Restoration of normal L-type Ca2+ channel function during timothy syndrome by ablation of an anchoring protein

Circulation Research

Volumn 109, Issue 3, 2011, Pages 255-261

  Cheng, Edward P ^a   Yuan, Can ^a   Navedo, Manuel F ^a   Dixon, Rose E ^a   Nieves Cintrón, Madeline ^a   Scott, John D ^b   Santana, Luis F ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

Author keywords

arrhythmias; CaV1.2 channels; calcium; EC coupling

Indexed keywords

CALCIUM CHANNEL L TYPE; CYCLIC AMP DEPENDENT PROTEIN KINASE ANCHORING PROTEIN;

ANIMAL CELL; ARTICLE; CHANNEL GATING; HEART ARRHYTHMIA; LONG QT SYNDROME; MOLECULAR IMAGING; MOUSE; MUSCLE CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN FUNCTION; PROTEIN MODIFICATION;

A KINASE ANCHOR PROTEINS; ACTION POTENTIALS; AGE FACTORS; ANIMALS; ARRHYTHMIAS, CARDIAC; CALCIUM; CALCIUM CHANNELS, L-TYPE; CARDIOMEGALY; ION CHANNEL GATING; LONG QT SYNDROME; MICE; MICE, TRANSGENIC; MYOCARDIAL CONTRACTION; MYOCYTES, CARDIAC; PROTEIN INTERACTION DOMAINS AND MOTIFS; SYNDACTYLY;

EID: 79961025662     PISSN: 00097330     EISSN: 15244571     Source Type: Journal    
DOI: 10.1161/CIRCRESAHA.111.248252     Document Type: Article

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