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Journal Abstract Search

65 related items for PubMed ID: 15312178

  • 1.
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  • 2. Oxidative inactivation of calcineurin by Cu,Zn superoxide dismutase G93A, a mutant typical of familial amyotrophic lateral sclerosis.
    Ferri A, Gabbianelli R, Casciati A, Celsi F, Rotilio G, Carrì MT.
    J Neurochem; 2001 Nov; 79(3):531-8. PubMed ID: 11701756
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  • 3. ALS patients with mutations in the SOD1 gene have an unique metabolomic profile in the cerebrospinal fluid compared with ALS patients without mutations.
    Wuolikainen A, Andersen PM, Moritz T, Marklund SL, Antti H.
    Mol Genet Metab; 2012 Mar; 105(3):472-8. PubMed ID: 22264771
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  • 4. Oxidative modulation of nuclear factor-kappaB in human cells expressing mutant fALS-typical superoxide dismutases.
    Casciati A, Ferri A, Cozzolino M, Celsi F, Nencini M, Rotilio G, Carrì MT.
    J Neurochem; 2002 Dec; 83(5):1019-29. PubMed ID: 12437573
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  • 6. Pharmacological treatment of ALS.
    Münch C, Ludolph AC.
    Neurol Neurochir Pol; 2001 Dec; 35(1 Suppl):41-50. PubMed ID: 11732279
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  • 8. Neuroprotective effect of activity-dependent neurotrophic factor against toxicity from familial amyotrophic lateral sclerosis-linked mutant SOD1 in vitro and in vivo.
    Chiba T, Hashimoto Y, Tajima H, Yamada M, Kato R, Niikura T, Terashita K, Schulman H, Aiso S, Kita Y, Matsuoka M, Nishimoto I.
    J Neurosci Res; 2004 Nov 15; 78(4):542-52. PubMed ID: 15478191
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  • 10. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S, Funakoshi H, Nakamura T, Kato M, Nakano I, Hirano A, Ohama E.
    Acta Neuropathol; 2003 Aug 15; 106(2):112-20. PubMed ID: 12707786
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  • 13. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
    García-Redondo A, Bustos F, Juan Y Seva B, Del Hoyo P, Jiménez S, Campos Y, Martín MA, Rubio JC, Cañadillas F, Arenas J, Esteban J.
    Muscle Nerve; 2002 Aug 15; 26(2):274-8. PubMed ID: 12210393
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  • 15. Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country.
    Khoris J, Moulard B, Briolotti V, Hayer M, Durieux A, Clavelou P, Malafosse A, Rouleau GA, Camu W.
    Eur J Neurol; 2000 Mar 15; 7(2):207-11. PubMed ID: 10809943
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  • 16. 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 15; 61(5):427-34. PubMed ID: 17469116
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  • 17. 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 15; 8(6):933-41. PubMed ID: 11741389
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  • 18. A novel Akt/PKB-interacting protein promotes cell adhesion and inhibits familial amyotrophic lateral sclerosis-linked mutant SOD1-induced neuronal death via inhibition of PP2A-mediated dephosphorylation of Akt/PKB.
    Nawa M, Kanekura K, Hashimoto Y, Aiso S, Matsuoka M.
    Cell Signal; 2008 Mar 15; 20(3):493-505. PubMed ID: 18160256
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  • 19. 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 15; 104(4):993-1005. PubMed ID: 18233996
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