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231 related items for PubMed ID: 9217978

  • 1. Mouse models of human CAG repeat disorders.
    Burright EN, Orr HT, Clark HB.
    Brain Pathol; 1997 Jul; 7(3):965-77. PubMed ID: 9217978
    [Abstract] [Full Text] [Related]

  • 2. The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
    Robitaille Y, Lopes-Cendes I, Becher M, Rouleau G, Clark AW.
    Brain Pathol; 1997 Jul; 7(3):901-26. PubMed ID: 9217975
    [Abstract] [Full Text] [Related]

  • 3. Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues.
    Timchenko LT, Caskey CT.
    FASEB J; 1996 Dec; 10(14):1589-97. PubMed ID: 9002550
    [Abstract] [Full Text] [Related]

  • 4. Trinucleotide repeats in neurogenetic disorders.
    Paulson HL, Fischbeck KH.
    Annu Rev Neurosci; 1996 Dec; 19():79-107. PubMed ID: 8833437
    [Abstract] [Full Text] [Related]

  • 5. Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.
    Ranum LP, Lundgren JK, Schut LJ, Ahrens MJ, Perlman S, Aita J, Bird TD, Gomez C, Orr HT.
    Am J Hum Genet; 1995 Sep; 57(3):603-8. PubMed ID: 7668288
    [Abstract] [Full Text] [Related]

  • 6. The repeat expansion detection method in the analysis of diseases with CAG/CTG repeat expansion: usefulness and limitations.
    Martorell L, Pujana MA, Volpini V, Sanchez A, Joven J, Vilella E, Estivill X.
    Hum Mutat; 1997 Sep; 10(6):486-8. PubMed ID: 9401013
    [Abstract] [Full Text] [Related]

  • 7. [The advances in research on phosphorylation of polyglutamine disease].
    Zhou YF, Jiang H, Tang JG, Tang BS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):414-7. PubMed ID: 18683139
    [Abstract] [Full Text] [Related]

  • 8. Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeats in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy.
    Tanaka F, Sobue G, Doyu M, Ito Y, Yamamoto M, Shimada N, Yamamoto K, Riku S, Hshizume Y, Mitsuma T.
    J Neurol Sci; 1996 Jan; 135(1):43-50. PubMed ID: 8926495
    [Abstract] [Full Text] [Related]

  • 9. Clinical aspects of CAG repeat diseases.
    Nance MA.
    Brain Pathol; 1997 Jul; 7(3):881-900. PubMed ID: 9217974
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Inherited neurodegenerative disorders caused by CAG/polyglutamine tract expansions: symposium introduction.
    La Spada AR, Clark AW.
    Brain Pathol; 1997 Jul; 7(3):877-80. PubMed ID: 9217973
    [Abstract] [Full Text] [Related]

  • 12. 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; 36(3):258-9. PubMed ID: 10204858
    [Abstract] [Full Text] [Related]

  • 13. Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
    Silveira I, Coutinho P, Maciel P, Gaspar C, Hayes S, Dias A, Guimarães J, Loureiro L, Sequeiros J, Rouleau GA.
    Am J Med Genet; 1998 Mar 28; 81(2):134-8. PubMed ID: 9613852
    [Abstract] [Full Text] [Related]

  • 14. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.
    Koshy BT, Zoghbi HY.
    Brain Pathol; 1997 Jul 28; 7(3):927-42. PubMed ID: 9217976
    [Abstract] [Full Text] [Related]

  • 15. Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA).
    Ito Y, Tanaka F, Yamamoto M, Doyu M, Nagamatsu M, Riku S, Mitsuma T, Sobue G.
    Neurochem Res; 1998 Jan 28; 23(1):25-32. PubMed ID: 9482263
    [Abstract] [Full Text] [Related]

  • 16. Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
    Silveira I, Lopes-Cendes I, Kish S, Maciel P, Gaspar C, Coutinho P, Botez MI, Teive H, Arruda W, Steiner CE, Pinto-Júnior W, Maciel JA, Jerin S, Sack G, Andermann E, Sudarsky L, Rosenberg R, MacLeod P, Chitayat D, Babul R, Sequeiros J, Rouleau GA.
    Neurology; 1996 Jan 28; 46(1):214-8. PubMed ID: 8559378
    [Abstract] [Full Text] [Related]

  • 17. 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 28; 38(1):68-72. PubMed ID: 7611728
    [Abstract] [Full Text] [Related]

  • 18. Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families.
    Ramesar RS, Bardien S, Beighton P, Bryer A.
    Hum Genet; 1997 Jul 28; 100(1):131-7. PubMed ID: 9225982
    [Abstract] [Full Text] [Related]

  • 19. Sequence variation and size ranges of CAG repeats in the Machado-Joseph disease, spinocerebellar ataxia type 1 and androgen receptor genes.
    Rubinsztein DC, Leggo J, Coetzee GA, Irvine RA, Buckley M, Ferguson-Smith MA.
    Hum Mol Genet; 1995 Sep 28; 4(9):1585-90. PubMed ID: 8541843
    [Abstract] [Full Text] [Related]

  • 20. Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD).
    Haberhausen G, Damian MS, Leweke F, Müller U.
    J Neurol Sci; 1995 Sep 28; 132(1):71-5. PubMed ID: 8523034
    [Abstract] [Full Text] [Related]

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