BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

310 related articles for article (PubMed ID: 27207688)

  • 1. 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]  

  • 2. Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay.
    Zhao M; Cheah FSH; Chen M; Lee CG; Law HY; Chong SS
    PLoS One; 2017; 12(7):e0180984. PubMed ID: 28700716
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Huntington Disease: Molecular Diagnostics Approach.
    Bastepe M; Xin W
    Curr Protoc Hum Genet; 2015 Oct; 87():9.26.1-9.26.23. PubMed ID: 26439718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Study of Triplet-Primed PCR for Identification of CAG Repeat Expansion in the HTT Gene in a Cohort of 503 Indian Cases with Huntington's Disease Symptoms.
    Chheda P; Chanekar M; Salunkhe Y; Dama T; Pais A; Pande S; Bendre R; Shah N
    Mol Diagn Ther; 2018 Jun; 22(3):353-359. PubMed ID: 29619771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation.
    Ciosi M; Cumming SA; Chatzi A; Larson E; Tottey W; Lomeikaite V; Hamilton G; Wheeler VC; Pinto RM; Kwak S; Morton AJ; Monckton DG
    J Huntingtons Dis; 2021; 10(1):53-74. PubMed ID: 33579864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triplet repeat primed PCR simplifies testing for Huntington disease.
    Jama M; Millson A; Miller CE; Lyon E
    J Mol Diagn; 2013 Mar; 15(2):255-62. PubMed ID: 23414820
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping.
    Zhao M; Cheah FSH; Tan ASC; Lian M; Phang GP; Agarwal A; Chong SS
    Sci Rep; 2019 Nov; 9(1):16481. PubMed ID: 31712634
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Methods of determination of the number of CTG/CAG repeats in trinucleotide repeats in the human genome].
    Falk M; Froster U; Vojtísková M
    Cas Lek Cesk; 2003; 142(10):609-14. PubMed ID: 14635426
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes.
    Ciosi M; Maxwell A; Cumming SA; Hensman Moss DJ; Alshammari AM; Flower MD; Durr A; Leavitt BR; Roos RAC; ; ; Holmans P; Jones L; Langbehn DR; Kwak S; Tabrizi SJ; Monckton DG
    EBioMedicine; 2019 Oct; 48():568-580. PubMed ID: 31607598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative semi-automated analysis of (CAG) repeats in the Huntington disease gene: use of internal standards.
    Williams LC; Hegde MR; Herrera G; Stapleton PM; Love DR
    Mol Cell Probes; 1999 Aug; 13(4):283-9. PubMed ID: 10441201
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single-step scalable-throughput molecular screening for Huntington disease.
    Teo CR; Wang W; Yang Law H; Lee CG; Chong SS
    Clin Chem; 2008 Jun; 54(6):964-72. PubMed ID: 18403567
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.
    Williams LC; Hegde MR; Nagappan R; Faull RL; Giles J; Winship I; Snow K; Love DR
    Genet Test; 2000; 4(1):55-60. PubMed ID: 10794362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Use of capillary electrophoresis for accurate determination of CAG repeats causing Huntington disease. An oligonucleotide design avoiding shadow bands.
    Blanco S; Suarez A; Gandia-Pla S; Gómez-Llorente C; Antúnez A; Gómez-Capilla JA; Fárez-Vidal ME
    Scand J Clin Lab Invest; 2008; 68(7):577-84. PubMed ID: 19378429
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.
    Mariani LL; Tesson C; Charles P; Cazeneuve C; Hahn V; Youssov K; Freeman L; Grabli D; Roze E; Noël S; Peuvion JN; Bachoud-Levi AC; Brice A; Stevanin G; Durr A
    JAMA Neurol; 2016 Sep; 73(9):1105-14. PubMed ID: 27400454
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout.
    Magri S; Nanetti L; Mongelli A; Rizzo E; Taroni F; Mariotti C; Gellera C
    Am J Med Genet A; 2021 Feb; 185(2):397-400. PubMed ID: 33247537
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel allele-specific quantification methods reveal no effects of adult onset CAG repeats on HTT mRNA and protein levels.
    Shin A; Shin B; Shin JW; Kim KH; Atwal RS; Hope JM; Gillis T; Leszyk JD; Shaffer SA; Lee R; Kwak S; MacDonald ME; Gusella JF; Seong IS; Lee JM
    Hum Mol Genet; 2017 Apr; 26(7):1258-1267. PubMed ID: 28165127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nonisotopic method for accurate detection of (CAG)n repeats causing Huntington disease.
    Muglia M; Leone O; Annesi G; Gabriele AL; Imbrogno E; Grandinetti C; Conforti FL; Naso F; Brancati C
    Clin Chem; 1996 Oct; 42(10):1601-3. PubMed ID: 8855141
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simple procedure for automatic detection of unstable alleles in the myotonic dystrophy and Huntington's disease loci.
    Falk M; Vojtísková M; Lukás Z; Kroupová I; Froster U
    Genet Test; 2006; 10(2):85-97. PubMed ID: 16792511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Attenuated huntingtin gene CAG nucleotide repeat size in individuals with Lynch syndrome.
    Dalene Skarping K; Arning L; Petersén Å; Nguyen HP; Gebre-Medhin S
    Sci Rep; 2024 Feb; 14(1):4300. PubMed ID: 38383663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.