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 *

278 related articles for article (PubMed ID: 8366869)

  • 21. [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]  

  • 22. 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]  

  • 23. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
    Orr HT; Chung MY; Banfi S; Kwiatkowski TJ; Servadio A; Beaudet AL; McCall AE; Duvick LA; Ranum LP; Zoghbi HY
    Nat Genet; 1993 Jul; 4(3):221-6. PubMed ID: 8358429
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A study on Huntington's disease associated trinucleotide repeat within the Chinese population.
    Soong BW; Wang JT
    Proc Natl Sci Counc Repub China B; 1995 Jul; 19(3):137-42. PubMed ID: 7480359
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.
    Wang CK; Wu YR; Hwu WL; Chen CM; Ro LS; Chen ST; Gwinn-Hardy K; Yang CC; Wu RM; Chen TF; Wang HC; Chao MC; Chiu MJ; Lu CJ; Lee-Chen GJ
    Eur Neurol; 2004; 52(2):96-100. PubMed ID: 15273431
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population.
    Barron LH; Rae A; Holloway S; Brock DJ; Warner JP
    Hum Mol Genet; 1994 Jan; 3(1):173-5. PubMed ID: 8162020
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Enzymatic amplification of synthetic oligodeoxyribonucleotides: implications for triplet repeat expansions in the human genome.
    Behn-Krappa A; Doerfler W
    Hum Mutat; 1994; 3(1):19-24. PubMed ID: 8118462
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.
    Cell; 1993 Mar; 72(6):971-83. PubMed ID: 8458085
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Molecular diagnosis of Huntington's disease in Mexican patients by polymerase chain reaction.
    Cisneros Vega B; Alonso Vilatela ME; Yescas Gomez P; Silva Arreola G; Montañez Ojeda C
    Arch Med Res; 1996; 27(1):87-92. PubMed ID: 8867374
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Huntington's disease: trinucleotide disease or polyglutamine disease?].
    Ide K; Nukina N; Kanazawa I
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1540-1. PubMed ID: 8752457
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Pre-symptomatic diagnosis of Huntington disease by polymerase chain reaction].
    Tóth T; Németi M; Papp Z
    Orv Hetil; 1996 Mar; 137(9):451-4. PubMed ID: 8714037
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Epidemiology of Huntington's disease in Slovenia.
    Peterlin B; Kobal J; Teran N; Flisar D; Lovrecić L
    Acta Neurol Scand; 2009 Jun; 119(6):371-5. PubMed ID: 18976322
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
    Langbehn DR; Brinkman RR; Falush D; Paulsen JS; Hayden MR;
    Clin Genet; 2004 Apr; 65(4):267-77. PubMed ID: 15025718
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular detection of new mutations, resolution of ambiguous results and complex genetic counseling issues in Huntington disease.
    Alford RL; Ashizawa T; Jankovic J; Caskey CT; Richards CS
    Am J Med Genet; 1996 Dec; 66(3):281-6. PubMed ID: 8985488
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research Group.
    Lucotte G; Aouizérate A; Loreille O; Gérard N; Turpin JC
    Genet Couns; 1994; 5(4):321-8. PubMed ID: 7888133
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Huntington's disease--advances in gene mapping].
    Nakamura S
    Nihon Rinsho; 1993 Sep; 51(9):2481-7. PubMed ID: 8411732
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.