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 *

113 related articles for article (PubMed ID: 8581556)

  • 1. Origins and evolution of Huntington disease chromosomes.
    Andrew SE; Hayden MR
    Neurodegeneration; 1995 Sep; 4(3):239-44. PubMed ID: 8581556
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.
    Squitieri F; Andrew SE; Goldberg YP; Kremer B; Spence N; Zeisler J; Nichol K; Theilmann J; Greenberg J; Goto J
    Hum Mol Genet; 1994 Dec; 3(12):2103-14. PubMed ID: 7881406
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease.
    Almqvist E; Spence N; Nichol K; Andrew SE; Vesa J; Peltonen L; Anvret M; Goto J; Kanazawa I; Goldberg YP
    Hum Mol Genet; 1995 Feb; 4(2):207-14. PubMed ID: 7757069
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease.
    Myers RH; MacDonald ME; Koroshetz WJ; Duyao MP; Ambrose CM; Taylor SA; Barnes G; Srinidhi J; Lin CS; Whaley WL
    Nat Genet; 1993 Oct; 5(2):168-73. PubMed ID: 8252042
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.
    Kremer B; Almqvist E; Theilmann J; Spence N; Telenius H; Goldberg YP; Hayden MR
    Am J Hum Genet; 1995 Aug; 57(2):343-50. PubMed ID: 7668260
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene.
    Zühlke C; Riess O; Bockel B; Lange H; Thies U
    Hum Mol Genet; 1993 Dec; 2(12):2063-7. PubMed ID: 8111374
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease.
    Novelletto A; Persichetti F; Sabbadini G; Mandich P; Bellone E; Ajmar F; Pergola M; Del Senno L; MacDonald ME; Gusella JF
    Hum Mol Genet; 1994 Jan; 3(1):93-8. PubMed ID: 8162059
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of CAG repeat expansion in Huntington's disease gene (IT 15) in a Hungarian population.
    Jakab K; Gárdián G; Endreffy E; Kalmár T; Bachrati C; Vécsei L; Raskó I
    Eur Neurol; 1999; 41(2):107-10. PubMed ID: 10023115
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 4p16.3 haplotype modifying age at onset of Huntington disease.
    Nørremølle A; Budtz-Jørgensen E; Fenger K; Nielsen JE; Sørensen SA; Hasholt L
    Clin Genet; 2009 Mar; 75(3):244-50. PubMed ID: 19250382
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.
    De Rooij KE; De Koning Gans PA; Skraastad MI; Belfroid RD; Vegter-Van Der Vlis M; Roos RA; Bakker E; Van Ommen GJ; Den Dunnen JT; Losekoot M
    J Med Genet; 1993 Dec; 30(12):996-1002. PubMed ID: 8133511
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing.
    Andrew SE; Goldberg YP; Theilmann J; Zeisler J; Hayden MR
    Hum Mol Genet; 1994 Jan; 3(1):65-7. PubMed ID: 8162053
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular genetics of Huntington's disease].
    Goto J; Masuda N; Watanabe M; Kanazawa I
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1529-31. PubMed ID: 8752453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis in patients with possible but apparently sporadic Huntington's disease.
    Davis MB; Bateman D; Quinn NP; Marsden CD; Harding AE
    Lancet; 1994 Sep; 344(8924):714-7. PubMed ID: 7915776
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.
    Kremer B; Goldberg P; Andrew SE; Theilmann J; Telenius H; Zeisler J; Squitieri F; Lin B; Bassett A; Almqvist E
    N Engl J Med; 1994 May; 330(20):1401-6. PubMed ID: 8159192
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The molecular genetics of Huntington's disease.
    Goldberg YP; Telenius H; Hayden MR
    Curr Opin Neurol; 1994 Aug; 7(4):325-32. PubMed ID: 7952241
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Late-onset Huntington disease with intermediate CAG repeats: true or false?
    Groen JL; de Bie RM; Foncke EM; Roos RA; Leenders KL; Tijssen MA
    J Neurol Neurosurg Psychiatry; 2010 Feb; 81(2):228-30. PubMed ID: 20145031
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
    García-Planells J; Burguera JA; Solís P; Millán JM; Ginestar D; Palau F; Espinós C
    Hum Mutat; 2005 May; 25(5):453-9. PubMed ID: 15832309
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.
    Telenius H; Kremer HP; Theilmann J; Andrew SE; Almqvist E; Anvret M; Greenberg C; Greenberg J; Lucotte G; Squitieri F
    Hum Mol Genet; 1993 Oct; 2(10):1535-40. PubMed ID: 8268906
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype.
    Rubinsztein DC; Leggo J; Goodburn S; Barton DE; Ferguson-Smith MA
    Hum Mol Genet; 1995 Feb; 4(2):203-6. PubMed ID: 7757068
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.