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January 5, 2004BloodOpen Access

5′-Flanking region polymorphisms of CYP2C9 and their relationship to S-warfarin metabolism in white and Japanese patients

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Authors

HTHarumi TakahashiKobe UniversityIIIchiro IeiriFukuoka International UniversityGWG. WilkinsonGeorgia Institute of Technology

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Takahashi et al. (2004) studied this question.

synapsesocial.com/papers/6a1996cf3e4c9aaeb7f64627https://doi.org/10.1182/blood-2003-07-2521
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Hydroxylation of warfarin by human cDNA-expressed cytochrome P-450: a role for P-4502C9 in the etiology of (S)-warfarin-drug interactions1992 · 602 citations
  2. 2Metabolism of warfarin enantiomers in Japanese patients with heart disease having different CYP2C9 and CYP2C19 genotypes*1998 · 184 citations
  3. 3Comparisons between in-vitro and in-vivo metabolism of (S)-warfarin: catalytic activities of cDNA-expressed CYP2C9, its Leu359 variant and their mixture versus unbound clearance in patients with the corresponding CYP2C9 genotypes1998 · 163 citations
  4. 4Population differences in S‐warfarin metabolism between <i>CYP2C9</i> genotype‐matched Caucasian and Japanese patients2003 · 190 citations
  5. 5Genetic polymorphisms and functional characterization of the 5′-flanking region of the human CYP2C9 gene: In vitro and in vivo studies2001 · 82 citations