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Journal Abstract Search

202 related items for PubMed ID: 33465527

  • 1. SOD1 oligomers in amyotrophic lateral sclerosis.
    Choi ES, Dokholyan NV.
    Curr Opin Struct Biol; 2021 Feb; 66():225-230. PubMed ID: 33465527
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  • 3. Large SOD1 aggregates, unlike trimeric SOD1, do not impact cell viability in a model of amyotrophic lateral sclerosis.
    Zhu C, Beck MV, Griffith JD, Deshmukh M, Dokholyan NV.
    Proc Natl Acad Sci U S A; 2018 May 01; 115(18):4661-4665. PubMed ID: 29666246
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  • 4. 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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  • 5. SOD1 in neurotoxicity and its controversial roles in SOD1 mutation-negative ALS.
    Hayashi Y, Homma K, Ichijo H.
    Adv Biol Regul; 2016 Jan 08; 60():95-104. PubMed ID: 26563614
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  • 6. Nonnative SOD1 trimer is toxic to motor neurons in a model of amyotrophic lateral sclerosis.
    Proctor EA, Fee L, Tao Y, Redler RL, Fay JM, Zhang Y, Lv Z, Mercer IP, Deshmukh M, Lyubchenko YL, Dokholyan NV.
    Proc Natl Acad Sci U S A; 2016 Jan 19; 113(3):614-9. PubMed ID: 26719414
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  • 7. Silence superoxide dismutase 1 (SOD1): a promising therapeutic target for amyotrophic lateral sclerosis (ALS).
    Abati E, Bresolin N, Comi G, Corti S.
    Expert Opin Ther Targets; 2020 Apr 19; 24(4):295-310. PubMed ID: 32125907
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  • 8. Perspective on SOD1 mediated toxicity in Amyotrophic Lateral Sclerosis.
    Sangwan S, Eisenberg DS.
    Postepy Biochem; 2016 Apr 19; 62(3):362-369. PubMed ID: 28132491
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  • 9. Unveiling the double-edged sword: SOD1 trimers possess tissue-selective toxicity and bind septin-7 in motor neuron-like cells.
    Choi ES, Hnath B, Sha CM, Dokholyan NV.
    Structure; 2024 Oct 03; 32(10):1776-1792.e5. PubMed ID: 39208794
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  • 10. Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS).
    Sangwan S, Zhao A, Adams KL, Jayson CK, Sawaya MR, Guenther EL, Pan AC, Ngo J, Moore DM, Soriaga AB, Do TD, Goldschmidt L, Nelson R, Bowers MT, Koehler CM, Shaw DE, Novitch BG, Eisenberg DS.
    Proc Natl Acad Sci U S A; 2017 Aug 15; 114(33):8770-8775. PubMed ID: 28760994
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  • 11. [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 Aug 15; 139(7):1015-1019. PubMed ID: 31257248
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  • 12. ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis.
    Parakh S, Jagaraj CJ, Vidal M, Ragagnin AMG, Perri ER, Konopka A, Toth RP, Galper J, Blair IP, Thomas CJ, Walker AK, Yang S, Spencer DM, Atkin JD.
    Hum Mol Genet; 2018 Apr 15; 27(8):1311-1331. PubMed ID: 29409023
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  • 13. ALS-Related Mutant SOD1 Aggregates Interfere with Mitophagy by Sequestering the Autophagy Receptor Optineurin.
    Tak YJ, Park JH, Rhim H, Kang S.
    Int J Mol Sci; 2020 Oct 13; 21(20):. PubMed ID: 33065963
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  • 14. CNS-derived extracellular vesicles from superoxide dismutase 1 (SOD1)G93A ALS mice originate from astrocytes and neurons and carry misfolded SOD1.
    Silverman JM, Christy D, Shyu CC, Moon KM, Fernando S, Gidden Z, Cowan CM, Ban Y, Stacey RG, Grad LI, McAlary L, Mackenzie IR, Foster LJ, Cashman NR.
    J Biol Chem; 2019 Mar 08; 294(10):3744-3759. PubMed ID: 30635404
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  • 19. Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations.
    Jeon GS, Shim YM, Lee DY, Kim JS, Kang M, Ahn SH, Shin JY, Geum D, Hong YH, Sung JJ.
    Mol Neurobiol; 2019 Mar 08; 56(3):2007-2021. PubMed ID: 29982983
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