Richard Robitaille

Affiliations: 
Université de Montréal, Montréal, Canada 
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"Richard Robitaille"
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Publications

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Bose P, Tremblay E, Maios C, et al. (2021) Correction to: The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics
Martineau É, Arbour D, Vallée J, et al. (2020) Properties of Glial Cell at the Neuromuscular Junction are Incompatible with synaptic repair in the SOD1 ALS mouse model. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Martineau É, Di Polo A, Vande Velde C, et al. (2020) Sex-specific differences in motor unit remodeling in a mouse model of ALS. Eneuro
Aubertin-Leheudre M, Pion CH, Vallée J, et al. (2019) Improved Human Muscle Biopsy Method To Study Neuromuscular Junction Structure And Functions With Aging. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences
Bose P, Tremblay E, Maois C, et al. (2019) The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics
Darabid H, St-Pierre-See A, Robitaille R. (2018) Purinergic-Dependent Glial Regulation of Synaptic Plasticity of Competing Terminals and Synapse Elimination at the Neuromuscular Junction. Cell Reports. 25: 2070-2082.e6
Martineau É, Di Polo A, Vande Velde C, et al. (2018) Dynamic neuromuscular remodeling precedes motor-unit loss in a mouse model of ALS. Elife. 7
Matos M, Bosson A, Riebe I, et al. (2018) Astrocytes detect and upregulate transmission at inhibitory synapses of somatostatin interneurons onto pyramidal cells. Nature Communications. 9: 4254
Daghfous G, Auclair F, Clotten F, et al. (2018) GABAergic modulation of olfactomotor transmission in lampreys. Plos Biology. 16: e2005512
Martineau É, Polo AD, Velde CV, et al. (2018) Author response: Dynamic neuromuscular remodeling precedes motor-unit loss in a mouse model of ALS Elife
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