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Article

Significant genetic linkage of MDR1 polymorphisms at positions 3435 and 2677: functional relevance to pharmacokinetics of digoxin.

Pharmaceutical research - 1 Oct 2002

Horinouchi Masanori, Sakaeda Toshiyuki, Nakamura Tsutomu, Morita Yoshinori, Tamura Takao, Aoyama Nobuo, Kasuga Masato, Okumura Katsuhiko

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Share to ATP Binding Cassette Transporter, Subfamily B, Member 1
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Genetic

Share to Polymorphism, Single Nucleotide

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Identifiers

PMID: 12425480
DOI: 10.1023/a:1020433422259

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Significant genetic linkage of MDR1 polymorphisms at positions 3435 and 2677: functional relevance to pharmacokinetics of digoxin.PMID 12425480Read ↗

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MDR1 genotype-related pharmacokinetics: fact or fiction?Semantic proximity Read ↗

Digoxin pharmacokinetics and MDR1 genetic polymorphisms.Semantic proximity Read ↗

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P-glycoprotein: tissue distribution, substrates, and functional consequences of genetic variations.Semantic proximity Read ↗

Meta-analysis of the influence of MDR1 C3435T polymorphism on digoxin pharmacokinetics and MDR1 gene expression.Semantic proximity Read ↗

Pharmacogenetics of drug transporters and its impact on the pharmacotherapy.Semantic proximity Read ↗

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