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1 chrome P450 or phase II conjugating enzymes (UDP-glucuronosyltransferase).
2 m deficiency of the hepatic enzyme bilirubin-UDP-glucuronosyltransferase.
3 otransferases, glutathione transferases, and UDP-glucuronosyltransferases.
4 ucuronic acid in the liver via the action of UDP-glucuronosyltransferases.
7 P4501A1, glutathione S-transferase Ya1, and UDP-glucuronosyltransferase 1*6 are apparently potentiat
9 nits (pfu) intravenously) in adult bilirubin-UDP-glucuronosyltransferase-1 (BUGT1)-deficient Gunn rat
10 olerance to adenoviral antigens in bilirubin-UDP-glucuronosyltransferase-1 (BUGT1)-deficient Gunn rat
11 via gastroduodenostomy tubes into bilirubin-UDP-glucuronosyltransferase-1 (BUGT1)-deficient jaundice
12 tyltransferase (pSV2-CAT) or human bilirubin-UDP-glucuronosyltransferase-1 (pSVK3-hBUGT1) genes were
13 iplex promoter spanning 218 kb, the phase II UDP-glucuronosyltransferase 1A (UGT1) gene encodes at le
14 us result in part from delayed expression of UDP-glucuronosyltransferase 1A1 (UGT1A1) and the inabili
16 valuated the impact of oral iAs treatment on UDP-glucuronosyltransferase 1A1 (UGT1A1) expression and
17 e evaluated the impact of lactational TCS on UDP-glucuronosyltransferase 1A1 (UGT1A1) expression and
22 lpha), CAR, cytochrome P-450 2b10 (Cyp2b10), UDP-glucuronosyltransferase 1a1 (Ugt1a1), sulfotransfera
23 hich in turn is detoxified primarily through UDP-glucuronosyltransferase 1A1 (UGT1A1)-catalyzed glucu
25 tributed isozymes encoded at the UGT1 locus, UDP-glucuronosyltransferase 1A10 (UGT1A10) metabolizes a
26 nstitutive or ligand-induced CYP1A1; CYP1A2; UDP glucuronosyltransferase 1A2; NAD(P)H dehydrogenase,
30 feration and stemness by inducing the enzyme UDP-glucuronosyltransferase 2B15 (UGT2B15), which promot
34 obably due to interindividual differences in UDP-glucuronosyltransferase activity and/or excretion pa
36 ecombinant adenovirus (Ad), adenovirus human UDP-glucuronosyltransferase (Ad-hBUGT1) carrying the hBU
39 ss heme oxygenase, biliverdin reductase, and UDP-glucuronosyltransferases, and there was concordance
40 adenoviral antigens, we immunized bilirubin-UDP-glucuronosyltransferase (BUGT)-deficient jaundiced G
42 rlying developmental effects of a microsomal UDP-glucuronosyltransferase-encoding gene from pea (Pisu
43 Heterogeneity in uridine 5'-diphosphate (UDP) glucuronosyltransferase expression across the human
44 ion resulted in a reduced level of bilirubin UDP-glucuronosyltransferase expression in the liver.
45 genetic inhibition of hepatic conjugation by UDP glucuronosyltransferase family 1 member A1 (UGT1A1),
46 observed across a 200 kb region spanning the UDP-glucuronosyltransferase family, including UGT1A1, an
48 ved hydrophobic region in the bilirubin-type UDP-glucuronosyltransferase isozyme was first uncovered
50 l as related detoxification enzymes, notably UDP-glucuronosyltransferases, suggesting a network of as
51 was attributed to metabolic deactivation by UDP-glucuronosyltransferases that were expressed in RASW
54 en is associated with a reduction in hepatic UDP glucuronosyltransferase (UGT) 1A1 activity that can
58 e of constitutional genetic variation at the UDP-glucuronosyltransferase (UGT) 1A1 locus in breast ca
59 etabolized solely through glucuronidation by UDP-glucuronosyltransferase (UGT) 1A1, it is now known t
60 ts induce the bilirubin-metabolizing enzyme--UDP-glucuronosyltransferase (UGT) 1A1--to prevent the on
61 of the rabbit liver dexamethasone-inducible UDP-glucuronosyltransferase (UGT) 2B13 RNA is related in
63 nvestigate the inhibitory effects of TKIs on UDP-glucuronosyltransferase (UGT) activities, and to qua
64 o indinavir-mediated impairment of bilirubin UDP-glucuronosyltransferase (UGT) activity and would be
65 drogen glucuronidation, catalyzed by the two UDP-glucuronosyltransferase (UGT) enzymes UGT2B15 and UG
66 ts of the UGT1A gene, encoding half of human UDP-glucuronosyltransferase (UGT) enzymes, undergo alter
68 and endoxifen, is by glucuronidation via the UDP-glucuronosyltransferase (UGT) family of enzymes.
69 AHA metabolism is by glucuronidation via the UDP-glucuronosyltransferase (UGT) family of enzymes.
70 protein-protein interactions between several UDP-glucuronosyltransferase (UGT) isoforms and cytochrom
74 e 1 (NQO1), glutathione S-transferase (GST), UDP-glucuronosyltransferase (UGT), and phenol sulfotrans
75 and hepatic glutathione S-transferase (GST), UDP-glucuronosyltransferase (UGT), and sulfotransferase
78 ent in vitro studies have suggested that the UDP-glucuronosyltransferases (UGT) 2B10 and 2B17 play ma
82 T), gamma-glutamylcysteine synthetase (GCS), UDP-glucuronosyltransferases (UGT),epoxide hydrolase, as
84 variable exons arrayed in tandem, including UDP glucuronosyltransferase (UGT1), plectin, neuronal ni
86 r glioma-associated protein 1 (GLI1) and the UDP glucuronosyltransferase (UGT1A) family of enzymes ar
87 Crigler-Najjar syndrome model animal lacking UDP-glucuronosyltransferase (UGT1A1), was used as recipi
91 on of two androgen-inactivating enzymes, the UDP-glucuronosyltransferases UGT2B15 and UGT2B17, was as
94 e efficient in drug conjugation catalyzed by UDP-glucuronosyltransferases (UGTs) and now report on th
100 ffinity label [beta-32P]5-azido-UDP-GlcUA to UDP-glucuronosyltransferases (UGTs) in intact, but not i
101 g rapid, reversible down-regulation of human UDP-glucuronosyltransferases (UGTs) in LS180 cells follo
102 eta-D-glucopyranosides (glucuronides) by the UDP-glucuronosyltransferases (UGTs) is a significant met
103 ferator-activated receptor alpha (PPARalpha)-UDP-glucuronosyltransferases (UGTs) signalling is an imp
104 human liver microsomes and human recombinant UDP-glucuronosyltransferases (UGTs) was characterized an
112 tipraz both induce an unidentified rat liver UDP-glucuronosyltransferase with activity toward benzo(a