A population and family study of CYP1A2 using caffeine urinary metabolites
- 1 January 1995
- journal article
- pharmacokinetics and-disposition
- Published by Springer Nature in European Journal of Clinical Pharmacology
- Vol. 47 (5) , 423-430
- https://doi.org/10.1007/bf00196856
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Determination of CYP1A2 and NAT2 phenotypes in human populations by analysis of caffeine urinary metabolitesPharmacogenetics, 1992
- Identification of the Ah Receptor Nuclear Translocator Protein (Arnt) as a Component of the DNA Binding Form of the Ah ReceptorScience, 1992
- Biotransformation of caffeine, paraxanthine, theobromine and theophylline by cDNA-expressed human CYP1A2 and CYP2E1Pharmacogenetics, 1992
- Diurnal Effect on Caffeine ClearanceThe Journal of Clinical Pharmacology, 1992
- Foreign compound metabolism capacity in man measured from metabolites of dietary caffeineCarcinogenesis: Integrative Cancer Research, 1992
- Human AH locus polymorphism and cancer: inducibility of CYP1A1 and other genes by combustion products and dioxinPharmacogenetics, 1991
- Oxidation of toxic and carcinogenic chemicals by human cytochrome P-450 enzymesChemical Research in Toxicology, 1991
- Cloning of a Factor Required for Activity of the Ah (Dioxin) ReceptorScience, 1991
- Racial differences in serum cotinine levels among smokers in the Coronary Artery Risk Development in (Young) Adults study.American Journal of Public Health, 1990
- Inducible, receptor-dependent protein-DNA interactions at a dioxin-responsive transcriptional enhancer.Proceedings of the National Academy of Sciences, 1988