These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

179 related items for PubMed ID: 36376198

  • 1. Pathogenicity classification of SOD1 variants of uncertain significance by in vitro aggregation propensity.
    Chen LX, Xu HF, Lin HX, Yang XX, Li HF, Wu ZY.
    Neurobiol Aging; 2023 Mar; 123():182-190. PubMed ID: 36376198
    [Abstract] [Full Text] [Related]

  • 2. Does wild-type Cu/Zn-superoxide dismutase have pathogenic roles in amyotrophic lateral sclerosis?
    Furukawa Y, Tokuda E.
    Transl Neurodegener; 2020 Aug 19; 9(1):33. PubMed ID: 32811540
    [Abstract] [Full Text] [Related]

  • 3. Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells.
    Oh YK, Shin KS, Yuan J, Kang SJ.
    J Neurochem; 2008 Feb 19; 104(4):993-1005. PubMed ID: 18233996
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. SOD1 aggregation and ALS: role of metallation states and disulfide status.
    Sheng Y, Chattopadhyay M, Whitelegge J, Valentine JS.
    Curr Top Med Chem; 2012 Feb 19; 12(22):2560-72. PubMed ID: 23339308
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [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 Feb 19; 139(7):1015-1019. PubMed ID: 31257248
    [Abstract] [Full Text] [Related]

  • 9. Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?
    Kabashi E, Valdmanis PN, Dion P, Rouleau GA.
    Ann Neurol; 2007 Dec 19; 62(6):553-9. PubMed ID: 18074357
    [Abstract] [Full Text] [Related]

  • 10. Co-deposition of SOD1, TDP-43 and p62 proteinopathies in ALS: evidence for multifaceted pathways underlying neurodegeneration.
    Trist BG, Fifita JA, Hogan A, Grima N, Smith B, Troakes C, Vance C, Shaw C, Al-Sarraj S, Blair IP, Double KL.
    Acta Neuropathol Commun; 2022 Aug 25; 10(1):122. PubMed ID: 36008843
    [Abstract] [Full Text] [Related]

  • 11. The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).
    Crippa V, Sau D, Rusmini P, Boncoraglio A, Onesto E, Bolzoni E, Galbiati M, Fontana E, Marino M, Carra S, Bendotti C, De Biasi S, Poletti A.
    Hum Mol Genet; 2010 Sep 01; 19(17):3440-56. PubMed ID: 20570967
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Amyloidogenic regions in beta-strands II and III modulate the aggregation and toxicity of SOD1 in living cells.
    McAlary L, Nan JR, Shyu C, Sher M, Plotkin SS, Cashman NR.
    Open Biol; 2024 Jun 01; 14(6):230418. PubMed ID: 38835240
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Superoxide dismutase 1 encoding mutations linked to ALS adopts a spectrum of misfolded states.
    Prudencio M, Borchelt DR.
    Mol Neurodegener; 2011 Nov 17; 6():77. PubMed ID: 22094223
    [Abstract] [Full Text] [Related]

  • 18. Functional links between SQSTM1 and ALS2 in the pathogenesis of ALS: cumulative impact on the protection against mutant SOD1-mediated motor dysfunction in mice.
    Hadano S, Mitsui S, Pan L, Otomo A, Kubo M, Sato K, Ono S, Onodera W, Abe K, Chen X, Koike M, Uchiyama Y, Aoki M, Warabi E, Yamamoto M, Ishii T, Yanagawa T, Shang HF, Yoshii F.
    Hum Mol Genet; 2016 Aug 01; 25(15):3321-3340. PubMed ID: 27439389
    [Abstract] [Full Text] [Related]

  • 19. A copper-deficient form of mutant Cu/Zn-superoxide dismutase as an early pathological species in amyotrophic lateral sclerosis.
    Tokuda E, Nomura T, Ohara S, Watanabe S, Yamanaka K, Morisaki Y, Misawa H, Furukawa Y.
    Biochim Biophys Acta Mol Basis Dis; 2018 Jun 01; 1864(6 Pt A):2119-2130. PubMed ID: 29551730
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.