Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions-Reference-Cited by-同舟云学术

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Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions

Published:2009-10-17 Issue:22 Volume:583 Page:3600-3604
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Zanou Nadège,Iwata Yuko,Schakman Olivier,Lebacq Jean,Wakabayashi Shigeo,Gailly Philippe

Funder

Association française contre les myopathies

Association belge contre les maladies neuro-musculaires

General Direction of Scientific Research of the French Community of Belgium

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Reference51 articles.

1. Function and genetics of dystrophin and dystrophin-related proteins in muscle;Blake;Physiol. Rev.,2002

2. Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse;Gillis;J. Muscle Res. Cell Motil.,1999

3. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene;Monaco;Nature,1986

4. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987

5. Membrane organization of the dystrophin–glycoprotein complex;Ervasti;Cell,1991

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