Editorial: Ion channels as a target for drug design

Current Pharmaceutical Design

Volumn 12, Issue 18, 2006, Pages 2187-

  Tai, Kwok Keung ^a  

^a LONG BEACH MEMORIAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIARRHYTHMIC AGENT; CALCIUM ACTIVATED POTASSIUM CHANNEL; CALCIUM CHANNEL T TYPE; ENZYME INHIBITOR; ION CHANNEL; MUTANT PROTEIN; POTASSIUM CHANNEL BLOCKING AGENT; POTASSIUM CHANNEL HERG; SODIUM CHANNEL; TRANSMEMBRANE CONDUCTANCE REGULATOR; VOLTAGE GATED CHANNEL FORMING PROTEIN; VOLTAGE GATED POTASSIUM CHANNEL;

ALPHA CHAIN; APOPTOSIS; CHANNEL GATING; CYSTIC FIBROSIS; DIARRHEA; DRUG DESIGN; DRUG POTENCY; DRUG TARGETING; EDITORIAL; ENZYME INHIBITION; EPILEPSY; HEART REPOLARIZATION; HEART RHYTHM; HUMAN; HYPERTENSION; IN VIVO STUDY; INDUSTRIALIZATION; INSULIN DEPENDENT DIABETES MELLITUS; KIDNEY EPITHELIUM; MITOCHONDRION; MORTALITY; MULTIPLE SCLEROSIS; NOCICEPTION; PAIN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; REPOLARIZATION; SYNAPTIC TRANSMISSION; T LYMPHOCYTE ACTIVATION;

EID: 33745146858     PISSN: 13816128     EISSN: None     Source Type: Journal    
DOI: 10.2174/138161206777585166     Document Type: Editorial

References (7)

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7. Panaghie G, Abbott GW. The Impact of Ancillary Subunits on Small-Molecule Interactions with Voltage-Gated Potassium Channels. Curr Pharm Des 2006; 12(18): 2285-2302.