R. Gaudet

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.

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.

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

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

KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2.

A. Mes-Masson, B. Brais, H. Van Esch, 2011, American journal of human genetics.

Renal and cardiac oxidative/nitrosative stress in salt-loaded pregnant rat.

R. Gaudet, M. Brochu, J. St-Louis, 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

Restless legs syndrome‐associated MEIS1 risk variant influences iron homeostasis

J. Montplaisir, G. Rouleau, G. Turecki, 2011, Annals of neurology.

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 .

Mitochondrial dysfunction and Purkinje cell loss in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)

E. Shoubridge, B. Brais, M. Duchen, 2012, Proceedings of the National Academy of Sciences.

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

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

Renal and cardiac Na+-K +-ATPase and aconitase in a rat model of fetal programming.

R. Gaudet, M. Brochu, 2009, Methods in molecular biology.

Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay.

E. Shoubridge, B. Brais, P. McPherson, 2015, Human molecular genetics.

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.

Sacs R272C missense homozygous mice develop an ataxia phenotype

Brenda Toscano Márquez, A. Watt, B. Brais, 2019, Molecular Brain.