BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 26781906)

  • 1. Three-dimensional polyacrylamide gel-based DNA microarray method effectively identifies UDP-glucuronosyltransferase 1A1 gene polymorphisms for the correct diagnosis of Gilbert's syndrome.
    Song J; Sun M; Li J; Zhou D; Wu X
    Int J Mol Med; 2016 Mar; 37(3):575-80. PubMed ID: 26781906
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 13(1):670-9. PubMed ID: 24615032
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 17(4):229-36. PubMed ID: 17496722
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.
    Shiu TY; Huang HH; Lin HH; Shih YL; Chu HC; Chang WK; Hsieh TY
    Liver Int; 2015 Aug; 35(8):2050-6. PubMed ID: 25611851
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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; 45(2):202-5. PubMed ID: 25887876
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 106(5):E59. PubMed ID: 11061796
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 35(7):432-439. PubMed ID: 31017737
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome.
    Maruo Y; D'Addario C; Mori A; Iwai M; Takahashi H; Sato H; Takeuchi Y
    Hum Genet; 2004 Nov; 115(6):525-6. PubMed ID: 15378351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients.
    Te HS; Schiano TD; Das S; Kuan SF; DasGupta K; Conjeevaram HS; Baker AL
    Transplantation; 2000 May; 69(9):1882-6. PubMed ID: 10830226
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 48(5):4953-4959. PubMed ID: 34089128
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response.
    Huang MJ; Chen PL; Huang CS
    Kaohsiung J Med Sci; 2022 Aug; 38(8):729-738. PubMed ID: 35942604
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Combined test for UGT1A1 -3279T-->G and A(TA)nTAA polymorphisms best predicts Gilbert's syndrome in Italian pediatric patients.
    Ferraris A; D'Amato G; Nobili V; Torres B; Marcellini M; Dallapiccola B
    Genet Test; 2006; 10(2):121-5. PubMed ID: 16792515
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Single-step identification of all length polymorphisms in the UGT1A1 gene promoter.
    Skarke C; Grösch S; Geisslinger G; Lötsch J
    Int J Clin Pharmacol Ther; 2004 Mar; 42(3):133-8. PubMed ID: 15049432
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.
    Fesenko EE; Heydarov RN; Stepanova EV; Abramov ME; Chudinov AV; Zasedatelev AS; Mikhailovich VM
    Clin Chem Lab Med; 2013 Jun; 51(6):1177-84. PubMed ID: 23241680
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of concomitant Gilbert's syndrome and hereditary spherocytosis.
    Lee HJ; Moon HS; Lee ES; Kim SH; Sung JK; Lee BS; Jeong HY; Lee HY; Eu YJ
    Korean J Hepatol; 2010 Sep; 16(3):321-4. PubMed ID: 20924216
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [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; 90(24):1690-3. PubMed ID: 20979879
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 33(3):348-51. PubMed ID: 11019988
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.