Common mutant alleles of CYP2D6 causing the defect of CYP2D6 enzyme activity in a Japanese population.
作者信息
Ishiguro Akihiro, Kubota Takahiro, Sasaki Hiroshi, Yamada Yasuhiko, Iga Tatsuji
出版信息
Br J Clin Pharmacol. 2003 Apr;55(4):414-5. doi: 10.1046/j.1365-2125.2003.01782.x.
Abstract
摘要
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Common mutant alleles of CYP2D6 causing the defect of CYP2D6 enzyme activity in a Japanese population.在日本人群中导致CYP2D6酶活性缺陷的CYP2D6常见突变等位基因。
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本文引用的文献
1
Frequent occurrence of CYP2D6*10 duplication allele in a Japanese population.
Mutat Res. 2002 Aug 29;505(1-2):83-5. doi: 10.1016/s0027-5107(02)00122-7.
2
CYP2D6 genotypes in a Japanese population: low frequencies of CYP2D6 gene duplication but high frequency of CYP2D6*10.
Pharmacogenetics. 2000 Aug;10(6):567-70. doi: 10.1097/00008571-200008000-00010.
3
Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes.正常日本人群中CYP2D6突变等位基因的频率以及不同CYP2D6基因型中右美沙芬O-去甲基化的代谢活性。
Br J Clin Pharmacol. 2000 Jul;50(1):31-4. doi: 10.1046/j.1365-2125.2000.00209.x.
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A new variant CYP2D6 allele (CYP2D6*21) with a single base insertion in exon 5 in a Japanese population associated with a poor metabolizer phenotype.
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CYP2D6 phenotype-genotype relationships in African-Americans and Caucasians in Los Angeles.洛杉矶非裔美国人和高加索人中CYP2D6的表型-基因型关系
Pharmacogenetics. 1998 Dec;8(6):529-41. doi: 10.1097/00008571-199812000-00010.
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A new CYP2D6 allele with a nine base insertion in exon 9 in a Japanese population associated with poor metabolizer phenotype.在日本人群中发现一种新的CYP2D6等位基因，其外显子9中有9个碱基插入，与代谢不良表型相关。
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