BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 32007587)

  • 1. Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis.
    Wang J; Yin J; Xue M; Lyu J; Wan Y
    Gene; 2020 Apr; 736():144409. PubMed ID: 32007587
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of Neonatal Hyperbilirubinemia with UGT1A1 Gene Polymorphisms: A Meta-Analysis.
    Yu Z; Zhu K; Wang L; Liu Y; Sun J
    Med Sci Monit; 2015 Oct; 21():3104-14. PubMed ID: 26467199
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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; 14(4):256-9. PubMed ID: 22537951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis.
    Mehrad-Majd H; Haerian MS; Akhtari J; Ravanshad Y; Azarfar A; Mamouri G
    J Matern Fetal Neonatal Med; 2019 May; 32(10):1575-1585. PubMed ID: 29179591
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan.
    Liu W; Chang LW; Xie M; Li WB; Rong ZH; Wu L; Chen L
    J Huazhong Univ Sci Technolog Med Sci; 2017 Oct; 37(5):740-743. PubMed ID: 29058288
    [TBL] [Abstract][Full Text] [Related]  

  • 7. UGT1A1*28 gene polymorphism was not associated with the risk of neonatal hyperbilirubinemia: a meta-analysis.
    Li H; Zhang P
    J Matern Fetal Neonatal Med; 2021 Dec; 34(24):4064-4071. PubMed ID: 31818155
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice.
    Halis H; Ergin H; Köseler A; Atalay EÖ
    J Matern Fetal Neonatal Med; 2017 Nov; 30(22):2658-2664. PubMed ID: 27842454
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility.
    Li Z; Song L; Hao L
    BMC Med Genet; 2020 Nov; 21(1):218. PubMed ID: 33158427
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 65(6):675-80. PubMed ID: 19430380
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neonatal hyperbilirubinemia and Gly71Arg mutation of UGT1A1 gene: a Chinese case-control study followed by systematic review of existing evidence.
    Long J; Zhang S; Fang X; Luo Y; Liu J
    Acta Paediatr; 2011 Jul; 100(7):966-71. PubMed ID: 21272068
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Association between UGT 1A1 Gly71Arg (G71R) polymorphism and neonatal hyperbilirubinemia.
    Prachukthum S; Gamnarai P; Kangsadalampai S
    J Med Assoc Thai; 2012 Jan; 95 Suppl 1():S13-7. PubMed ID: 23964438
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Mutations in UGT1A1 gene in neonates with hyperbilirubinemia of Guangxi Heiyi Zhuang nationality].
    Wu XJ; Zhong DN; Ye DZ; Zhong Y; Xie XZ
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 May; 16(5):483-8. PubMed ID: 24856997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice.
    Chou HC; Chen MH; Yang HI; Su YN; Hsieh WS; Chen CY; Chen HL; Chang MH; Tsao PN
    Pediatr Res; 2011 Feb; 69(2):170-4. PubMed ID: 20975617
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association between uridin diphosphate glucuronosylotransferase 1A1 (UGT1A1) gene polymorphism and neonatal hyperbilirubinemia.
    Mazur-Kominek K; Romanowski T; Bielawski K; Kiełbratowska B; Preis K; Domżalska-Popadiuk I; Słomińska-Frączek M; Sznurkowska K; Renke J; Plata-Nazar K; Śledzińska K; Sikorska-Wiśniewska G; Góra-Gębka M; Liberek A
    Acta Biochim Pol; 2017; 64(2):351-356. PubMed ID: 28399191
    [TBL] [Abstract][Full Text] [Related]  

  • 17. UDP-glucuronosyltransferase promoter polymorphism in Iranian neonates with idiopathic hyperbilirubinemia.
    Kaveh M; Esmailnia T; Nayeri F; Nili F; Davari Tanha F; Ghajarzdeh M
    Acta Med Iran; 2013; 51(11):789-92. PubMed ID: 24390949
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia.
    Huang MJ; Lin YC; Liu K; Chang PF; Huang CS
    Pediatr Neonatol; 2020 Oct; 61(5):506-512. PubMed ID: 32571672
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis.
    Zhou JF; Luo JY; Zhu WB; Yang CY; Zeng YL; Qiu XL
    J Matern Fetal Neonatal Med; 2021 Jan; 34(1):12-23. PubMed ID: 30700176
    [No Abstract]   [Full Text] [Related]  

  • 20. Association between the Specific UGT1A1 Promoter Sequence Variant (c-3279T>G) and Unconjugated Neonatal Hyperbilirubinemia.
    Tomerak RH; Helal NF; Shaker OG; Yousef MA
    J Trop Pediatr; 2016 Dec; 62(6):457-463. PubMed ID: 27318112
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.