These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 10352000)

  • 1. Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population.
    Biondi ML; Turri O; Dilillo D; Stival G; Guagnellini E
    Clin Chem; 1999 Jun; 45(6 Pt 1):897-8. PubMed ID: 10352000
    [No Abstract]   [Full Text] [Related]  

  • 2. Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.
    Dabke PS; Colah RB; Ghosh KK; Nadkarni AH
    Hematology; 2014 Oct; 19(7):388-92. PubMed ID: 24620945
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unusual presentation of Gilbert disease with high levels of unconjugated bilirubin. Report of two cases.
    Flores-Villalba E; Rodriguez-Montalvo C; Bosques-Padilla F; Arredondo-Saldaña G; Zertuche-Maldonado T; Torre-Flores L
    Rev Esp Enferm Dig; 2016 Apr; 108(4):228-30. PubMed ID: 26181050
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic basis of fasting hyperbilirubinemia.
    Ishihara T; Gabazza EC; Adachi Y; Sato H; Maruo Y
    Gastroenterology; 1999 May; 116(5):1272. PubMed ID: 10220526
    [No Abstract]   [Full Text] [Related]  

  • 5. TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.
    Sampietro M; Lupica L; Perrero L; Romano R; Molteni V; Fiorelli G
    Ital J Gastroenterol Hepatol; 1998 Apr; 30(2):194-8. PubMed ID: 9675658
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effect of bilirubin UDP glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries.
    Doyama H; Okada T; Kobayashi T; Suzuki A; Takeda Y; Mabuchi H
    Hepatology; 2000 Sep; 32(3):563-8. PubMed ID: 10960450
    [TBL] [Abstract][Full Text] [Related]  

  • 7. TATA-Box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with clinical diagnosis of Gilbert Syndrome.
    Costa E; Vieira E; Santos-Silva E; Barbot J; dos Santos R
    Haematologica; 2002 Apr; 87(4):ELT21. PubMed ID: 11940506
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects.
    Borlak J; Thum T; Landt O; Erb K; Hermann R
    Hepatology; 2000 Oct; 32(4 Pt 1):792-5. PubMed ID: 11003624
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic lesions in the UGT1A1 genes among Gilbert's syndrome patients from India.
    Chiddarwar AS; D'Silva SZ; Colah RB; Ghosh K; Mukherjee MB
    Mol Biol Rep; 2018 Dec; 45(6):2733-2739. PubMed ID: 30105552
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1.
    Persico M; Persico E; Bakker CT; Rigato I; Amoroso A; Torella R; Bosma PJ; Tiribelli C; Ostrow JD
    Hepatology; 2001 Mar; 33(3):627-32. PubMed ID: 11230743
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.
    Moyer AM; Skierka JM; Kotzer KE; Kluge ML; Black JL; Baudhuin LM
    Mol Diagn Ther; 2017 Jun; 21(3):327-335. PubMed ID: 28213806
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.
    Rodrigues C; Vieira E; Santos R; de Carvalho J; Santos-Silva A; Costa E; Bronze-da-Rocha E
    Blood Cells Mol Dis; 2012 Mar; 48(3):166-72. PubMed ID: 22325916
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.
    Hsieh SY; Wu YH; Lin DY; Chu CM; Wu M; Liaw YF
    Am J Gastroenterol; 2001 Apr; 96(4):1188-93. PubMed ID: 11316168
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic variation in UGT1A1 typical of Gilbert syndrome is associated with unconjugated hyperbilirubinemia in patients receiving tocilizumab.
    Lee JS; Wang J; Martin M; Germer S; Kenwright A; Benayed R; Spleiss O; Platt A; Pilson R; Hemmings A; Weinblatt ME; Kaplowitz N; Krasnow J
    Pharmacogenet Genomics; 2011 Jul; 21(7):365-74. PubMed ID: 21412181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
    Sampietro M; Lupica L; Perrero L; Comino A; Martinez di Montemuros F; Cappellini MD; Fiorelli G
    Br J Haematol; 1997 Nov; 99(2):437-9. PubMed ID: 9375769
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gilbert's syndrome: a possible cause of hyperbilirubinemia after orthotopic liver transplantation.
    Lachaux A; Aboufadel A; Chambon M; Boillot O; Le Gall C; Gille D; Hermier M
    Transplant Proc; 1996 Oct; 28(5):2846. PubMed ID: 8908094
    [No Abstract]   [Full Text] [Related]  

  • 18. The genetic basis of Gilbert's syndrome.
    Sato H; Adachi Y; Koiwai O
    Lancet; 1996 Mar; 347(9001):557-8. PubMed ID: 8596313
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals.
    Radoi VE; Ursu RI; Poenaru E; Arsene C; Bohiltea CL; Bohiltea R
    J Gastrointestin Liver Dis; 2017 Mar; 26(1):25-28. PubMed ID: 28338110
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.