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92 related items for PubMed ID: 15033789

  • 1. Early activation of antioxidant mechanisms in muscle of mutant Cu/Zn-superoxide dismutase-linked amyotrophic lateral sclerosis mice.
    Jokic N, Di Scala F, Dupuis L, Rene F, Muller A, Gonzalez De Aguilar JL, Loeffler JP.
    Ann N Y Acad Sci; 2003 Dec; 1010():552-6. PubMed ID: 15033789
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  • 2. Progressive impairment of CaV1.1 function in the skeletal muscle of mice expressing a mutant type 1 Cu/Zn superoxide dismutase (G93A) linked to amyotrophic lateral sclerosis.
    Beqollari D, Romberg CF, Dobrowolny G, Martini M, Voss AA, Musarò A, Bannister RA.
    Skelet Muscle; 2016 Dec; 6():24. PubMed ID: 27340545
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  • 3. Oxidative stress and antioxidant enzyme upregulation in SOD1-G93A mouse skeletal muscle.
    Mahoney DJ, Kaczor JJ, Bourgeois J, Yasuda N, Tarnopolsky MA.
    Muscle Nerve; 2006 Jun; 33(6):809-16. PubMed ID: 16583367
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  • 4. Cu/Zn superoxide dismutase (SOD1) mutations associated with familial amyotrophic lateral sclerosis (ALS) affect cellular free radical release in the presence of oxidative stress.
    Cookson MR, Menzies FM, Manning P, Eggett CJ, Figlewicz DA, McNeil CJ, Shaw PJ.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):75-85. PubMed ID: 12215229
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  • 6. Differential gene expression in a cell culture model of SOD1-related familial motor neurone disease.
    Kirby J, Menzies FM, Cookson MR, Bushby K, Shaw PJ.
    Hum Mol Genet; 2002 Aug 15; 11(17):2061-75. PubMed ID: 12165567
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  • 7. Effect of overexpression of wild-type and mutant Cu/Zn-superoxide dismutases on oxidative stress and cell death induced by hydrogen peroxide, 4-hydroxynonenal or serum deprivation: potentiation of injury by ALS-related mutant superoxide dismutases and protection by Bcl-2.
    Lee M, Hyun DH, Halliwell B, Jenner P.
    J Neurochem; 2001 Jul 15; 78(2):209-20. PubMed ID: 11461956
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  • 10. Equine motor neuron disease is not linked to Cu/Zn superoxide dismutase mutations: sequence analysis of the equine Cu/Zn superoxide dismutase cDNA.
    de la Rúa-Domènech R, Wiedmann M, Mohammed HO, Cummings JF, Divers TJ, Batt CA.
    Gene; 1996 Oct 31; 178(1-2):83-8. PubMed ID: 8921896
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  • 11. Analysis of the cytosolic proteome in a cell culture model of familial amyotrophic lateral sclerosis reveals alterations to the proteasome, antioxidant defenses, and nitric oxide synthetic pathways.
    Allen S, Heath PR, Kirby J, Wharton SB, Cookson MR, Menzies FM, Banks RE, Shaw PJ.
    J Biol Chem; 2003 Feb 21; 278(8):6371-83. PubMed ID: 12475980
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  • 12. Neuronal tissue-specific ribonucleoprotein complex formation on SOD1 mRNA: alterations by ALS SOD1 mutations.
    Ge WW, Leystra-Lantz C, Sanelli TR, McLean J, Wen W, Strong W, Strong MJ.
    Neurobiol Dis; 2006 Aug 21; 23(2):342-50. PubMed ID: 16730180
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  • 15. Mutant SOD1-induced neuronal toxicity is mediated by increased mitochondrial superoxide levels.
    Zimmerman MC, Oberley LW, Flanagan SW.
    J Neurochem; 2007 Aug 21; 102(3):609-18. PubMed ID: 17394531
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  • 16. Interleukin-6 Deficiency Does Not Affect Motor Neuron Disease Caused by Superoxide Dismutase 1 Mutation.
    Han Y, Ripley B, Serada S, Naka T, Fujimoto M.
    PLoS One; 2016 Aug 21; 11(4):e0153399. PubMed ID: 27070121
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  • 17. Wild-type human SOD1 overexpression does not accelerate motor neuron disease in mice expressing murine Sod1 G86R.
    Audet JN, Gowing G, Julien JP.
    Neurobiol Dis; 2010 Oct 21; 40(1):245-50. PubMed ID: 20573565
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  • 19. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network.
    Wei R, Bhattacharya A, Hamilton RT, Jernigan AL, Chaudhuri AR.
    Biochem Biophys Res Commun; 2013 Aug 16; 438(1):218-23. PubMed ID: 23886956
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  • 20. The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS.
    Urushitani M, Ezzi SA, Matsuo A, Tooyama I, Julien JP.
    FASEB J; 2008 Jul 16; 22(7):2476-87. PubMed ID: 18337461
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