BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 9002673)

  • 1. Trinucleotide repeats in the human genome: size distributions for all possible triplets and detection of expanded disease alleles in a group of Huntington disease individuals by the repeat expansion detection method.
    Hofferbert S; Schanen NC; Chehab F; Francke U
    Hum Mol Genet; 1997 Jan; 6(1):77-83. PubMed ID: 9002673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations.
    Martorell L; Pujana MA; Volpini V; Sanchez A; Joven J; Vilella E; Estivill X
    Hum Mutat; 1997; 10(6):486-8. PubMed ID: 9401013
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Age-, tissue- and length-dependent bidirectional somatic CAG•CTG repeat instability in an allelic series of R6/2 Huntington disease mice.
    Larson E; Fyfe I; Morton AJ; Monckton DG
    Neurobiol Dis; 2015 Apr; 76():98-111. PubMed ID: 25662336
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Enhanced Detection and Sizing of the HTT CAG Repeat Expansion in Huntington Disease Using an Improved Triplet-Primed PCR Assay.
    Zhao M; Lee CG; Law HY; Chong SS
    Neurodegener Dis; 2016; 16(5-6):348-51. PubMed ID: 27207688
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unstable familial transmissions of Huntington disease alleles with 27-35 CAG repeats (intermediate alleles).
    Semaka A; Collins JA; Hayden MR
    Am J Med Genet B Neuropsychiatr Genet; 2010 Jan; 153B(1):314-20. PubMed ID: 19455596
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expansion of a (CAG)n repeat region in a sporadic case of HD.
    Bozza A; Malagù S; Calzolari E; Novelletto A; Pavoni M; del Senno L
    Acta Neurol Scand; 1995 Aug; 92(2):132-4. PubMed ID: 7484060
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Predictive testing for Huntington disease: interpretation and significance of intermediate alleles.
    Semaka A; Creighton S; Warby S; Hayden MR
    Clin Genet; 2006 Oct; 70(4):283-94. PubMed ID: 16965319
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease.
    Semaka A; Kay C; Doty C; Collins JA; Bijlsma EK; Richards F; Goldberg YP; Hayden MR
    J Med Genet; 2013 Oct; 50(10):696-703. PubMed ID: 23896435
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array.
    Holmes SE; Wentzell JS; Seixas AI; Callahan C; Silveira I; Ross CA; Margolis RL
    Hum Genet; 2006 Sep; 120(2):193-200. PubMed ID: 16783570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of CAG repeats in pre-eclampsia/eclampsia using the repeat expansion detection method.
    Freed KA; Cooper DW; Brennecke SP; Moses EK
    Mol Hum Reprod; 2005 Jul; 11(7):481-7. PubMed ID: 16123075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.
    Yapijakis C; Vassilopoulos D; Tzagournisakis M; Maris T; Fesdjian C; Papageorgiou C; Plaitakis A
    Eur J Hum Genet; 1995; 3(4):228-34. PubMed ID: 8528671
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide scan for CAG/CTG repeat expansions in Pimas with early onset of type 2 diabetes mellitus.
    Wolford JK; Bogardus C; Prochazka M
    Mol Genet Metab; 1999 Jan; 66(1):62-7. PubMed ID: 9973549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of the (CAG)n repeat causing Huntington's disease in a Mexican population.
    Alonso ME; Yescas P; Cisneros B; Martínez C; Silva G; Ochoa A; Montañez C
    Clin Genet; 1997 Apr; 51(4):225-30. PubMed ID: 9184242
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.
    Koshy BT; Zoghbi HY
    Brain Pathol; 1997 Jul; 7(3):927-42. PubMed ID: 9217976
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene (
    De Luca A; Morella A; Consoli F; Fanelli S; Thibert JR; Statt S; Latham GJ; Squitieri F
    Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33567536
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
    Veitch NJ; Ennis M; McAbney JP; ; Shelbourne PF; Monckton DG
    DNA Repair (Amst); 2007 Jun; 6(6):789-96. PubMed ID: 17293170
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease.
    Djoussé L; Knowlton B; Hayden M; Almqvist EW; Brinkman R; Ross C; Margolis R; Rosenblatt A; Durr A; Dode C; Morrison PJ; Novelletto A; Frontali M; Trent RJ; McCusker E; Gómez-Tortosa E; Mayo D; Jones R; Zanko A; Nance M; Abramson R; Suchowersky O; Paulsen J; Harrison M; Yang Q; Cupples LA; Gusella JF; MacDonald ME; Myers RH
    Am J Med Genet A; 2003 Jun; 119A(3):279-82. PubMed ID: 12784292
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The CAG repeat at the Huntington disease gene in the Portuguese population: insights into its dynamics and to the origin of the mutation.
    Costa MDC; Magalhães P; Guimarães L; Maciel P; Sequeiros J; Sousa A
    J Hum Genet; 2006; 51(3):189-195. PubMed ID: 16372132
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.
    Leeflang EP; Zhang L; Tavaré S; Hubert R; Srinidhi J; MacDonald ME; Myers RH; de Young M; Wexler NS; Gusella JF
    Hum Mol Genet; 1995 Sep; 4(9):1519-26. PubMed ID: 8541834
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular interpretation of expanded RED products in bipolar disorder by CAG/CTG repeats located at chromosomes 17q and 18q.
    Verheyen GR; Del-Favero J; Mendlewicz J; Lindblad K; Van Zand K; Aalbregtse M; Schalling M; Souery D; Van Broeckhoven C
    Neurobiol Dis; 1999 Oct; 6(5):424-32. PubMed ID: 10527808
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.