BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

315 related articles for article (PubMed ID: 7715297)

  • 1. 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; 345(8955):958-9. PubMed ID: 7715297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Co-occurrence of three different mutations in the bilirubin UDP-glucuronosyltransferase gene in a Chinese family with Crigler-Najjar syndrome type I and Gilbert's syndrome.
    Maruo Y; Poon KK; Ito M; Iwai M; Takahashi H; Mori A; Sato H; Takeuchi Y
    Clin Genet; 2003 Nov; 64(5):420-3. PubMed ID: 14616765
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 333(18):1171-5. PubMed ID: 7565971
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 1406(3):267-73. PubMed ID: 9630669
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.
    Sampietro M; Iolascon A
    Haematologica; 1999 Feb; 84(2):150-7. PubMed ID: 10091414
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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; 146(32):1488-90. PubMed ID: 12198827
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias.
    Clarke DJ; Moghrabi N; Monaghan G; Cassidy A; Boxer M; Hume R; Burchell B
    Clin Chim Acta; 1997 Oct; 266(1):63-74. PubMed ID: 9435989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 16(4):297-306. PubMed ID: 11013440
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
    Takeuchi K; Kobayashi Y; Tamaki S; Ishihara T; Maruo Y; Araki J; Mifuji R; Itani T; Kuroda M; Sato H; Kaito M; Adachi Y
    J Gastroenterol Hepatol; 2004 Sep; 19(9):1023-8. PubMed ID: 15304120
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.
    Koiwai O; Nishizawa M; Hasada K; Aono S; Adachi Y; Mamiya N; Sato H
    Hum Mol Genet; 1995 Jul; 4(7):1183-6. PubMed ID: 8528206
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].
    Kim YH; Yeon JE; Jung GM; Kim HJ; Kim JS; Byun KS; Bak YT; Lee CH
    Taehan Kan Hakhoe Chi; 2002 Jun; 8(2):132-8. PubMed ID: 12499798
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 36(1):91-7. PubMed ID: 16269258
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unconjugated bilirubin and an increased proportion of bilirubin monoconjugates in the bile of patients with Gilbert's syndrome and Crigler-Najjar disease.
    Fevery J; Blanckaert N; Heirwegh KP; Préaux AM; Berthelot P
    J Clin Invest; 1977 Nov; 60(5):970-9. PubMed ID: 409736
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.
    Costa E
    Blood Cells Mol Dis; 2006; 36(1):77-80. PubMed ID: 16386929
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Liver bilirubin UDP-glucuronosyltransferase activity in chronic nonhemolytic unconjugated hyperbilirubinemia of adults.
    Watanabe A; Wakabayashi H; Kuwabara Y; Yamamoto H; Hattori S; Tsuji T
    Res Exp Med (Berl); 1998 Apr; 197(6):329-36. PubMed ID: 9638795
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.
    Yildiz D; Alan S; Kilic A; Yaman A; Erdeve O; Kuloglu Z; Atasay B; Arsan S
    Genet Couns; 2013; 24(3):273-7. PubMed ID: 24341141
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gilbert's syndrome phenotypically expressed as Crigler-Najjar syndrome type II.
    Seo YS; Keum B; Park S; Kim du R; Kwon YD; Kim YS; Jeen YT; Chun HJ; Um SH; Kim CD; Ryu HS
    Scand J Gastroenterol; 2007 Apr; 42(4):540-1. PubMed ID: 17454871
    [No Abstract]   [Full Text] [Related]  

  • 18. UDP-glucuronosyltransferase in Gilbert's syndrome.
    Debinski HS; Lee CS; Dhillon AP; Mackenzie P; Rhode J; Desmond PV
    Pathology; 1996 Aug; 28(3):238-41. PubMed ID: 8912353
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The genetic basis of Gilbert's syndrome.
    Sato H; Adachi Y; Koiwai O
    Lancet; 1996 Mar; 347(9001):557-8. PubMed ID: 8596313
    [No Abstract]   [Full Text] [Related]  

  • 20. Assessment of UGT polymorphisms and neonatal jaundice.
    Bartlett MG; Gourley GR
    Semin Perinatol; 2011 Jun; 35(3):127-33. PubMed ID: 21641485
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.