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Volumn 72, Issue 2, 2002, Pages 209-219
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Role of human MDR1 gene polymorphism in bioavailability and interaction of digoxin, a substrate of P-glycoprotein
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Author keywords
[No Author keywords available]
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Indexed keywords
CLARITHROMYCIN;
DIGOSIN;
DIGOXIN;
GLYCOPROTEIN P;
MULTIDRUG RESISTANCE PROTEIN 1;
ADULT;
ALLELE;
ARTICLE;
CLINICAL TRIAL;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
DOSE RESPONSE;
DRUG ABSORPTION;
DRUG BIOAVAILABILITY;
DRUG BLOOD LEVEL;
DRUG CLEARANCE;
DRUG DISPOSITION;
GENETIC POLYMORPHISM;
GENOTYPE;
HUMAN;
KIDNEY CLEARANCE;
MALE;
NORMAL HUMAN;
PRIORITY JOURNAL;
ADMINISTRATION, ORAL;
ADULT;
ALLELES;
ANTI-BACTERIAL AGENTS;
AREA UNDER CURVE;
ASIAN CONTINENTAL ANCESTRY GROUP;
BIOLOGICAL AVAILABILITY;
CARDIOTONIC AGENTS;
CLARITHROMYCIN;
CYTOCHROME P-450 ENZYME SYSTEM;
DIGOXIN;
DRUG ADMINISTRATION SCHEDULE;
DRUG INTERACTIONS;
ENZYME INHIBITORS;
GENES, MDR;
GENOTYPE;
HUMANS;
INJECTIONS, INTRAVENOUS;
JAPAN;
MALE;
P-GLYCOPROTEIN;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, GENETIC;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
REFERENCE VALUES;
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EID: 0036693051
PISSN: 00099236
EISSN: None
Source Type: Journal
DOI: 10.1067/mcp.2002.126177 Document Type: Article |
Times cited : (263)
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References (52)
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