BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 19732760)

  • 1. Haplotypes in the UGT1A1 gene and their role as genetic determinants of bilirubin concentration in healthy German volunteers.
    Borucki K; Weikert C; Fisher E; Jakubiczka S; Luley C; Westphal S; Dierkes J
    Clin Biochem; 2009 Nov; 42(16-17):1635-41. PubMed ID: 19732760
    [TBL] [Abstract][Full Text] [Related]  

  • 2. UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.
    D'Silva S; Colah RB; Ghosh K; Mukherjee MB
    Gene; 2013 Jan; 513(1):36-9. PubMed ID: 23147267
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Intra-ethnic differences in genetic variants of the UGT-glucuronosyltransferase 1A1 gene in Chinese populations.
    Zhang A; Xing Q; Qin S; Du J; Wang L; Yu L; Li X; Xu L; Xu M; Feng G; He L
    Pharmacogenomics J; 2007 Oct; 7(5):333-8. PubMed ID: 17060921
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Racial variability in haplotype frequencies of UGT1A1 and glucuronidation activity of a novel single nucleotide polymorphism 686C> T (P229L) found in an African-American.
    Kaniwa N; Kurose K; Jinno H; Tanaka-Kagawa T; Saito Y; Saeki M; Sawada J; Tohkin M; Hasegawa R
    Drug Metab Dispos; 2005 Mar; 33(3):458-65. PubMed ID: 15572581
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups.
    Innocenti F; Grimsley C; Das S; Ramírez J; Cheng C; Kuttab-Boulos H; Ratain MJ; Di Rienzo A
    Pharmacogenetics; 2002 Dec; 12(9):725-33. PubMed ID: 12464801
    [TBL] [Abstract][Full Text] [Related]  

  • 6. UDP-Glucuronosyltransferase 1A1 gene polymorphisms and total bilirubin levels in an ethnically diverse cohort of women.
    Hong AL; Huo D; Kim HJ; Niu Q; Fackenthal DL; Cummings SA; John EM; West DW; Whittemore AS; Das S; Olopade OI
    Drug Metab Dispos; 2007 Aug; 35(8):1254-61. PubMed ID: 17478602
    [TBL] [Abstract][Full Text] [Related]  

  • 7. UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: relationships to serum bilirubin concentrations.
    Lampe JW; Bigler J; Horner NK; Potter JD
    Pharmacogenetics; 1999 Jun; 9(3):341-9. PubMed ID: 10471066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The impact of the UGT1A1*60 allele on bilirubin serum concentrations.
    Pasternak AL; Crews KR; Caudle KE; Smith C; Pei D; Cheng C; Broeckel U; Gaur AH; Hankins J; Relling MV; Haidar CE
    Pharmacogenomics; 2017 Jan; 18(1):5-16. PubMed ID: 27967321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns.
    Nguyen TT; Zhao W; Yang X; Zhong DN
    Pediatr Res; 2020 Dec; 88(6):940-944. PubMed ID: 32126570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.
    Ostanek B; Furlan D; Mavec T; Lukac-Bajalo J
    Blood Cells Mol Dis; 2007; 38(2):78-82. PubMed ID: 17196409
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 560(1):1-10. PubMed ID: 15099818
    [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. A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.
    Yusoff S; Takeuchi A; Ashi C; Tsukada M; Ma'amor NH; Zilfalil BA; Yusoff NM; Nakamura T; Hirai M; Harahap IS; Gunadi ; Lee MJ; Nishimura N; Takaoka Y; Morikawa S; Morioka I; Yokoyama N; Matsuo M; Nishio H; van Rostenberghe H
    Pediatr Res; 2010 Apr; 67(4):401-6. PubMed ID: 20057336
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Does bilirubin level correspond to interaction of c.-3279T>G and A(TA)7TAA variants in UGT1A1 gene?
    Slachtova L; Kemlink D; Martasek P; Kabicek P
    Cell Mol Biol (Noisy-le-grand); 2009 Feb; 55(1):98-101. PubMed ID: 19268007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. UGT1A polymorphisms in a Swedish cohort and a human diversity panel, and the relation to bilirubin plasma levels in males and females.
    Mercke Odeberg J; Andrade J; Holmberg K; Hoglund P; Malmqvist U; Odeberg J
    Eur J Clin Pharmacol; 2006 Oct; 62(10):829-37. PubMed ID: 16909274
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Association of polymorphisms in four bilirubin metabolism genes with serum bilirubin in three Asian populations.
    Lin R; Wang X; Wang Y; Zhang F; Wang Y; Fu W; Yu T; Li S; Xiong M; Huang W; Jin L
    Hum Mutat; 2009 Apr; 30(4):609-15. PubMed ID: 19243019
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.
    Rodrigues C; Vieira E; Santos R; de Carvalho J; Santos-Silva A; Costa E; Bronze-da-Rocha E
    Blood Cells Mol Dis; 2012 Mar; 48(3):166-72. PubMed ID: 22325916
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Close association of UGT1A9 IVS1+399C>T with UGT1A1*28, *6, or *60 haplotype and its apparent influence on 7-ethyl-10-hydroxycamptothecin (SN-38) glucuronidation in Japanese.
    Saito Y; Sai K; Maekawa K; Kaniwa N; Shirao K; Hamaguchi T; Yamamoto N; Kunitoh H; Ohe Y; Yamada Y; Tamura T; Yoshida T; Minami H; Ohtsu A; Matsumura Y; Saijo N; Sawada J
    Drug Metab Dispos; 2009 Feb; 37(2):272-6. PubMed ID: 18981166
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.