162 related articles for article (PubMed ID: 36520959)
1. UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia.
Yang H; Li H; Xia Q; Dai W; Li X; Liu Y; Nie J; Yang F; Sun Y; Feng L; Yang L
PLoS One; 2022; 17(12):e0279059. PubMed ID: 36520959
[TBL] [Abstract][Full Text] [Related]
2. UGT1A1 gene mutations and neonatal hyperbilirubinemia in Guangxi Heiyi Zhuang and Han populations.
Wu XJ; Zhong DN; Xie XZ; Ye DZ; Gao ZY
Pediatr Res; 2015 Nov; 78(5):585-8. PubMed ID: 26200705
[TBL] [Abstract][Full Text] [Related]
3. UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China.
Yang H; Lin F; Chen ZK; Zhang L; Xu JX; Wu YH; Gu JY; Ma YB; Li JD; Yang LY
BMC Pediatr; 2021 Jun; 21(1):259. PubMed ID: 34074250
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Clinical Significance of UGT1A1 Genetic Analysis in Chinese Neonates with Severe Hyperbilirubinemia.
Yang H; Wang Q; Zheng L; Zheng XB; Lin M; Zhan XF; Yang LY
Pediatr Neonatol; 2016 Aug; 57(4):310-7. PubMed ID: 26727668
[TBL] [Abstract][Full Text] [Related]
7. Cord blood bilirubin level in relation to bilirubin UDP-glucuronosyltransferase gene missense allele in Chinese neonates.
Sun G; Wu M; Cao J; Du L
Acta Paediatr; 2007 Nov; 96(11):1622-5. PubMed ID: 17888052
[TBL] [Abstract][Full Text] [Related]
8. [Predictive value of umbilical cord blood bilirubin level for subsequent neonatal jaundice].
Sun G; Wang YL; Liang JF; Du LZ
Zhonghua Er Ke Za Zhi; 2007 Nov; 45(11):848-52. PubMed ID: 18282419
[TBL] [Abstract][Full Text] [Related]
9. Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene: the common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese.
Kanai M; Kijima K; Shirahata E; Sasaki A; Akaba K; Umetsu K; Tezuka N; Kurachi H; Aikawa S; Hayasaka K
Pediatr Int; 2005 Apr; 47(2):137-41. PubMed ID: 15771689
[TBL] [Abstract][Full Text] [Related]
10. Homozygous variant of UGT1A1 gene mutation and severe neonatal hyperbilirubinemia.
Boo NY; Wong FL; Wang MK; Othman A
Pediatr Int; 2009 Aug; 51(4):488-93. PubMed ID: 19674361
[TBL] [Abstract][Full Text] [Related]
11. Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity.
Cozzi L; Nuti F; Degrassi I; Civeriati D; Paolella G; Nebbia G
Ital J Pediatr; 2022 Apr; 48(1):59. PubMed ID: 35436954
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population.
Yamamoto A; Nishio H; Waku S; Yokoyama N; Yonetani M; Uetani Y; Nakamura H
Kobe J Med Sci; 2002 Aug; 48(3-4):73-7. PubMed ID: 12502904
[TBL] [Abstract][Full Text] [Related]
14. Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.
Maruo Y; Morioka Y; Fujito H; Nakahara S; Yanagi T; Matsui K; Mori A; Sato H; Tukey RH; Takeuchi Y
J Pediatr; 2014 Jul; 165(1):36-41.e1. PubMed ID: 24650397
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population.
Atasilp C; Kanjanapipak J; Vichayaprasertkul J; Jinda P; Tiyasirichokchai R; Srisawasdi P; Prempunpong C; Chamnanphon M; Puangpetch A; Vanwong N; Klongthalay S; Jantararoungtong T; Sukasem C
BMC Pediatr; 2022 May; 22(1):243. PubMed ID: 35501760
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Gene Mutation in Neonatal Jaundice - Mutations in UGT1A1 and OATP2 Genes.
Min J; Jie L; Caiyun Y; Ying L; Xuefang Y
Indian J Pediatr; 2016 Jul; 83(7):723-5. PubMed ID: 26960716
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
