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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
19 lpha), CAR, cytochrome P-450 2b10 (Cyp2b10), UDP-glucuronosyltransferase 1a1 (Ugt1a1), sulfotransfera
20 hich in turn is detoxified primarily through UDP-glucuronosyltransferase 1A1 (UGT1A1)-catalyzed glucu
21 tributed isozymes encoded at the UGT1 locus, UDP-glucuronosyltransferase 1A10 (UGT1A10) metabolizes a
22 nstitutive or ligand-induced CYP1A1; CYP1A2; UDP glucuronosyltransferase 1A2; NAD(P)H dehydrogenase,
29 obably due to interindividual differences in UDP-glucuronosyltransferase activity and/or excretion pa
31 ecombinant adenovirus (Ad), adenovirus human UDP-glucuronosyltransferase (Ad-hBUGT1) carrying the hBU
33 ss heme oxygenase, biliverdin reductase, and UDP-glucuronosyltransferases, and there was concordance
34 adenoviral antigens, we immunized bilirubin-UDP-glucuronosyltransferase (BUGT)-deficient jaundiced G
36 rlying developmental effects of a microsomal UDP-glucuronosyltransferase-encoding gene from pea (Pisu
37 Heterogeneity in uridine 5'-diphosphate (UDP) glucuronosyltransferase expression across the human
38 ion resulted in a reduced level of bilirubin UDP-glucuronosyltransferase expression in the liver.
39 observed across a 200 kb region spanning the UDP-glucuronosyltransferase family, including UGT1A1, an
40 ved hydrophobic region in the bilirubin-type UDP-glucuronosyltransferase isozyme was first uncovered
42 l as related detoxification enzymes, notably UDP-glucuronosyltransferases, suggesting a network of as
45 en is associated with a reduction in hepatic UDP glucuronosyltransferase (UGT) 1A1 activity that can
49 e of constitutional genetic variation at the UDP-glucuronosyltransferase (UGT) 1A1 locus in breast ca
50 etabolized solely through glucuronidation by UDP-glucuronosyltransferase (UGT) 1A1, it is now known t
51 ts induce the bilirubin-metabolizing enzyme--UDP-glucuronosyltransferase (UGT) 1A1--to prevent the on
52 of the rabbit liver dexamethasone-inducible UDP-glucuronosyltransferase (UGT) 2B13 RNA is related in
54 nvestigate the inhibitory effects of TKIs on UDP-glucuronosyltransferase (UGT) activities, and to qua
55 o indinavir-mediated impairment of bilirubin UDP-glucuronosyltransferase (UGT) activity and would be
56 drogen glucuronidation, catalyzed by the two UDP-glucuronosyltransferase (UGT) enzymes UGT2B15 and UG
57 ts of the UGT1A gene, encoding half of human UDP-glucuronosyltransferase (UGT) enzymes, undergo alter
58 and endoxifen, is by glucuronidation via the UDP-glucuronosyltransferase (UGT) family of enzymes.
59 AHA metabolism is by glucuronidation via the UDP-glucuronosyltransferase (UGT) family of enzymes.
60 protein-protein interactions between several UDP-glucuronosyltransferase (UGT) isoforms and cytochrom
64 e 1 (NQO1), glutathione S-transferase (GST), UDP-glucuronosyltransferase (UGT), and phenol sulfotrans
65 and hepatic glutathione S-transferase (GST), UDP-glucuronosyltransferase (UGT), and sulfotransferase
68 ent in vitro studies have suggested that the UDP-glucuronosyltransferases (UGT) 2B10 and 2B17 play ma
71 T), gamma-glutamylcysteine synthetase (GCS), UDP-glucuronosyltransferases (UGT),epoxide hydrolase, as
73 variable exons arrayed in tandem, including UDP glucuronosyltransferase (UGT1), plectin, neuronal ni
75 r glioma-associated protein 1 (GLI1) and the UDP glucuronosyltransferase (UGT1A) family of enzymes ar
79 on of two androgen-inactivating enzymes, the UDP-glucuronosyltransferases UGT2B15 and UGT2B17, was as
83 e efficient in drug conjugation catalyzed by UDP-glucuronosyltransferases (UGTs) and now report on th
89 ffinity label [beta-32P]5-azido-UDP-GlcUA to UDP-glucuronosyltransferases (UGTs) in intact, but not i
90 g rapid, reversible down-regulation of human UDP-glucuronosyltransferases (UGTs) in LS180 cells follo
91 eta-D-glucopyranosides (glucuronides) by the UDP-glucuronosyltransferases (UGTs) is a significant met
92 ferator-activated receptor alpha (PPARalpha)-UDP-glucuronosyltransferases (UGTs) signalling is an imp
93 human liver microsomes and human recombinant UDP-glucuronosyltransferases (UGTs) was characterized an
101 tipraz both induce an unidentified rat liver UDP-glucuronosyltransferase with activity toward benzo(a
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