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204 related items for PubMed ID: 38906973

  • 1. Progressive degeneration in a new Drosophila model of spinocerebellar ataxia type 7.
    Sujkowski A, Ranxhi B, Bangash ZR, Chbihi ZM, Prifti MV, Qadri Z, Alam N, Todi SV, Tsou WL.
    Sci Rep; 2024 Jun 21; 14(1):14332. PubMed ID: 38906973
    [Abstract] [Full Text] [Related]

  • 2. Progressive degeneration in a new Drosophila model of Spinocerebellar Ataxia type 7.
    Sujkowski AL, Ranxhi B, Prifti MV, Alam N, Todi SV, Tsou WL.
    Res Sq; 2023 Nov 23. PubMed ID: 38045332
    [Abstract] [Full Text] [Related]

  • 3. Progressive degeneration in a new Drosophila model of Spinocerebellar Ataxia type 7.
    Sujkowski AL, Ranxhi B, Prifti MV, Alam N, Todi SV, Tsou WL.
    bioRxiv; 2023 Nov 11. PubMed ID: 37986914
    [Abstract] [Full Text] [Related]

  • 4. Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
    Niewiadomska-Cimicka A, Trottier Y.
    Neurotherapeutics; 2019 Oct 11; 16(4):1074-1096. PubMed ID: 31432449
    [Abstract] [Full Text] [Related]

  • 5. Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7.
    Niu C, Prakash TP, Kim A, Quach JL, Huryn LA, Yang Y, Lopez E, Jazayeri A, Hung G, Sopher BL, Brooks BP, Swayze EE, Bennett CF, La Spada AR.
    Sci Transl Med; 2018 Oct 31; 10(465):. PubMed ID: 30381411
    [Abstract] [Full Text] [Related]

  • 6. Molecular Mechanisms and Therapeutic Strategies in Spinocerebellar Ataxia Type 7.
    Karam A, Trottier Y.
    Adv Exp Med Biol; 2018 Oct 31; 1049():197-218. PubMed ID: 29427104
    [Abstract] [Full Text] [Related]

  • 7. SUMOylation by SUMO2 is implicated in the degradation of misfolded ataxin-7 via RNF4 in SCA7 models.
    Marinello M, Werner A, Giannone M, Tahiri K, Alves S, Tesson C, den Dunnen W, Seeler JS, Brice A, Sittler A.
    Dis Model Mech; 2019 Jan 11; 12(1):. PubMed ID: 30559154
    [Abstract] [Full Text] [Related]

  • 8. A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes.
    Latouche M, Lasbleiz C, Martin E, Monnier V, Debeir T, Mouatt-Prigent A, Muriel MP, Morel L, Ruberg M, Brice A, Stevanin G, Tricoire H.
    J Neurosci; 2007 Mar 07; 27(10):2483-92. PubMed ID: 17344386
    [Abstract] [Full Text] [Related]

  • 9. Differential degradation of full-length and cleaved ataxin-7 fragments in a novel stable inducible SCA7 model.
    Yu X, Ajayi A, Boga NR, Ström AL.
    J Mol Neurosci; 2012 Jun 07; 47(2):219-33. PubMed ID: 22367614
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. Altered p53 and NOX1 activity cause bioenergetic defects in a SCA7 polyglutamine disease model.
    Ajayi A, Yu X, Wahlo-Svedin C, Tsirigotaki G, Karlström V, Ström AL.
    Biochim Biophys Acta; 2015 Nov 09; 1847(4-5):418-428. PubMed ID: 25647692
    [Abstract] [Full Text] [Related]

  • 13. Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration.
    Garden GA, La Spada AR.
    Cerebellum; 2008 Nov 09; 7(2):138-49. PubMed ID: 18418675
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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]

  • 16. Aggregation of Polyglutamine-expanded Ataxin 7 Protein Specifically Sequesters Ubiquitin-specific Protease 22 and Deteriorates Its Deubiquitinating Function in the Spt-Ada-Gcn5-Acetyltransferase (SAGA) Complex.
    Yang H, Liu S, He WT, Zhao J, Jiang LL, Hu HY.
    J Biol Chem; 2015 Sep 04; 290(36):21996-2004. PubMed ID: 26195632
    [Abstract] [Full Text] [Related]

  • 17. Transcriptome Profiling Identifies Multiplexin as a Target of SAGA Deubiquitinase Activity in Glia Required for Precise Axon Guidance During Drosophila Visual Development.
    Ma J, Brennan KJ, D'Aloia MR, Pascuzzi PE, Weake VM.
    G3 (Bethesda); 2016 Aug 09; 6(8):2435-45. PubMed ID: 27261002
    [Abstract] [Full Text] [Related]

  • 18. The Molecular Basis of Spinocerebellar Ataxia Type 7.
    Goswami R, Bello AI, Bean J, Costanzo KM, Omer B, Cornelio-Parra D, Odah R, Ahluwalia A, Allan SK, Nguyen N, Shores T, Aziz NA, Mohan RD.
    Front Neurosci; 2022 Aug 09; 16():818757. PubMed ID: 35401096
    [Abstract] [Full Text] [Related]

  • 19. Spinocerebellar ataxia Type 7: clinical and genetic study of a new Moroccan family (case report).
    Bouzid FZ, Mansouri M, Abdelaziz C, Louhab N, Bernard S, Strubi-Vuillaume I, Dafir K, Aboussair N.
    Pan Afr Med J; 2021 Aug 09; 38():162. PubMed ID: 33995769
    [Abstract] [Full Text] [Related]

  • 20. Cell Death Mechanisms in a Mouse Model of Retinal Degeneration in Spinocerebellar Ataxia 7.
    Lebon C, Behar-Cohen F, Torriglia A.
    Neuroscience; 2019 Feb 21; 400():72-84. PubMed ID: 30625334
    [Abstract] [Full Text] [Related]

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