Truncation of murine CaV1.2 at Asp 1904 increases Ca V1.3 expression in embryonic atrial cardiomyocytes

Pflugers Archiv European Journal of Physiology

Volumn 465, Issue 7, 2013, Pages 955-964

  Ding, Jie ^a   Domes, Katrin ^a   Hofmann, Franz ^a   Wegener, Jörg W ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

adrenergic regulation; C terminus; Heart; L type Ca2+ current

Indexed keywords

ASPARTIC ACID; CALCIUM CHANNEL CAV1.2; CALCIUM CHANNEL CAV1.3; CALCIUM CHANNEL L TYPE; MESSENGER RNA; UNCLASSIFIED DRUG; CACNA1D PROTEIN, MOUSE; CALCIUM CHANNEL BLOCKING AGENT; CAV1.2 PROTEIN, MOUSE; FORSKOLIN; CACNA1C PROTEIN, MOUSE;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CALCIUM CURRENT; CARBOXY TERMINAL SEQUENCE; CHANNEL GATING; CONTROLLED STUDY; EMBRYO; GENE EXPRESSION; HEART MUSCLE CELL; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; UPREGULATION; WESTERN BLOTTING; WILD TYPE; ACTION POTENTIAL; ANIMAL; CHEMISTRY; CYTOLOGY; DRUG EFFECT; FETUS HEART; GENE DELETION; GENETIC TRANSCRIPTION; GENETICS; HEART ATRIUM; HEART VENTRICLE; METABOLISM; PHYSIOLOGY; PROTEIN TERTIARY STRUCTURE; DRUG EFFECTS;

ACTION POTENTIALS; ANIMALS; ASPARTIC ACID; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS, L-TYPE; COLFORSIN; FETAL HEART; GENE DELETION; HEART ATRIA; HEART VENTRICLES; MICE; MYOCYTES, CARDIAC; PROTEIN STRUCTURE, TERTIARY; TRANSCRIPTION, GENETIC;

EID: 84879841554     PISSN: 00316768     EISSN: 14322013     Source Type: Journal    
DOI: 10.1007/s00424-012-1212-x     Document Type: Article

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