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Journal Abstract Search

473 related items for PubMed ID: 22072931

  • 1. 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; 12(10):6980-7003. PubMed ID: 22072931
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. 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 25; 56(3):2007-2021. PubMed ID: 29982983
    [Abstract] [Full Text] [Related]

  • 4. 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 25; 7(4):e35050. PubMed ID: 22493728
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  • 5. 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 25; 61(5):427-34. PubMed ID: 17469116
    [Abstract] [Full Text] [Related]

  • 6. TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations.
    Maekawa S, Leigh PN, King A, Jones E, Steele JC, Bodi I, Shaw CE, Hortobagyi T, Al-Sarraj S.
    Neuropathology; 2009 Dec 25; 29(6):672-83. PubMed ID: 19496940
    [Abstract] [Full Text] [Related]

  • 7. Tar DNA binding protein of 43 kDa (TDP-43), 14-3-3 proteins and copper/zinc superoxide dismutase (SOD1) interact to modulate NFL mRNA stability. Implications for altered RNA processing in amyotrophic lateral sclerosis (ALS).
    Volkening K, Leystra-Lantz C, Yang W, Jaffee H, Strong MJ.
    Brain Res; 2009 Dec 11; 1305():168-82. PubMed ID: 19815002
    [Abstract] [Full Text] [Related]

  • 8. Extracellular wildtype and mutant SOD1 induces ER-Golgi pathology characteristic of amyotrophic lateral sclerosis in neuronal cells.
    Sundaramoorthy V, Walker AK, Yerbury J, Soo KY, Farg MA, Hoang V, Zeineddine R, Spencer D, Atkin JD.
    Cell Mol Life Sci; 2013 Nov 11; 70(21):4181-95. PubMed ID: 23765103
    [Abstract] [Full Text] [Related]

  • 9. Mislocalization of TDP-43 in the G93A mutant SOD1 transgenic mouse model of ALS.
    Shan X, Vocadlo D, Krieger C.
    Neurosci Lett; 2009 Jul 17; 458(2):70-4. PubMed ID: 19379791
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  • 11. Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS.
    Robertson J, Sanelli T, Xiao S, Yang W, Horne P, Hammond R, Pioro EP, Strong MJ.
    Neurosci Lett; 2007 Jun 13; 420(2):128-32. PubMed ID: 17543992
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  • 12. The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.
    Lu Y, Tang C, Zhu L, Li J, Liang H, Zhang J, Xu R.
    Int J Biol Sci; 2016 Jun 13; 12(9):1140-9. PubMed ID: 27570488
    [Abstract] [Full Text] [Related]

  • 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 13; 119(3):335-44. PubMed ID: 20111867
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  • 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 13; 300(5):107207. PubMed ID: 38522514
    [Abstract] [Full Text] [Related]

  • 16. TDP-43 physically interacts with amyotrophic lateral sclerosis-linked mutant CuZn superoxide dismutase.
    Higashi S, Tsuchiya Y, Araki T, Wada K, Kabuta T.
    Neurochem Int; 2010 Dec 13; 57(8):906-13. PubMed ID: 20933032
    [Abstract] [Full Text] [Related]

  • 17. 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 13; 104(4):993-1005. PubMed ID: 18233996
    [Abstract] [Full Text] [Related]

  • 18. [Implications of successful immunotherapy in ALS model mice].
    Urushitani M.
    Brain Nerve; 2008 Jun 13; 60(6):643-51. PubMed ID: 18567360
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  • 20. Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.
    Zhang F, Ström AL, Fukada K, Lee S, Hayward LJ, Zhu H.
    J Biol Chem; 2007 Jun 01; 282(22):16691-9. PubMed ID: 17403682
    [Abstract] [Full Text] [Related]

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