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Items: 1 to 20 of 123

1.

Gilbert syndrome: the UGT1A1*28 promoter polymorphism as a biomarker of multifactorial diseases and drug metabolism.

Gil J, Sąsiadek MM.

Biomark Med. 2012 Apr;6(2):223-30. doi: 10.2217/BMM.12.4. Review.

PMID:
22448797
2.

Predicting the risk of sporadic elevated bilirubin levels and diagnosing Gilbert's syndrome by genotyping UGT1A1*28 promoter polymorphism.

Rauchschwalbe SK, Zühlsdorf MT, Schühly U, Kuhlmann J.

Int J Clin Pharmacol Ther. 2002 Jun;40(6):233-40.

PMID:
12078936
3.

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.

Rodrigues C, Vieira E, Santos R, de Carvalho J, Santos-Silva A, Costa E, Bronze-da-Rocha E.

Blood Cells Mol Dis. 2012 Mar 15;48(3):166-72. doi: 10.1016/j.bcmd.2012.01.004.

PMID:
22325916
4.

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.

PMID:
17196409
5.

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
6.

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
7.

Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype.

Rauchschwalbe SK, Zühlsdorf MT, Wensing G, Kuhlmann J.

Int J Clin Pharmacol Ther. 2004 Feb;42(2):73-7.

PMID:
15180166
8.

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
9.

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.

Dabke PS, Colah RB, Ghosh KK, Nadkarni AH.

Hematology. 2014 Oct;19(7):388-92. doi: 10.1179/1607845413Y.0000000142.

PMID:
24620945
10.

Snapback primer genotyping of the Gilbert syndrome UGT1A1 (TA)(n) promoter polymorphism by high-resolution melting.

Farrar JS, Palais RA, Wittwer CT.

Clin Chem. 2011 Sep;57(9):1303-10. doi: 10.1373/clinchem.2011.166306.

11.

(TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.

Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A.

Haematologica. 1999 Feb;84(2):106-9.

12.

Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.

Fesenko EE, Heydarov RN, Stepanova EV, Abramov ME, Chudinov AV, Zasedatelev AS, Mikhailovich VM.

Clin Chem Lab Med. 2013 Jun;51(6):1177-84. doi: 10.1515/cclm-2012-0656.

PMID:
23241680
13.
14.

[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].

Kraemer D, Scheurlen M.

Med Klin (Munich). 2002 Sep 15;97(9):528-32. Review. German.

PMID:
12371080
17.

Single-step identification of all length polymorphisms in the UGT1A1 gene promoter.

Skarke C, Grösch S, Geisslinger G, Lötsch J.

Int J Clin Pharmacol Ther. 2004 Mar;42(3):133-8.

PMID:
15049432
19.

Rapid allelic discrimination by TaqMan PCR for the detection of the Gilbert's syndrome marker UGT1A1*28.

Ehmer U, Lankisch TO, Erichsen TJ, Kalthoff S, Freiberg N, Wehmeier M, Manns MP, Strassburg CP.

J Mol Diagn. 2008 Nov;10(6):549-52. doi: 10.2353/jmoldx.2008.080036.

20.

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.

Maruo Y, D'Addario C, Mori A, Iwai M, Takahashi H, Sato H, Takeuchi Y.

Hum Genet. 2004 Nov;115(6):525-6.

PMID:
15378351

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