PHARMACOKINETICS OF CITALOPRAM IN RELATION TO GENETIC POLYMORPHISM OF CYP2C19-Reference-Cited by-同舟云学术

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PHARMACOKINETICS OF CITALOPRAM IN RELATION TO GENETIC POLYMORPHISM OF CYP2C19

Published:2003-09-15 Issue:10 Volume:31 Page:1255-1259
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Yu Bang-Ning,Chen Guo-Lin,He Nan,Ouyang Dong-Sheng,Chen Xiao-Ping,Liu Zhao-Qian,Zhou Hong-Hao

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference26 articles.

1. The hydroxylation of omeprazole correlates with S-mephenytoin metabolism: A population study*

2. Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and S-mephenytoin

3. Debrisoquine/Sparteine Hydroxylation Genotype and Phenotype: Analysis of Common Mutations and Alleles ofCYP2D6in a European Population

4. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans.

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5. Pharmacokinetic and pharmacodynamic interactions between daridorexant, a dual orexin receptor antagonist, and citalopram in healthy subjects;European Neuropsychopharmacology;2021-10

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