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Export 118 results:
Filtres: Author is J-P Julien  [Enlever les filtres]
Zhao W, Beers DR, Henkel JS, Zhang W, Urushitani M, J-P Julien, et al. Extracellular mutant SOD1 induces microglial-mediated motoneuron injury. Glia. 2010;58(2):231-43.
Takeuchi S, Fujiwara N, Ido A, Oono M, Takeuchi Y, Tateno M, et al. Induction of protective immunity by vaccination with wild-type apo superoxide dismutase 1 in mutant SOD1 transgenic mice. J Neuropathol Exp Neurol. 2010;69(10):1044-56.
Gros-Louis F, Soucy G, Larivière R, J-P Julien. Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS. J Neurochem. 2010;113(5):1188-99.
Ezzi SA, Larivière R, Urushitani M, J-P Julien. Neuronal over-expression of chromogranin A accelerates disease onset in a mouse model of ALS. J Neurochem. 2010;115(5):1102-11.
Dequen F, Filali M, Larivière RC, Perrot R, Hisanaga S-, J-P Julien. Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E. Hum Mol Genet. 2010;19(13):2616-29.
Barclay M, J-P Julien, Ryan AF, Housley GD. Type III intermediate filament peripherin inhibits neuritogenesis in type II spiral ganglion neurons in vitro. Neurosci Lett. 2010;478(2):51-5.
Bosco DA, Morfini G, N Karabacak M, Song Y, Gros-Louis F, Pasinelli P, et al. Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS. Nat Neurosci. 2010;13(11):1396-403.
Audet J-, Gowing G, J-P Julien. Wild-type human SOD1 overexpression does not accelerate motor neuron disease in mice expressing murine Sod1 G86R. Neurobiol Dis. 2010;40(1):245-50.
Gowing G, Philips T, Van Wijmeersch B, Audet J-, Dewil M, Van Den Bosch L, et al. Ablation of proliferating microglia does not affect motor neuron degeneration in amyotrophic lateral sclerosis caused by mutant superoxide dismutase. J Neurosci. 2008;28(41):10234-44.
Gros-Louis F, Kriz J, Kabashi E, McDearmid J, Millecamps S, Urushitani M, et al. Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish. Hum Mol Genet. 2008;17(17):2691-702.
Millecamps S, J-P Julien. [Dysfunction of axonal transport in neuropathies and motor neuron diseases]. Med Sci (Paris). 2008;24(1):65-71.
Urushitani M, Ezzi SA, Matsuo A, Tooyama I, J-P Julien. The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS. FASEB J. 2008;22(7):2476-87.
Dequen F, Bomont P, Gowing G, Cleveland DW, J-P Julien. Modest loss of peripheral axons, muscle atrophy and formation of brain inclusions in mice with targeted deletion of gigaxonin exon 1. J Neurochem. 2008;107(1):253-64.
Barrette B, Hébert M-, Filali M, Lafortune K, Vallières N, Gowing G, et al. Requirement of myeloid cells for axon regeneration. J Neurosci. 2008;28(38):9363-76.
Eriksson KS, Zhang S, Lin L, Larivière RC, J-P Julien, Mignot E. The type III neurofilament peripherin is expressed in the tuberomammillary neurons of the mouse. BMC Neurosci. 2008;9:26.

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