BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 9621515)

  • 1. Analysis of bilirubin uridine 5'-diphosphate (UDP)-glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome type II.
    Yamamoto K; Soeda Y; Kamisako T; Hosaka H; Fukano M; Sato H; Fujiyama Y; Adachi Y; Satoh Y; Bamba T
    J Hum Genet; 1998; 43(2):111-4. PubMed ID: 9621515
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new type of defect in the gene for bilirubin uridine 5'-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I.
    Aono S; Yamada Y; Keino H; Sasaoka Y; Nakagawa T; Onishi S; Mimura S; Koiwai O; Sato H
    Pediatr Res; 1994 Jun; 35(6):629-32. PubMed ID: 7936809
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation.
    Servedio V; d'Apolito M; Maiorano N; Minuti B; Torricelli F; Ronchi F; Zancan L; Perrotta S; Vajro P; Boschetto L; Iolascon A
    Hum Mutat; 2005 Mar; 25(3):325. PubMed ID: 15712364
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I.
    Bosma PJ; Chowdhury NR; Goldhoorn BG; Hofker MH; Oude Elferink RP; Jansen PL; Chowdhury JR
    Hepatology; 1992 May; 15(5):941-7. PubMed ID: 1568736
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait.
    Koiwai O; Aono S; Adachi Y; Kamisako T; Yasui Y; Nishizawa M; Sato H
    Hum Mol Genet; 1996 May; 5(5):645-7. PubMed ID: 8733132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene.
    Iolascon A; Meloni A; Coppola B; Rosatelli MC
    J Med Genet; 2000 Sep; 37(9):712-3. PubMed ID: 11182932
    [No Abstract]   [Full Text] [Related]  

  • 8. Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease.
    Ciotti M; Chen F; Rubaltelli FF; Owens IS
    Biochim Biophys Acta; 1998 Jul; 1407(1):40-50. PubMed ID: 9639672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II.
    Aono S; Yamada Y; Keino H; Hanada N; Nakagawa T; Sasaoka Y; Yazawa T; Sato H; Koiwai O
    Biochem Biophys Res Commun; 1993 Dec; 197(3):1239-44. PubMed ID: 8280139
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A mutation in bilirubin uridine 5'-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II.
    Bosma PJ; Goldhoorn B; Oude Elferink RP; Sinaasappel M; Oostra BA; Jansen PL
    Gastroenterology; 1993 Jul; 105(1):216-20. PubMed ID: 8514037
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.
    Maruo Y; Nakahara S; Yanagi T; Nomura A; Mimura Y; Matsui K; Sato H; Takeuchi Y
    J Gastroenterol Hepatol; 2016 Feb; 31(2):403-8. PubMed ID: 26250421
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase.
    Seppen J; Bosma PJ; Goldhoorn BG; Bakker CT; Chowdhury JR; Chowdhury NR; Jansen PL; Oude Elferink RP
    J Clin Invest; 1994 Dec; 94(6):2385-91. PubMed ID: 7989595
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Crigler-Najjar syndrome type 2.
    Huang CS; Tan N; Yang SS; Sung YC; Huang MJ
    J Formos Med Assoc; 2006 Nov; 105(11):950-3. PubMed ID: 17098698
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Identification of two single base substitutions in the UGT1 gene locus which abolish bilirubin uridine diphosphate glucuronosyltransferase activity in vitro.
    Erps LT; Ritter JK; Hersh JH; Blossom D; Martin NC; Owens IS
    J Clin Invest; 1994 Feb; 93(2):564-70. PubMed ID: 7906695
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Three Japanese patients with Crigler-Najjar syndrome type I carry an identical nonsense mutation in the gene for UDP-glucuronosyltransferase.
    Koiwai O; Yasui Y; Hasada K; Aono S; Sato H; Fujikake M; Aoki T
    Jpn J Hum Genet; 1995 Sep; 40(3):253-7. PubMed ID: 8527799
    [No Abstract]   [Full Text] [Related]  

  • 20. Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.
    Maruo Y; Sato H; Yamano T; Doida Y; Shimada M
    J Pediatr; 1998 Jun; 132(6):1045-7. PubMed ID: 9627603
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.