-
2
-
-
0001177611
-
The uridine diphosphate glucuronosyltransferase multigene family: Function and regulation
-
Clarke DJ, Burchell B. The uridine diphosphate glucuronosyltransferase multigene family: function and regulation. Handb Exper Pharmcol 1994; 112: 3-43
-
(1994)
Handb Exper Pharmcol
, vol.112
, pp. 3-43
-
-
Clarke, D.J.1
Burchell, B.2
-
3
-
-
0001643397
-
UDP-glucuronosyltransferases
-
Sipes IG, Gandolfi AJ, Mcqueen CA, editors. Amsterdam: Pergamon Elsevier Science
-
Burchell B, McGurk K, Brierley CH, et al. UDP-glucuronosyltransferases. In: Sipes IG, Gandolfi AJ, Mcqueen CA, editors. Comprehensive toxicology. Vol. 3. Amsterdam: Pergamon Elsevier Science, 1997: 401-35
-
(1997)
Comprehensive Toxicology
, vol.3
, pp. 401-435
-
-
Burchell, B.1
McGurk, K.2
Brierley, C.H.3
-
4
-
-
0027692685
-
Human UDP-glucuronosyltransferases: Chemical defence, jaundice and gene therapy
-
Brierley CH, Burchell B. Human UDP-glucuronosyltransferases: chemical defence, jaundice and gene therapy. Bioessays 1993; 15: 749-54
-
(1993)
Bioessays
, vol.15
, pp. 749-754
-
-
Brierley, C.H.1
Burchell, B.2
-
5
-
-
0026532030
-
Acyl glucuronides revisited: Is the glucuronidation process a toxification as well as detoxification mechanism?
-
Spahn-Langguth H, Benet LZ. Acyl glucuronides revisited: is the glucuronidation process a toxification as well as detoxification mechanism? Drug Metab Rev 1992; 24: 5-48
-
(1992)
Drug Metab Rev
, vol.24
, pp. 5-48
-
-
Spahn-Langguth, H.1
Benet, L.Z.2
-
6
-
-
0028875109
-
Specificity of human UDP-glucuronosyltransferases and xenobiotic glucuronidation
-
Burchell B, Brierley CH, Rance D. Specificity of human UDP-glucuronosyltransferases and xenobiotic glucuronidation. Life Sci 1995; 57: 1819-31
-
(1995)
Life Sci
, vol.57
, pp. 1819-1831
-
-
Burchell, B.1
Brierley, C.H.2
Rance, D.3
-
7
-
-
0027242397
-
Validation and use of cloned, expressed human drug metabolising enzymes in heterologous cells for analysis of drug metabolism and drug-drug interactions
-
Remmel RP, Burchell B. Validation and use of cloned, expressed human drug metabolising enzymes in heterologous cells for analysis of drug metabolism and drug-drug interactions. Biochem Pharmacol 1993; 46: 559-66
-
(1993)
Biochem Pharmacol
, vol.46
, pp. 559-566
-
-
Remmel, R.P.1
Burchell, B.2
-
8
-
-
0035115599
-
Genetic multiplicity of the human UDP-glucuronosyltransferases and regulation in the gastrointestinal tract
-
Tukey RH, Strassburg CP. Genetic multiplicity of the human UDP-glucuronosyltransferases and regulation in the gastrointestinal tract. Mol Pharmacol 2001; 59: 405-14
-
(2001)
Mol Pharmacol
, vol.59
, pp. 405-414
-
-
Tukey, R.H.1
Strassburg, C.P.2
-
9
-
-
0032707765
-
Structural and functional studies of UDP-Glucuronosyltransferases
-
Radominska-Pandya A, Czernik PJ, Little JM, et al. Structural and functional studies of UDP-Glucuronosyltransferases. Drug Metab Rev 1999; 31: 817-99
-
(1999)
Drug Metab Rev
, vol.31
, pp. 817-899
-
-
Radominska-Pandya, A.1
Czernik, P.J.2
Little, J.M.3
-
10
-
-
0025773294
-
The UDP glucuronosyltransferase gene superfamily: Suggested nomenclature based on evolutionary divergence
-
Burchell B, Nebert DW, Nelson DR, et al. The UDP glucuronosyltransferase gene superfamily: suggested nomenclature based on evolutionary divergence. DNA Cell Biol 1991; 10: 487-94
-
(1991)
DNA Cell Biol
, vol.10
, pp. 487-494
-
-
Burchell, B.1
Nebert, D.W.2
Nelson, D.R.3
-
11
-
-
8544224973
-
The UDP glycosyltransferase gene superfamily: Recommended nomenclature update based on evolutionary divergence
-
Mackenzie P, Owens IS, Burchell B, et al. The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence. Pharmacogenetics 1997; 7: 255-69
-
(1997)
Pharmacogenetics
, vol.7
, pp. 255-269
-
-
Mackenzie, P.1
Owens, I.S.2
Burchell, B.3
-
12
-
-
0026665547
-
Chromosomal assignment of human phenol and bilirubin UDP-glucuronosyltransferase genes (UGT1A Subfamily)
-
Moghrabi N, Sutherland L, Wooster R, et al. Chromosomal assignment of human phenol and bilirubin UDP-glucuronosyltransferase genes (UGT1A Subfamily). Ann Hum Genet 1992; 56: 83-93
-
(1992)
Ann Hum Genet
, vol.56
, pp. 83-93
-
-
Moghrabi, N.1
Sutherland, L.2
Wooster, R.3
-
13
-
-
0026879233
-
The novel bilirubin/phenol UDP-glucuronosyltransferase UGT 1 gene locus: Implications for multiple nonhemolytic familial hyperbilirubinaemia phenotypes
-
Owens IS, Ritter JK. The novel bilirubin/phenol UDP-glucuronosyltransferase UGT 1 gene locus: implications for multiple nonhemolytic familial hyperbilirubinaemia phenotypes. Pharmacogenetics 1992; 2: 93-108
-
(1992)
Pharmacogenetics
, vol.2
, pp. 93-108
-
-
Owens, I.S.1
Ritter, J.K.2
-
14
-
-
0025861217
-
Cloning and stable expression of a new member of the human liver phenol/bilirubin UDP-glucuronosyltransferase cDNA family
-
Wooster R, Sutherland L, Ebner T, et al. Cloning and stable expression of a new member of the human liver phenol/bilirubin UDP-glucuronosyltransferase cDNA family. Biochem J 1991; 278: 465-9
-
(1991)
Biochem J
, vol.278
, pp. 465-469
-
-
Wooster, R.1
Sutherland, L.2
Ebner, T.3
-
15
-
-
0034966656
-
Thirteen UDP-glucuronosyltransferase genes are encoded at the human UGT1 gene complex locus
-
Gong Q-H, Cho JW, Huang T, et al. Thirteen UDP-glucuronosyltransferase genes are encoded at the human UGT1 gene complex locus. Pharmacogenetics 2001; 11: 357-68
-
(2001)
Pharmacogenetics
, vol.11
, pp. 357-368
-
-
Gong, Q.-H.1
Cho, J.W.2
Huang, T.3
-
17
-
-
0026736260
-
Localization of a bile acid UDP-glucuronosyltransferase gene UGT2B to chromosome 4 using the polymerase chain reaction
-
Monaghan G, Povey S, Burchell B, et al. Localization of a bile acid UDP-glucuronosyltransferase gene UGT2B to chromosome 4 using the polymerase chain reaction. Genomics 1992; 13: 908-9
-
(1992)
Genomics
, vol.13
, pp. 908-909
-
-
Monaghan, G.1
Povey, S.2
Burchell, B.3
-
18
-
-
0028136583
-
Isolation of a human YAC contig encompassing a cluster of UGT2 genes and its regional localization to chromosome 4q13
-
Monaghan G, Clarke DJ, Povey S, et al. Isolation of a human YAC contig encompassing a cluster of UGT2 genes and its regional localization to chromosome 4q13. Genomics 1994; 23: 496-9
-
(1994)
Genomics
, vol.23
, pp. 496-499
-
-
Monaghan, G.1
Clarke, D.J.2
Povey, S.3
-
19
-
-
0034050743
-
Genomic organisation of the UGT2B gene cluster on human chromosome 4q13
-
Reidy M, Wang J-Y, Miller AP, et al. Genomic organisation of the UGT2B gene cluster on human chromosome 4q13. Pharmacogenetics 2000; 10: 251-60
-
(2000)
Pharmacogenetics
, vol.10
, pp. 251-260
-
-
Reidy, M.1
Wang, J.-Y.2
Miller, A.P.3
-
20
-
-
0035103197
-
Relative enzymatic activity, protein stability, and tissue distribution of human steroid-metabolizing UGT2B subfamily members
-
Turgeon D, Carrier J-S, Levesque E, et al. Relative enzymatic activity, protein stability, and tissue distribution of human steroid-metabolizing UGT2B subfamily members. Endocrinology 2001; 142: 778-87
-
(2001)
Endocrinology
, vol.142
, pp. 778-787
-
-
Turgeon, D.1
Carrier, J.-S.2
Levesque, E.3
-
21
-
-
0033564554
-
Cloning and characterization of a novel human olfactory UGT
-
Jedlitschky G, Cassidy AJ, Sales M, et al. Cloning and characterization of a novel human olfactory UGT. Biochem J 1999; 340: 837-43
-
(1999)
Biochem J
, vol.340
, pp. 837-843
-
-
Jedlitschky, G.1
Cassidy, A.J.2
Sales, M.3
-
22
-
-
0025284207
-
The UDP-glucuronosyltransferases: A family of detoxifying enzymes
-
Tephly TR, Burchell B. The UDP-glucuronosyltransferases: a family of detoxifying enzymes. Trends Pharmacol Sci 1990; 11: 276-9
-
(1990)
Trends Pharmacol Sci
, vol.11
, pp. 276-279
-
-
Tephly, T.R.1
Burchell, B.2
-
23
-
-
0027991904
-
Investigation of the substrate-specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation
-
Senafi SB, Clarke DJ, Burchell B. Investigation of the substrate-specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation. Biochem J 1994; 303: 233-40
-
(1994)
Biochem J
, vol.303
, pp. 233-240
-
-
Senafi, S.B.1
Clarke, D.J.2
Burchell, B.3
-
24
-
-
0025831505
-
Interindividual variability in the glucuronidation and sulphation of ethinyloestradiol in human liver
-
Temellini A, Giuliani L, Pacifici GM. Interindividual variability in the glucuronidation and sulphation of ethinyloestradiol in human liver. Br J Clin Pharmacol 1991; 31: 661-4
-
(1991)
Br J Clin Pharmacol
, vol.31
, pp. 661-664
-
-
Temellini, A.1
Giuliani, L.2
Pacifici, G.M.3
-
25
-
-
0035154231
-
Evidence for significant differences in microsomal drug glucuronidation by canine and human liver and kidney
-
Soars MG, Riley RJ, Findlay KAB, et al. Evidence for significant differences in microsomal drug glucuronidation by canine and human liver and kidney. Drug Metab Dispos 2001; 29: 121-6
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 121-126
-
-
Soars, M.G.1
Riley, R.J.2
Findlay, K.A.B.3
-
26
-
-
0024390969
-
UDP-glucuronyltransferases in "genetic factors influencing the metabolism of foreign compounds"
-
Burchell B, Coughtrie MWH. UDP-glucuronyltransferases in "genetic factors influencing the metabolism of foreign compounds". Pharmacol Ther 1989; 43: 261-89
-
(1989)
Pharmacol Ther
, vol.43
, pp. 261-289
-
-
Burchell, B.1
Coughtrie, M.W.H.2
-
27
-
-
0003144221
-
Expression and co-induction of CYP1A1 and UGT1*6 in human lungs
-
Vainio H, Elovaara E, Luukkanen L, et al. Expression and co-induction of CYP1A1 and UGT1*6 in human lungs. Eur J Drug Metab Pharmacokinet 1995; Special Issue: 47-8
-
(1995)
Eur J Drug Metab Pharmacokinet
, Issue.SPEC. ISSUE
, pp. 47-48
-
-
Vainio, H.1
Elovaara, E.2
Luukkanen, L.3
-
28
-
-
0032705773
-
Ethnic differences in N-glucuronidation of nicotine and cotinine
-
Benowitz NL, Perez-Stable E, Fong I, et al. Ethnic differences in N-glucuronidation of nicotine and cotinine. J Pharmacol Exp Ther 1999; 291: 1196-203
-
(1999)
J Pharmacol Exp Ther
, vol.291
, pp. 1196-1203
-
-
Benowitz, N.L.1
Perez-Stable, E.2
Fong, I.3
-
29
-
-
0029092399
-
Metabolism of clomipramine in a Japanese psychiatric population: Hydroxylation, desmethylation, and glucuronidation
-
Shimoda K, Noguchi T, Ozeki Y, et al. Metabolism of clomipramine in a Japanese psychiatric population: hydroxylation, desmethylation, and glucuronidation. Neuropsychopharmacology 1995; 12: 323-33
-
(1995)
Neuropsychopharmacology
, vol.12
, pp. 323-333
-
-
Shimoda, K.1
Noguchi, T.2
Ozeki, Y.3
-
30
-
-
0028018821
-
The influence of environmental and genetic factors on CYP2D6, CYP1A2 and UDP-glucuronosyltransferases in man using sparteine, caffeine, and paracetamol as probes
-
Bock KW, Schrenk D, Forster A, et al. The influence of environmental and genetic factors on CYP2D6, CYP1A2 and UDP-glucuronosyltransferases in man using sparteine, caffeine, and paracetamol as probes. Pharmacogenetics 1994; 4: 209-18
-
(1994)
Pharmacogenetics
, vol.4
, pp. 209-218
-
-
Bock, K.W.1
Schrenk, D.2
Forster, A.3
-
31
-
-
0025873406
-
Urinary glucuronide excretion of fenofibric and clofibric acid glucuronides in man: Is it polymorphic
-
Liu HF, Vincentviry M, Galteau MM, et al. Urinary glucuronide excretion of fenofibric and clofibric acid glucuronides in man: is it polymorphic. Eur J Clin Pharmacol 1991; 41: 153-9
-
(1991)
Eur J Clin Pharmacol
, vol.41
, pp. 153-159
-
-
Liu, H.F.1
Vincentviry, M.2
Galteau, M.M.3
-
32
-
-
0028821440
-
Lack of a genetic polymorphism in the glucuronidation of fenofibric acid
-
Vincent-Viry M, Cossy C, Galteau MM, et al. Lack of a genetic polymorphism in the glucuronidation of fenofibric acid. Pharmacogenetics 1995; 5: 50-2
-
(1995)
Pharmacogenetics
, vol.5
, pp. 50-52
-
-
Vincent-Viry, M.1
Cossy, C.2
Galteau, M.M.3
-
33
-
-
0027234212
-
Dextromethorphan O-demethylation and dextrorphan glucuronidation in a French population
-
Duche JC, Querol-Ferrer V, Barre J, et al. Dextromethorphan O-demethylation and dextrorphan glucuronidation in a French population. Int J Clin Pharmacol Ther Toxicol 1993; 31: 392-8
-
(1993)
Int J Clin Pharmacol Ther Toxicol
, vol.31
, pp. 392-398
-
-
Duche, J.C.1
Querol-Ferrer, V.2
Barre, J.3
-
34
-
-
0030838552
-
Variability of diphenhydramine N-glucuronidation in healthy subjects
-
Fischer D, Breyer-Pfaff U. Variability of diphenhydramine N-glucuronidation in healthy subjects. Eur J Drug Metab Pharmacokinet 1997; 22: 151-4
-
(1997)
Eur J Drug Metab Pharmacokinet
, vol.22
, pp. 151-154
-
-
Fischer, D.1
Breyer-Pfaff, U.2
-
35
-
-
0030847925
-
Intra-individual variation in serum AZT is not related to intestinal absorption or small intestinal inflammatory changes in human HIV-infected subjects
-
Sherwood RA, Marsden JT, Stein CA, et al. Intra-individual variation in serum AZT is not related to intestinal absorption or small intestinal inflammatory changes in human HIV-infected subjects. Antivir Chem Chemother 1997; 8: 327-32
-
(1997)
Antivir Chem Chemother
, vol.8
, pp. 327-332
-
-
Sherwood, R.A.1
Marsden, J.T.2
Stein, C.A.3
-
36
-
-
0001517022
-
Interindividual variation in the levels of certain urinary polycyclic aromatic hydrocarbon metabolites following medicinal exposure to coal tar ointment
-
Bowman ED, Rothman N, Hackl C, et al. Interindividual variation in the levels of certain urinary polycyclic aromatic hydrocarbon metabolites following medicinal exposure to coal tar ointment. Biomarkers 1997; 2: 321-7
-
(1997)
Biomarkers
, vol.2
, pp. 321-327
-
-
Bowman, E.D.1
Rothman, N.2
Hackl, C.3
-
37
-
-
0035197725
-
Interindividual variability in acetaminophen glucuronidation by human liver microsomes: Identification of relevant acetaminophen UDP-glucuronosyltransferase isoforms
-
Court MH, Duan SX, Van Moltke LL, et al. Interindividual variability in acetaminophen glucuronidation by human liver microsomes: identification of relevant acetaminophen UDP-glucuronosyltransferase isoforms. J Pharmacol Exp Ther 2001; 299: 988-1006
-
(2001)
J Pharmacol Exp Ther
, vol.299
, pp. 988-1006
-
-
Court, M.H.1
Duan, S.X.2
Van Moltke, L.L.3
-
38
-
-
0036266930
-
Hepatocyte nuclear factor-1α is a causal factor responsible for interindividual differences in the expression of UDP-Glucuronosyltransferase 2B7 mRNA in human livers
-
Toide K, Takahashi Y, Yamazaki H, et al. Hepatocyte nuclear factor-1α is a causal factor responsible for interindividual differences in the expression of UDP-Glucuronosyltransferase 2B7 mRNA in human livers. Drug Metab Dispos 2002; 30: 613-5
-
(2002)
Drug Metab Dispos
, vol.30
, pp. 613-615
-
-
Toide, K.1
Takahashi, Y.2
Yamazaki, H.3
-
39
-
-
0343924387
-
Regulation of the human bilirubin UDP-Glucuronosyltransferase gene
-
Brierley CH, Senafi SB, Clarke D, et al. Regulation of the human bilirubin UDP-Glucuronosyltransferase gene. Adv Enzyme Regul 1996; 36: 85-97
-
(1996)
Adv Enzyme Regul
, vol.36
, pp. 85-97
-
-
Brierley, C.H.1
Senafi, S.B.2
Clarke, D.3
-
40
-
-
0030765649
-
Disruption of the c/ebpα gene in adult mouse liver
-
Lee Y-H, Sauer B, Johnson PF, et al. Disruption of the c/ebpα gene in adult mouse liver. Mol Cell Biol 1997; 17: 6014-22
-
(1997)
Mol Cell Biol
, vol.17
, pp. 6014-6022
-
-
Lee, Y.-H.1
Sauer, B.2
Johnson, P.F.3
-
41
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
-
Bosma PJ, Roy Chowdhury J, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 1995; 333: 1171-218
-
(1995)
N Engl J Med
, vol.333
, pp. 1171-1218
-
-
Bosma, P.J.1
Roy Chowdhury, J.2
Bakker, C.3
-
42
-
-
0030030762
-
Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
-
Monaghan G, Ryan MF, et al. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996; 347: 578-81
-
(1996)
Lancet
, vol.347
, pp. 578-581
-
-
Monaghan, G.1
Ryan, M.F.2
-
43
-
-
18444399926
-
Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinaemia
-
Sugatani J, Yamakawa K, Yoshinari K, et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinaemia, Biochem Biophys Res Commun 2002; 292: 492-7
-
(2002)
Biochem Biophys Res Commun
, vol.292
, pp. 492-497
-
-
Sugatani, J.1
Yamakawa, K.2
Yoshinari, K.3
-
44
-
-
12244271026
-
Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups
-
Innocenti F, Grimsley C, Das S, et al. Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups. Pharmacogenetics 2002; 12: 725-33
-
(2002)
Pharmacogenetics
, vol.12
, pp. 725-733
-
-
Innocenti, F.1
Grimsley, C.2
Das, S.3
-
45
-
-
0028811175
-
Interindividual variability in the glucuronidation of (S) oxazepam contrasted with that of (R) oxazepam
-
Patel M, Tang BK, Grant DM, et al. Interindividual variability in the glucuronidation of (S) oxazepam contrasted with that of (R) oxazepam. Pharmacogenetics 1995; 5: 287-97
-
(1995)
Pharmacogenetics
, vol.5
, pp. 287-297
-
-
Patel, M.1
Tang, B.K.2
Grant, D.M.3
-
46
-
-
0033645752
-
Genetic polymorphism of UDP-glucuronosyltransferase 2B7 (UGT2B7) at amino acid 268: Ethnic diversity of alleles and potential clinical significance
-
Bhasker CR, McKinnon W, Stone A, et al. Genetic polymorphism of UDP-glucuronosyltransferase 2B7 (UGT2B7) at amino acid 268: ethnic diversity of alleles and potential clinical significance. Pharmacogenetics 2000; 10: 679-85
-
(2000)
Pharmacogenetics
, vol.10
, pp. 679-685
-
-
Bhasker, C.R.1
McKinnon, W.2
Stone, A.3
-
47
-
-
0029015847
-
Gilbert's syndrome is caused by heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase
-
Koiwai O, Nishizawa M, Hasada K, et al. Gilbert's syndrome is caused by heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase. Hum Mol Genet 1995; 4: 1183-6
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1183-1186
-
-
Koiwai, O.1
Nishizawa, M.2
Hasada, K.3
-
48
-
-
0030699360
-
Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: Pharmacological implications
-
Ciotti M, Marrone A, Potter C, et al. Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: pharmacological implications. Pharmacogenetics 1997; 7: 485-95
-
(1997)
Pharmacogenetics
, vol.7
, pp. 485-495
-
-
Ciotti, M.1
Marrone, A.2
Potter, C.3
-
49
-
-
0033789766
-
Structural heterogeneity at the UDP-glucuronosyltransferase 1 locus: Functional consequences of three novel missense mutations in the human UGT1A7 gene
-
Guillemette C, Ritter JK, Auyeung DJ, et al. Structural heterogeneity at the UDP-glucuronosyltransferase 1 locus: functional consequences of three novel missense mutations in the human UGT1A7 gene. Pharmacogenetics 2000; 10: 629-44
-
(2000)
Pharmacogenetics
, vol.10
, pp. 629-644
-
-
Guillemette, C.1
Ritter, J.K.2
Auyeung, D.J.3
-
50
-
-
0034765595
-
Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene
-
Vogel A, Kneip S, Barut A, et al. Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene. Gastroenterology 2001; 121: 1136-44
-
(2001)
Gastroenterology
, vol.121
, pp. 1136-1144
-
-
Vogel, A.1
Kneip, S.2
Barut, A.3
-
51
-
-
0012356560
-
The tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with oralaryngeal cancer risk in Caucasian and African Americans
-
Zheng Z, Guillemette C, Park JY, et al. The tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with oralaryngeal cancer risk in Caucasian and African Americans. J Natl Cancer Inst 2001; 29: 1343-8
-
(2001)
J Natl Cancer Inst
, vol.29
, pp. 1343-1348
-
-
Zheng, Z.1
Guillemette, C.2
Park, J.Y.3
-
52
-
-
0036016310
-
Identification and functional characterization of UDP-glucuronosyltransferases UGT1A8*1, UGT1A8*2 and UGT1A8*3
-
Huang Y-H, Galijatovic A, Nguyen N, et al. Identification and functional characterization of UDP-glucuronosyltransferases UGT1A8*1. UGT1A8*2 and UGT1A8*3. Pharmacogenetics 2002; 12: 287-97
-
(2002)
Pharmacogenetics
, vol.12
, pp. 287-297
-
-
Huang, Y.-H.1
Galijatovic, A.2
Nguyen, N.3
-
53
-
-
0032812606
-
Characterization and substrate specificity of UGT2B4 (E458), a UDP-Glucuronosyltransferase encoded by a polymorphic gene
-
Levesque E, Beaulieu M, Hum D, et al. Characterization and substrate specificity of UGT2B4 (E458), a UDP-Glucuronosyltransferase encoded by a polymorphic gene. Pharmacogenetics 1999; 9: 207-16
-
(1999)
Pharmacogenetics
, vol.9
, pp. 207-216
-
-
Levesque, E.1
Beaulieu, M.2
Hum, D.3
-
54
-
-
0036842042
-
Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9
-
Court MH, Duan SX, Guillemette C, et al. Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9. Drug Metab Dispos 2002; 30: 1257-65
-
(2002)
Drug Metab Dispos
, vol.30
, pp. 1257-1265
-
-
Court, M.H.1
Duan, S.X.2
Guillemette, C.3
-
55
-
-
0030795936
-
T1: Islation and characterization of UGT2B15(Y-85): A UDP-glucuronosyltransferase encoded by a polymorphic gene
-
Levesque E, Beaulieu M, Green MD, et al. T1: islation and characterization of UGT2B15(Y-85): A UDP-glucuronosyltransferase encoded by a polymorphic gene. Pharmacogenetics 1997; 7: 317-25
-
(1997)
Pharmacogenetics
, vol.7
, pp. 317-325
-
-
Levesque, E.1
Beaulieu, M.2
Green, M.D.3
-
56
-
-
0030728222
-
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias
-
Clarke DJ, Moghrabi N, Monaghan G, et al. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias. Clin Chim Acta 1997; 266: 63-74
-
(1997)
Clin Chim Acta
, vol.266
, pp. 63-74
-
-
Clarke, D.J.1
Moghrabi, N.2
Monaghan, G.3
-
57
-
-
0001400656
-
Chronic unconjugated hyperbilirubinaemia without overt signs of hemolysis in adolescents and adults
-
Arias IM. Chronic unconjugated hyperbilirubinaemia without overt signs of hemolysis in adolescents and adults. J Clin Invest 1962; 41: 2233-45
-
(1962)
J Clin Invest
, vol.41
, pp. 2233-2245
-
-
Arias, I.M.1
-
58
-
-
0012343828
-
Studies on the inheritance of Crigler-Najjar syndrome by the menthol test
-
Szabo L, Ebrey P. Studies on the inheritance of Crigler-Najjar syndrome by the menthol test. Acta Paediatr Scand 1963; 4: 153-8
-
(1963)
Acta Paediatr Scand
, vol.4
, pp. 153-158
-
-
Szabo, L.1
Ebrey, P.2
-
59
-
-
0014579106
-
Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyltransferase deficiency: Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity
-
Arias IM, Gartner LM, Cohen M, et al. Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyltransferase deficiency: clinical, biochemical, pharmacologic and genetic evidence for heterogeneity. Am J Med 1969; 47: 395-409
-
(1969)
Am J Med
, vol.47
, pp. 395-409
-
-
Arias, I.M.1
Gartner, L.M.2
Cohen, M.3
-
60
-
-
0012355291
-
Bilirubin metabolism in congenital nonhemolytic jaundice
-
Bloomer JR, Berk PD, Howe RB, et al. Bilirubin metabolism in congenital nonhemolytic jaundice. Pediatr Res 1971; 5: 256-64
-
(1971)
Pediatr Res
, vol.5
, pp. 256-264
-
-
Bloomer, J.R.1
Berk, P.D.2
Howe, R.B.3
-
61
-
-
0034458006
-
Characterization of the UGTs catalysing thyroid hormone glucuronidation in man
-
Findlay K, Burchell B. Characterization of the UGTs catalysing thyroid hormone glucuronidation in man. J Clin Endocrinol 2000; 85: 2879-83
-
(2000)
J Clin Endocrinol
, vol.85
, pp. 2879-2883
-
-
Findlay, K.1
Burchell, B.2
-
62
-
-
0030221217
-
The glucuronidation of exogenous and endogenous compounds by stably expressed rat and human UDP-glucuronosyltransferase 1.1
-
King CD, Green MD, Rios GR, et al. The glucuronidation of exogenous and endogenous compounds by stably expressed rat and human UDP-glucuronosyltransferase 1.1. Arch Biochem Biophys 1996; 332: 92-100
-
(1996)
Arch Biochem Biophys
, vol.332
, pp. 92-100
-
-
King, C.D.1
Green, M.D.2
Rios, G.R.3
-
63
-
-
0027521059
-
Human bilirubin UDP-glucuronosyltransferase catalyses the glucuronidation of ethinylestradiol
-
Ebner T, Burchell B, Remmel RP. Human bilirubin UDP-glucuronosyltransferase catalyses the glucuronidation of ethinylestradiol. Mol Pharmacol 1993; 43: 649-54
-
(1993)
Mol Pharmacol
, vol.43
, pp. 649-654
-
-
Ebner, T.1
Burchell, B.2
Remmel, R.P.3
-
64
-
-
0032519431
-
Genetic predisposition to the metabolism of irinotecan (CPT11)
-
Iyer L, King CD, Whitington PF, et al. Genetic predisposition to the metabolism of irinotecan (CPT11). J Clin Invest 1998; 101: 847-54
-
(1998)
J Clin Invest
, vol.101
, pp. 847-854
-
-
Iyer, L.1
King, C.D.2
Whitington, P.F.3
-
65
-
-
0027422955
-
Cosegration of intragenic markers with a novel mutation that causes Crigler-Najjar Syndrome type 1: Implications for carrier detection and prenatal diagnosis
-
Moghrabi N, Clarke DJ, Burchell B, et al. Cosegration of intragenic markers with a novel mutation that causes Crigler-Najjar Syndrome type 1: implications for carrier detection and prenatal diagnosis. Am J Hum Genet 1993; 53: 722-9
-
(1993)
Am J Hum Genet
, vol.53
, pp. 722-729
-
-
Moghrabi, N.1
Clarke, D.J.2
Burchell, B.3
-
66
-
-
0019846078
-
Pathogenesis of Gilbert's syndrome
-
Fevery J. Pathogenesis of Gilbert's syndrome. Eur J Clin Invest 1981; 11: 417-8
-
(1981)
Eur J Clin Invest
, vol.11
, pp. 417-418
-
-
Fevery, J.1
-
68
-
-
0023187951
-
Normal pathways for glucuronidation, sulphation and oxidation of paracetamol in Gilbert's syndrome
-
Ullrich D, Sieg A, Blume R, et al. Normal pathways for glucuronidation, sulphation and oxidation of paracetamol in Gilbert's syndrome. Eur J Clin Invest 1987; 17: 237-40
-
(1987)
Eur J Clin Invest
, vol.17
, pp. 237-240
-
-
Ullrich, D.1
Sieg, A.2
Blume, R.3
-
69
-
-
0026545451
-
Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome
-
De Morais SMF, Uetrecht JP, Wells PG. Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome. Gastroenterology 1992; 102: 577-86
-
(1992)
Gastroenterology
, vol.102
, pp. 577-586
-
-
De Morais, S.M.F.1
Uetrecht, J.P.2
Wells, P.G.3
-
70
-
-
0033841077
-
Association of human liver bilirubin UDP-glucuronosyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene
-
Raijmakers MT, Jansen PL, Steegers EA, et al. Association of human liver bilirubin UDP-glucuronosyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene. J Hepatol 2000; 33: 348-51
-
(2000)
J Hepatol
, vol.33
, pp. 348-351
-
-
Raijmakers, M.T.1
Jansen, P.L.2
Steegers, E.A.3
-
72
-
-
0036157862
-
Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1*28 is a common allele in Indians
-
Balram C, Sabapathy K, Fei G, et al. Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1*28 is a common allele in Indians. Pharmacogenetics 2002; 12: 81-3
-
(2002)
Pharmacogenetics
, vol.12
, pp. 81-83
-
-
Balram, C.1
Sabapathy, K.2
Fei, G.3
-
73
-
-
0031850241
-
TATA-box promoter mutant in the promoter of UDP-glucuronosyltransferase gene in Italian patients with Gilbert's syndrome
-
Sampietro M, Lupica L, Perrero L, et al. TATA-box promoter mutant in the promoter of UDP-glucuronosyltransferase gene in Italian patients with Gilbert's syndrome. Ital J Gastroenterol Hepatol 1998; 30: 194-8
-
(1998)
Ital J Gastroenterol Hepatol
, vol.30
, pp. 194-198
-
-
Sampietro, M.1
Lupica, L.2
Perrero, L.3
-
74
-
-
0033054393
-
Contribution of the TATA-Box genotype (Gilbert's syndrome) to serum bilirubin concentrations in the Italian population
-
Biondi ML, Turri O, Dilillo E, et al. Contribution of the TATA-Box genotype (Gilbert's syndrome) to serum bilirubin concentrations in the Italian population. Clin Chem 1999; 45: 897-8
-
(1999)
Clin Chem
, vol.45
, pp. 897-898
-
-
Biondi, M.L.1
Turri, O.2
Dilillo, E.3
-
75
-
-
0032493441
-
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism
-
Beutler E, Gelbert T, Demina A, et al. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism. Proc Natl Acad Sci U S A 1998; 95: 8170-4
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbert, T.2
Demina, A.3
-
76
-
-
17744374081
-
Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects [letter]
-
te Morsche RHM, Zusterzeel PLM, Raijmakers MTM, et al. Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects [letter]. Hepatology 2001; 33: 765
-
(2001)
Hepatology
, vol.33
, pp. 765
-
-
Te Morsche, R.H.M.1
Zusterzeel, P.L.M.2
Raijmakers, M.T.M.3
-
77
-
-
0033802568
-
Molecular diagnosis of a familial nonhemolytic hyperbilirubinaemia (Gilbert healthy subjects)
-
Borlak J, Thum T, Landt O, et al. Molecular diagnosis of a familial nonhemolytic hyperbilirubinaemia (Gilbert healthy subjects). Hepatology 2000; 32: 792-5
-
(2000)
Hepatology
, vol.32
, pp. 792-795
-
-
Borlak, J.1
Thum, T.2
Landt, O.3
-
78
-
-
0031595660
-
The UGT1A1*28 allele is relatively rare in a Japanese population
-
Ando Y, Chida M, Nakayama K, et al. The UGT1A1*28 allele is relatively rare in a Japanese population. Pharmacogenet 1998; 8: 357-60
-
(1998)
Pharmacogenet
, vol.8
, pp. 357-360
-
-
Ando, Y.1
Chida, M.2
Nakayama, K.3
-
79
-
-
0030053274
-
The genetic basis of Gilbert's syndrome
-
Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert's syndrome. Lancet 1996; 347: 557-8
-
(1996)
Lancet
, vol.347
, pp. 557-558
-
-
Sato, H.1
Adachi, Y.2
Koiwai, O.3
-
80
-
-
0031719562
-
Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
-
Akaba K, Kimura T, Sasaki A, et al. Neonatal hyperbilirubinaemia and mutation of bilirubin UDP-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese. Biochem Mol Biol Int 1998; 46: 21-6
-
(1998)
Biochem Mol Biol Int
, vol.46
, pp. 21-26
-
-
Akaba, K.1
Kimura, T.2
Sasaki, A.3
-
81
-
-
0031864410
-
Contribution of two missense mutation (G71R and Y486D) of the bilirubin UDP-glucuronosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II
-
Yamamoto K, Sato H, Fujiyama Y, et al. Contribution of two missense mutation (G71R and Y486D) of the bilirubin UDP-glucuronosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II. Biochim Biophys Acta 1998; 1406: 267-73
-
(1998)
Biochim Biophys Acta
, vol.1406
, pp. 267-273
-
-
Yamamoto, K.1
Sato, H.2
Fujiyama, Y.3
-
82
-
-
0028904620
-
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
Aono S, Adachi Y, Uyama E, et al. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. Lancet 1995; 345: 958-9
-
(1995)
Lancet
, vol.345
, pp. 958-959
-
-
Aono, S.1
Adachi, Y.2
Uyama, E.3
-
83
-
-
0033816138
-
Variations of the bilirubin in uridine-diphosphoglucuronosyltransferase 1A1 gene in healthy Taiwanese
-
Huang C-S, Luo G-A, Huang M-H, et al. Variations of the bilirubin in uridine-diphosphoglucuronosyltransferase 1A1 gene in healthy Taiwanese. Pharmacogenetics 2000; 10: 539-44
-
(2000)
Pharmacogenetics
, vol.10
, pp. 539-544
-
-
Huang, C.-S.1
Luo, G.-A.2
Huang, M.-H.3
-
84
-
-
0029774577
-
Evidence for overlapping active sites for 17α-Ethinylestradiol and bilirubin in the human major bilirubin UDPglucuronosyltransferase
-
Ciotti M, Owens IS. Evidence for overlapping active sites for 17α-Ethinylestradiol and bilirubin in the human major bilirubin UDPglucuronosyltransferase. Biochem 1996; 35: 10119-24
-
(1996)
Biochem
, vol.35
, pp. 10119-10124
-
-
Ciotti, M.1
Owens, I.S.2
-
85
-
-
0033661491
-
Tissue distribution and interindividual variation in human UDP-glucuronosyltransferase activity: Relationship between UGT1A1 promoter genotype and variability in a liver bank
-
Fisher MB, Vanden Branden M, Findlay K, et al. Tissue distribution and interindividual variation in human UDP-glucuronosyltransferase activity: relationship between UGT1A1 promoter genotype and variability in a liver bank. Pharmacogenetics 2000; 10: 727-39
-
(2000)
Pharmacogenetics
, vol.10
, pp. 727-739
-
-
Fisher, M.B.1
Vanden Branden, M.2
Findlay, K.3
-
86
-
-
0030716924
-
Severe CPT-11 toxicity in patients with Gilbert's syndrome: Two case reports
-
Wasserman E, Myara A, Lokiec F, et al. Severe CPT-11 toxicity in patients with Gilbert's syndrome: two case reports. Ann Oncol 1997; 810: 1049-51
-
(1997)
Ann Oncol
, vol.810
, pp. 1049-1051
-
-
Wasserman, E.1
Myara, A.2
Lokiec, F.3
-
87
-
-
0030958098
-
Pharmacokinetic and pharmacodynamic evaluation of the topoisomerase inhibitor irinotecan in cancer patients
-
Gupta E, Mick R, Ramirez J, et al. Pharmacokinetic and pharmacodynamic evaluation of the topoisomerase inhibitor irinotecan in cancer patients. J Clin Oncol 1997; 15: 1502-10
-
(1997)
J Clin Oncol
, vol.15
, pp. 1502-1510
-
-
Gupta, E.1
Mick, R.2
Ramirez, J.3
-
88
-
-
0031926749
-
Pathophysiology and therapy of irinotecan-induced onset diarrhoea in patients with advanced colorectal cancer
-
Saliba F, Higipantelli R, Misset JL, et al. Pathophysiology and therapy of irinotecan-induced onset diarrhoea in patients with advanced colorectal cancer. J Clin Oncol 1998; 16: 2745-51
-
(1998)
J Clin Oncol
, vol.16
, pp. 2745-2751
-
-
Saliba, F.1
Higipantelli, R.2
Misset, J.L.3
-
89
-
-
0031661579
-
UGT1A1 genotypes and glucuronidation of SN-38, the active metabolite of irinotecan
-
Ando Y, Saka H, Asai G, et al. UGT1A1 genotypes and glucuronidation of SN-38, the active metabolite of irinotecan. Ann Oncol 1998; 9: 845-7
-
(1998)
Ann Oncol
, vol.9
, pp. 845-847
-
-
Ando, Y.1
Saka, H.2
Asai, G.3
-
90
-
-
0032934383
-
Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism
-
Iyer L, Hall D, Das S, et al. Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism. Clin Pharmacol Ther 1999; 65: 576-82
-
(1999)
Clin Pharmacol Ther
, vol.65
, pp. 576-582
-
-
Iyer, L.1
Hall, D.2
Das, S.3
-
91
-
-
0036025450
-
UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity
-
Iyer L, Das S, Janisch L, et al. UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity. Pharmacogenomics J 2002; 2: 43-7
-
(2002)
Pharmacogenomics J
, vol.2
, pp. 43-47
-
-
Iyer, L.1
Das, S.2
Janisch, L.3
-
92
-
-
0036148810
-
Polymorphisms of UDP-glucuronosyltransferase and pharmacokinetics of irinotecan
-
Ando Y, Ueoka H, Sugiyama T, et al. Polymorphisms of UDP-glucuronosyltransferase and pharmacokinetics of irinotecan. Ther Drug Monit 2002; 24: 111-6
-
(2002)
Ther Drug Monit
, vol.24
, pp. 111-116
-
-
Ando, Y.1
Ueoka, H.2
Sugiyama, T.3
-
93
-
-
0033600191
-
Glucuronidation of 7-Ethyl-10-hydroxycamptothecin (SN38) by the human UDP-glucuronosyltransferases encoded at the UGT1 locus
-
Ciotti M, Basu N, Brangi M, et al. Glucuronidation of 7-Ethyl-10-hydroxycamptothecin (SN38) by the human UDP-glucuronosyltransferases encoded at the UGT1 locus. Biochem Biophys Res Commun 1999; 260: 199-202
-
(1999)
Biochem Biophys Res Commun
, vol.260
, pp. 199-202
-
-
Ciotti, M.1
Basu, N.2
Brangi, M.3
-
94
-
-
0034778246
-
Human liver UDP-glucuronosyltransferase isoforms involved in the glucuronidfation of 7-ethyl-10-hydroxycamptothecin
-
Hanioka N, Ozawa S, Jinno H, et al. Human liver UDP-glucuronosyltransferase isoforms involved in the glucuronidfation of 7-ethyl-10-hydroxycamptothecin. Xenobiotica 2001; 31: 687-99
-
(2001)
Xenobiotica
, vol.31
, pp. 687-699
-
-
Hanioka, N.1
Ozawa, S.2
Jinno, H.3
-
95
-
-
0031827877
-
Inhibition of intestinal microflora beta-glucuronidase modifes the distribution of the active metabolite of the antitumor agent, irinotecan hydrochloride (CPT-11) in rats
-
Takasuna K, Hagiwara T, Hirohashi M, et al. Inhibition of intestinal microflora beta-glucuronidase modifes the distribution of the active metabolite of the antitumor agent, irinotecan hydrochloride (CPT-11) in rats. Cancer Chemother Pharmacol 1998; 42: 280-6
-
(1998)
Cancer Chemother Pharmacol
, vol.42
, pp. 280-286
-
-
Takasuna, K.1
Hagiwara, T.2
Hirohashi, M.3
-
96
-
-
0035147198
-
Chemotherapy-induced unconjugated hyperbilirubinaemia caused by a mutation of the bilirubin uridine-5′-diphosphate glucuronosyltransferase gene
-
Maruo Y, Sata H, Bamba N, et al. Chemotherapy-induced unconjugated hyperbilirubinaemia caused by a mutation of the bilirubin uridine-5′-diphosphate glucuronosyltransferase gene. J Pediatr Hematol Oncol 2001; 23: 45-7
-
(2001)
J Pediatr Hematol Oncol
, vol.23
, pp. 45-47
-
-
Maruo, Y.1
Sata, H.2
Bamba, N.3
-
97
-
-
0037986926
-
Relationship between UDP-glucuronosyltransferase 1A1 genotype and total bilirubin elevation in healthy subjects receiving BMS-232632 and saquinavir
-
Sep 17-21. Toronto, Canada
-
O'Mara EM, Mummanemi V, Burchell B, et al. Relationship between UDP-glucuronosyltransferase 1A1 genotype and total bilirubin elevation in healthy subjects receiving BMS-232632 and saquinavir [abstract]. 40th ICAAC Meeting; 2000 Sep 17-21. Toronto, Canada
-
(2000)
40th ICAAC Meeting
-
-
O'Mara, E.M.1
Mummanemi, V.2
Burchell, B.3
-
99
-
-
0028567847
-
Disposition of Lorazepam in Gilbert's Syndrome: Effects of fasting, feeding, and enterohepatic circulation
-
Herman RJ, Chaudhary A, Szakacs CB. Disposition of Lorazepam in Gilbert's Syndrome: effects of fasting, feeding, and enterohepatic circulation. J Clin Pharmacol 1994; 34: 978-84
-
(1994)
J Clin Pharmacol
, vol.34
, pp. 978-984
-
-
Herman, R.J.1
Chaudhary, A.2
Szakacs, C.B.3
-
100
-
-
0001747399
-
Hereditary jaundice and disorders of bilirubin metabolism
-
Scriver CR, Beaudet A, Sly W, et al., editors. New York: McGraw-Hill
-
Chowdhury RJ, Wolkoff A, Chowdhury RN, et al. Hereditary jaundice and disorders of bilirubin metabolism. In: Scriver CR, Beaudet A, Sly W, et al., editors. The metabolic basis of inherited disease. New York: McGraw-Hill, 1995; 2161-208
-
(1995)
The Metabolic Basis of Inherited Disease
, pp. 2161-2208
-
-
Chowdhury, R.J.1
Wolkoff, A.2
Chowdhury, R.N.3
-
101
-
-
0018574014
-
Postnatal development of uridine, diphosphate glucuronosyltransferase activity towads bilirubin and 2-aminophenol in human liver
-
Onishi S, Kawade N, Itoh S, et al. Postnatal development of uridine, diphosphate glucuronosyltransferase activity towads bilirubin and 2-aminophenol in human liver. Biochem J 1979; 184: 705-7
-
(1979)
Biochem J
, vol.184
, pp. 705-707
-
-
Onishi, S.1
Kawade, N.2
Itoh, S.3
-
102
-
-
0000621679
-
Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α,20β-diol in maternal milk that inhibits glucuronide formation in vitro
-
Arias IM, Gartner LM, Seifter S, et al. Prolonged neonatal unconjugated hyperbilirubinaemia associated with breast-feeding and a steroid, pregnane-3α,20β-diol in maternal milk that inhibits glucuronide formation in vitro. J Clin Invest 1964; 43: 2037-47
-
(1964)
J Clin Invest
, vol.43
, pp. 2037-2047
-
-
Arias, I.M.1
Gartner, L.M.2
Seifter, S.3
-
103
-
-
0017861029
-
Clinical study of prolonged jaundice in breast and bottle-fed babies
-
Winfield CR, MacFaul R. Clinical study of prolonged jaundice in breast and bottle-fed babies. Arch Dis Child 1978; 54: 506-7
-
(1978)
Arch Dis Child
, vol.54
, pp. 506-507
-
-
Winfield, C.R.1
MacFaul, R.2
-
105
-
-
0023936363
-
Jaundice in the healthy newborn infant: A new approach to an old problem
-
Maisels MK, Gifford K, Antle CE, et al. Jaundice in the healthy newborn infant: a new approach to an old problem. Pediatrics 1988; 81: 505-11
-
(1988)
Pediatrics
, vol.81
, pp. 505-511
-
-
Maisels, M.K.1
Gifford, K.2
Antle, C.E.3
-
106
-
-
0020639259
-
Neonatal jaundice in full-term infants: Role of breast-feeding and other causes
-
Maisels MJ, Gifford K. Neonatal jaundice in full-term infants: role of breast-feeding and other causes. Am J Dis Child 1983; 137: 561-2
-
(1983)
Am J Dis Child
, vol.137
, pp. 561-562
-
-
Maisels, M.J.1
Gifford, K.2
-
107
-
-
0031949264
-
Gilbert's syndrome accelerates development of neonatal jaundice
-
Bancroft JD, Kreamer B, Gourley GR. Gilbert's syndrome accelerates development of neonatal jaundice. J Paediatr 1998; 132: 656-60
-
(1998)
J Paediatr
, vol.132
, pp. 656-660
-
-
Bancroft, J.D.1
Kreamer, B.2
Gourley, G.R.3
-
108
-
-
0033510908
-
Gilbert's syndrome is a contributory factor in very prolonged unconjugated hyperbilirubinaema of the newborn
-
Monaghan G, McLellan A, McGeechan A, et al. Gilbert's syndrome is a contributory factor in very prolonged unconjugated hyperbilirubinaema of the newborn. J Pediatr 1999; 134: 441-6
-
(1999)
J Pediatr
, vol.134
, pp. 441-446
-
-
Monaghan, G.1
McLellan, A.2
McGeechan, A.3
-
109
-
-
0016242097
-
Navajo jaundice: A variant of neonatal hyperbilirubinaemia associated with breast-feeding
-
Saland J, McNamara H, Cohen MI. Navajo jaundice: a variant of neonatal hyperbilirubinaemia associated with breast-feeding. J Pediatr 1974; 85: 271-5
-
(1974)
J Pediatr
, vol.85
, pp. 271-275
-
-
Saland, J.1
McNamara, H.2
Cohen, M.I.3
-
110
-
-
0018216093
-
Jaundice and breast-feeding among Alaska Eskimo newborns
-
Fisher Q, Cohen MI, Curda L. Jaundice and breast-feeding among Alaska Eskimo newborns. Am J Dis Child 1978; 132: 859-63
-
(1978)
Am J Dis Child
, vol.132
, pp. 859-863
-
-
Fisher, Q.1
Cohen, M.I.2
Curda, L.3
-
111
-
-
0027085807
-
Jaundice in Navajo neonates
-
Johnson JD. Jaundice in Navajo neonates. Clin Paediatr (Phila) 1992; 12: 716-8
-
(1992)
Clin Paediatr (Phila)
, vol.12
, pp. 716-718
-
-
Johnson, J.D.1
-
112
-
-
0031705604
-
Severe neonatal hyperbilirubinaemia: A potential complication of glucose-6-phosphate dehydrogenase deficiency
-
Kaplan M, Hammerman C. Severe neonatal hyperbilirubinaemia: a potential complication of glucose-6-phosphate dehydrogenase deficiency. Clin Perinatol 1998; 25: 575-92
-
(1998)
Clin Perinatol
, vol.25
, pp. 575-592
-
-
Kaplan, M.1
Hammerman, C.2
-
113
-
-
0030691028
-
Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinaemia
-
Kaplan M, Renbaum P, Levy-Lahad E, et al. Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinaemia. Proc Natl Acad Sci U S A 1997; 94: 12128-32
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 12128-12132
-
-
Kaplan, M.1
Renbaum, P.2
Levy-Lahad, E.3
-
114
-
-
0030663191
-
The expression of UDP-glucuronosyltransferase is a major determinant ofbilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
-
Sanpietro M, Lupica L, Perrero L, et al. The expression of UDP-glucuronosyltransferase is a major determinant ofbilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 1997; 99: 437-9
-
(1997)
Br J Haematol
, vol.99
, pp. 437-439
-
-
Sanpietro, M.1
Lupica, L.2
Perrero, L.3
-
115
-
-
0032845453
-
Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome
-
Gollanello R, Cipollino MD, Carboni G, et al. Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome. Eur J Pediatr 1999; 158: 914-6
-
(1999)
Eur J Pediatr
, vol.158
, pp. 914-916
-
-
Gollanello, R.1
Cipollino, M.D.2
Carboni, G.3
-
116
-
-
0034686969
-
Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates
-
Kaplan M, Hammerman C, Renbaum P, et al. Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates. Lancet 2000; 356: 652-3
-
(2000)
Lancet
, vol.356
, pp. 652-653
-
-
Kaplan, M.1
Hammerman, C.2
Renbaum, P.3
-
117
-
-
0008435402
-
Coinheritance of Gilbert's syndrome increases the risk of developing gallstones in patients with hereditary spherocytosis
-
del Guidice EM, Perotta S, Nobili B, et al. Coinheritance of Gilbert's syndrome increases the risk of developing gallstones in patients with hereditary spherocytosis. Blood 1999; 94: 2259-62
-
(1999)
Blood
, vol.94
, pp. 2259-2262
-
-
Del Guidice, E.M.1
Perotta, S.2
Nobili, B.3
-
118
-
-
0033943506
-
Gilbert's syndrome accounts for the phenotypic variability of congenital dyserthropoietic anaemia type II
-
Perrotta S, del Giudice EM, Carbane R, et al. Gilbert's syndrome accounts for the phenotypic variability of congenital dyserthropoietic anaemia type II. J Pediatr 2000; 136: 556-9
-
(2000)
J Pediatr
, vol.136
, pp. 556-559
-
-
Perrotta, S.1
Del Giudice, E.M.2
Carbane, R.3
-
119
-
-
0036204931
-
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism
-
Kaplan M, Hammerman C, Rubaltelli FF, et al. Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism. Hepatology 2002; 35: 905-11
-
(2002)
Hepatology
, vol.35
, pp. 905-911
-
-
Kaplan, M.1
Hammerman, C.2
Rubaltelli, F.F.3
-
120
-
-
0032884336
-
Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert's Syndrome
-
Trioche P, Chalas J, Francoual J, et al. Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert's Syndrome. Arch Dis Child 1999; 81: 301-3
-
(1999)
Arch Dis Child
, vol.81
, pp. 301-303
-
-
Trioche, P.1
Chalas, J.2
Francoual, J.3
-
121
-
-
0032852420
-
Co-inherited Gilbert's syndrome: A factor determining hyperbilirubinaemia in homozygous beta-thalassemia
-
Galanello R, Cipollina MD, Dessi C, et al. Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinaemia in homozygous beta-thalassemia. Haematologica 1999; 84: 103-5
-
(1999)
Haematologica
, vol.84
, pp. 103-105
-
-
Galanello, R.1
Cipollina, M.D.2
Dessi, C.3
-
122
-
-
4243464375
-
UDP-glucuronosyltransferase (UGT1A1) promoter polymorphism and bilirubin levels in patients with sickle cell disease [abstract 861]
-
McKie K, Kutlar F, Sromek S, et al. UDP-glucuronosyltransferase (UGT1A1) promoter polymorphism and bilirubin levels in patients with sickle cell disease [abstract 861]. Blood 1999; 94: P197a
-
(1999)
Blood
, vol.94
-
-
McKie, K.1
Kutlar, F.2
Sromek, S.3
-
123
-
-
4244134019
-
The effect of UDP-glucuronosyltransferase (UGT1A1) promoter polymorphisms on serum bilirubin levels and cholelthiasis in patients with sickle cell anaemia [abstract 2865]
-
Passon RG, Howard TA, Zimmerman SA, et al. The effect of UDP-glucuronosyltransferase (UGT1A1) promoter polymorphisms on serum bilirubin levels and cholelthiasis in patients with sickle cell anaemia [abstract 2865]. Blood 1999; 94: P645a
-
(1999)
Blood
, vol.94
-
-
Passon, R.G.1
Howard, T.A.2
Zimmerman, S.A.3
-
124
-
-
0033849474
-
Effect of bilirubin UDP-glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries
-
Doyama H, Okada T, Kobayashi T, et al. Effect of bilirubin UDP-glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries. Hepatology 2000; 32: 563-8
-
(2000)
Hepatology
, vol.32
, pp. 563-568
-
-
Doyama, H.1
Okada, T.2
Kobayashi, T.3
-
125
-
-
0034652640
-
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans
-
Guillemette C, Millikan RC, Newman B, et al. Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and association with breast cancer among African Americans. Cancer Res 2000; 60: 950-6
-
(2000)
Cancer Res
, vol.60
, pp. 950-956
-
-
Guillemette, C.1
Millikan, R.C.2
Newman, B.3
-
126
-
-
0027256828
-
Paracetamol glucuronidation by recombinant rat and human phenol UDP-glucuronosyltransferase
-
Bock KW, Forster A, Gschaidmeier H, et al. Paracetamol glucuronidation by recombinant rat and human phenol UDP-glucuronosyltransferase. Biochem Pharmacol 1993; 45: 1809-14
-
(1993)
Biochem Pharmacol
, vol.45
, pp. 1809-1814
-
-
Bock, K.W.1
Forster, A.2
Gschaidmeier, H.3
-
127
-
-
0025840257
-
Interethnic differences in drug glucuronidation: A comparison of paracetamol metabolism in Caucasians and Chinese
-
Osborne NJ, Tonkin AL, Miners JO. Interethnic differences in drug glucuronidation: a comparison of paracetamol metabolism in Caucasians and Chinese. Br J Clin Pharmacol 1991; 32: 765-7
-
(1991)
Br J Clin Pharmacol
, vol.32
, pp. 765-767
-
-
Osborne, N.J.1
Tonkin, A.L.2
Miners, J.O.3
-
128
-
-
0027530118
-
Substrate specificities of two stably expressed human liver UDP-glucuronosyltransferases of the UGT1 gene family
-
Ebner T, Burchell B. Substrate specificities of two stably expressed human liver UDP-glucuronosyltransferases of the UGT1 gene family. Drug Metab Dispos 1993; 21: 50-5
-
(1993)
Drug Metab Dispos
, vol.21
, pp. 50-55
-
-
Ebner, T.1
Burchell, B.2
-
130
-
-
0033786733
-
The COMT inhibitors and entacapone and tolcapone are good substrates for UGT1A4 and UGT1A9
-
Lautala P, Ethell B, Burchell B, et al. The COMT inhibitors and entacapone and tolcapone are good substrates for UGT1A4 and UGT1A9. Drug Metab Dispos 2000; 28: 1385-9
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 1385-1389
-
-
Lautala, P.1
Ethell, B.2
Burchell, B.3
-
131
-
-
0032502764
-
Expression of the UDP-glucuronosyltransferase 1A locus in human colon
-
Strassburg CP, Mann MP, Tukey RH. Expression of the UDP-glucuronosyltransferase 1A locus in human colon. J Biol Chem 1998; 273: 8719-26
-
(1998)
J Biol Chem
, vol.273
, pp. 8719-8726
-
-
Strassburg, C.P.1
Mann, M.P.2
Tukey, R.H.3
-
132
-
-
0024579299
-
Expression of a human liver cDNA encoding hydeoxycholic acid UDP-glucuronosyltransferase in cell culture
-
Fournel-Gigleux S, Jackson MR, Wooster R, et al. Expression of a human liver cDNA encoding hydeoxycholic acid UDP-glucuronosyltransferase in cell culture. FEBS Lett 1989; 243: 119-22
-
(1989)
FEBS Lett
, vol.243
, pp. 119-122
-
-
Fournel-Gigleux, S.1
Jackson, M.R.2
Wooster, R.3
-
133
-
-
0027431814
-
Glucuronidation of hyodeoxycholic acid in human liver: Evidence for a selective role of UGT2B4
-
Pillot T, Ouzzine M, Fournel-Gigleux S, et al. Glucuronidation of hyodeoxycholic acid in human liver: evidence for a selective role of UGT2B4. J Biol Chem 1993; 268: 25636-42
-
(1993)
J Biol Chem
, vol.268
, pp. 25636-25642
-
-
Pillot, T.1
Ouzzine, M.2
Fournel-Gigleux, S.3
-
134
-
-
0027433317
-
Complementary deoxyribonucleic acid cloning and expression of a human liver uridine diphosphate-glucuronosyltranferase glucuronidating carboxylic acid-containing drugs
-
Jin CJ, Miners JO, Lillywhite KJ, et al. Complementary deoxyribonucleic acid cloning and expression of a human liver uridine diphosphate-glucuronosyltranferase glucuronidating carboxylic acid-containing drugs. J Pharmacol Exp Ther 1993; 264: 475-9
-
(1993)
J Pharmacol Exp Ther
, vol.264
, pp. 475-479
-
-
Jin, C.J.1
Miners, J.O.2
Lillywhite, K.J.3
-
135
-
-
0026591504
-
Two human liver cDNAs encode UDP-glucuronosyltransferase with 2 log differences in activity toward parallel substrates including hyodeoxycholic acid and certain estrogen derivatives
-
Ritter JK, Chen F, Sheen YY, et al. Two human liver cDNAs encode UDP-glucuronosyltransferase with 2 log differences in activity toward parallel substrates including hyodeoxycholic acid and certain estrogen derivatives. Biochem 1992; 31: 3409-14
-
(1992)
Biochem
, vol.31
, pp. 3409-3414
-
-
Ritter, J.K.1
Chen, F.2
Sheen, Y.Y.3
-
136
-
-
0031570313
-
The regio- and stereo-selectivity of C19 and C21 hydroxysteroid glucuronidation by UGT2B7 and UGT2B11
-
Jin CJ, Mackenzie PI, Miners JO. The regio- and stereo-selectivity of C19 and C21 hydroxysteroid glucuronidation by UGT2B7 and UGT2B11. Arch Biochem Biophys 1997; 341: 207-11
-
(1997)
Arch Biochem Biophys
, vol.341
, pp. 207-211
-
-
Jin, C.J.1
Mackenzie, P.I.2
Miners, J.O.3
-
138
-
-
0028837971
-
(S) Oxazepam glucuronidation is inhibited by ketoprofen and other substrates of UGT 2B7
-
Patel M, Tang BK, Kalow W, (S) Oxazepam glucuronidation is inhibited by ketoprofen and other substrates of UGT 2B7. Pharmacogentics 1995; 5: 43-29
-
(1995)
Pharmacogentics
, vol.5
, pp. 43-29
-
-
Patel, M.1
Tang, B.K.2
Kalow, W.3
-
139
-
-
0031894377
-
The glucuronidation of opioids, other xenobiotics and androgens by human UGT2B7Y(268) and UGT2B7H(268)
-
Coffman BL, King CD, Rios GR, et al. The glucuronidation of opioids, other xenobiotics and androgens by human UGT2B7Y(268) and UGT2B7H(268). Drug Metab Dispos 1998; 26: 73-7
-
(1998)
Drug Metab Dispos
, vol.26
, pp. 73-77
-
-
Coffman, B.L.1
King, C.D.2
Rios, G.R.3
-
140
-
-
0024355675
-
Interindividual and interethnic differences in the demethylation and glucuronidation of codeine
-
Yue QY, Svensson JO, Alm C, et al. Interindividual and interethnic differences in the demethylation and glucuronidation of codeine. Br J Clin Pharmacol 1989; 28: 629-37
-
(1989)
Br J Clin Pharmacol
, vol.28
, pp. 629-637
-
-
Yue, Q.Y.1
Svensson, J.O.2
Alm, C.3
-
141
-
-
0029003283
-
Codeine metabolism in three oriental populations: A pilot study in Chinese, Japanese and Koreans
-
Yue Q-Y, Svensson J-O, Sawe J, et al. Codeine metabolism in three oriental populations: a pilot study in Chinese. Japanese and Koreans. Pharmacogenetics 1995; 5: 173-7
-
(1995)
Pharmacogenetics
, vol.5
, pp. 173-177
-
-
Yue, Q.-Y.1
Svensson, J.-O.2
Sawe, J.3
-
142
-
-
0028031001
-
Stable expression of a human liver UDP-glucuronosyltransferase (UGT2B15) with activity toward steroid and xenobiotic substrates
-
Green MD, Oturu EM, Tephly TR. Stable expression of a human liver UDP-glucuronosyltransferase (UGT2B15) with activity toward steroid and xenobiotic substrates. Drug Metab Dispos 1994; 22: 799-805
-
(1994)
Drug Metab Dispos
, vol.22
, pp. 799-805
-
-
Green, M.D.1
Oturu, E.M.2
Tephly, T.R.3
-
143
-
-
0033637811
-
Determination of genetic polymorphisms in UGT2B15 by allele-specific PCR
-
MacLeod SL, Nowell SA, Lang NP. Determination of genetic polymorphisms in UGT2B15 by allele-specific PCR. Ann Surg Oncol 2000; 7: 777-82
-
(2000)
Ann Surg Oncol
, vol.7
, pp. 777-782
-
-
MacLeod, S.L.1
Nowell, S.A.2
Lang, N.P.3
-
144
-
-
0034118356
-
Prevalence of polymorphisms in the human UDP-glucuronosyltransferase 2B family: UGT2B4 ((DE)-E-458), UGT2B7 ((HY)-Y-268), and UGT2B15((DY)-Y-85)
-
Lampe JW, Bigler J, Bush AC, et al. Prevalence of polymorphisms in the human UDP-glucuronosyltransferase 2B family: UGT2B4 ((DE)-E-458), UGT2B7 ((HY)-Y-268), and UGT2B15((DY)-Y-85). Cancer Epidemiol Biomarkers Prev 2000; 9: 329-33
-
(2000)
Cancer Epidemiol Biomarkers Prev
, vol.9
, pp. 329-333
-
-
Lampe, J.W.1
Bigler, J.2
Bush, A.C.3
|