The auxiliary subunit γ1 of the skeletal muscle L-type Ca2+ channel is an endogenous Ca2+ antagonist

Proceedings of the National Academy of Sciences of the United States of America

Volumn 104, Issue 45, 2007, Pages 17885-17890

  Andronache, Zoita ^a   Ursu, Daniel ^a   Lehnert, Simone ^b   Freichel, Marc ^b   Flockerzi, Veit ^b   Melzer, Werner ^a  

^a UNIVERSITY OF ULM   (Germany)

^b SAARLAND UNIVERSITY   (Germany)

Author keywords

Accessory subunits; Dihydropyridine receptor; Excitation contraction coupling; Mouse skeletal muscle; Phenylalkylamine

Indexed keywords

1,4 DIHYDROPYRIDINE RECEPTOR; BENZOTHIAZEPINE DERIVATIVE; CALCIUM ANTAGONIST; CALCIUM CHANNEL L TYPE; CALCIUM ION; DEVAPAMIL; DILTIAZEM; ISRADIPINE; PHENYLALKYLAMINE; PROTEIN SUBUNIT; RYANODINE RECEPTOR 1;

ALLOSTERISM; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CALCIUM TRANSPORT; CONTROLLED STUDY; DRUG BINDING; EXCITATION CONTRACTION COUPLING; KNOCKOUT MOUSE; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; SKELETAL MUSCLE;

ANIMALS; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS, L-TYPE; HINDLIMB; MICE; MICE, KNOCKOUT; MUSCLE FIBERS; MUSCLE, SKELETAL; PATCH-CLAMP TECHNIQUES; PROTEIN SUBUNITS;

MUS;

EID: 36749099052     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0704340104     Document Type: Article

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