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Eichelbaum, M., M. Ingelman-Sundberg, and W.E. Evans, Pharmacogenomics and individualized drug therapy. Annu. Rev. Med.,. 5 7: pp.119-137 (2006).
Hu, Y.F., et al., CYP3A5* 3 and CYP3A4* 18 single nucleotide polymorphisms in a Chinese population. Clinica chimica acta,. 3 5 3(1): pp.187-192(2005).
Lamba, J.K., et al., Genetic contribution to variable human CYP3A-mediated metabolism. Advanced drug delivery reviews,. 5 4(10): pp.1271-1294(2002).
Shih, P.S. and J.D. Huang, Pharmacokinetics of midazolam and 1-hydroxymidazolam in Chinese with different CYP3A5 genotypes. Drug metabolism and disposition,. 3 0(12): pp.1491-1496(2002).
Keshava, C., E.C. McCanlies, and A. Weston, CYP3A4 polymorphisms-potential risk factors for breast and prostate cancer: a HuGE review. American journal of epidemiology, 1 6 0(9): pp.825-841(2004).
Bork, R., et al., Characterization of mRNA species related to human liver cytochrome P-450 nifedipine oxidase and the regulation of catalytic activity. Journal of Biological Chemistry, 2 6 4(2): pp.910-919(1989).
Beaune, P.H., et al., Isolation and sequence determination of a cDNA clone related to human cytochrome P-450 nifedipine oxidase. Proceedings of the National Academy of Sciences, 8 3(21): p.8064(1989).
Linder, M.W., R.A. Prough, and R. Valdes Jr, Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. Clinical Chemistry,. 4 3(2): pp.254-266(1997).
Hashimoto, H., et al., Gene structure of CYP3A4, an adult-specific form of cytochrome P450 in human livers, and its transcriptional control. European Journal of Biochemistry, 2 1 8(2): pp.585-595(1993).
Rebbeck, T.R., et al., Modification of clinical presentation of prostate tumors by a novel genetic variant in CYP3A4. Journal of the National Cancer Institute, 9 0(16): p.12251229(1998).
Amirimani, B., et al., Increased transcriptional activity of the CYP3A4* 1B promoter variant. Environmental and molecular mutagenesis, 4 2(4): pp.299-305(2003).
Felix, C.A., et al., Association of CYP3A4 genotype with treatment-related leukemia. Proceedings of the National Academy of Sciences, 9 5(22): p.13176(1998).
von Moltke, L.L., et al., Unusually low clearance of two CYP3A substrates, alprazolam and trazodone, in a volunteer subject with wild-type CYP3A4 promoter region. The Journal of Clinical Pharmacology, 4 0(2): pp.200-204(2000).
Sata, F., et al., CYP3A4 allelic variants with amino acid substitutions in exons 7 and 12: evidence for an allelic variant with altered catalytic activity. Clinical Pharmacology & Therapeutics, 6 7(1): pp.48-56(2000).
Ball, S.E., et al., Population distribution and effects on drug metabolism of a genetic variant in the 5 promotor region of CYP3A4. Clinical Pharmacology & Therapeutics, 6 6(3): p.288294 (1999).
Cavalli, S.A., M.H. Hirata, and R.D.C. Hirata, Detection of MboII polymorphism at the 5 promoter region of CYP3A4. Clinical chemistry, 4 7(2): pp.348-351(2001).
Arvanitidis, K., et al., Genetic polymorphisms of drug-metabolizing enzymes CYP2D6, CYP2C9, CYP2C19 and CYP3A5 in the Greek population. Fundamental & clinical pharmacology, 2 1(4): pp.419-426 (2007).
Miao, J., et al., Association of genotypes of the CYP3A cluster with midazolam disposition in vivo. The pharmacogenomics journal, 9(5): pp.319-326(2009).
Oliveira, E., et al., Pharmacogenetically relevant polymorphisms in Portugal. Pharmacogenomics, 8(7): pp.703-712(2007).
Wolbold, R., et al., Sex is a major determinant of CYP3A4 expression in human liver. Hepatology, 38(4): pp.978-988(2003).