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459 related items for PubMed ID: 18418675

  • 1. Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration.
    Garden GA, La Spada AR.
    Cerebellum; 2008; 7(2):138-49. PubMed ID: 18418675
    [Abstract] [Full Text] [Related]

  • 2. Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration.
    Furrer SA, Mohanachandran MS, Waldherr SM, Chang C, Damian VA, Sopher BL, Garden GA, La Spada AR.
    J Neurosci; 2011 Nov 09; 31(45):16269-78. PubMed ID: 22072678
    [Abstract] [Full Text] [Related]

  • 3. Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7.
    Furrer SA, Waldherr SM, Mohanachandran MS, Baughn TD, Nguyen KT, Sopher BL, Damian VA, Garden GA, La Spada AR.
    Hum Mol Genet; 2013 Mar 01; 22(5):890-903. PubMed ID: 23197655
    [Abstract] [Full Text] [Related]

  • 4. Spinocerebellar ataxia 7 (SCA7).
    Lebre AS, Brice A.
    Cytogenet Genome Res; 2003 Mar 01; 100(1-4):154-63. PubMed ID: 14526176
    [Abstract] [Full Text] [Related]

  • 5. Disease progression despite early loss of polyglutamine protein expression in SCA7 mouse model.
    Helmlinger D, Abou-Sleymane G, Yvert G, Rousseau S, Weber C, Trottier Y, Mandel JL, Devys D.
    J Neurosci; 2004 Feb 25; 24(8):1881-7. PubMed ID: 14985428
    [Abstract] [Full Text] [Related]

  • 6. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.
    Tang B, Liu C, Shen L, Dai H, Pan Q, Jing L, Ouyang S, Xia J.
    Arch Neurol; 2000 Apr 25; 57(4):540-4. PubMed ID: 10768629
    [Abstract] [Full Text] [Related]

  • 7. Insights into the molecular basis of polyglutamine neurodegeneration from studies of a spinocerebellar ataxia type 7 mouse model.
    Grote SK, La Spada AR.
    Cytogenet Genome Res; 2003 Apr 25; 100(1-4):164-74. PubMed ID: 14526177
    [Abstract] [Full Text] [Related]

  • 8. Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.
    Katagiri S, Hayashi T, Takeuchi T, Yamada H, Gekka T, Kawabe K, Kurita A, Tsuneoka H.
    Doc Ophthalmol; 2015 Jun 25; 130(3):189-95. PubMed ID: 25643591
    [Abstract] [Full Text] [Related]

  • 9. AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse Model.
    Niewiadomska-Cimicka A, Fievet L, Surdyka M, Jesion E, Keime C, Singer E, Eisenmann A, Kalinowska-Poska Z, Nguyen HHP, Fiszer A, Figiel M, Trottier Y.
    Int J Mol Sci; 2024 Apr 15; 25(8):. PubMed ID: 38673939
    [Abstract] [Full Text] [Related]

  • 10. Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice.
    Yvert G, Lindenberg KS, Picaud S, Landwehrmeyer GB, Sahel JA, Mandel JL.
    Hum Mol Genet; 2000 Oct 12; 9(17):2491-506. PubMed ID: 11030754
    [Abstract] [Full Text] [Related]

  • 11. Interference of Crx-dependent transcription by ataxin-7 involves interaction between the glutamine regions and requires the ataxin-7 carboxy-terminal region for nuclear localization.
    Chen S, Peng GH, Wang X, Smith AC, Grote SK, Sopher BL, La Spada AR.
    Hum Mol Genet; 2004 Jan 01; 13(1):53-67. PubMed ID: 14613968
    [Abstract] [Full Text] [Related]

  • 12. [The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].
    Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H.
    Yi Chuan; 2007 Jun 01; 29(6):688-92. PubMed ID: 17650485
    [Abstract] [Full Text] [Related]

  • 13. A novel central nervous system-enriched spinocerebellar ataxia type 7 gene product.
    Einum DD, Clark AM, Townsend JJ, Ptacek LJ, Fu YH.
    Arch Neurol; 2003 Jan 01; 60(1):97-103. PubMed ID: 12533095
    [Abstract] [Full Text] [Related]

  • 14. Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration.
    Palhan VB, Chen S, Peng GH, Tjernberg A, Gamper AM, Fan Y, Chait BT, La Spada AR, Roeder RG.
    Proc Natl Acad Sci U S A; 2005 Jun 14; 102(24):8472-7. PubMed ID: 15932940
    [Abstract] [Full Text] [Related]

  • 15. SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell types.
    Yvert G, Lindenberg KS, Devys D, Helmlinger D, Landwehrmeyer GB, Mandel JL.
    Hum Mol Genet; 2001 Aug 01; 10(16):1679-92. PubMed ID: 11487572
    [Abstract] [Full Text] [Related]

  • 16. Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
    Karam A, Trottier Y.
    Adv Exp Med Biol; 2018 Aug 01; 1049():197-218. PubMed ID: 29427104
    [Abstract] [Full Text] [Related]

  • 17. Spinocerebellar ataxia type 7.
    Martin JJ.
    Handb Clin Neurol; 2012 Aug 01; 103():475-91. PubMed ID: 21827908
    [Abstract] [Full Text] [Related]

  • 18. Spinocerebellar ataxia type 7 (SCA7) - correlations between phenotype and genotype in one large Belgian family.
    Martin J, Van Regemorter N, Del-Favero J, Löfgren A, Van Broeckhoven C.
    J Neurol Sci; 1999 Sep 15; 168(1):37-46. PubMed ID: 10500272
    [Abstract] [Full Text] [Related]

  • 19. The autophagy/lysosome pathway is impaired in SCA7 patients and SCA7 knock-in mice.
    Alves S, Cormier-Dequaire F, Marinello M, Marais T, Muriel MP, Beaumatin F, Charbonnier-Beaupel F, Tahiri K, Seilhean D, El Hachimi K, Ruberg M, Stevanin G, Barkats M, den Dunnen W, Priault M, Brice A, Durr A, Corvol JC, Sittler A.
    Acta Neuropathol; 2014 Nov 15; 128(5):705-22. PubMed ID: 24859968
    [Abstract] [Full Text] [Related]

  • 20. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families.
    Brusco A, Gellera C, Cagnoli C, Saluto A, Castucci A, Michielotto C, Fetoni V, Mariotti C, Migone N, Di Donato S, Taroni F.
    Arch Neurol; 2004 May 15; 61(5):727-33. PubMed ID: 15148151
    [Abstract] [Full Text] [Related]

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