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Journal Abstract Search

121 related items for PubMed ID: 10222776

  • 21. Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.
    Mangiarini L, Sathasivam K, Mahal A, Mott R, Seller M, Bates GP.
    Nat Genet; 1997 Feb; 15(2):197-200. PubMed ID: 9020849
    [Abstract] [Full Text] [Related]

  • 22. Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1.
    Watase K, Venken KJ, Sun Y, Orr HT, Zoghbi HY.
    Hum Mol Genet; 2003 Nov 01; 12(21):2789-95. PubMed ID: 12952864
    [Abstract] [Full Text] [Related]

  • 23. [Molecular genetics of Machado-Joseph disease].
    Kawakami H, Maruyama H, Nakamura S.
    Nihon Rinsho; 1996 Mar 01; 54(3):854-60. PubMed ID: 8904248
    [Abstract] [Full Text] [Related]

  • 24. Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci.
    MacMillan JC, Voisey J, Healey SC, Martin NG.
    J Med Genet; 1999 Mar 01; 36(3):258-9. PubMed ID: 10204858
    [Abstract] [Full Text] [Related]

  • 25. Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract.
    Maciel P, Gaspar C, Guimarães L, Goto J, Lopes-Cendes I, Hayes S, Arvidsson K, Dias A, Sequeiros J, Sousa A, Rouleau GA.
    Eur J Hum Genet; 1999 Mar 01; 7(2):147-56. PubMed ID: 10196697
    [Abstract] [Full Text] [Related]

  • 26.
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    [No Abstract] [Full Text] [Related]

  • 27. Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies.
    Mittal U, Srivastava AK, Jain S, Jain S, Mukerji M.
    Arch Neurol; 2005 Apr 01; 62(4):637-40. PubMed ID: 15824265
    [Abstract] [Full Text] [Related]

  • 28. Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.
    Igarashi S, Takiyama Y, Cancel G, Rogaeva EA, Sasaki H, Wakisaka A, Zhou YX, Takano H, Endo K, Sanpei K, Oyake M, Tanaka H, Stevanin G, Abbas N, Dürr A, Rogaev EI, Sherrington R, Tsuda T, Ikeda M, Cassa E, Nishizawa M, Benomar A, Julien J, Weissenbach J, Wang GX, Agid Y, St George-Hyslop PH, Brice A, Tsuji S.
    Hum Mol Genet; 1996 Jul 01; 5(7):923-32. PubMed ID: 8817326
    [Abstract] [Full Text] [Related]

  • 29. Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.
    Martins S, Pearson CE, Coutinho P, Provost S, Amorim A, Dubé MP, Sequeiros J, Rouleau GA.
    Hum Genet; 2014 Oct 01; 133(10):1311-8. PubMed ID: 25026993
    [Abstract] [Full Text] [Related]

  • 30. The relationship between trinucleotide repeat length and phenotypic variation in Machado-Joseph disease.
    Matsumura R, Takayanagi T, Fujimoto Y, Murata K, Mano Y, Horikawa H, Chuma T.
    J Neurol Sci; 1996 Jul 01; 139(1):52-7. PubMed ID: 8836972
    [Abstract] [Full Text] [Related]

  • 31. Studies of the CAG repeat in the Machado-Joseph disease gene in Taiwan.
    Hsieh M, Tsai HF, Lu TM, Yang CY, Wu HM, Li SY.
    Hum Genet; 1997 Aug 01; 100(2):155-62. PubMed ID: 9254842
    [Abstract] [Full Text] [Related]

  • 32. Molecular and clinical correlations in spinocerebellar ataxia type 3 and Machado-Joseph disease.
    Matilla T, McCall A, Subramony SH, Zoghbi HY.
    Ann Neurol; 1995 Jul 01; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 33. Relationship of (CAG)nC configuration to repeat instability of the Machado-Joseph disease gene.
    Matsumura R, Takayanagi T, Murata K, Futamura N, Hirano M, Ueno S.
    Hum Genet; 1996 Dec 01; 98(6):643-5. PubMed ID: 8931692
    [Abstract] [Full Text] [Related]

  • 34. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.
    Cancel G, Abbas N, Stevanin G, Dürr A, Chneiweiss H, Néri C, Duyckaerts C, Penet C, Cann HM, Agid Y.
    Am J Hum Genet; 1995 Oct 01; 57(4):809-16. PubMed ID: 7573040
    [Abstract] [Full Text] [Related]

  • 35. Searching for modulating effects of SCA2, SCA6 and DRPLA CAG tracts on the Machado-Joseph disease (SCA3) phenotype.
    Jardim L, Silveira I, Pereira ML, do Céu Moreira M, Mendonça P, Sequeiros J, Giugliani R.
    Acta Neurol Scand; 2003 Mar 01; 107(3):211-4. PubMed ID: 12614315
    [Abstract] [Full Text] [Related]

  • 36. Non-Mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats.
    Rubinsztein DC, Leggo J.
    J Med Genet; 1997 Mar 01; 34(3):234-6. PubMed ID: 9132496
    [Abstract] [Full Text] [Related]

  • 37. The genomic structure and expression of MJD, the Machado-Joseph disease gene.
    Ichikawa Y, Goto J, Hattori M, Toyoda A, Ishii K, Jeong SY, Hashida H, Masuda N, Ogata K, Kasai F, Hirai M, Maciel P, Rouleau GA, Sakaki Y, Kanazawa I.
    J Hum Genet; 2001 Mar 01; 46(7):413-22. PubMed ID: 11450850
    [Abstract] [Full Text] [Related]

  • 38. Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis.
    Ikeuchi T, Igarashi S, Takiyama Y, Onodera O, Oyake M, Takano H, Koide R, Tanaka H, Tsuji S.
    Am J Hum Genet; 1996 Apr 01; 58(4):730-3. PubMed ID: 8644735
    [Abstract] [Full Text] [Related]

  • 39. Mosaicism of the CAG repeat in CNS tissue in relation to age at death in spinocerebellar ataxia type 1 and Machado-Joseph disease patients.
    Maciel P, Lopes-Cendes I, Kish S, Sequeiros J, Rouleau GA.
    Am J Hum Genet; 1997 Apr 01; 60(4):993-6. PubMed ID: 9106546
    [No Abstract] [Full Text] [Related]

  • 40. Machado-Joseph disease: cerebellar ataxia and autonomic dysfunction in a patient with the shortest known expanded allele (56 CAG repeat units) of the MJD1 gene.
    Takiyama Y, Sakoe K, Nakano I, Nishizawa M.
    Neurology; 1997 Aug 01; 49(2):604-6. PubMed ID: 9270607
    [Abstract] [Full Text] [Related]

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