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Items: 1 to 20 of 411

1.

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, et al.

N Engl J Med. 1995 Nov 2;333(18):1171-5.

2.

[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].

Drenth JP, Peters WH, Jansen JB.

Ned Tijdschr Geneeskd. 2002 Aug 10;146(32):1488-90. Review. Dutch.

PMID:
12198827
3.
4.

TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.

Sampietro M, Lupica L, Perrero L, Romano R, Molteni V, Fiorelli G.

Ital J Gastroenterol Hepatol. 1998 Apr;30(2):194-8.

PMID:
9675658
5.

Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients.

Te HS, Schiano TD, Das S, Kuan SF, DasGupta K, Conjeevaram HS, Baker AL.

Transplantation. 2000 May 15;69(9):1882-6.

PMID:
10830226
6.
7.

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. Review.

PMID:
11013440
8.

Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.

Sampietro M, Iolascon A.

Haematologica. 1999 Feb;84(2):150-7. Review.

9.

[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].

Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, Bak YT, Lee CH.

Taehan Kan Hakhoe Chi. 2002 Jun;8(2):132-8. Korean.

10.

Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.

Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y.

J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8.

PMID:
15304120
11.

Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.

Hsieh SY, Wu YH, Lin DY, Chu CM, Wu M, Liaw YF.

Am J Gastroenterol. 2001 Apr;96(4):1188-93.

PMID:
11316168
12.
13.

Liver bilirubin UDP-glucuronosyltransferase activity in chronic nonhemolytic unconjugated hyperbilirubinemia of adults.

Watanabe A, Wakabayashi H, Kuwabara Y, Yamamoto H, Hattori S, Tsuji T.

Res Exp Med (Berl). 1998 Apr;197(6):329-36.

PMID:
9638795
14.

Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.

Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, Koiwai O, Sato H.

Lancet. 1995 Apr 15;345(8955):958-9.

PMID:
7715297
15.

Gilbert's syndrome--a legitimate genetic anomaly?

Schmid R.

N Engl J Med. 1995 Nov 2;333(18):1217-8. No abstract available.

PMID:
7565981
16.

UDP-glucuronosyltransferase in Gilbert's syndrome.

Debinski HS, Lee CS, Dhillon AP, Mackenzie P, Rhode J, Desmond PV.

Pathology. 1996 Aug;28(3):238-41.

PMID:
8912353
17.
18.

Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias.

Clarke DJ, Moghrabi N, Monaghan G, Cassidy A, Boxer M, Hume R, Burchell B.

Clin Chim Acta. 1997 Oct 9;266(1):63-74.

PMID:
9435989
19.
20.

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.

Monaghan G, Ryan M, Seddon R, Hume R, Burchell B.

Lancet. 1996 Mar 2;347(9001):578-81.

PMID:
8596320

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