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 *

219 related articles for article (PubMed ID: 19932091)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Genotyping UGT1A1(TA)(n) polymorphism rare variants by high resolution melting curve analysis.
    Ostanek B; Furlan D; Bratanič B
    Clin Chim Acta; 2011 Feb; 412(5-6):489-90. PubMed ID: 21134365
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. UGT1A1 (TA)n genotyping in sickle-cell disease: high resolution melting (HRM) curve analysis or direct sequencing, what is the best way?
    Thomas V; Mazard B; Garcia C; Lacan P; Gagnieu MC; Joly P
    Clin Chim Acta; 2013 Sep; 424():258-60. PubMed ID: 23827693
    [TBL] [Abstract][Full Text] [Related]  

  • 8. TaqMan real time PCR for the Detection of the Gilbert's Syndrome Markers UGT1A1*28; UGT1A1*36 and UGT1A1*37.
    Daprà V; Alliaudi C; Galliano I; Dini M; Curcio GL; Calvi C; Archetti M; Gavatorta M; Bergallo M
    Mol Biol Rep; 2021 May; 48(5):4953-4959. PubMed ID: 34089128
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 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. [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]  

  • 14. Snapback primer genotyping of the Gilbert syndrome UGT1A1 (TA)(n) promoter polymorphism by high-resolution melting.
    Farrar JS; Palais RA; Wittwer CT
    Clin Chem; 2011 Sep; 57(9):1303-10. PubMed ID: 21771946
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.
    Fesenko EE; Heydarov RN; Stepanova EV; Abramov ME; Chudinov AV; Zasedatelev AS; Mikhailovich VM
    Clin Chem Lab Med; 2013 Jun; 51(6):1177-84. PubMed ID: 23241680
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism.
    Iyer L; Hall D; Das S; Mortell MA; Ramírez J; Kim S; Di Rienzo A; Ratain MJ
    Clin Pharmacol Ther; 1999 May; 65(5):576-82. PubMed ID: 10340924
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.