Expression of the muscular dystrophy-associated caveolin-3P104L mutant in adult mouse skeletal muscle specifically alters the Ca2+ channel function of the dihydropyridine receptor

Pflugers Archiv European Journal of Physiology

Volumn 457, Issue 2, 2008, Pages 361-375

  Weiss, Norbert ^a   Couchoux, Harold ^a   Legrand, Claude ^a   Berthier, Christine ^a   Allard, Bruno ^a   Jacquemond, Vincent ^a  

^a UNIVERSITÉ LYON 1   (France)

Author keywords

Calcium channel; Caveolin 3; Skeletal muscle

Indexed keywords

1,4 DIHYDROPYRIDINE RECEPTOR; CALCIUM; CALCIUM CHANNEL; CALCIUM CHANNEL L TYPE; CAVEOLIN 3; VOLTAGE GATED CALCIUM CHANNEL;

ADULT ANIMAL; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CALCIUM CELL LEVEL; CONTROLLED STUDY; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; MOUSE; MUSCULAR DYSTROPHY; MUTANT; MUTATION; NONHUMAN; PRIORITY JOURNAL; REGULATORY MECHANISM; SKELETAL MUSCLE; WESTERN BLOTTING;

ANIMALS; CALCIUM CHANNELS, L-TYPE; CALCIUM SIGNALING; CAVEOLIN 3; CELL MEMBRANE; ELECTROPORATION; GENE TRANSFER TECHNIQUES; HUMANS; KINETICS; MALE; MEMBRANE POTENTIALS; MICE; MUSCLE CONTRACTION; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES, LIMB-GIRDLE; MUTATION; RECOMBINANT FUSION PROTEINS;

EID: 56649095921     PISSN: 00316768     EISSN: 14322013     Source Type: Journal    
DOI: 10.1007/s00424-008-0528-z     Document Type: Article

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