Targeted inactivation of αi2 or αi3 disrupts activation of the cardiac muscarinic K+ channel, IK+Ach, in intact cells

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

Volumn 94, Issue 15, 1997, Pages 7921-7926

  Sowell, Margaret O ^a   Ye, Chianping ^a   Ricupero, Dennis A ^a   Hansen, Sherry ^a   Quinn, Stephen J ^a   Vassilev, Peter M ^a   Mortensen, Richard M ^a  

^a BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE; CARBACHOL; GUANINE NUCLEOTIDE BINDING PROTEIN; GUANOSINE TRIPHOSPHATASE; MUSCARINIC RECEPTOR; POTASSIUM CHANNEL; ADENOSINE RECEPTOR; POTASSIUM CHANNEL BLOCKING AGENT;

ARTICLE; BINDING SITE; CHRONOTROPISM; ELECTROPHYSIOLOGY; GENE EXPRESSION; HEART CONTRACTION; HEART MUSCLE CELL; HUMAN; HUMAN CELL; IMMUNOBLOTTING; PRIORITY JOURNAL; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; CELL LINE; DRUG ANTAGONISM; GENETICS; HEART MUSCLE; METABOLISM; MUTATION;

CARBACHOL; CELL LINE; GTP-BINDING PROTEINS; MUTATION; MYOCARDIUM; POTASSIUM CHANNEL BLOCKERS; POTASSIUM CHANNELS; RECEPTORS, PURINERGIC P1;

EID: 0030610849     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.15.7921     Document Type: Article

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