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Items: 1 to 20 of 137

2.

Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.

Hsieh TY, Shiu TY, Chu NF, Chao TY, Chu HC, Chang WK, Chao YC, Huang HH.

Genet Mol Res. 2014 Jan 28;13(1):670-9. doi: 10.4238/2014.January.28.12.

3.

Linkage disequilibrium of UGT1A1 *6 and UGT1A1 *28 in relation to UGT1A6 and UGT1A7 polymorphisms.

Urawa N, Kobayashi Y, Araki J, Sugimoto R, Iwasa M, Kaito M, Adachi Y.

Oncol Rep. 2006 Oct;16(4):801-6.

PMID:
16969497
4.

Identification and characterization of a functional TATA box polymorphism of the UDP glucuronosyltransferase 1A7 gene.

Lankisch TO, Vogel A, Eilermann S, Fiebeler A, Krone B, Barut A, Manns MP, Strassburg CP.

Mol Pharmacol. 2005 May;67(5):1732-9. Epub 2005 Feb 16.

5.

Drug-mediated toxicity caused by genetic deficiency of UDP-glucuronosyltransferases.

Burchell B, Soars M, Monaghan G, Cassidy A, Smith D, Ethell B.

Toxicol Lett. 2000 Mar 15;112-113:333-40. Review.

PMID:
10720749
6.
7.

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
8.
9.

Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.

Shiu TY, Huang HH, Lin HH, Shih YL, Chu HC, Chang WK, Hsieh TY.

Liver Int. 2015 Aug;35(8):2050-6. doi: 10.1111/liv.12785. Epub 2015 Feb 6.

PMID:
25611851
10.

Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults.

Teng HC, Huang MJ, Tang KS, Yang SS, Tseng CS, Huang CS.

Clin Genet. 2007 Oct;72(4):321-8.

PMID:
17850628
11.

Gilbert's disease and atazanavir: from phenotype to UDP-glucuronosyltransferase haplotype.

Lankisch TO, Moebius U, Wehmeier M, Behrens G, Manns MP, Schmidt RE, Strassburg CP.

Hepatology. 2006 Nov;44(5):1324-32.

PMID:
17058217
12.

Gilbert's Syndrome and irinotecan toxicity: combination with UDP-glucuronosyltransferase 1A7 variants increases risk.

Lankisch TO, Schulz C, Zwingers T, Erichsen TJ, Manns MP, Heinemann V, Strassburg CP.

Cancer Epidemiol Biomarkers Prev. 2008 Mar;17(3):695-701. doi: 10.1158/1055-9965.EPI-07-2517.

13.

UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.

Ostanek B, Furlan D, Mavec T, Lukac-Bajalo J.

Blood Cells Mol Dis. 2007 Mar-Apr;38(2):78-82. Epub 2006 Dec 28.

PMID:
17196409
14.

Analysis of inherited genetic variations at the UGT1 locus in the French-Canadian population.

Ménard V, Girard H, Harvey M, Pérusse L, Guillemette C.

Hum Mutat. 2009 Apr;30(4):677-87. doi: 10.1002/humu.20946.

PMID:
19204906
15.

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
16.

Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.

Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I, Din Z, Cassidy A, Hume R, Burchell B.

J Pediatr. 1999 Apr;134(4):441-6.

PMID:
10190918
17.

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
18.

Gilbert's syndrome and hyperbilirubinemia in protease inhibitor therapy--an extended haplotype of genetic variants increases risk in indinavir treatment.

Lankisch TO, Behrens G, Ehmer U, Möbius U, Rockstroh J, Wehmeier M, Kalthoff S, Freiberg N, Manns MP, Schmidt RE, Strassburg CP.

J Hepatol. 2009 May;50(5):1010-8. doi: 10.1016/j.jhep.2008.12.030. Epub 2009 Mar 5.

PMID:
19303655
19.
20.

Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.

Hsieh TY, Shiu TY, Huang SM, Lin HH, Lee TC, Chen PJ, Chu HC, Chang WK, Jeng KS, Lai MM, Chao YC.

Pharmacogenet Genomics. 2007 Apr;17(4):229-36.

PMID:
17496722

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