell Biochem. Biophys.,2013

5. Alterations of dystrophin-associated glycoproteins in the heart lacking dystrophin or dystrophin and utrophin;Sharpe;J. Muscle Res. Cell Motil.,2013

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