Publications
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Filtres: Author is Soucy, Geneviève [Enlever les filtres]
, « Monoclonal full-length antibody against TAR DNA-binding protein 43 reduces related proteinopathy in neurons. », JCI Insight, 2020.
, « Transmission of ALS pathogenesis by the cerebrospinal fluid », Acta neuropathologica communications, vol. 8, nᵒ 1, p. 65 - 65, 2020.
, « Transmission of ALS pathogenesis by the cerebrospinal fluid. », Acta Neuropathol Commun, vol. 8, nᵒ 1, p. 65, 2020.
, « Virus-mediated delivery of antibody targeting TAR DNA-binding protein-43 mitigates associated neuropathology. », J Clin Invest, vol. 129, nᵒ 4, p. 1581-1595, 2019.
, « Exosome secretion is a key pathway for clearance of pathological TDP-43. », Brain, vol. 139, nᵒ Pt 12, p. 3187-3201, 2016.
, « IL-10 Controls Early Microglial Phenotypes and Disease Onset in ALS Caused by Misfolded Superoxide Dismutase 1. », J Neurosci, vol. 36, nᵒ 3, p. 1031-48, 2016.
, « Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. », Hum Mol Genet, 2016.
, « Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. », Hum Mol Genet, vol. 25, nᵒ 21, p. 4771-4786, 2016.
, « Adeno-associated virus-mediated delivery of a recombinant single-chain antibody against misfolded superoxide dismutase for treatment of amyotrophic lateral sclerosis. », Mol Ther, vol. 22, nᵒ 3, p. 498-510, 2014.
, « Loss of glial neurofascin155 delays developmental synapse elimination at the neuromuscular junction. », J Neurosci, vol. 34, nᵒ 38, p. 12904-18, 2014.
, « Ablation of proliferating cells in the CNS exacerbates motor neuron disease caused by mutant superoxide dismutase. », PLoS One, vol. 7, nᵒ 4, p. e34932, 2012.
, « 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, vol. 113, nᵒ 5, p. 1188-99, 2010.
, « Absence of tumor necrosis factor-alpha does not affect motor neuron disease caused by superoxide dismutase 1 mutations. », J Neurosci, vol. 26, nᵒ 44, p. 11397-402, 2006.
