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 *

372 related articles for article (PubMed ID: 11003624)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Gilbert's syndrome--a frequent cause of unconjugated hyperbilirubinemia in children after orthotopic liver transplantation.
    Kathemann S; Lainka E; Baba HA; Hoyer PF; Gerner P
    Pediatr Transplant; 2012 Mar; 16(2):201-4. PubMed ID: 22360405
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Gilbert's disease and atazanavir: from phenotype to UDP-glucuronosyltransferase haplotype.
    Lankisch TO; Moebius U; Wehmeier M; Behrens G; Manns MP; Schmidt RE; Strassburg CP
    Hepatology; 2006 Nov; 44(5):1324-32. PubMed ID: 17058217
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Use of double gradient denaturing gradient gel electrophoresis to detect (AT)n polymorphisms in the UDP-glucuronosyltransferase 1 gene promoter associated with Gilbert's syndrome.
    Gürtler V; Parkin JD; Mayall BC
    Electrophoresis; 1999 Oct; 20(14):2841-3. PubMed ID: 10546817
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Dependence of blood biochemical parameters on various genotypes of the UGT1A1 gene associated with gilbert's syndrome.
    Sidorenko DV; Nazarov VD; Volnikova EG; Kondrasheva EA; Peshkova NG; Kovaleva IS; Kokorina OS; Svatkovskaya IB; Lapin SV
    Klin Lab Diagn; 2022 Feb; 67(2):69-75. PubMed ID: 35192750
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis.
    Minucci A; Concolino P; Giardina B; Zuppi C; Capoluongo E
    Clin Chim Acta; 2010 Feb; 411(3-4):246-9. PubMed ID: 19932091
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].
    Kim YH; Yeon JE; Jung GM; Kim HJ; Kim JS; Byun KS; Bak YT; Lee CH
    Taehan Kan Hakhoe Chi; 2002 Jun; 8(2):132-8. PubMed ID: 12499798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid allelic discrimination by TaqMan PCR for the detection of the Gilbert's syndrome marker UGT1A1*28.
    Ehmer U; Lankisch TO; Erichsen TJ; Kalthoff S; Freiberg N; Wehmeier M; Manns MP; Strassburg CP
    J Mol Diagn; 2008 Nov; 10(6):549-52. PubMed ID: 18832463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gilbert syndrome associated with beta-thalassemia.
    Tzetis M; Kanavakis E; Tsezou A; Ladis V; Pateraki E; Georgakopoulou T; Kavazarakis E; Maragoudaki E; Karpathios T; Kitsiou-Tzeli S
    Pediatr Hematol Oncol; 2001 Dec; 18(8):477-84. PubMed ID: 11764096
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people.
    Zhang M; Wang H; Huang Y; Xu X; Liu W; Ning Q; Chen T; Qi J
    Gene; 2021 May; 781():145526. PubMed ID: 33631237
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
    Bosma PJ; Chowdhury JR; Bakker C; Gantla S; de Boer A; Oostra BA; Lindhout D; Tytgat GN; Jansen PL; Oude Elferink RP
    N Engl J Med; 1995 Nov; 333(18):1171-5. PubMed ID: 7565971
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.