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Journal Abstract Search

257 related items for PubMed ID: 19303655

  • 1. 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. PubMed ID: 19303655
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  • 7. Gilbert-Meulengracht's syndrome and pharmacogenetics: is jaundice just the tip of the iceberg?
    Strassburg CP.
    Drug Metab Rev; 2010 Feb; 42(1):168-81. PubMed ID: 20070246
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  • 10. Relationship between hyperbilirubinaemia and UDP-glucuronosyltransferase 1A1 (UGT1A1) polymorphism in adult HIV-infected Thai patients treated with indinavir.
    Boyd MA, Srasuebkul P, Ruxrungtham K, Mackenzie PI, Uchaipichat V, Stek M, Lange JM, Phanuphak P, Cooper DA, Udomuksorn W, Miners JO.
    Pharmacogenet Genomics; 2006 May; 16(5):321-9. PubMed ID: 16609363
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  • 11. A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
    Nakagawa T, Mure T, Yusoff S, Ono E, Kusuma Harahap IS, Morikawa S, Morioka I, Takeshima Y, Nishio H, Matsuo M.
    Kobe J Med Sci; 2011 Jul 20; 57(1):E26-31. PubMed ID: 22169899
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  • 13. 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 20; 72(4):321-8. PubMed ID: 17850628
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  • 14. [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 20; 8(2):132-8. PubMed ID: 12499798
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  • 16. 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 20; 96(4):1188-93. PubMed ID: 11316168
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  • 19. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
    Kaplan M.
    J Perinatol; 2001 Dec 20; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413
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  • 20. Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome.
    Huang MJ, Chen YC, Huang YY, Yang SS, Chen PL, Huang CS.
    Kaohsiung J Med Sci; 2019 Jul 20; 35(7):432-439. PubMed ID: 31017737
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