Induction of P-450 in workers exposed to dioxin.
暂无分享,去创建一个
W. Halperin | M. Sweeney | M. Fingerhut | B. Tang | W. Kalow | K. Wille | B. Timpkins | K. K. Wille | Brent Timpkins
[1] P. Harper,et al. The Ah receptor: mediator of the toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds. , 1994, Toxicology letters.
[2] B. Tang,et al. The use of caffeine for enzyme assays: A critical appraisal , 1993, Clinical pharmacology and therapeutics.
[3] S. Loft,et al. Foreign compound metabolism capacity in man measured from metabolites of dietary caffeine. , 1992, Carcinogenesis.
[4] R. Hayes,et al. Determination of CYP1A2 and NAT2 phenotypes in human populations by analysis of caffeine urinary metabolites. , 1992, Pharmacogenetics.
[5] F. Gonzalez,et al. Biotransformation of caffeine, paraxanthine, theobromine and theophylline by cDNA-expressed human CYP1A2 and CYP2E1. , 1992, Pharmacogenetics.
[6] S. Loft,et al. Interaction of smoking, uptake of polycyclic aromatic hydrocarbons, and cytochrome P450IA2 activity among foundry workers. , 1992, British journal of industrial medicine.
[7] B. Tang,et al. Use of caffeine metabolite ratios to explore CYP1A2 and xanthine oxidase activities , 1991, Clinical pharmacology and therapeutics.
[8] P. A. Honchar,et al. Cancer mortality in workers exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin. , 1991, The New England journal of medicine.
[9] B. Tang,et al. Caffeine as a metabolic probe: Exploration of the enzyme‐inducing effect of cigarette smoking , 1991, Clinical pharmacology and therapeutics.
[10] D. Schoeller,et al. The caffeine breath test and caffeine urinary metabolite ratios in the Michigan cohort exposed to polybrominated biphenyls: a preliminary study. , 1990, Environmental health perspectives.
[11] R. Hornung,et al. Estimation of Average Concentration in the Presence of Nondetectable Values , 1990 .
[12] W. Halperin,et al. Comparison of serum levels of 2,3,7,8-TCDD in TCP production workers and in an unexposed comparison group , 1990 .
[13] A. Okey. Enzyme induction in the cytochrome P-450 system. , 1990, Pharmacology & therapeutics.
[14] M. Butler,et al. Human cytochrome P-450PA (P-450IA2), the phenacetin O-deethylase, is primarily responsible for the hepatic 3-demethylation of caffeine and N-oxidation of carcinogenic arylamines. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[15] D. Nebert,et al. Human CYP1A2: sequence, gene structure, comparison with the mouse and rat orthologous gene, and differences in liver 1A2 mRNA expression. , 1989, Molecular endocrinology.
[16] E. Silbergeld,et al. Dioxins and the Ah receptor. , 1989, American journal of industrial medicine.
[17] D A Marlow,et al. Levels of polychlorinated dibenzo-p-dioxins and dibenzofurans in workers exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin. , 1989, American journal of industrial medicine.
[18] B. Tang,et al. An alternative test for acetylator phenotyping with caffeine , 1987, Clinical pharmacology and therapeutics.
[19] S. Spielberg,et al. A urinary metabolite ratio that reflects systemic caffeine clearance , 1987, Clinical pharmacology and therapeutics.
[20] D. Grant,et al. Biotransformation of caffeine, paraxanthine, theophylline, and theobromine by polycyclic aromatic hydrocarbon-inducible cytochrome(s) P-450 in human liver microsomes. , 1987, Drug metabolism and disposition: the biological fate of chemicals.
[21] M. Denison,et al. Induction of drug-metabolizing enzymes: mechanisms and consequences. , 1986, Clinical biochemistry.
[22] D. Grant,et al. A simple test for acetylator phenotype using caffeine. , 1984, British journal of clinical pharmacology.
[23] A Poland,et al. 2,3,7,8-tetrachlorodibenzo-p-dioxin and related halogenated aromatic hydrocarbons: examination of the mechanism of toxicity. , 1982, Annual review of pharmacology and toxicology.
[24] E. Glover,et al. Chlorinated dibenzo-p-dioxins: potent inducers of delta-aminolevulinic acid synthetase and aryl hydrocarbon hydroxylase. II. A study of the structure-activity relationship. , 1973, Molecular pharmacology.
[25] D. Nebert,et al. Aryl hydrocarbon hydroxylase induction by polycyclic hydrocarbons: simple autosomal dominant trait in the mouse. , 1972, Nature: New biology.