Chapter 4 – Xenobiotic Metabolism
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[1] H. Jörnvall,et al. Nomenclature of alcohol dehydrogenases. , 1995, Alcohol and alcoholism.
[2] F. Oesch,et al. Asp, Asp, and His Form the Catalytic Triad of Rat Soluble Epoxide Hydrolase (*) , 1996, The Journal of Biological Chemistry.
[3] B. Hammock,et al. Bioactivation of leukotoxins to their toxic diols by epoxide hydrolase , 1997, Nature Medicine.
[4] G. Siest,et al. The UDP glucuronosyltransferase gene superfamily: suggested nomenclature based on evolutionary divergence. , 1991, DNA and cell biology.
[5] M. Coughtrie. Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism? , 1996, Human & experimental toxicology.
[6] J. Ritter,et al. Gene structure at the human UGT1 locus creates diversity in isozyme structure, substrate specificity, and regulation. , 1995, Progress in nucleic acid research and molecular biology.
[7] R. Armstrong,et al. The catalytic mechanism of microsomal epoxide hydrolase involves an ester intermediate , 1993 .
[8] W. Dekant,et al. Biotransformation and membrane transport in nephrotoxicity. , 1996, Critical reviews in toxicology.
[9] R. Armstrong,et al. Enzyme-catalyzed detoxication reactions: mechanisms and stereochemistry. , 1987, CRC critical reviews in biochemistry.
[10] F. Guengerich,et al. Human cytochrome P-450 enzymes. , 1992, Life sciences.
[11] J. Brockmöller,et al. Combined analysis of inherited polymorphisms in arylamine N-acetyltransferase 2, glutathione S-transferases M1 and T1, microsomal epoxide hydrolase, and cytochrome P450 enzymes as modulators of bladder cancer risk. , 1996, Cancer research.
[12] T. Vales,et al. Selective suppression of cytochrome P-450 gene expression by interleukins 1 and 6 in rat liver. , 1994, Biochimica et biophysica acta.
[13] R. Weinshilboum,et al. Sulfation pharmacogenetics in humans. , 1994, Chemico-biological interactions.
[14] K. Bock. Roles of UDP-glucuronosyltransferases in chemical carcinogenesis. , 1991, Critical reviews in biochemistry and molecular biology.
[15] Y. Fujii‐Kuriyama,et al. Regulation of CYP1A1 expression , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[16] F. Guengerich,et al. New applications of bacterial systems to problems in toxicology. , 1996, Critical reviews in toxicology.
[17] C. Bradfield,et al. Ah receptor signaling pathways. , 1996, Annual review of cell and developmental biology.
[18] T A Jones,et al. Structural analysis of human alpha-class glutathione transferase A1-1 in the apo-form and in complexes with ethacrynic acid and its glutathione conjugate. , 1995, Structure.
[19] J R Cashman,et al. Pharmacokinetics and molecular detoxication. , 1996, Environmental health perspectives.
[20] S. Loft,et al. Foreign compound metabolism capacity in man measured from metabolites of dietary caffeine. , 1992, Carcinogenesis.
[21] B. Mannervik,et al. Glutathione transferases--structure and catalytic activity. , 1988, CRC critical reviews in biochemistry.
[22] O. Hankinson. The aryl hydrocarbon receptor complex. , 1995, Annual review of pharmacology and toxicology.
[23] P. Mackenzie,et al. Steroid UDP glucuronosyltransferases: characterization and regulation. , 1996, The Journal of endocrinology.
[24] F. Gonzalez,et al. Targeted disruption of specific cytochromes P450 and xenobiotic receptor genes. , 1996, Methods in enzymology.
[25] D W Nebert,et al. P450 superfamily: update on new sequences, gene mapping, accession numbers and nomenclature. , 1996, Pharmacogenetics.
[26] E. Maser,et al. The identification of 11 beta-hydroxysteroid dehydrogenase as carbonyl reductase of the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone. , 1996, European journal of biochemistry.
[27] N. Vermeulen,et al. Metabolism and kinetics of trichloroethylene in relation to toxicity and carcinogenicity. Relevance of the mercapturic acid pathway. , 1995, Chemical research in toxicology.
[28] F. Oesch,et al. Sequence similarity of mammalian epoxide hydrolases to the bacterial haloalkane dehalogenase and other related proteins , 1994, FEBS letters.
[29] R. Estabrook. The remarkable P450s: a historical overview of these versatile hemeprotein catalysts , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[30] W. Pearson,et al. Nomenclature for human glutathione transferases. , 1992, The Biochemical journal.
[31] C. Wolf,et al. Recombinant DNA technology as an investigative tool in drug metabolism research , 1996 .
[32] S. Okino,et al. Induction of cytochrome P4501A1: a model for analyzing mammalian gene transcription , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[33] F. Kadlubar,et al. Cytochrome P-450 and acetyltransferase expression as biomarkers of carcinogen-DNA adduct levels and human cancer susceptibility. , 1996, Progress in clinical and biological research.
[34] R. Armstrong. Glutathione S-transferases: reaction mechanism, structure, and function. , 1991, Chemical research in toxicology.
[35] M. J. Coon,et al. Cytochrome P450 2: peroxidative reactions of diversozymes. , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[36] J. Hayes,et al. The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance. , 1995, Critical reviews in biochemistry and molecular biology.
[37] C. Smith,et al. Genetic polymorphisms in xenobiotic metabolism. , 1994, European journal of cancer.
[38] B. Ketterer. Effects of genetic polymorphism and enzyme induction in the glutathione S-transferase family on chemical safety and risk assessment. , 1996, Environmental toxicology and pharmacology.
[39] F. Gonzalez,et al. Role of human cytochromes P450 in the metabolic activation of chemical carcinogens and toxins. , 1994, Drug metabolism reviews.
[40] Ortiz de Montellano,et al. Cytochrome P-450: Structure, Mechanism, and Biochemistry , 1986 .
[41] J R Cashman,et al. Structural and catalytic properties of the mammalian flavin-containing monooxygenase. , 1995, Chemical research in toxicology.
[42] B. Ketterer,et al. The role of glutathione and glutathione transferases in chemical carcinogenesis. , 1990, Critical reviews in biochemistry and molecular biology.
[43] R. Huber,et al. X-ray crystal structures of cytosolic glutathione S-transferases. Implications for protein architecture, substrate recognition and catalytic function. , 1994, European journal of biochemistry.
[44] G L Gilliland,et al. The three-dimensional structure of a glutathione S-transferase from the mu gene class. Structural analysis of the binary complex of isoenzyme 3-3 and glutathione at 2.2-A resolution. , 1992, Biochemistry.
[45] F. Oesch,et al. Gene evolution of epoxide hydrolases and recommended nomenclature. , 1995, DNA and cell biology.
[46] M. Ingelman-Sundberg,et al. Genetic polymorphism of human cytochrome P450 2E1. , 1996, Methods in enzymology.
[47] J. Goldstein,et al. Biochemistry and molecular biology of the human CYP2C subfamily. , 1994, Pharmacogenetics.
[48] C. Bloomfield,et al. Increased risk for myelodysplastic syndromes in individuals with glutathione transferase theta 1 (GSTT1) gene defect , 1996, The Lancet.
[49] D. Nebert,et al. Cytochrome P450: evolution and functional diversity. , 1994, Progress in liver diseases.
[50] D W Nebert,et al. Human drug-metabolizing enzyme polymorphisms: effects on risk of toxicity and cancer. , 1996, DNA and cell biology.