Not logged in Share Save
Share Save
Share Save
Inhibition of the kinase WNK1/HSN2 ameliorates neuropathic pain by restoring GABA inhibition Kahle, Kristopher T.; Schmouth, Jean-Francois; Lavastre, Valerie; Latremoliere, Alban; Zhang, Jinwei; Andrews, Nick; Omura, Takao; Laganiere, Janet; Rochefort, Daniel; Hince, Pascale; Castonguay, Genevieve; Gaudet, Rebecca; 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. Share Save
Share Save
Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models Stochmanski, Shawn J.; Therrien, Martine; Laganiere, Janet; Rochefort, Daniel; Laurent, Sandra; Karemera, Liliane; Gaudet, Rebecca; Vyboh, Kishanda; Van Meyel, Don J.; Di Cristo, Graziella; Dion, Patrick A.; Gaspar, Claudia; Rouleau, Guy A. Share Save
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 Salin-Cantegrel, Adele; Riviere, Jean-Baptiste; Shekarabi, Masoud; Rasheed, Sarah; DaCal, Sandra; Laganiere, Janet; Gaudet, Rebecca; Rochefort, Daniel; Lesca, Gaetan; Gaspar, Claudia; Dion, Patrick A.; Lapointe, Jean-Yves; Rouleau, Guy A. Share Save
HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3 Salin-Cantegrel, Adele; Shekarabi, Masoud; Holbert, Sebastien; Dion, Patrick; Rochefort, Daniel; Laganiere, Janet; Dacal, Sandra; Hince, Pascale; Karemera, Liliane; Gaspar, Claudia; Lapointe, Jean-Yves; Rouleau, Guy A. Share Save
Mutations in the nervous system-specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II Shekarabi, Masoud; Girard, Nathalie; Riviere, Jean-Baptiste; Dion, Patrick; Houle, Martin; Toulouse, Andre; Lafreniere, Ronald G.; Vercauteren, Freya; Hince, Pascale; Laganiere, Janet; Rochefort, Daniel; Faivre, Laurence; Samuels, Mark; Rouleau, Guy A. Share Save
Share Save
Share Save
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice Dion, P; Shanmugam, V; Gaspar, C; Messaed, C; Meijer, I; Toulouse, A; Laganiere, J; Roussel, J; Rochefort, D; Laganiere, S; Allen, C; Karpati, G; Bouchard, JP; Braisd, B; Rouleau, GA Share Save
Share Save