123 related articles for article (PubMed ID: 17264799)
21. Three Japanese patients with Crigler-Najjar syndrome type I carry an identical nonsense mutation in the gene for UDP-glucuronosyltransferase.
Koiwai O; Yasui Y; Hasada K; Aono S; Sato H; Fujikake M; Aoki T
Jpn J Hum Genet; 1995 Sep; 40(3):253-7. PubMed ID: 8527799
[No Abstract] [Full Text] [Related]
22. Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I.
Rosatelli MC; Meloni A; Faa V; Saba L; Crisponi G; Clemente MG; Meloni G; Piga MT; Cao A
J Med Genet; 1997 Feb; 34(2):122-5. PubMed ID: 9039987
[TBL] [Abstract][Full Text] [Related]
23. Genetic diversity at the UGT1 locus is amplified by a novel 3' alternative splicing mechanism leading to nine additional UGT1A proteins that act as regulators of glucuronidation activity.
Girard H; Lévesque E; Bellemare J; Journault K; Caillier B; Guillemette C
Pharmacogenet Genomics; 2007 Dec; 17(12):1077-89. PubMed ID: 18004212
[TBL] [Abstract][Full Text] [Related]
24. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini.
Ritter JK; Chen F; Sheen YY; Tran HM; Kimura S; Yeatman MT; Owens IS
J Biol Chem; 1992 Feb; 267(5):3257-61. PubMed ID: 1339448
[TBL] [Abstract][Full Text] [Related]
25. Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2.
Moghrabi N; Clarke DJ; Boxer M; Burchell B
Genomics; 1993 Oct; 18(1):171-3. PubMed ID: 8276413
[No Abstract] [Full Text] [Related]
26. Variability and function of family 1 uridine-5'-diphosphate glucuronosyltransferases (UGT1A).
Strassburg CP; Kalthoff S; Ehmer U
Crit Rev Clin Lab Sci; 2008; 45(6):485-530. PubMed ID: 19003600
[TBL] [Abstract][Full Text] [Related]
27. Takashi Iyanagi: UGT1 gene complex: from Gunn rat to human.
Ikushiro S
Drug Metab Rev; 2010 Feb; 42(1):14-22. PubMed ID: 19845429
[TBL] [Abstract][Full Text] [Related]
28. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
Bosma PJ; Chowdhury JR; Bakker C; Gantla S; de Boer A; Oostra BA; Lindhout D; Tytgat GN; Jansen PL; Oude Elferink RP
N Engl J Med; 1995 Nov; 333(18):1171-5. PubMed ID: 7565971
[TBL] [Abstract][Full Text] [Related]
29. Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase.
Seppen J; Bosma PJ; Goldhoorn BG; Bakker CT; Chowdhury JR; Chowdhury NR; Jansen PL; Oude Elferink RP
J Clin Invest; 1994 Dec; 94(6):2385-91. PubMed ID: 7989595
[TBL] [Abstract][Full Text] [Related]
30. The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence.
Mackenzie PI; Owens IS; Burchell B; Bock KW; Bairoch A; Bélanger A; Fournel-Gigleux S; Green M; Hum DW; Iyanagi T; Lancet D; Louisot P; Magdalou J; Chowdhury JR; Ritter JK; Schachter H; Tephly TR; Tipton KF; Nebert DW
Pharmacogenetics; 1997 Aug; 7(4):255-69. PubMed ID: 9295054
[TBL] [Abstract][Full Text] [Related]
31. UDP-glucuronosyltransferases: gene structures of UGT1 and UGT2 families.
Owens IS; Basu NK; Banerjee R
Methods Enzymol; 2005; 400():1-22. PubMed ID: 16399340
[TBL] [Abstract][Full Text] [Related]
32. Isolation and characterization of the monkey UDP-glucuronosyltransferase cDNA clone monUGT1A01 active on bilirubin and estrogens.
Vallée M; Albert C; Beaudry G; Hum DW; Bélanger A
J Steroid Biochem Mol Biol; 2001 Jun; 77(4-5):239-49. PubMed ID: 11457662
[TBL] [Abstract][Full Text] [Related]
33. Complete correction of hyperbilirubinemia in the Gunn rat model of Crigler-Najjar syndrome type I following transient in vivo adenovirus-mediated expression of human bilirubin UDP-glucuronosyltransferase.
Askari FK; Hitomi Y; Mao M; Wilson JM
Gene Ther; 1996 May; 3(5):381-8. PubMed ID: 9156798
[TBL] [Abstract][Full Text] [Related]
34. Adaptive evolution of multiple-variable exons and structural diversity of drug-metabolizing enzymes.
Li C; Wu Q
BMC Evol Biol; 2007 May; 7():69. PubMed ID: 17475008
[TBL] [Abstract][Full Text] [Related]
35. Characterization of two baboon surfactant protein A genes.
Gao E; Wang Y; McCormick SM; Li J; Seidner SR; Mendelson CR
Am J Physiol; 1996 Oct; 271(4 Pt 1):L617-30. PubMed ID: 8897910
[TBL] [Abstract][Full Text] [Related]
36. Cloning and sequencing of baboon and cynomolgus monkey intra-acrosomal protein SP-10: homology with human SP-10 and a mouse sperm antigen (MSA-63).
Freemerman AJ; Wright RM; Flickinger CJ; Herr JC
Mol Reprod Dev; 1993 Feb; 34(2):140-8. PubMed ID: 8442953
[TBL] [Abstract][Full Text] [Related]
37. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR
Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440
[TBL] [Abstract][Full Text] [Related]
38. Genetic variations and haplotypes of UDP-glucuronosyltransferase 1A locus in a Korean population.
Yea SS; Lee SS; Kim WY; Liu KH; Kim H; Shon JH; Cha IJ; Shin JG
Ther Drug Monit; 2008 Feb; 30(1):23-34. PubMed ID: 18223459
[TBL] [Abstract][Full Text] [Related]
39. An investigation of human and rat liver microsomal mycophenolic acid glucuronidation: evidence for a principal role of UGT1A enzymes and species differences in UGT1A specificity.
Miles KK; Stern ST; Smith PC; Kessler FK; Ali S; Ritter JK
Drug Metab Dispos; 2005 Oct; 33(10):1513-20. PubMed ID: 16033946
[TBL] [Abstract][Full Text] [Related]
40. Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes.
Iyer L; King CD; Whitington PF; Green MD; Roy SK; Tephly TR; Coffman BL; Ratain MJ
J Clin Invest; 1998 Feb; 101(4):847-54. PubMed ID: 9466980
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
