CYP1A2 F21L and F186L polymorphisms in an Italian population sample.
暂无分享,去创建一个
[1] R. V. Schaik. Cancer treatment and pharmacogenetics of cytochrome P450 enzymes , 2005, Investigational New Drugs.
[2] M. Nakajima,et al. Cytochrome P450-mediated metabolism of estrogens and its regulation in human. , 2005, Cancer letters.
[3] Kazuo Komamura,et al. Six Novel Nonsynonymous CYP1A2 Gene Polymorphisms: Catalytic Activities of the Naturally Occurring Variant Enzymes , 2004, Journal of Pharmacology and Experimental Therapeutics.
[4] D. Nebert,et al. Uroporphyrin accumulation in hepatoma cells expressing human or mouse CYP1A2: relation to the role of CYP1A2 in human porphyria cutanea tarda. , 2003, Biochemical pharmacology.
[5] H. Yamazaki,et al. A population phenotyping study of three drug‐metabolizing enzymes in Kyushu, Japan, with use of the caffeine test , 2002, Clinical pharmacology and therapeutics.
[6] K. Kyvik,et al. The interindividual differences in the 3-demthylation of caffeine alias CYP1A2 is determined by both genetic and environmental factors. , 2002, Pharmacogenetics.
[7] J. Barrett,et al. Polymorphisms in the cytochrome P450 CYP1A2 gene (CYP1A2) in colorectal cancer patients and controls: allele frequencies, linkage disequilibrium and influence on caffeine metabolism. , 2003, British journal of clinical pharmacology.
[8] M. Lai,et al. Detection of a novel cytochrome P-450 1A2 polymorphism (F21L) in Chinese. , 1999, Drug metabolism and disposition: the biological fate of chemicals.