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 *

172 related articles for article (PubMed ID: 7480359)

  • 41. Huntington's disease: diagnosis by amplification of the CAG repeat.
    Upton JD; Avery S; Parkin P; George PM
    N Z Med J; 1995 Mar; 108(995):78-80. PubMed ID: 7891947
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Abnormal gene product identified in Huntington's disease lymphocytes and brain.
    Ide K; Nukina N; Masuda N; Goto J; Kanazawa I
    Biochem Biophys Res Commun; 1995 Apr; 209(3):1119-25. PubMed ID: 7733967
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian species.
    Pêcheux C; Gall AL; Kaplan JC; Dodé C
    Ann Genet; 1996; 39(2):81-6. PubMed ID: 8766138
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.
    Stine OC; Pleasant N; Franz ML; Abbott MH; Folstein SE; Ross CA
    Hum Mol Genet; 1993 Oct; 2(10):1547-9. PubMed ID: 8268907
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.
    Mandich P; Di Maria E; Bellone E; Ajmar F; Abbruzzese G
    Eur Neurol; 1996; 36(6):348-52. PubMed ID: 8954302
    [TBL] [Abstract][Full Text] [Related]  

  • 46. 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]  

  • 47. Trinucleotide repeat length and progression of illness in Huntington's disease.
    Kieburtz K; MacDonald M; Shih C; Feigin A; Steinberg K; Bordwell K; Zimmerman C; Srinidhi J; Sotack J; Gusella J
    J Med Genet; 1994 Nov; 31(11):872-4. PubMed ID: 7853373
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Population and family studies of CAG repeats in the IT-15 gene].
    Malysheva OV; Ivashchenko TE; Baranov VS
    Genetika; 2001 Mar; 37(3):402-6. PubMed ID: 11357373
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Molecular analysis of late onset Huntington's disease.
    Kremer B; Squitieri F; Telenius H; Andrew SE; Theilmann J; Spence N; Goldberg YP; Hayden MR
    J Med Genet; 1993 Dec; 30(12):991-5. PubMed ID: 8133510
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [The gene responsible for Huntington's disease in Spanish families: its diagnostic value and the relation between trinucleotide expansion and the clinical characteristics].
    Benítez J; Fernández E; García Ruiz P; Robledo M; Ayuso C; García Yébenes J
    Rev Clin Esp; 1994 Aug; 194(8):591-3. PubMed ID: 7938836
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. [Huntington chorea. Molecular genetic principles, mutation detection and predictive diagnosis].
    Zühlke C; Thies U
    Nervenarzt; 1996 Jan; 67(1):25-35. PubMed ID: 8676985
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat.
    Ambrose CM; Duyao MP; Barnes G; Bates GP; Lin CS; Srinidhi J; Baxendale S; Hummerich H; Lehrach H; Altherr M; Wasmuth J; Buckler A; Church D; Housman D; Berks M; Micklem G; Durbin R; Dodge A; Read A; Gusella J; MacDonald ME
    Somat Cell Mol Genet; 1994 Jan; 20(1):27-38. PubMed ID: 8197474
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. 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]  

  • 57. Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.
    Nance MA; Mathias-Hagen V; Breningstall G; Wick MJ; McGlennen RC
    Neurology; 1999 Jan; 52(2):392-4. PubMed ID: 9932964
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The genetic analysis of Turkish patients with Huntington's disease.
    Ataç FB; Elibol B; Schaefer F
    Acta Neurol Scand; 1999 Sep; 100(3):195-8. PubMed ID: 10478585
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Diagnosis of "sporadic" Huntington's disease.
    Dürr A; Dodé C; Hahn V; Pêcheux C; Pillon B; Feingold J; Kaplan JC; Agid Y; Brice A
    J Neurol Sci; 1995 Mar; 129(1):51-5. PubMed ID: 7751845
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 9.