Modulation of recombinant human cardiac L-type Ca2+ channel α(1C) subunits by redox agents and hypoxia

Journal of Physiology

Volumn 514, Issue 3, 1999, Pages 629-637

  Fearon, I M ^a   Palmer, A C V ^a   Balmforth, A J ^a   Ball, S G ^a   Varadi, G ^b   Peers, C ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

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

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALCIUM ION; CHLOROMERCURIBENZENESULFONIC ACID; DITHIOTHREITOL; THIOMERSAL; CALCIUM CHANNEL ALPHA 1C L TYPE; CALCIUM CHANNEL L TYPE; UNCLASSIFIED DRUG;

ARTICLE; CALCIUM CURRENT; HUMAN; HUMAN CELL; HYPOXIA; KIDNEY CELL CULTURE; PATCH CLAMP; PRIORITY JOURNAL; CHANNEL GATING; CONTROLLED STUDY; COUPLING FACTOR; EMBRYO; HEK293 CELL LINE; METABOLIC REGULATION; MODULATION; OXIDATION REDUCTION STATE; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; WHOLE CELL PATCH CLAMP;

ANOXIA; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS; CALCIUM CHANNELS, L-TYPE; CELL LINE; CYSTEINE; ELECTRIC STIMULATION; ELECTROPHYSIOLOGY; HEART; HUMANS; MEMBRANE POTENTIALS; MYOCARDIUM; OXIDANTS; OXIDATION-REDUCTION; PATCH-CLAMP TECHNIQUES; RECOMBINANT PROTEINS; REDUCING AGENTS;

EID: 0033082894     PISSN: 00223751     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1469-7793.1999.629ad.x     Document Type: Article

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