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Journal Abstract Search

411 related items for PubMed ID: 32958236

  • 1. The prion-like nature of amyotrophic lateral sclerosis.
    McAlary L, Yerbury JJ, Cashman NR.
    Prog Mol Biol Transl Sci; 2020; 175():261-296. PubMed ID: 32958236
    [Abstract] [Full Text] [Related]

  • 2. From molecule to molecule and cell to cell: prion-like mechanisms in amyotrophic lateral sclerosis.
    Grad LI, Fernando SM, Cashman NR.
    Neurobiol Dis; 2015 May; 77():257-65. PubMed ID: 25701498
    [Abstract] [Full Text] [Related]

  • 3. TDP-43 or FUS-induced misfolded human wild-type SOD1 can propagate intercellularly in a prion-like fashion.
    Pokrishevsky E, Grad LI, Cashman NR.
    Sci Rep; 2016 Mar 01; 6():22155. PubMed ID: 26926802
    [Abstract] [Full Text] [Related]

  • 4. [Prion-like Properties of Misfolded Cu/Zn-superoxide Dismutase in Amyotrophic Lateral Sclerosis: Update and Perspectives].
    Tokuda E, Marklund SL, Furukawa Y.
    Yakugaku Zasshi; 2019 Mar 01; 139(7):1015-1019. PubMed ID: 31257248
    [Abstract] [Full Text] [Related]

  • 5. Aberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosis.
    Pokrishevsky E, Grad LI, Yousefi M, Wang J, Mackenzie IR, Cashman NR.
    PLoS One; 2012 Mar 01; 7(4):e35050. PubMed ID: 22493728
    [Abstract] [Full Text] [Related]

  • 6. Prion-Like Propagation of Protein Misfolding and Aggregation in Amyotrophic Lateral Sclerosis.
    McAlary L, Plotkin SS, Yerbury JJ, Cashman NR.
    Front Mol Neurosci; 2019 Mar 01; 12():262. PubMed ID: 31736708
    [Abstract] [Full Text] [Related]

  • 7. Prion-like mechanisms in amyotrophic lateral sclerosis.
    Ayers JI, Cashman NR.
    Handb Clin Neurol; 2018 Mar 01; 153():337-354. PubMed ID: 29887144
    [Abstract] [Full Text] [Related]

  • 8. Protein misfolding in the late-onset neurodegenerative diseases: common themes and the unique case of amyotrophic lateral sclerosis.
    Mulligan VK, Chakrabartty A.
    Proteins; 2013 Aug 01; 81(8):1285-303. PubMed ID: 23508986
    [Abstract] [Full Text] [Related]

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  • 11. Prion Properties of SOD1 in Amyotrophic Lateral Sclerosis and Potential Therapy.
    Sibilla C, Bertolotti A.
    Cold Spring Harb Perspect Biol; 2017 Oct 03; 9(10):. PubMed ID: 28096265
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  • 13. Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.
    Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A.
    Acta Neuropathol; 2010 Mar 03; 119(3):335-44. PubMed ID: 20111867
    [Abstract] [Full Text] [Related]

  • 14. From nucleation to widespread propagation: A prion-like concept for ALS.
    Maniecka Z, Polymenidou M.
    Virus Res; 2015 Sep 02; 207():94-105. PubMed ID: 25656065
    [Abstract] [Full Text] [Related]

  • 15. Tryptophan residues in TDP-43 and SOD1 modulate the cross-seeding and toxicity of SOD1.
    Pokrishevsky E, DuVal MG, McAlary L, Louadi S, Pozzi S, Roman A, Plotkin SS, Dijkstra A, Julien JP, Allison WT, Cashman NR.
    J Biol Chem; 2024 May 02; 300(5):107207. PubMed ID: 38522514
    [Abstract] [Full Text] [Related]

  • 16. Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology.
    Allison WT, DuVal MG, Nguyen-Phuoc K, Leighton PLA.
    Int J Mol Sci; 2017 Oct 24; 18(10):. PubMed ID: 29064456
    [Abstract] [Full Text] [Related]

  • 17. Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.
    Bastow EL, Gourlay CW, Tuite MF.
    Biochem Soc Trans; 2011 Oct 24; 39(5):1482-7. PubMed ID: 21936838
    [Abstract] [Full Text] [Related]

  • 18. The relevance of contact-independent cell-to-cell transfer of TDP-43 and SOD1 in amyotrophic lateral sclerosis.
    Hanspal MA, Dobson CM, Yerbury JJ, Kumita JR.
    Biochim Biophys Acta Mol Basis Dis; 2017 Nov 24; 1863(11):2762-2771. PubMed ID: 28711596
    [Abstract] [Full Text] [Related]

  • 19. Protein aggregates and regional disease spread in ALS is reminiscent of prion-like pathogenesis.
    Verma A.
    Neurol India; 2013 Nov 24; 61(2):107-10. PubMed ID: 23644307
    [Abstract] [Full Text] [Related]

  • 20. Modeling ALS and FTLD proteinopathies in yeast: an efficient approach for studying protein aggregation and toxicity.
    Kryndushkin D, Shewmaker F.
    Prion; 2011 Nov 24; 5(4):250-7. PubMed ID: 22052354
    [Abstract] [Full Text] [Related]

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