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Journal Abstract Search

251 related items for PubMed ID: 12139570

  • 21. 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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  • 22. [From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].
    Drenth JP, Peters WH, Jansen JB.
    Ned Tijdschr Geneeskd; 2002 Aug 10; 146(32):1488-90. PubMed ID: 12198827
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  • 23. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.
    Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, Koiwai O, Sato H.
    Lancet; 1995 Apr 15; 345(8955):958-9. PubMed ID: 7715297
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  • 24. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
    Kaplan M.
    J Perinatol; 2001 Dec 15; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413
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  • 26. TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UGT1A1*37.
    Daprà V, Alliaudi C, Galliano I, Dini M, Curcio GL, Calvi C, Archetti M, Gavatorta M, Bergallo M.
    Mol Biol Rep; 2021 May 15; 48(5):4953-4959. PubMed ID: 34089128
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  • 27. [Genetic analysis of the UGT1A1 gene mutation sites in a Chinese family suffered from Gilbert's syndrome].
    Yu LH, Gao J, Wang CL, Wang J, Gao Y, Yuan QL, Sun ZX, Wang HY, Zhang CG.
    Yi Chuan; 2006 Jan 15; 28(1):11-6. PubMed ID: 16469709
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  • 28. Dual hereditary jaundice: simultaneous occurrence of mutations causing Gilbert's and Dubin-Johnson syndrome.
    Cebecauerova D, Jirasek T, Budisova L, Mandys V, Volf V, Novotna Z, Subhanova I, Hrebicek M, Elleder M, Jirsa M.
    Gastroenterology; 2005 Jul 15; 129(1):315-20. PubMed ID: 16012956
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  • 29. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
    Hsieh TY, Shiu TY, Huang SM, Lin HH, Lee TC, Chen PJ, Chu HC, Chang WK, Jeng KS, Lai MM, Chao YC.
    Pharmacogenet Genomics; 2007 Apr 15; 17(4):229-36. PubMed ID: 17496722
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  • 32. Pharmacogenetics of Gilbert's syndrome.
    Strassburg CP.
    Pharmacogenomics; 2008 Jun 15; 9(6):703-15. PubMed ID: 18518849
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  • 34. [Clinical and genetic analyses of UGT1A1 gene from a Chinese family with Gilbert's syndrome].
    Peng XX, Jiang J.
    Zhonghua Yi Xue Za Zhi; 2010 Jun 22; 90(24):1690-3. PubMed ID: 20979879
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  • 36. Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2.
    Tesapirat L, Nilyanimit P, Wanlapakorn N, Poovorawan Y.
    Genet Mol Res; 2015 Apr 13; 14(2):3293-9. PubMed ID: 25966095
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  • 38. 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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  • 39. (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 23; 84(2):106-9. PubMed ID: 10091406
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  • 40. Gilbert's syndrome--a frequent cause of unconjugated hyperbilirubinemia in children after orthotopic liver transplantation.
    Kathemann S, Lainka E, Baba HA, Hoyer PF, Gerner P.
    Pediatr Transplant; 2012 Mar 23; 16(2):201-4. PubMed ID: 22360405
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