Tissue-specific, inducible, and hormonal control of the human UDP-glucuronosyltransferase-1 (UGT1) locus.
about
Triclocarban mediates induction of xenobiotic metabolism through activation of the constitutive androstane receptor and the estrogen receptor alphaNrf2-Keap1 signaling pathway regulates human UGT1A1 expression in vitro and in transgenic UGT1 miceOrganic anion transporting polypeptide 1a/1b-knockout mice provide insights into hepatic handling of bilirubin, bile acids, and drugsDevelopmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus.Use of transgenic mice in UDP-glucuronosyltransferase (UGT) studiesHuman UGT1A4 and UGT1A3 conjugate 25-hydroxyvitamin D3: metabolite structure, kinetics, inducibility, and interindividual variability.A humanized UGT1 mouse model expressing the UGT1A1*28 allele for assessing drug clearance by UGT1A1-dependent glucuronidationStudies on induction of lamotrigine metabolism in transgenic UGT1 mice.Importance of UDP-glucuronosyltransferase 1A1 expression in skin and its induction by UVB in neonatal hyperbilirubinemiaDrug-metabolizing enzyme, transporter, and nuclear receptor genetically modified mouse models.Inhibition of human UGT2B7 gene expression in transgenic mice by the constitutive androstane receptor.Clinical therapeutics in pregnancy.UDP-glucuronosyltransferase expression in mouse liver is increased in obesity- and fasting-induced steatosisParacetamol pharmacokinetics and metabolism in young women.Pregnane-x-receptor controls hepatic glucuronidation during pregnancy and neonatal development in humanized UGT1 mice.Reduced expression of UGT1A1 in intestines of humanized UGT1 mice via inactivation of NF-κB leads to hyperbilirubinemia.Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia.Hormones, seizures, and lamotrigine: Oh, my!Human UGT1A8 and UGT1A10 mRNA are expressed in primary human hepatocytesLamotrigine in pregnancy: clearance, therapeutic drug monitoring, and seizure frequency.Alterations in drug disposition during pregnancy: implications for drug therapy.Phytochemical regulation of UDP-glucuronosyltransferases: implications for cancer prevention.Identification of human UDP-glucuronosyltransferases catalyzing hepatic 1alpha,25-dihydroxyvitamin D3 conjugation.Intestinal glucuronidation protects against chemotherapy-induced toxicity by irinotecan (CPT-11).Developmental onset of bilirubin-induced neurotoxicity involves Toll-like receptor 2-dependent signaling in humanized UDP-glucuronosyltransferase1 mice.UDP-glucuronosyltransferases (UGTs): from purification of Ah-receptor-inducible UGT1A6 to coordinate regulation of subsets of CYPs, UGTs, and ABC transporters by nuclear receptors.Regulation of endobiotics glucuronidation by ligand-activated transcription factors: physiological function and therapeutic potential.UDP-glucuronosyltransferases (UGTs) in neuro-olfactory tissues: expression, regulation, and function.Contributions of the Ah receptor to bilirubin homeostasis and its antioxidative and atheroprotective functions.Genetic polymorphism in metabolism and host defense enzymes: implications for human health risk assessment.Nuclear receptors and endobiotics glucuronidation: the good, the bad, and the UGT.Genetically humanized mouse models of drug metabolizing enzymes and transporters and their applications.Transcriptional regulation of human UDP-glucuronosyltransferase genes.Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia.Human CYP1A1GFP expression in transgenic mice serves as a biomarker for environmental toxicant exposure.Glucuronidation of drugs in humanized UDP-glucuronosyltransferase 1 mice: Similarity with glucuronidation in human liver microsomes.Intestinal NCoR1, a regulator of epithelial cell maturation, controls neonatal hyperbilirubinemia.Effect of aging on glucuronidation of valproic acid in human liver microsomes and the role of UDP-glucuronosyltransferase UGT1A4, UGT1A8, and UGT1A10Induction of mouse UDP-glucuronosyltransferase mRNA expression in liver and intestine by activators of aryl-hydrocarbon receptor, constitutive androstane receptor, pregnane X receptor, peroxisome proliferator-activated receptor alpha, and nuclear faIsothiocyanates induce UGT1A1 in humanized UGT1 mice in a CAR dependent fashion that is highly dependent upon oxidative stress.
P2860
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P2860
Tissue-specific, inducible, and hormonal control of the human UDP-glucuronosyltransferase-1 (UGT1) locus.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@en
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@nl
type
label
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@en
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@nl
prefLabel
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@en
Tissue-specific, inducible, an ...... syltransferase-1 (UGT1) locus.
@nl
P2093
P2860
P356
P1476
Tissue-specific, inducible, an ...... osyltransferase-1 (UGT1) locus
@en
P2093
Deirdre Beaton
Erin Brace-Sinnokrak
Jocelyn Trottier
Joseph K Ritter
Kathy Senekeo-Effenberger
Nghia Nguyen
Olivier Barbier
Robert H Tukey
Rory P Remmel
Shujuan Chen
P2860
P304
37547-37557
P356
10.1074/JBC.M506683200
P407
P577
2005-09-09T00:00:00Z