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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

171 related items for PubMed ID: 17196409

  • 1. UGT1A1(TA)n promoter polymorphism--a new case of a (TA)8 allele in Caucasians.
    Ostanek B, Furlan D, Mavec T, Lukac-Bajalo J.
    Blood Cells Mol Dis; 2007; 38(2):78-82. PubMed ID: 17196409
    [Abstract] [Full Text] [Related]

  • 2. (TA)8 allele in the UGT1A1 gene promoter of a Caucasian with Gilbert's syndrome.
    Iolascon A, Faienza MF, Centra M, Storelli S, Zelante L, Savoia A.
    Haematologica; 1999 Feb; 84(2):106-9. PubMed ID: 10091406
    [Abstract] [Full Text] [Related]

  • 3. Development of a new DHPLC assay for genotyping UGT1A (TA)n polymorphism associated with Gilbert's syndrome.
    Mlakar SJ, Ostanek B.
    Biochem Med (Zagreb); 2011 Feb; 21(2):167-73. PubMed ID: 22135857
    [Abstract] [Full Text] [Related]

  • 4. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene.
    Raijmakers MT, Jansen PL, Steegers EA, Peters WH.
    J Hepatol; 2000 Sep; 33(3):348-51. PubMed ID: 11019988
    [Abstract] [Full Text] [Related]

  • 5. UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: relationships to serum bilirubin concentrations.
    Lampe JW, Bigler J, Horner NK, Potter JD.
    Pharmacogenetics; 1999 Jun; 9(3):341-9. PubMed ID: 10471066
    [Abstract] [Full Text] [Related]

  • 6. Bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1) gene promoter polymorphisms and HPRT, glycophorin A, and micronuclei mutant frequencies in human blood.
    Grant DJ, Hall IJ, Eastmond DA, Jones IM, Bell DA.
    Mutat Res; 2004 May 09; 560(1):1-10. PubMed ID: 15099818
    [Abstract] [Full Text] [Related]

  • 7. 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 09; 35(8):2050-6. PubMed ID: 25611851
    [Abstract] [Full Text] [Related]

  • 8. 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 09; 106(5):E59. PubMed ID: 11061796
    [Abstract] [Full Text] [Related]

  • 9. 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 23; 67(2):69-75. PubMed ID: 35192750
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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 20; 781():145526. PubMed ID: 33631237
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. 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 02; 347(9001):578-81. PubMed ID: 8596320
    [Abstract] [Full Text] [Related]

  • 17. 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 02; 26(1):25-28. PubMed ID: 28338110
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 48(3):166-72. PubMed ID: 22325916
    [Abstract] [Full Text] [Related]

  • 19. 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 28; 13(1):670-9. PubMed ID: 24615032
    [Abstract] [Full Text] [Related]

  • 20. 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 28; 48(5):4953-4959. PubMed ID: 34089128
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.