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Journal Abstract Search

139 related items for PubMed ID: 7565981

  • 21. Inherited disorders of bilirubin metabolism.
    Bosma PJ.
    J Hepatol; 2003 Jan; 38(1):107-17. PubMed ID: 12480568
    [No Abstract] [Full Text] [Related]

  • 22. Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
    Canu G, Minucci A, Zuppi C, Capoluongo E.
    Blood Cells Mol Dis; 2013 Apr; 50(4):273-80. PubMed ID: 23403257
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  • 23. Liver bilirubin UDP-glucuronosyltransferase activity in chronic nonhemolytic unconjugated hyperbilirubinemia of adults.
    Watanabe A, Wakabayashi H, Kuwabara Y, Yamamoto H, Hattori S, Tsuji T.
    Res Exp Med (Berl); 1998 Apr; 197(6):329-36. PubMed ID: 9638795
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  • 24. Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type II syndrome.
    Labrune P, Myara A, Chalas J, Le Bihan B, Capel L, Francoual J.
    Hum Mutat; 2002 Nov; 20(5):399-401. PubMed ID: 12402338
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  • 28. Genetic inheritance of Gilbert's syndrome.
    Bosma P, Chowdhury JR, Jansen PH.
    Lancet; 1995 Jul 29; 346(8970):314-5. PubMed ID: 7630272
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  • 29. 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.
    Ann Clin Lab Sci; 2015 Jul 29; 45(2):202-5. PubMed ID: 25887876
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  • 30. [Molecular diagnosis of heritable unconjugated hyperbilirubinemias].
    Mammaev SN.
    Klin Lab Diagn; 2005 Dec 29; (12):8-13. PubMed ID: 16498946
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  • 31. Kernicterus in an adult who is heterozygous for Crigler-Najjar syndrome and homozygous for Gilbert-type genetic defect.
    Chalasani N, Chowdhury NR, Chowdhury JR, Boyer TD.
    Gastroenterology; 1997 Jun 29; 112(6):2099-103. PubMed ID: 9178703
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  • 34. The novel UGT1 gene complex links bilirubin, xenobiotics, and therapeutic drug metabolism by encoding UDP-glucuronosyltransferase isozymes with a common carboxyl terminus.
    Owens IS, Ritter JK, Yeatman MT, Chen F.
    J Pharmacokinet Biopharm; 1996 Oct 29; 24(5):491-508. PubMed ID: 9131487
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  • 39. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.
    Koiwai O, Nishizawa M, Hasada K, Aono S, Adachi Y, Mamiya N, Sato H.
    Hum Mol Genet; 1995 Jul 29; 4(7):1183-6. PubMed ID: 8528206
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  • 40. Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
    Maruo Y, Sato H, Yamano T, Doida Y, Shimada M.
    J Pediatr; 1998 Jun 29; 132(6):1045-7. PubMed ID: 9627603
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