BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 17888052)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. [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]  

  • 13. [
    Yao X; Zhong DN; Peng YC
    Zhongguo Dang Dai Er Ke Za Zhi; 2022 Jul; 24(7):792-796. PubMed ID: 35894195
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 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. [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]  

  • 18. 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]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.