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Year | Number of Results |
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1994 | 1 |
1997 | 1 |
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The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans.
J Biol Chem. 1994 Jun 3;269(22):15419-22.
J Biol Chem. 1994.
PMID: 8195181
Free article.
High frequencies of CYP2C19 mutations and poor metabolism of proguanil in Vanuatu.
Kaneko A, Kaneko O, Taleo G, Björkman A, Kobayakawa T.
Kaneko A, et al.
Lancet. 1997 Mar 29;349(9056):921-2. doi: 10.1016/S0140-6736(05)62696-7.
Lancet. 1997.
PMID: 9093256
No abstract available.
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Cytochrome P450 2C19 loss-of-function polymorphism, but not CYP3A4 IVS10 + 12G/A and P2Y12 T744C polymorphisms, is associated with response variability to dual antiplatelet treatment in high-risk vascular patients.
Giusti B, Gori AM, Marcucci R, Saracini C, Sestini I, Paniccia R, Valente S, Antoniucci D, Abbate R, Gensini GF.
Giusti B, et al.
Pharmacogenet Genomics. 2007 Dec;17(12):1057-64. doi: 10.1097/FPC.0b013e3282f1b2be.
Pharmacogenet Genomics. 2007.
PMID: 18004210
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Frequencies of genotypes and alleles of the functional SNPs in CYP2C19 and CYP2E1 in mainland Chinese Kazakh, Uygur and Han populations.
Wang SM, Zhu AP, Li D, Wang Z, Zhang P, Zhang GL.
Wang SM, et al.
J Hum Genet. 2009 Jun;54(6):372-5. doi: 10.1038/jhg.2009.41. Epub 2009 May 15.
J Hum Genet. 2009.
PMID: 19444287
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