Substitutions of the S4DIV R2 residue (R1451) in Na(V)1.4 lead to complex forms of paramyotonia congenita and periodic paralyses

Por Poulin, Hugo, Gosselin-Badaroudine, Pascal, Vicart, Savine, Habbout, Karima, Sternberg, Damien, Giuliano, Serena, Fontaine, Bertrand, Bendahhou, Saïd, Nicole, Sophie, Chahine, Mohamed
Publicado no Sci Rep (2018)

A recessive Na(v)1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis

Por Habbout, Karima, Poulin, Hugo, Rivier, François, Giuliano, Serena, Sternberg, Damien, Fontaine, Bertrand, Eymard, Bruno, Morales, Raul Juntas, Echenne, Bernard, King, Louise, Hanna, Michael G., Männikkö, Roope, Chahine, Mohamed, Nicole, Sophie, Bendahhou, Said
Publicado no Neurology (2016)

Inhibition of CHK 1 (Checkpoint Kinase 1) Elicits Therapeutic Effects in Pulmonary Arterial Hypertension

Por Bourgeois, Alice, Bonnet, Sébastien, Breuils-Bonnet, Sandra, Habbout, Karima, Paradis, Renée, Tremblay, Eve, Lampron, Marie-Claude, Orcholski, Mark E., Potus, Francois, Bertero, Thomas, Peterlini, Thibaut, Chan, Stephen Y., Norris., Karen A, Paulin, Roxane, Provencher, Steeve, Boucherat, Olivier
Publicado no Arterioscler Thromb Vasc Biol (2019)

Implication of EZH2 in the Pro-Proliferative and Apoptosis-Resistant Phenotype of Pulmonary Artery Smooth Muscle Cells in PAH: A Transcriptomic and Proteomic Approach

Por Habbout, Karima, Omura, Junichi, Awada, Charifa, Bourgeois, Alice, Grobs, Yann, Krishna, Vinod, Breuils-Bonnet, Sandra, Tremblay, Eve, Mkannez, Ghada, Martineau, Sandra, Nadeau, Valérie, Roux-Dalvai, Florence, Orcholski, Mark, Jeyaseelan, Jey, Gutstein, David, Potus, François, Provencher, Steeve, Bonnet, Sébastien, Paulin, Roxane, Boucherat, Olivier
Publicado no Int J Mol Sci (2021)