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Journal Abstract Search

348 related items for PubMed ID: 33923808

  • 41. A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis.
    Maier M, Welt T, Wirth F, Montrasio F, Preisig D, McAfoose J, Vieira FG, Kulic L, Späni C, Stehle T, Perrin S, Weber M, Hock C, Nitsch RM, Grimm J.
    Sci Transl Med; 2018 Dec 05; 10(470):. PubMed ID: 30518612
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  • 43. 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 05; 1863(11):2762-2771. PubMed ID: 28711596
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  • 44. 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 05; 300(5):107207. PubMed ID: 38522514
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  • 45. 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
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  • 47. Superoxide Dismutase 1 (SOD1)-Derived Peptide Inhibits Amyloid Aggregation of Familial Amyotrophic Lateral Sclerosis SOD1 Mutants.
    Banerjee V, Shani T, Katzman B, Vyazmensky M, Papo N, Israelson A, Engel S.
    ACS Chem Neurosci; 2016 Nov 16; 7(11):1595-1606. PubMed ID: 27540759
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  • 50. The prion-like nature of amyotrophic lateral sclerosis.
    McAlary L, Yerbury JJ, Cashman NR.
    Prog Mol Biol Transl Sci; 2020 Nov 16; 175():261-296. PubMed ID: 32958236
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  • 51. Misfolded superoxide dismutase-1 in CSF from amyotrophic lateral sclerosis patients.
    Zetterström P, Andersen PM, Brännström T, Marklund SL.
    J Neurochem; 2011 Apr 16; 117(1):91-9. PubMed ID: 21226712
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  • 54. P2X7 receptor activation mediates superoxide dismutase 1 (SOD1) release from murine NSC-34 motor neurons.
    Bartlett R, Ly D, Cashman NR, Sluyter R, Yerbury JJ.
    Purinergic Signal; 2022 Dec 16; 18(4):451-467. PubMed ID: 35478453
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  • 55. The molecular tweezer CLR01 inhibits aberrant superoxide dismutase 1 (SOD1) self-assembly in vitro and in the G93A-SOD1 mouse model of ALS.
    Malik R, Meng H, Wongkongkathep P, Corrales CI, Sepanj N, Atlasi RS, Klärner FG, Schrader T, Spencer MJ, Loo JA, Wiedau M, Bitan G.
    J Biol Chem; 2019 Mar 08; 294(10):3501-3513. PubMed ID: 30602569
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  • 58. Protein misdirection inside and outside motor neurons in Amyotrophic Lateral Sclerosis (ALS): a possible clue for therapeutic strategies.
    Ido A, Fukuyama H, Urushitani M.
    Int J Mol Sci; 2011 Mar 08; 12(10):6980-7003. PubMed ID: 22072931
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  • 59. Mutant SOD1 instability: implications for toxicity in amyotrophic lateral sclerosis.
    Tiwari A, Hayward LJ.
    Neurodegener Dis; 2005 Mar 08; 2(3-4):115-27. PubMed ID: 16909016
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  • 60. Spinal cord homogenates from SOD1 familial amyotrophic lateral sclerosis induce SOD1 aggregation in living cells.
    Pokrishevsky E, Hong RH, Mackenzie IR, Cashman NR.
    PLoS One; 2017 Mar 08; 12(9):e0184384. PubMed ID: 28877271
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