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Journal Abstract Search

196 related items for PubMed ID: 21558795

  • 21. Prevention of mutant SOD1 motoneuron degeneration by copper chelators in vitro.
    Azzouz M, Poindron P, Guettier S, Leclerc N, Andres C, Warter JM, Borg J.
    J Neurobiol; 2000 Jan; 42(1):49-55. PubMed ID: 10623900
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  • 22. The effect of peripheral nerve injury on disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Sharp PS, Dick JR, Greensmith L.
    Neuroscience; 2005 Jan; 130(4):897-910. PubMed ID: 15652988
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  • 27. Depressed excitability and ion currents linked to slow exocytotic fusion pore in chromaffin cells of the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.
    Calvo-Gallardo E, de Pascual R, Fernández-Morales JC, Arranz-Tagarro JA, Maroto M, Nanclares C, Gandía L, de Diego AM, Padín JF, García AG.
    Am J Physiol Cell Physiol; 2015 Jan 01; 308(1):C1-19. PubMed ID: 25377090
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  • 30. Transcriptomic indices of fast and slow disease progression in two mouse models of amyotrophic lateral sclerosis.
    Nardo G, Iennaco R, Fusi N, Heath PR, Marino M, Trolese MC, Ferraiuolo L, Lawrence N, Shaw PJ, Bendotti C.
    Brain; 2013 Nov 01; 136(Pt 11):3305-32. PubMed ID: 24065725
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  • 31. The human G93A-SOD1 mutation in a pre-symptomatic rat model of amyotrophic lateral sclerosis increases the vulnerability to a mild spinal cord compression.
    Jokic N, Yip PK, Michael-Titus A, Priestley JV, Malaspina A.
    BMC Genomics; 2010 Nov 15; 11():633. PubMed ID: 21078175
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  • 32. Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice.
    Locatelli F, Corti S, Papadimitriou D, Fortunato F, Del Bo R, Donadoni C, Nizzardo M, Nardini M, Salani S, Ghezzi S, Strazzer S, Bresolin N, Comi GP.
    Ann Neurol; 2007 Jul 15; 62(1):81-92. PubMed ID: 17503505
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  • 33. Collapsin response mediator protein 4a (CRMP4a) is upregulated in motoneurons of mutant SOD1 mice and can trigger motoneuron axonal degeneration and cell death.
    Duplan L, Bernard N, Casseron W, Dudley K, Thouvenot E, Honnorat J, Rogemond V, De Bovis B, Aebischer P, Marin P, Raoul C, Henderson CE, Pettmann B.
    J Neurosci; 2010 Jan 13; 30(2):785-96. PubMed ID: 20071543
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  • 34. Altered reaction of facial motoneurons to axonal damage in the presymptomatic phase of a murine model of familial amyotrophic lateral sclerosis.
    Mariotti R, Cristino L, Bressan C, Boscolo S, Bentivoglio M.
    Neuroscience; 2002 Jan 13; 115(2):331-5. PubMed ID: 12421599
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  • 35. Wild-type microglia extend survival in PU.1 knockout mice with familial amyotrophic lateral sclerosis.
    Beers DR, Henkel JS, Xiao Q, Zhao W, Wang J, Yen AA, Siklos L, McKercher SR, Appel SH.
    Proc Natl Acad Sci U S A; 2006 Oct 24; 103(43):16021-6. PubMed ID: 17043238
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  • 36. Mutant copper-zinc superoxide dismutase (SOD1) induces protein secretion pathway alterations and exosome release in astrocytes: implications for disease spreading and motor neuron pathology in amyotrophic lateral sclerosis.
    Basso M, Pozzi S, Tortarolo M, Fiordaliso F, Bisighini C, Pasetto L, Spaltro G, Lidonnici D, Gensano F, Battaglia E, Bendotti C, Bonetto V.
    J Biol Chem; 2013 May 31; 288(22):15699-711. PubMed ID: 23592792
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  • 37. alpha-Amino-3-hydroxy-5-methyl-isoxazole-4-propionate receptors in spinal cord motor neurons are altered in transgenic mice overexpressing human Cu,Zn superoxide dismutase (Gly93-->Ala) mutation.
    Pieri M, Gaetti C, Spalloni A, Cavalcanti S, Mercuri N, Bernardi G, Longone P, Zona C.
    Neuroscience; 2003 May 31; 122(1):47-58. PubMed ID: 14596848
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  • 39. Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.
    Li QX, Mok SS, Laughton KM, McLean CA, Volitakis I, Cherny RA, Cheung NS, White AR, Masters CL.
    Aging Cell; 2006 Apr 31; 5(2):153-65. PubMed ID: 16626394
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