Function of human cytochrome P450s: characterization of the orphans.
暂无分享,去创建一个
F Peter Guengerich | F. Guengerich | Z. Wu | Zhong-Liu Wu | Cheryl J Bartleson | C. Bartleson | F. Guengerich | Cheryl J. Bartleson
[1] K. Anderson,et al. Radiometric analysis of biological oxidations in man: sex differences in estradiol metabolism. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[2] M. Kaiser-Kupfer,et al. Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2. , 2004, American journal of human genetics.
[3] M. Waterman,et al. Characterization of the CYP4A11 gene, a second CYP4A gene in humans. , 2003, Archives of biochemistry and biophysics.
[4] 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.
[5] J. Brockmöller,et al. Interindividual variability and tissue-specificity in the expression of cytochrome P450 3A mRNA. , 2002, Drug metabolism and disposition: the biological fate of chemicals.
[6] F. Gonzalez,et al. The CYP2A3 gene product catalyzes coumarin 7-hydroxylation in human liver microsomes. , 1990, Biochemistry.
[7] Jun-yan Hong,et al. HUMAN CYTOCHROME P450 2S1: LACK OF ACTIVITY IN THE METABOLIC ACTIVATION OF SEVERAL CIGARETTE SMOKE CARCINOGENS AND IN THE METABOLISM OF NICOTINE , 2005, Drug Metabolism and Disposition.
[8] H. Strobel,et al. Expression and characterization of human cytochrome P450 4F11: Putative role in the metabolism of therapeutic drugs and eicosanoids. , 2004, Toxicology and applied pharmacology.
[9] A. Fersht. Structure and mechanism in protein science , 1998 .
[10] F. Guengerich,et al. Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity. , 2001, Chemical research in toxicology.
[11] F. Guengerich,et al. Cytochrome P450 3A4-catalyzed Testosterone 6β-Hydroxylation Stereochemistry, Kinetic Deuterium Isotope Effects, and Rate-limiting Steps* , 2005, Journal of Biological Chemistry.
[12] M. Ingelman-Sundberg,et al. Characterization of a novel CYP2A7/CYP2A6 hybrid allele (CYP2A6*12) that causes reduced CYP2A6 activity , 2002, Human mutation.
[13] J. Schenkman,et al. Expression patterns of mouse and human CYP orthologs (families 1-4) during development and in different adult tissues. , 2005, Archives of biochemistry and biophysics.
[14] H. Cui,et al. Liver-specific Deletion of the NADPH-Cytochrome P450 Reductase Gene , 2003, Journal of Biological Chemistry.
[15] E. Rieber,et al. Identification of a Novel Mammary-Restricted Cytochrome P450, CYP4Z1, with Overexpression in Breast Carcinoma , 2004, Cancer Research.
[16] T. Rebbeck,et al. CYP3A4, CYP3A5, and CYP3A43 Genotypes and Haplotypes in the Etiology and Severity of Prostate Cancer , 2004, Cancer Research.
[17] J. Halpert,et al. cDNA cloning and initial characterization of CYP3A43, a novel human cytochrome P450. , 2001, Molecular pharmacology.
[18] D. Waxman,et al. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. , 1986, The Journal of biological chemistry.
[19] M. Taimi,et al. CYP2U1, a Novel Human Thymus- and Brain-specific Cytochrome P450, Catalyzes ω- and (ω-1)-Hydroxylation of Fatty Acids* , 2004, Journal of Biological Chemistry.
[20] J. Schenkman,et al. Comparative expression profiling of 40 mouse cytochrome P450 genes in embryonic and adult tissues. , 2003, Archives of biochemistry and biophysics.
[21] Eric F. Johnson,et al. Differential regulation of human CYP4A genes by peroxisome proliferators and dexamethasone. , 2003, Archives of biochemistry and biophysics.
[22] J. Lafitte,et al. First report of a genetic polymorphism of the cytochrome P450 3A43 (CYP3A43) gene: Identification of a loss‐of‐function variant , 2004, Human mutation.
[23] Eric F. Johnson,et al. Conditional regulation of the human CYP4X1 and CYP4Z1 genes. , 2005, Archives of biochemistry and biophysics.
[24] F. Guengerich,et al. Cooperativity in oxidations catalyzed by cytochrome P450 3A4. , 1997, Biochemistry.
[25] M. Ingelman-Sundberg,et al. Cloning and tissue distribution of a novel human cytochrome p450 of the CYP3A subfamily, CYP3A43. , 2001, Biochemical and biophysical research communications.
[26] D. Kelly,et al. The Diversity and Importance of Microbial Cytochromes P450 , 2005 .
[27] D. Harder,et al. Identification of a novel cytochrome P450, CYP4X1, with unique localization specific to the brain. , 2002, Biochemical and biophysical research communications.
[28] M Ingelman-Sundberg,et al. Identification and tissue distribution of the novel human cytochrome P450 2S1 (CYP2S1). , 2001, Biochemical and biophysical research communications.
[29] William B. Jakoby,et al. Enzymatic basis of detoxication , 1980 .
[30] O. Hankinson,et al. Identification of a novel dioxin-inducible cytochrome P450. , 2002, Molecular pharmacology.
[31] R. Evans,et al. The RXR heterodimers and orphan receptors , 1995, Cell.
[32] A. Hayes. Principles and methods of toxicology , 1982 .
[33] D. Kroetz,et al. REGULATION AND INHIBITION OF ARACHIDONIC ACID ω-HYDROXYLASES AND 20-HETE FORMATION , 2005 .
[34] F. Gonzalez,et al. Study of P450 function using gene knockout and transgenic mice. , 2003, Archives of biochemistry and biophysics.
[35] K. Husgafvel‐Pursiainen,et al. Identification of genetic polymorphisms of CYP2S1 in a Finnish Caucasian population. , 2004, Mutation research.
[36] M. Ingelman-Sundberg,et al. Characterization and tissue distribution of a novel human cytochrome P450-CYP2U1. , 2004, Biochemical and biophysical research communications.
[37] F. Guengerich,et al. Human cytochrome P-450 enzymes. , 1992, Life sciences.
[38] Ortiz de Montellano,et al. Cytochrome P-450: Structure, Mechanism, and Biochemistry , 1986 .
[39] R. Tyndale,et al. Implications of CYP2A6 Genetic Variation for Smoking Behaviors and Nicotine Dependence , 2005, Clinical pharmacology and therapeutics.
[40] C. Wolf,et al. Inactivation of the Hepatic Cytochrome P450 System by Conditional Deletion of Hepatic Cytochrome P450 Reductase* , 2003, The Journal of Biological Chemistry.
[41] D. Liebler,et al. P-Mod: an algorithm and software to map modifications to peptide sequences using tandem MS data. , 2005, Journal of proteome research.
[42] B. Møller,et al. Cytochrome P450s in Plants , 2005 .
[43] M. Sarfarazi,et al. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. , 1997, Human molecular genetics.
[44] H. Yamazaki,et al. Aryl hydrocarbon hydroxylase represents CYP1B1, and not CYP1A1, in human freshly isolated white cells: trimodal distribution of Japanese population according to induction of CYP1B1 mRNA by environmental dioxins. , 2003, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.
[45] Gillian Smith,et al. Cutaneous expression of cytochrome P450 CYP2S1: individuality in regulation by therapeutic agents for psoriasis and other skin diseases , 2003, The Lancet.
[46] D. Russell,et al. Clinical importance of the cytochromes P450 , 2002, The Lancet.
[47] B. Lake,et al. Expression and alternative splicing of the cytochrome P-450 CYP2A7. , 1995, The Biochemical journal.