BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

210 related articles for article (PubMed ID: 23388413)

  • 1. Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism.
    Kaga A; Ohkubo Y; Watanabe Y; Saito S; Matsuki T; Usuda H; Kanda S; Suzuki Y; Tanabu M; Kure S
    BMC Res Notes; 2013 Feb; 6():51. PubMed ID: 23388413
    [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. Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.
    Shiu TY; Huang HH; Lin HH; Shih YL; Chu HC; Chang WK; Hsieh TY
    Liver Int; 2015 Aug; 35(8):2050-6. PubMed ID: 25611851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
    Takeuchi K; Kobayashi Y; Tamaki S; Ishihara T; Maruo Y; Araki J; Mifuji R; Itani T; Kuroda M; Sato H; Kaito M; Adachi Y
    J Gastroenterol Hepatol; 2004 Sep; 19(9):1023-8. PubMed ID: 15304120
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetic basis of Gilbert's syndrome.
    Burchell B; Hume R
    J Gastroenterol Hepatol; 1999 Oct; 14(10):960-6. PubMed ID: 10530490
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.
    Monaghan G; McLellan A; McGeehan A; Li Volti S; Mollica F; Salemi I; Din Z; Cassidy A; Hume R; Burchell B
    J Pediatr; 1999 Apr; 134(4):441-6. PubMed ID: 10190918
    [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. 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]  

  • 9. Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.
    Žaja O; Tiljak MK; Štefanović M; Tumbri J; Jurčić Z
    J Matern Fetal Neonatal Med; 2014 May; 27(8):844-50. PubMed ID: 23981182
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.
    Hsieh TY; Shiu TY; Chu NF; Chao TY; Chu HC; Chang WK; Chao YC; Huang HH
    Genet Mol Res; 2014 Jan; 13(1):670-9. PubMed ID: 24615032
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.
    Monaghan G; Ryan M; Seddon R; Hume R; Burchell B
    Lancet; 1996 Mar; 347(9001):578-81. PubMed ID: 8596320
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
    Kaplan M
    J Perinatol; 2001 Dec; 21 Suppl 1():S30-4; discussion S35-9. PubMed ID: 11803413
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice].
    Seco ML; del Río E; Barceló MJ; Remacha A; Ginovart G; Moliner E; Baiget M
    An Esp Pediatr; 2002 Feb; 56(2):139-43. PubMed ID: 11827650
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.
    D'Angelo R; Rinaldi C; Donato L; Nicocia G; Sidoti A
    Ann Clin Lab Sci; 2015; 45(2):202-5. PubMed ID: 25887876
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effect of UDP-glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome.
    Huang MJ; Chen YC; Huang YY; Yang SS; Chen PL; Huang CS
    Kaohsiung J Med Sci; 2019 Jul; 35(7):432-439. PubMed ID: 31017737
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.
    Hsieh TY; Shiu TY; Huang SM; Lin HH; Lee TC; Chen PJ; Chu HC; Chang WK; Jeng KS; Lai MM; Chao YC
    Pharmacogenet Genomics; 2007 Apr; 17(4):229-36. PubMed ID: 17496722
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.