Similar articles for PMID: 17496722

Year	Number of Results
1850	2
1891	2
1948	1
1957	1
1967	1
1978	1
1993	1
1994	1
1995	4
1996	5
1997	4
1998	7
1999	11
2000	17
2001	10
2002	15
2003	11
2004	13
2005	8
2006	12
2007	11
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2009	8
2010	16
2011	13
2012	15
2013	16
2014	13
2015	11
2016	6
2017	8
2018	7
2019	4
2020	6
2021	10
2022	10
2023	3
2024	0

1

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. Hsieh TY, et al. Pharmacogenet Genomics. 2007 Apr;17(4):229-36. doi: 10.1097/FPC.0b013e328012d0da. Pharmacogenet Genomics. 2007. PMID: 17496722

2

The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.

D'Angelo R, Rinaldi C, Donato L, Nicocia G, Sidoti A. D'Angelo R, et al. Ann Clin Lab Sci. 2015 Spring;45(2):202-5. Ann Clin Lab Sci. 2015. PMID: 25887876

3

[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. Kim YH, et al. Taehan Kan Hakhoe Chi. 2002 Jun;8(2):132-8. Taehan Kan Hakhoe Chi. 2002. PMID: 12499798 Korean.

4

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. Hsieh TY, et al. Genet Mol Res. 2014 Jan 28;13(1):670-9. doi: 10.4238/2014.January.28.12. Genet Mol Res. 2014. PMID: 24615032 Free article.

5

TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UGT1A1*37.

Daprà V, Alliaudi C, Galliano I, Dini M, Curcio GL, Calvi C, Archetti M, Gavatorta M, Bergallo M. Daprà V, et al. Mol Biol Rep. 2021 May;48(5):4953-4959. doi: 10.1007/s11033-021-06454-2. Epub 2021 Jun 4. Mol Biol Rep. 2021. PMID: 34089128

6

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. Sampietro M, et al. Ital J Gastroenterol Hepatol. 1998 Apr;30(2):194-8. Ital J Gastroenterol Hepatol. 1998. PMID: 9675658 Clinical Trial.

7

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. Takeuchi K, et al. J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8. doi: 10.1111/j.1440-1746.2004.03370.x. J Gastroenterol Hepatol. 2004. PMID: 15304120

8

Rare TA repeats in promoter TATA box of the UDP glucuronosyltranferase (UGT1A1) gene in Croatian subjects.

Nikolac N, Simundic AM, Topic E, Jurcic Z, Stefanovic M, Dumic J, Goreta SS. Nikolac N, et al. Clin Chem Lab Med. 2008;46(2):174-8. doi: 10.1515/CCLM.2008.035. Clin Chem Lab Med. 2008. PMID: 18324905

9

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. Bosma PJ, et al. N Engl J Med. 1995 Nov 2;333(18):1171-5. doi: 10.1056/NEJM199511023331802. N Engl J Med. 1995. PMID: 7565971 Free article.

10

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. Shiu TY, et al. Liver Int. 2015 Aug;35(8):2050-6. doi: 10.1111/liv.12785. Epub 2015 Feb 6. Liver Int. 2015. PMID: 25611851

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