Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
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Regulation and function of family 1 and family 2 UDP-glucuronosyltransferase genes (UGT1A, UGT2B) in human oesophagusAnimal models of human response to dioxinsIdentification of a rat oltipraz-inducible UDP-glucuronosyltransferase (UGT1A7) with activity towards benzo(a)pyrene-7,8-dihydrodiolIsolation and characterization of the monkey UGT2B30 gene that encodes a uridine diphosphate-glucuronosyltransferase enzyme active on mineralocorticoid, glucocorticoid, androgen and oestrogen hormonesImplications for risk assessment of suggested nongenotoxic mechanisms of chemical carcinogenesis.Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.Dietary Dihydromethysticin Increases Glucuronidation of 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanol in A/J Mice, Potentially Enhancing Its DetoxificationPotential role of UGT pharmacogenetics in cancer treatment and prevention: focus on tamoxifen.UGT1A1*28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case-control study.Expression of UDP-glucuronosyltransferase 1A in bladder cancer: association with prognosis and regulation by estrogen.Androgen receptor signals regulate UDP-glucuronosyltransferases in the urinary bladder: a potential mechanism of androgen-induced bladder carcinogenesis.Cytosylglucuronic acid synthase (cytosine: UDP-glucuronosyltransferase) from Streptomyces griseochromogenes, the first prokaryotic UDP-glucuronosyltransferase.Induction of cytochrome P4501 as an indicator of potential chemical carcinogenesis.Expression of a functionally active human hepatic UDP-glucuronosyltransferase (UGT1A6) lacking the N-terminal signal sequence in the endoplasmic reticulum.Opposite regulation of bilirubin and 4-nitrophenol UDP-glucuronosyltransferase mRNA levels by 3,3',5 triiodo-L-thyronine in rat liver.In vitro effects of some antibiotics on glutathione reductase from sheep liver.Identification of aspartic acid and histidine residues mediating the reaction mechanism and the substrate specificity of the human UDP-glucuronosyltransferases 1A.Inhibition of aflatoxin B1- and N-nitrosodiethylamine-induced liver preneoplastic foci in rats fed naturally occurring allyl sulfides.
P2860
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P2860
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
description
article científic
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article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on January 1991
@en
vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@en
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@nl
type
label
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@en
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@nl
prefLabel
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@en
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@nl
P2860
P1476
Roles of UDP-glucuronosyltransferases in chemical carcinogenesis.
@en
P2093
P2860
P304
P356
10.3109/10409239109081125
P577
1991-01-01T00:00:00Z