Inhibition of recombinant human cardiac L-type Ca2+ channel α(1C) subunits by 3-isobutyl-1-methylxanthine

European Journal of Pharmacology

Volumn 342, Issue 2-3, 1998, Pages 353-358

  Fearon, Ian M ^a   Palmer, Adrian C V ^a   Balmforth, Anthony J ^a   Ball, Stephen G ^a   Mikala, Gabor ^b   Peers, Chris ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Ca2+ channel; Cyclic nucleotide; Isobutylmethylxanthine; Phosphodiesterase

Indexed keywords

CALCIUM CHANNEL; CYCLIC AMP DEPENDENT PROTEIN KINASE; CYCLIC GMP DEPENDENT PROTEIN KINASE; ISOBUTYLMETHYLXANTHINE; METHYLXANTHINE; PHOSPHODIESTERASE; ROLIPRAM;

ARTICLE; BASE PAIRING; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; ENZYME ACTIVATION; ENZYME ACTIVITY; ENZYME INHIBITION; HUMAN; HUMAN CELL; PATCH CLAMP; PRIORITY JOURNAL;

1-METHYL-3-ISOBUTYLXANTHINE; ADENOSINE; BARIUM; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS; CLONE CELLS; FLAVINS; HEART; HUMANS; MEMBRANE POTENTIALS; MYOCARDIUM; PATCH-CLAMP TECHNIQUES; PHOSPHODIESTERASE INHIBITORS; RECOMBINANT PROTEINS;

EID: 0032567754     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-2999(97)01497-0     Document Type: Article

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