Ohcanbohtosat - Gaudet, Rébecca

Comparative Analysis of the Expression Profile of Wnk1 and Wnk1/Hsn2 Splice Variants in Developing and Adult Mouse Tissues Dahkki Shekarabi, Masoud, Lafrenière, Ron G., Gaudet, Rébecca, Laganière, Janet, Marcinkiewicz, Martin M., Dion, Patrick A., Rouleau, Guy A.

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Sacs R272C missense homozygous mice develop an ataxia phenotype Dahkki Larivière, Roxanne, Sgarioto, Nicolas, Márquez, Brenda Toscano, Gaudet, Rébecca, Choquet, Karine, McKinney, R. Anne, Watt, Alanna J., Brais, Bernard

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Potassium-Chloride Cotransporter 3 Interacts with Vav2 to Synchronize the Cell Volume Decrease Response with Cell Protrusion Dynamics Dahkki Salin-Cantegrel, Adèle, Shekarabi, Masoud, Rasheed, Sarah, Charron, François M., Laganière, Janet, Gaudet, Rebecca, Dion, Patrick A., Lapointe, Jean-Yves, Rouleau, Guy A.

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Transit Defect of Potassium-Chloride Co-transporter 3 Is a Major Pathogenic Mechanism in Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum Dahkki Salin-Cantegrel, Adèle, Rivière, Jean-Baptiste, Shekarabi, Masoud, Rasheed, Sarah, DaCal, Sandra, Laganière, Janet, Gaudet, Rébecca, Rochefort, Daniel, Lesca, Gaëtan, Gaspar, Claudia, Dion, Patrick A., Lapointe, Jean-Yves, Rouleau, Guy A.

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Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay Dahkki Larivière, Roxanne, Gaudet, Rébecca, Gentil, Benoit J., Girard, Martine, Conte, Talita Cristiane, Minotti, Sandra, Leclerc-Desaulniers, Kim, Gehring, Kalle, McKinney, R. Anne, Shoubridge, Eric A., McPherson, Peter S., Durham, Heather D., Brais, Bernard

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Loss of Neuronal Potassium/Chloride Cotransporter 3 (KCC3) Is Responsible for the Degenerative Phenotype in a Conditional Mouse Model of Hereditary Motor and Sensory Neuropathy Ass... Dahkki Shekarabi, Masoud, Moldrich, Randal X., Rasheed, Sarah, Salin-Cantegrel, Adéle, Laganière, Janet, Rochefort, Daniel, Hince, Pascale, Huot, Karine, Gaudet, Rébecca, Kurniawan, Nyoman, Sotocinal, Susana G., Ritchie, Jennifer, Dion, Patrick A., Mogil, Jeffrey S., Richards, Linda J., Rouleau, Guy A.

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Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) Dahkki Girard, Martine, Larivière, Roxanne, Parfitt, David A., Deane, Emily C., Gaudet, Rebecca, Nossova, Nadya, Blondeau, Francois, Prenosil, George, Vermeulen, Esmeralda G. M., Duchen, Michael R., Richter, Andrea, Shoubridge, Eric A., Gehring, Kalle, McKinney, R. Anne, Brais, Bernard, Chapple, J. Paul, McPherson, Peter S.

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WNK1/HSN2 kinase inhibition ameliorates neuropathic pain by reducing maladaptive KCC2 inhibitory phosphorylation and restoring GABA inhibition Dahkki Kahle, Kristopher T., Schmouth, Jean-François, Lavastre, Valérie, Latremoliere, Alban, Zhang, Jinwei, Andrews, Nick, Laganière, Janet, Rochefort, Daniel, Hince, Pascale, Castonguay, Geneviève, Gaudet, Rébecca, Mapplebeck, Josiane C.S., Sotocinal, Susana G., Duan, JingJing, Ward, Catherine, Khanna, Arjun R., Mogil, Jeffrey S., Dion, Patrick A., Woolf, Clifford J., Inquimbert, Perrine, Rouleau, Guy A.

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KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2 Dahkki Rivière, Jean-Baptiste, Ramalingam, Siriram, Lavastre, Valérie, Shekarabi, Masoud, Holbert, Sébastien, Lafontaine, Julie, Srour, Myriam, Merner, Nancy, Rochefort, Daniel, Hince, Pascale, Gaudet, Rébecca, Mes-Masson, Anne-Marie, Baets, Jonathan, Houlden, Henry, Brais, Bernard, Nicholson, Garth A., Van Esch, Hilde, Nafissi, Shahriar, De Jonghe, Peter, Reilly, Mary M., Timmerman, Vincent, Dion, Patrick A., Rouleau, Guy A.

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