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Journal Abstract Search

291 related items for PubMed ID: 27842454

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  • 24. 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
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  • 27. [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
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  • 29. 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 Apr; 89(3):171-6. PubMed ID: 16210851
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  • 30. Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study.
    Zhou J, Yang C, Zhu W, Chen S, Zeng Y, Wang J, Zhao H, Chen Y, Lin F.
    Biomed Res Int; 2018 Apr; 2018():7803175. PubMed ID: 30298137
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  • 32. 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
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  • 33. 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
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  • 34. UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association?
    Alencastro de Azevedo L, Reverbel da Silveira T, Carvalho CG, Martins de Castro S, Giugliani R, Matte U.
    Pediatr Res; 2012 Aug; 72(2):169-73. PubMed ID: 22580719
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  • 35. Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism.
    Travan L, Lega S, Crovella S, Montico M, Panontin E, Demarini S.
    J Pediatr; 2014 Jul; 165(1):42-5. PubMed ID: 24726540
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  • 36. Revisiting ABO incompatibility as a risk factor for significant neonatal hyperbilirubinemia.
    Khurana R, Batra P, Faridi M, Khan N.
    Trop Doct; 2019 Jul; 49(3):201-204. PubMed ID: 30943888
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  • 38. 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
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  • 39. Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal period.
    Katayama Y, Yokota T, Zhao H, Wong RJ, Stevenson DK, Taniguchi-Ikeda M, Nakamura H, Iijima K, Morioka I.
    Pediatr Int; 2015 Aug; 57(4):645-9. PubMed ID: 25625535
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