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]