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Journal Abstract Search


389 related items for PubMed ID: 30614396

  • 1. The Expanding Clinical Universe of Polyglutamine Disease.
    Huang S, Zhu S, Li XJ, Li S.
    Neuroscientist; 2019 Oct; 25(5):512-520. PubMed ID: 30614396
    [Abstract] [Full Text] [Related]

  • 2. Autophagy and Polyglutamine Disease.
    Ren H, Hao Z, Wang G.
    Adv Exp Med Biol; 2020 Oct; 1207():149-161. PubMed ID: 32671744
    [Abstract] [Full Text] [Related]

  • 3. Polyglutamine (PolyQ) diseases: genetics to treatments.
    Fan HC, Ho LI, Chi CS, Chen SJ, Peng GS, Chan TM, Lin SZ, Harn HJ.
    Cell Transplant; 2014 Oct; 23(4-5):441-58. PubMed ID: 24816443
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  • 7. X-Linked Spinal and Bulbar Muscular Atrophy: From Clinical Genetic Features and Molecular Pathology to Mechanisms Underlying Disease Toxicity.
    Cortes CJ, La Spada AR.
    Adv Exp Med Biol; 2018 Oct; 1049():103-133. PubMed ID: 29427100
    [Abstract] [Full Text] [Related]

  • 8. [The Role of Mutant RNA in the Pathogenesis of Huntington's Disease and Other Polyglutamine Diseases].
    Bogomazova AN, Eremeev AV, Pozmogova GE, Lagarkova MA.
    Mol Biol (Mosk); 2019 Oct; 53(6):954-967. PubMed ID: 31876275
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  • 9.
    Lo DC, Hughes RE, La Spada AR, Weydt P, Pineda VV.
    ; 2011 Oct. PubMed ID: 21882412
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  • 10. Deubiquitinase USP7 contributes to the pathogenicity of spinal and bulbar muscular atrophy.
    Pluciennik A, Liu Y, Molotsky E, Marsh GB, Ranxhi B, Arnold FJ, St-Cyr S, Davidson B, Pourshafie N, Lieberman AP, Gu W, Todi SV, Merry DE.
    J Clin Invest; 2021 Jan 04; 131(1):. PubMed ID: 33170804
    [Abstract] [Full Text] [Related]

  • 11. Polyglutamine disease proteins: Commonalities and differences in interaction profiles and pathological effects.
    Bonsor M, Ammar O, Schnoegl S, Wanker EE, Silva Ramos E.
    Proteomics; 2024 Jun 04; 24(12-13):e2300114. PubMed ID: 38615323
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  • 13. Protein aggregation and pathogenesis of Huntington's disease: mechanisms and correlations.
    Wanker EE.
    Biol Chem; 2000 Jun 04; 381(9-10):937-42. PubMed ID: 11076024
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  • 14. The CAG-polyglutamine repeat diseases: a clinical, molecular, genetic, and pathophysiologic nosology.
    Stoyas CA, La Spada AR.
    Handb Clin Neurol; 2018 Jun 04; 147():143-170. PubMed ID: 29325609
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  • 17. Polyglutamine pathogenesis: emergence of unifying mechanisms for Huntington's disease and related disorders.
    Ross CA.
    Neuron; 2002 Aug 29; 35(5):819-22. PubMed ID: 12372277
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  • 18. Polyglutamine neurodegeneration: expanded glutamines enhance native functions.
    Orr HT.
    Curr Opin Genet Dev; 2012 Jun 29; 22(3):251-5. PubMed ID: 22284692
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  • 19. Possible Role of the Polyglutamine Elongation in Evolution of Amyloid-Related Evolvability.
    Hashimoto M, Ho G, Takamatsu Y, Wada R, Sugama S, Takenouchi T, Masliah E, Waragai M.
    J Huntingtons Dis; 2018 Jun 29; 7(4):297-307. PubMed ID: 30372687
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  • 20. Huntingtin aggregation and toxicity in Huntington's disease.
    Bates G.
    Lancet; 2003 May 10; 361(9369):1642-4. PubMed ID: 12747895
    [Abstract] [Full Text] [Related]


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