[1] Wrighton SA, vardonbradonM, Ring BJ.The human drug metabolizing cytochromes P450[J].J Pharm Biopharm, 1996, 24(5):461-473. [2] Fujihara J, Shiwaku K, Xue Y, et al.CYP1A2 polymorphism(C>A at position -163) in Ovambos, Koreans and Mongolians[J].Cell Biochem Funct, 2007, 25(5):491-494. [3] Aklillu E, Carrillo JA, Makonnen E, et al.Genetic polymorphism of CYP1A2 in Ethiopians affecting induction and expression:Characterization of novel haplotypes with single- nucleotide polymorphisms in intron 1[J].Mol Pharmacol, 2003, 64(3):659-669. [4] Murayama N, Soyama A, Saito Y, et al.Six novel nonsynonymous CYP1A2 gene polymorphisms:Catalytic activities of the naturally occurring variant enzymes[J].J Pharmacol Exp Ther, 2004, 308(3):1219-1219. [5] Allorge D, Chevalier D, Lo-Guidice JM, et al.Identifica-Chin J Clin Pharmacol Ther 2009 Oct;14(10) tion of a novel splice-site mutation in the CYP1A2 gene [J].Br J Clin Pharmacol, 2003, 56(3):341-344. [6] Skarke C, Kirchhof A, Geisslinger G, et al.Rapid genotyping for relevant CYP1A2 alleles by pyrosequencing[J]. Eur J Clin Pharmacol, 2005, 61(12):887-892. [7] Ghotbi R, Christensen M, Roh HK, et al.Comparisons of CYP1A2 genetic polymorphism, enzyme activity and the genotype-phenotype relationship in Swedes and Koreans [J].Eur J Clin Pharmacol, 2007, 63(6):537-546. [8] Grabar PB, Rozman B, Tomsic M, et al.Genetic polymorphism of CYP1A2 and the toxicity of leflunomide treatment in rheumatoid arthritis patients[J].Eur J Clin Pharmacol, 2008, 64(9):871-876. [9] Tay JKX, Tan CH, Chong SA, et al.Functional polymorphism of the cytochrome P450 1A2(CYP1A2) gene and prolonged QTc interval in schizophrenia[J].Prog Neuro- Psychopharmacol Biol Psychiatry, 2007, 31(6):1297-1302. [10] Obase Y, Shimoda T, Kawano T, et al.Polymorphisms in the CYP1A2 gene and theophylline metabolism in patients with asthma[J].Clin Parmacol Ther, 2003, 73(5):468-474. [11] Kivisto KT, Kroemer HK.Use of probe drugs as predictors of drug metabolism in humans[J].J Clin Pharmacol, 1997, 37(Suppl 1):S40-S48. [12] DeMorais SM, Wilkinson GR, Blaisdell J, et al.The major genetic defect responsible for the polymorphism of Smephenytoin metabolism in humans[J].J Biol Chem, 1994, 269(22):15419-15422. [13] DeMorais SM,Wilkinson GR, Blaisdell J, et al.Identification of a new genetic-defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese[J]. Mol Pharmacol, 1994, 46(4):594-598. [14] Xiao ZS, Goldstein JA, Xie HG, et al.Differences in the incidence of the CYP2C19 polymorphism affecting the Smephenytoin phenotype in Chinese Han and Bai populations and identification of a new rare CYP2C19 mutant allele[J].J Pharmacol Exp Ther, 1997, 281(1):604-609. [15] Ibeanu GC, Blaisdell J, Ferguson RJ, et al.A novel transversion in the intron 5 donor splice junction of CYP2C19 and a sequence polymorphism in exon 3 contribute to the poor metabolizer phenotype for the anticonvulsant drug Smephenytoin[J].J Pharmacol Exp Ther, 1999, 290(2): 635-640. [16] Yin OQR, Tomlinson B, Chow AHL, et al.Omeprazole as a CYP2C19 Marker in Chinese subjects:Assessment of its gene-dose effect and intrasubject variability [J].J Clin Pharmacol, 2004, 44(6):582-589. [17] 郑露, 邵建国.CYP2C19 的基因多态性与临床[J].第二军医大学学报, 2007, 28(11):1262-1265. [18] Rudberg I, Hermann M, Refsum H, et al.Serum concentrations of sertraline and N-desmethyl sertraline in relation to CYP2C19 genotype in psy chiatric patients[J].Eur J Clin Pharmacol, 2008, 64(12):1181-1188. [19] Sim SC, Risinger C, Dahl ML, et al.A common novel CYP2C19 gene variant causes ultrarapid drug metabolism relevant for the drug response to proton pump inhibitors and antidepressants[J].Clin Pharmacol Ther, 2006, 79(1):103-113. [20] Sugimoto K, Uno T, Yamazaki H, et al.Limited frequency of the CYP2C19*17 allele and its minor role in a Japanese population[J].Br J Clin Pharmacol, 2008, 65(3): 437-439. [21] King BP,Khan TI, Aithal GP, et al.Up stream and coding region CYP2C9 polymorphisms:correlation with warfarin dose and metabolism[J].Pharmacogenetics, 2004, 14(12):813-822. [22] Dickmann LJ, Rettie AE, Kneller MB, et al.Identification and functional characterization of a new CYP2C9 variant (CYP2C9*5) expressed among African Americans[J]. Mol Pharmacol, 2001, 60(2):382-387. [23] 李智, 王果, 周宏灏.CYP2C19 基因多态性及其功能意义研究进展[J].中国临床药理学与治疗学,2008, 13(6):601-609. [24] Xie HG, Prasad HC, Kim RB, et al.CYP2C19 allelic variants: ethnic distribution and functional significance [J]. Adv Drug Deliver Rev, 2002, 54(10):1257-1270. [25] VanderWeide J, Steijns LS, vanWeeldenMJ, et al.The effect of genetic polymorphism of cytochrome P450 CYP2C9 on phenytoin dose requirement[J].Pharmacogenetics, 2001, 11(4):287-291. [26] 李健, 文思远, 王睿, 等.细胞色素P450 CYP2C9 基因多态性对甲苯磺丁脲代谢动力学的影响[J].药学学报, 2005, 40(8):695-699. [27] Lindh JD, Holm L, Andersson ML, et al.Influence of CYP2C9 genotype on warfarin dose requirements-a systematic review and meta-analysis[J].Eur J Clin Pharmacol, 2009, 65(4):365-375. [28] Zhang YF, Zhong DF, Si DY, et al.Lornoxicam pharmacokinetics in relation to cytochrome P450 2C9 genotype [J].Br J Clin Pharmacol, 2005, 59(1):14-17. [29] Bae JW, Kim JH, Choi CI, et al.Effect of CYP2C9*3 allele on the pharmacokinetics of naproxen in Korean subjects[J].Arch Pharm Res, 2009, 32(2):269-273. [30] Shimada T, Tsumura F, Yamazaki H, et al.Characterization of (+ -) bufuralol hydroxylation activities in liver microsomes of Japanese and Caucasian subjects genotyped for CYP2D6[J].Pharmacogenetics, 2001, 11(2):143-156. [31] Evert B, Griese EU, Eichelbaum M.A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteine[J].Naunyn Schmiedebergs Arch Pharmacol, 1994, 350(4):434-439. [32] Sawamura K, Suzuki Y, Someya T, et al.Effects of dosage and CYP2D6-mutated allele on plasma concentration of paroxetine[J].Eur J Clin Pharmacol, 2004, 60(8):553-557. [33] Yin OP, Shi XJ, Tomlinson B, et al.Effect of CYP2D6*10 allele on the pharmacokinetics of loratadine in chinese subjects[J].Drug Metab Dispos, 2005, 33(9):1283-1287. [34] 李芹, 王睿, 郭雅, 等.中国人群CYP2D6 基因多态性对美托洛尔药代动力学的影响[J].中国临床药理学与治疗学, 2008, 13(7):796-802. [35] Shams MEE, Arneth B, Hiemke C, et al.CYP2D6 polymorphism and clinical effect of the antidepressant venlafaxine[J].J Clin Pharm Ther, 2006, 31(5):493-502. [36] 伍忠銮, 谢红光, 周宏灏.细胞色素P450 2E1 的研究进展[J].中国临床药理学杂志, 1997, 13(1):57-62. [37] Hu Y, Oscarson M, Johansson I, et al.Genetic polymorphism of human CYP2E1:characterization of two variant alleles[J].Mol Pharmacol, 1997, 51(3):370-376. [38] Howard LA, Ahluwalia JS, Lin SK, et al.CYP2E1*1D regulatory polymorphism:association with alcohol and nicotine dependence[J].Pharmacogenetics, 2003, 13(6): 321-328. [39] Sata F, Sapone A, Elizondo G, et al.CYP3A4 allelic variants with amino acid substitutions in exons 7 and 12:evidence for an allelic variant with altered catalytic activity [J].Clin Pharmacol Ther, 2000, 67(1):48-56. [40] Fukushima-Uesaka H, Saito Y,Watanabe H, et al.Haplotypes of CYP3A4 and their close linkage with CYP3A5 haplotypes in a Japanese population[J].Hum Mutat, 2004, 23(1):100-108. [41] Hsieh KP, Lin YY, Cheng CL, et al.Novel mutations of CYP3A4 in Chinese[J].Drug Metab Dispos, 2001, 29(3):268-273. [42] Wang A, Yu BN, Luo CH, et al.IIe118Val genetic polymorphism of CYP3A4 and its effects on lipid-lowering efficacy of simvastatin in Chinese hyperlipidemic patients[J]. Eur J Clin Pharmacol, 2005, 60(12):843-848. [43] Gao Y, Zhang LR, Fu Q.CYP3A4*1G polymorphism is associated with lipid-lowering efficacy of atorbvastatin but not of simvastatin[J].43] Gao Y, Zhang LR, Fu Q.CYP3A4*1G polymorphism is associated with lipid-lowering efficacy of atorbvastatin but not of simvastatin[J].Eur J Clin Pharmacol, 2008, 64(9):877-882. [44] Rodriguez-Antona C, Sayi JG, Gustafsson LL, et al.Phenotype- genotype variability in the human CYP3A locus as assessed by the probe drug quinine and analyses of variant CYP3A4 alleles[J].Biochem Biophys Res Commum, 2005, 338(1):299-305. [45] 姜敏, 熊玉卿.细胞色素氧化酶P450 3A4 与药物代谢[J].实用临床医学, 2006, 7(11):199-201 |