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Journal Abstract Search

620 related items for PubMed ID: 26586529

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  • 26. CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.
    Janzen E, Mendoza-Ferreira N, Hosseinibarkooie S, Schneider S, Hupperich K, Tschanz T, Grysko V, Riessland M, Hammerschmidt M, Rigo F, Bennett CF, Kye MJ, Torres-Benito L, Wirth B.
    Brain; 2018 Aug 01; 141(8):2343-2361. PubMed ID: 29961886
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  • 27. Mitochondrial defects in the respiratory complex I contribute to impaired translational initiation via ROS and energy homeostasis in SMA motor neurons.
    Thelen MP, Wirth B, Kye MJ.
    Acta Neuropathol Commun; 2020 Dec 22; 8(1):223. PubMed ID: 33353564
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  • 28. Proteomic assessment of a cell model of spinal muscular atrophy.
    Wu CY, Whye D, Glazewski L, Choe L, Kerr D, Lee KH, Mason RW, Wang W.
    BMC Neurosci; 2011 Mar 08; 12():25. PubMed ID: 21385431
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  • 29. Time Is Motor Neuron: Therapeutic Window and Its Correlation with Pathogenetic Mechanisms in Spinal Muscular Atrophy.
    Govoni A, Gagliardi D, Comi GP, Corti S.
    Mol Neurobiol; 2018 Aug 08; 55(8):6307-6318. PubMed ID: 29294245
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  • 30. Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.
    Liu H, Beauvais A, Baker AN, Tsilfidis C, Kothary R.
    Dev Neurobiol; 2011 Feb 08; 71(2):153-69. PubMed ID: 20862739
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  • 31. Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy.
    Wen HL, Lin YT, Ting CH, Lin-Chao S, Li H, Hsieh-Li HM.
    Hum Mol Genet; 2010 May 01; 19(9):1766-78. PubMed ID: 20176735
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  • 35. Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches.
    Nizzardo M, Simone C, Dametti S, Salani S, Ulzi G, Pagliarani S, Rizzo F, Frattini E, Pagani F, Bresolin N, Comi G, Corti S.
    Sci Rep; 2015 Jun 30; 5():11746. PubMed ID: 26123042
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  • 36. Dysregulation of Aldh1a2 underlies motor neuron degeneration in spinal muscular atrophy.
    Kataoka M, Sahashi K, Tsujikawa K, Takeda JI, Hirunagi T, Iida M, Katsuno M.
    Neurosci Res; 2023 Sep 30; 194():58-65. PubMed ID: 37146794
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  • 37. Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy.
    Jablonka S, Karle K, Sandner B, Andreassi C, von Au K, Sendtner M.
    Hum Mol Genet; 2006 Feb 01; 15(3):511-8. PubMed ID: 16396995
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  • 39. Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy.
    Acsadi G, Lee I, Li X, Khaidakov M, Pecinova A, Parker GC, Hüttemann M.
    J Neurosci Res; 2009 Sep 01; 87(12):2748-56. PubMed ID: 19437551
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  • 40. Modeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs.
    Yoshida M, Kitaoka S, Egawa N, Yamane M, Ikeda R, Tsukita K, Amano N, Watanabe A, Morimoto M, Takahashi J, Hosoi H, Nakahata T, Inoue H, Saito MK.
    Stem Cell Reports; 2015 Apr 14; 4(4):561-8. PubMed ID: 25801509
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