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Journal Abstract Search

143 related items for PubMed ID: 21614935

  • 21. Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism is associated with choledocholithiasis in Taiwanese patients.
    Chu CH, Yang AM, Kao JH, Liu CY, Chang WH, Yang WS.
    J Gastroenterol Hepatol; 2009 Sep; 24(9):1559-61. PubMed ID: 19486253
    [Abstract] [Full Text] [Related]

  • 22. Association of neonatal hyperbilirubinemia with uridine diphosphate-glucuronosyltransferase 1A1 gene polymorphisms: meta-analysis.
    Long J, Zhang S, Fang X, Luo Y, Liu J.
    Pediatr Int; 2011 Aug; 53(4):530-40. PubMed ID: 21342357
    [Abstract] [Full Text] [Related]

  • 23. Quantitative method for determination of urobilinogen in stool and of urobilinogen and bilirubin in urine.
    BRERETON HG, LUCIA SP.
    Am J Clin Pathol; 1948 Nov; 18(11):887-90. PubMed ID: 18894814
    [No Abstract] [Full Text] [Related]

  • 24. [Diagnostic effectiveness of the determination of bilirubin and urobilinogen in urine].
    Kutter D.
    Z Med Lab Diagn; 1984 Nov; 25(8):423-6. PubMed ID: 6523997
    [No Abstract] [Full Text] [Related]

  • 25. Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects.
    Saito A, Kawamoto M, Kamatani N.
    J Hum Genet; 2009 Jun; 54(6):317-23. PubMed ID: 19343046
    [Abstract] [Full Text] [Related]

  • 26. INTESTINAL ABSORPTION OF BILE PIGMENTS. IV. UROBILINOGEN ABSORPTION IN MAN.
    LESTER R, SCHUMER W, SCHMID R.
    N Engl J Med; 1965 May 06; 272():939-43. PubMed ID: 14274450
    [No Abstract] [Full Text] [Related]

  • 27. 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 06; 35(7):432-439. PubMed ID: 31017737
    [Abstract] [Full Text] [Related]

  • 28. Tocilizumab-induced hyperbilirubinemia in Japanese patients with rheumatoid arthritis: its association with UDP glucuronosyltransferase 1A1 gene polymorphisms.
    Mori S, Terada K, Ueki Y.
    Mod Rheumatol; 2012 Aug 06; 22(4):515-23. PubMed ID: 21993917
    [Abstract] [Full Text] [Related]

  • 29. Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype.
    Rauchschwalbe SK, Zühlsdorf MT, Wensing G, Kuhlmann J.
    Int J Clin Pharmacol Ther; 2004 Feb 06; 42(2):73-7. PubMed ID: 15180166
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  • 34. [Genetic factors in the occurrence of neonatal unconjugated hyperbilirubinemia].
    Sun LL, Chen YS, Yu ZZ, Huang BX, Xu G, Ma DL, Li CG, Liu L, Liu XH.
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Apr 06; 14(4):256-9. PubMed ID: 22537951
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  • 36. UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.
    Agrawal SK, Kumar P, Rathi R, Sharma N, DAS R, Prasad R, Narang A.
    Pediatr Res; 2009 Jun 06; 65(6):675-80. PubMed ID: 19430380
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  • 37. UGT1AI*6 and UGT1A1*27 for individualized irinotecan chemotherapy.
    Ando Y, Fujita K, Sasaki Y, Hasegawa Y.
    Curr Opin Mol Ther; 2007 Jun 06; 9(3):258-62. PubMed ID: 17608024
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  • 39. Bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1) gene promoter polymorphisms and HPRT, glycophorin A, and micronuclei mutant frequencies in human blood.
    Grant DJ, Hall IJ, Eastmond DA, Jones IM, Bell DA.
    Mutat Res; 2004 May 09; 560(1):1-10. PubMed ID: 15099818
    [Abstract] [Full Text] [Related]

  • 40. A high urinary urobilinogen/serum total bilirubin ratio indicates acute hepatic porphyria in patients with abdominal pain.
    Song C, Liu Y.
    Sci Rep; 2023 Dec 04; 13(1):21330. PubMed ID: 38044386
    [Abstract] [Full Text] [Related]

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