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175 related items for PubMed ID: 35192750

  • 1. Dependence of blood biochemical parameters on various genotypes of the UGT1A1 gene associated with gilbert's syndrome.
    Sidorenko DV, Nazarov VD, Volnikova EG, Kondrasheva EA, Peshkova NG, Kovaleva IS, Kokorina OS, Svatkovskaya IB, Lapin SV.
    Klin Lab Diagn; 2022 Feb 23; 67(2):69-75. PubMed ID: 35192750
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  • 2. 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 23; 35(7):432-439. PubMed ID: 31017737
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  • 3. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.
    Monaghan G, Ryan M, Seddon R, Hume R, Burchell B.
    Lancet; 1996 Mar 02; 347(9001):578-81. PubMed ID: 8596320
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  • 4. 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 Mar 02; 45(2):202-5. PubMed ID: 25887876
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  • 5. (TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.
    Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A.
    Haematologica; 1999 Feb 02; 84(2):106-9. PubMed ID: 10091406
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  • 9. 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 02; 106(5):E59. PubMed ID: 11061796
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  • 11. Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.
    Hsieh TY, Shiu TY, Chu NF, Chao TY, Chu HC, Chang WK, Chao YC, Huang HH.
    Genet Mol Res; 2014 Jan 28; 13(1):670-9. PubMed ID: 24615032
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  • 15. Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.
    Horsfall LJ, Hardy R, Wong A, Kuh D, Swallow DM.
    J Hepatol; 2014 Dec 28; 61(6):1344-51. PubMed ID: 25086287
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  • 16. UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.
    Ostanek B, Furlan D, Mavec T, Lukac-Bajalo J.
    Blood Cells Mol Dis; 2007 Dec 28; 38(2):78-82. PubMed ID: 17196409
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  • 18. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene.
    Raijmakers MT, Jansen PL, Steegers EA, Peters WH.
    J Hepatol; 2000 Sep 28; 33(3):348-51. PubMed ID: 11019988
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