238 related articles for article (PubMed ID: 23964438)
1. 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]
2. [Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].
Gao ZY; Zhong DN; Liu Y; Liu YN; Wei LM
Zhonghua Er Ke Za Zhi; 2010 Sep; 48(9):646-9. PubMed ID: 21092520
[TBL] [Abstract][Full Text] [Related]
3. Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding.
Sato H; Uchida T; Toyota K; Kanno M; Hashimoto T; Watanabe M; Nakamura T; Tamiya G; Aoki K; Hayasaka K
J Hum Genet; 2013 Jan; 58(1):7-10. PubMed ID: 23014115
[TBL] [Abstract][Full Text] [Related]
4. Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients.
Narter F; Can G; Ergen A; Isbir T; Ince Z; Çoban A
J Matern Fetal Neonatal Med; 2011 Feb; 24(2):313-6. PubMed ID: 20528217
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. [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]
7. 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]
8. UGT1A1 gene and neonatal hyperbilirubinemia: a preliminary study from Bengkulu, Indonesia.
Amandito R; Putradista R; Jikesya C; Utaminingsih D; Rusin J; Rohsiswatmo R; Malik A
BMC Res Notes; 2018 Mar; 11(1):172. PubMed ID: 29534743
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Screening for G71R mutation of the UDP-glucuronosyltransferase 1 (UGT1A1) gene in neonates with pathologic and prolonged hyperbilirubinemia in Turkey.
Kilic I; Koseler A; Cakaloz I; Atalay E
Int J Clin Pharmacol Ther; 2010 Aug; 48(8):504-8. PubMed ID: 20650040
[TBL] [Abstract][Full Text] [Related]
11. Prevalence of uridine glucuronosyl transferase 1A1 (UGT1A1) mutations in Malay neonates with severe jaundice.
Azlin I; Wong FL; Ezham M; Hafiza A; Ainoon O
Malays J Pathol; 2011 Dec; 33(2):95-100. PubMed ID: 22299209
[TBL] [Abstract][Full Text] [Related]
12. Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population.
Yusoff S; Van Rostenberghe H; Yusoff NM; Talib NA; Ramli N; Ismail NZ; Ismail WP; Matsuo M; Nishio H
Biol Neonate; 2006; 89(3):171-6. PubMed ID: 16210851
[TBL] [Abstract][Full Text] [Related]
13. Bilirubin Uridine Diphosphate-glucuronosyltransferase Polymorphism as a Risk Factor for Prolonged Hyperbilirubinemia in Japanese Preterm Infants.
Yanagi T; Nakahara S; Maruo Y
J Pediatr; 2017 Nov; 190():159-162.e1. PubMed ID: 28888563
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia.
Huang CS; Chang PF; Huang MJ; Chen ES; Hung KL; Tsou KI
Pediatr Res; 2002 Oct; 52(4):601-5. PubMed ID: 12357057
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [OATP 1B1 T521C/A388G is an important polymorphism gene related to neonatal hyperbilirubinemia].
Zhang HX; Zhao X; Yang Z; Peng CY; Long R; Li GN; Li J; He ZK
Zhonghua Er Ke Za Zhi; 2010 Sep; 48(9):650-5. PubMed ID: 21092521
[TBL] [Abstract][Full Text] [Related]
19. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism.
Maruo Y; Nishizawa K; Sato H; Doida Y; Shimada M
Pediatrics; 1999 Jun; 103(6 Pt 1):1224-7. PubMed ID: 10353933
[TBL] [Abstract][Full Text] [Related]
20. Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates.
D'Silva S; Colah RB; Ghosh K; Mukherjee MB
Gene; 2014 Aug; 547(1):18-22. PubMed ID: 24865931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]