J. Laganière

发表

Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway

B. Brais, G. Rouleau, C. Néri, 2013, Cell Death and Disease.

Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy

B. Brais, G. Rouleau, A. Abu-Baker, 2007, Neurobiology of Disease.

Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.

B. Brais, G. Rouleau, J. Laganière, 2001, Human molecular genetics.

Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.

B. Brais, G. Rouleau, A. Abu-Baker, 2003, Human molecular genetics.

Cytoplasmic Targeting of Mutant Poly(A)‐Binding Protein Nuclear 1 Suppresses Protein Aggregation and Toxicity in Oculopharyngeal Muscular Dystrophy

B. Brais, G. Rouleau, A. Abu-Baker, 2005, Traffic.

Comparative Analysis of the Expression Profile of Wnk1 and Wnk1/Hsn2 Splice Variants in Developing and Adult Mouse Tissues

G. Rouleau, M. Shekarabi, J. Laganière, 2013, PloS one.

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.

G. Rouleau, M. Shekarabi, J. Laganière, 2008, Human molecular genetics.

Expanded ATXN3 frameshifting events are toxic in Drosophila and mammalian neuron models.

G. Rouleau, J. Laganière, R. Gaudet, 2012, Human molecular genetics.

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*

G. Rouleau, J. Rivière, M. Shekarabi, 2011, The Journal of Biological Chemistry.

MAJOR PATHOGENIC MECHANISM IN HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH AGENESIS OF THE CORPUS CALLOSUM

G. Rouleau, J. Rivière, M. Shekarabi, 2011 .

Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice

Simon E. Laganiere, J. Bouchard, B. Brais, 2005, Neurobiology of Disease.

hnRNP A1 and A/B Interaction with PABPN1 in Oculopharyngeal Muscular Dystrophy

B. Brais, G. Rouleau, J. Laganière, 2003, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

G. Rouleau, J. Rivière, L. Faivre, 2008, The Journal of clinical investigation.

CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation.

B. Brais, G. Rouleau, J. Laganière, 2000, Human molecular genetics.

Valproic acid is protective in cellular and worm models of oculopharyngeal muscular dystrophy

B. Brais, G. Rouleau, C. Néri, 2018, Neurology.

PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy

B. Brais, G. Rouleau, J. Laganière, 2000, Annals of neurology.

Neuron-Specific Expression of Mutant Superoxide Dismutase 1 in Transgenic Mice Does Not Lead to Motor Impairment

A. Pramatarova, J. Laganière, G. Rouleau, 2001, The Journal of Neuroscience.

Schwannomin Isoform-1 Interacts with Syntenin via PDZ Domains*

G. Rouleau, A. Chishti, J. Laganière, 2001, The Journal of Biological Chemistry.

Inhibition of the kinase WNK1/HSN2 ameliorates neuropathic pain by restoring GABA inhibition

Clifford J. Woolf, Guy A. Rouleau, G. Rouleau, 2016, Science Signaling.

KCC3 axonopathy: neuropathological features in the central and peripheral nervous system

G. Rouleau, M. Shekarabi, J. Laganière, 2016, Modern Pathology.

Potassium-Chloride Cotransporter 3 Interacts with Vav2 to Synchronize the Cell Volume Decrease Response with Cell Protrusion Dynamics

G. Rouleau, M. Shekarabi, J. Laganière, 2013, PloS one.

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 Associated with Agenesis of the Corpus Callosum

L. Richards, N. Kurniawan, G. Rouleau, 2012, The Journal of Neuroscience.

Cellular expression of the K+–Cl− cotransporter KCC3 in the central nervous system of mouse

G. Rouleau, M. Shekarabi, J. Laganière, 2011, Brain Research.