Potentiation of the cardiac L-type Ca2+ channel (α1C) by dihydropyridine agonist and strong depolarization occur via distinct mechanisms

Journal of General Physiology

Volumn 118, Issue 5, 2001, Pages 495-507

  Wilkens, C M ^a   Grabner, M ^a   Beam, K G ^a  

^a Department of Environmental and Radiological Health Sciences   (United States)

Author keywords

Facilitation; Ion channel modulation; Muscle

Indexed keywords

1,4 DIHYDROPYRIDINE DERIVATIVE; CALCIUM CHANNEL L TYPE; CALCIUM CHANNEL STIMULATING AGENT;

ANIMAL CELL; ARTICLE; CELL MEMBRANE DEPOLARIZATION; FACILITATION; GENE MUTATION; HEART DEPOLARIZATION; ION TRANSPORT; MOUSE; MYOTUBE; NONHUMAN;

ACTION POTENTIALS; ANIMALS; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS, L-TYPE; DIHYDROPYRIDINES; ELECTROPHYSIOLOGY; HEART; MEMBRANE POTENTIALS; MICE; MUTAGENESIS, SITE-DIRECTED; POINT MUTATION; POLYMERASE CHAIN REACTION;

EID: 0035174481     PISSN: 00221295     EISSN: None     Source Type: Journal    
DOI: 10.1085/jgp.118.5.495     Document Type: Article

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