Loss of caveolin-3 induced by the dystrophy-associated P104L mutation impairs L-type calcium channel function in mouse skeletal muscle cells
Author:
Publisher
Wiley
Subject
Physiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/jphysiol.2006.124198/fullpdf
Reference47 articles.
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2. Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease;Betz;Nat Genet,2001
3. Caveolin-1 contributes to assembly of store-operated Ca2+ influx channels by regulating plasma membrane localization of TRPC1;Brazer;J Biol Chem,2003
4. Inhibition of lipid raft-dependent signalling by a dystrophy-associated mutant of caveolin-3;Carozzi;J Biol Chem,2002
5. Appearance and evolution of calcium currents and contraction during the early post-fusional stages of rat skeletal muscle cells developing in primary culture;Cognard;Development,1993
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