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Journal Abstract Search

155 related items for PubMed ID: 15304109

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  • 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.
    Taehan Kan Hakhoe Chi; 2002 Jun; 8(2):132-8. PubMed ID: 12499798
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  • 5. Dual polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: a novel mechanism for hyperserotoninaemia in Gilbert's syndrome mimicking carcinoid syndrome?
    Lee P, Jones G, Seibel MJ.
    Eur J Gastroenterol Hepatol; 2007 Apr; 19(4):337-40. PubMed ID: 17353700
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  • 7. 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. PubMed ID: 25611851
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  • 9. Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.
    Sutomo R, Laosombat V, Sadewa AH, Yokoyama N, Nakamura H, Matsuo M, Nishio H.
    Pediatr Int; 2002 Aug; 44(4):427-32. PubMed ID: 12139570
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  • 13. 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. PubMed ID: 17496722
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  • 15. Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects.
    Te Morsche RH, Zusterzeel PL, Raijmakers MT, Roes EM, Steegers EA, Peters WH.
    Hepatology; 2001 Mar; 33(3):765. PubMed ID: 11230763
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  • 16. [Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice].
    Seco ML, del Río E, Barceló MJ, Remacha A, Ginovart G, Moliner E, Baiget M.
    An Esp Pediatr; 2002 Feb; 56(2):139-43. PubMed ID: 11827650
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  • 18. Frequency of Gilbert's syndrome associated with UGTA1 (TA)(7) polymorphism in Southern Italy.
    Iolascon A, Perrotta S, Coppola B, Carbone R, Miraglia Del Giudice E.
    Haematologica; 2000 Mar; 85(3):335-6. PubMed ID: 10702836
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