BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 18403567)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington's disease.
    Aziz NA; van Belzen MJ; Coops ID; Belfroid RD; Roos RA
    Eur J Med Genet; 2011; 54(4):e413-8. PubMed ID: 21540131
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
    Ma M; Yang Y; Shang H; Su D; Zhang H; Ma Y; Liu Y; Tao D; Zhang S
    J Neurol Sci; 2010 Nov; 298(1-2):57-60. PubMed ID: 20864123
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic diagnosis of Huntington disease].
    Mo YQ; Li LY; Lu GX
    Yi Chuan; 2005 Nov; 27(6):861-4. PubMed ID: 16378928
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
    Sułek-Piatkowska A; Krysa W; Zdzienicka E; Szirkowiec W; Hoffman-Zacharska D; Rajkiewicz M; Fidziańska E; Kowalska G; Zaremba J
    Neurol Neurochir Pol; 2008; 42(3):203-9. PubMed ID: 18651325
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An intergenerational contraction of a fully penetrant Huntington disease allele to a reduced penetrance allele: interpretation of results and significance for risk assessment and genetic counseling.
    Nahhas F; Garbern J; Feely S; Feldman GL
    Am J Med Genet A; 2009 Feb; 149A(4):732-6. PubMed ID: 19267413
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Counting CAG repeats in the Huntington's disease gene by restriction endonuclease EcoP15I cleavage.
    Möncke-Buchner E; Reich S; Mücke M; Reuter M; Messer W; Wanker EE; Krüger DH
    Nucleic Acids Res; 2002 Aug; 30(16):e83. PubMed ID: 12177311
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology.
    Uhlmann WR; Peñaherrera MS; Robinson WP; Milunsky JM; Nicholson JM; Albin RL
    Am J Med Genet A; 2015 May; 167A(5):1152-60. PubMed ID: 25736541
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.
    Masuda N; Goto J; Murayama N; Watanabe M; Kondo I; Kanazawa I
    J Med Genet; 1995 Sep; 32(9):701-5. PubMed ID: 8544189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
    Kenney C; Powell S; Jankovic J
    Mov Disord; 2007 Jan; 22(1):127-30. PubMed ID: 17115386
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Clinical characteristics of Huntington disease in two pedigrees and analysis of expanded CAG trinucleotide repeat].
    Cao GN; Bao XH; Lu HM; Zhang JJ; Ma YN; Gu WH; Xiong H; Qin J; Wu XR
    Beijing Da Xue Xue Bao Yi Xue Ban; 2011 Apr; 43(2):163-7. PubMed ID: 21503105
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.