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Journal Abstract Search

862 related items for PubMed ID: 15304120

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  • 2. Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
    Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y.
    J Gastroenterol Hepatol; 2016 Feb; 31(2):403-8. PubMed ID: 26250421
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  • 5. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.
    Yamamoto K, Sato H, Fujiyama Y, Doida Y, Bamba T.
    Biochim Biophys Acta; 1998 Apr 28; 1406(3):267-73. PubMed ID: 9630669
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  • 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 28; 16(4):297-306. PubMed ID: 11013440
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  • 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.
    N Engl J Med; 1995 Nov 02; 333(18):1171-5. PubMed ID: 7565971
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  • 10. Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.
    Sun L, Li M, Zhang L, Teng X, Chen X, Zhou X, Ma Z, Qi L, Wang P.
    Medicine (Baltimore); 2017 Nov 02; 96(45):e8620. PubMed ID: 29137095
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  • 11. Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.
    Udomuksorn W, Elliot DJ, Lewis BC, Mackenzie PI, Yoovathaworn K, Miners JO.
    Pharmacogenet Genomics; 2007 Dec 02; 17(12):1017-29. PubMed ID: 18004206
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  • 13. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias.
    Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M.
    Ann Hum Genet; 2013 Nov 02; 77(6):482-7. PubMed ID: 23992562
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  • 14. 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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  • 15. 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.
    Ital J Gastroenterol Hepatol; 1998 Apr 20; 30(2):194-8. PubMed ID: 9675658
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  • 16. Analysis of the UDP-glucuronosyltransferase gene in Portuguese patients with a clinical diagnosis of Gilbert and Crigler-Najjar syndromes.
    Costa E, Vieira E, Martins M, Saraiva J, Cancela E, Costa M, Bauerle R, Freitas T, Carvalho JR, Santos-Silva E, Barbot J, Dos Santos R.
    Blood Cells Mol Dis; 2006 Apr 20; 36(1):91-7. PubMed ID: 16269258
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  • 17. Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people.
    Zhang M, Wang H, Huang Y, Xu X, Liu W, Ning Q, Chen T, Qi J.
    Gene; 2021 May 20; 781():145526. PubMed ID: 33631237
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  • 18. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
    Sampietro M, Iolascon A.
    Haematologica; 1999 Feb 20; 84(2):150-7. PubMed ID: 10091414
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  • 19. 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. PubMed ID: 22325916
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