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Journal Abstract Search

1141 related items for PubMed ID: 17015226

  • 21. Amyotrophic lateral sclerosis: all roads lead to Rome.
    Gonzalez de Aguilar JL, Echaniz-Laguna A, Fergani A, René F, Meininger V, Loeffler JP, Dupuis L.
    J Neurochem; 2007 Jun; 101(5):1153-60. PubMed ID: 17250677
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  • 22. Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALS.
    Foust KD, Salazar DL, Likhite S, Ferraiuolo L, Ditsworth D, Ilieva H, Meyer K, Schmelzer L, Braun L, Cleveland DW, Kaspar BK.
    Mol Ther; 2013 Dec; 21(12):2148-59. PubMed ID: 24008656
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  • 23. Expression of N19S-SOD1, an SOD1 mutant found in sporadic amyotrophic lateral sclerosis patients, induces low-grade motoneuronal toxicity.
    Obata Y, Niikura T, Kanekura K, Hashimoto Y, Kawasumi M, Kita Y, Aiso S, Matsuoka M, Nishimoto I.
    J Neurosci Res; 2005 Sep 01; 81(5):720-9. PubMed ID: 16035108
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  • 24. 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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  • 25. Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMA.
    Kawahara Y, Sun H, Ito K, Hideyama T, Aoki M, Sobue G, Tsuji S, Kwak S.
    Neurosci Res; 2006 Jan 19; 54(1):11-4. PubMed ID: 16225946
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  • 27. Mutant SOD1-induced neuronal toxicity is mediated by increased mitochondrial superoxide levels.
    Zimmerman MC, Oberley LW, Flanagan SW.
    J Neurochem; 2007 Aug 19; 102(3):609-18. PubMed ID: 17394531
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  • 28. 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
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  • 30. 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
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  • 36. Absence of neurofilaments reduces the selective vulnerability of motor neurons and slows disease caused by a familial amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutant.
    Williamson TL, Bruijn LI, Zhu Q, Anderson KL, Anderson SD, Julien JP, Cleveland DW.
    Proc Natl Acad Sci U S A; 1998 Aug 04; 95(16):9631-6. PubMed ID: 9689132
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  • 37. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.
    Watanabe M, Dykes-Hoberg M, Culotta VC, Price DL, Wong PC, Rothstein JD.
    Neurobiol Dis; 2001 Dec 04; 8(6):933-41. PubMed ID: 11741389
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  • 39. The human G93A-superoxide dismutase-1 mutation, mitochondrial glutathione and apoptotic cell death.
    Muyderman H, Hutson PG, Matusica D, Rogers ML, Rush RA.
    Neurochem Res; 2009 Oct 04; 34(10):1847-56. PubMed ID: 19399611
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  • 40. Neuron-glia interactions underlie ALS-like axonal cytoskeletal pathology.
    King AE, Dickson TC, Blizzard CA, Woodhouse A, Foster SS, Chung RS, Vickers JC.
    Neurobiol Aging; 2011 Mar 04; 32(3):459-69. PubMed ID: 19427060
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