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

409 related items for PubMed ID: 35052556

  • 1. Hydrogen Peroxide and Amyotrophic Lateral Sclerosis: From Biochemistry to Pathophysiology.
    Sanghai N, Tranmer GK.
    Antioxidants (Basel); 2021 Dec 27; 11(1):. PubMed ID: 35052556
    [Abstract] [Full Text] [Related]

  • 2. 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 Dec 27; 7(4):e35050. PubMed ID: 22493728
    [Abstract] [Full Text] [Related]

  • 3. Pathological hydrogen peroxide triggers the fibrillization of wild-type SOD1 via sulfenic acid modification of Cys-111.
    Xu WC, Liang JZ, Li C, He ZX, Yuan HY, Huang BY, Liu XL, Tang B, Pang DW, Du HN, Yang Y, Chen J, Wang L, Zhang M, Liang Y.
    Cell Death Dis; 2018 Jan 22; 9(2):67. PubMed ID: 29358575
    [Abstract] [Full Text] [Related]

  • 4. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
    Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, Kwong LK, Forman MS, Ravits J, Stewart H, Eisen A, McClusky L, Kretzschmar HA, Monoranu CM, Highley JR, Kirby J, Siddique T, Shaw PJ, Lee VM, Trojanowski JQ.
    Ann Neurol; 2007 May 22; 61(5):427-34. PubMed ID: 17469116
    [Abstract] [Full Text] [Related]

  • 5. The role of heat shock proteins in Amyotrophic Lateral Sclerosis: The therapeutic potential of Arimoclomol.
    Kalmar B, Lu CH, Greensmith L.
    Pharmacol Ther; 2014 Jan 22; 141(1):40-54. PubMed ID: 23978556
    [Abstract] [Full Text] [Related]

  • 6. 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 22; 56(3):2007-2021. PubMed ID: 29982983
    [Abstract] [Full Text] [Related]

  • 7. 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 22; 1864(6 Pt A):2119-2130. PubMed ID: 29551730
    [Abstract] [Full Text] [Related]

  • 8. Wild-type Cu/Zn-superoxide dismutase is misfolded in cerebrospinal fluid of sporadic amyotrophic lateral sclerosis.
    Tokuda E, Takei YI, Ohara S, Fujiwara N, Hozumi I, Furukawa Y.
    Mol Neurodegener; 2019 Nov 19; 14(1):42. PubMed ID: 31744522
    [Abstract] [Full Text] [Related]

  • 9. Using yeast models to probe the molecular basis of amyotrophic lateral sclerosis.
    Bastow EL, Gourlay CW, Tuite MF.
    Biochem Soc Trans; 2011 Oct 19; 39(5):1482-7. PubMed ID: 21936838
    [Abstract] [Full Text] [Related]

  • 10. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.
    Tan CF, Eguchi H, Tagawa A, Onodera O, Iwasaki T, Tsujino A, Nishizawa M, Kakita A, Takahashi H.
    Acta Neuropathol; 2007 May 19; 113(5):535-42. PubMed ID: 17333220
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 14. Pathological roles of wild-type cu, zn-superoxide dismutase in amyotrophic lateral sclerosis.
    Furukawa Y.
    Neurol Res Int; 2012 May 19; 2012():323261. PubMed ID: 22830015
    [Abstract] [Full Text] [Related]

  • 15. Protein aggregation and therapeutic strategies in SOD1- and TDP-43- linked ALS.
    Tsekrekou M, Giannakou M, Papanikolopoulou K, Skretas G.
    Front Mol Biosci; 2024 May 19; 11():1383453. PubMed ID: 38855322
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. 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 19; 119(3):335-44. PubMed ID: 20111867
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. A pathological link between dysregulated copper binding in Cu/Zn-superoxide dismutase and amyotrophic lateral sclerosis.
    Furukawa Y.
    J Clin Biochem Nutr; 2022 Sep 19; 71(2):73-77. PubMed ID: 36213785
    [Abstract] [Full Text] [Related]

  • 20. Cu/Zn-superoxide dismutase and wild-type like fALS SOD1 mutants produce cytotoxic quantities of H2O2 via cysteine-dependent redox short-circuit.
    Bakavayev S, Chetrit N, Zvagelsky T, Mansour R, Vyazmensky M, Barak Z, Israelson A, Engel S.
    Sci Rep; 2019 Jul 25; 9(1):10826. PubMed ID: 31346243
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.