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Journal Abstract Search

251 related items for PubMed ID: 12139570

  • 1. 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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  • 2. Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.
    Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M.
    Pediatrics; 2000 Nov; 106(5):E59. PubMed ID: 11061796
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  • 3. 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 Nov; 45(2):202-5. PubMed ID: 25887876
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  • 6. 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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  • 9. 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 20; 35(8):2050-6. PubMed ID: 25611851
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  • 11. [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 20; 56(2):139-43. PubMed ID: 11827650
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  • 12. Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.
    Ferraris A, D'Amato G, Nobili V, Torres B, Marcellini M, Dallapiccola B.
    Genet Test; 2006 Feb 20; 10(2):121-5. PubMed ID: 16792515
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  • 17. 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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  • 18. 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 28; 35(7):432-439. PubMed ID: 31017737
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