The function of RNA-binding proteins at the synapse: implications for neurodegeneration

por Sephton, Chantelle F., Yu, Gang
Publicado 2015

Metabolic Networks Influencing Skeletal Muscle Fiber Composition

por Bourdeau Julien, Isabelle, Sephton, Chantelle F., Dutchak, Paul A.
Publicado 2018

Synaptic dysfunction in ALS and FTD: anatomical and molecular changes provide insights into mechanisms of disease

por Gelon, Pauline A., Dutchak, Paul A., Sephton, Chantelle F.
Publicado 2022

FUS contributes to mTOR-dependent inhibition of translation

por Sévigny, Myriam, Bourdeau Julien, Isabelle, Venkatasubramani, Janani Priya, Hui, Jeremy B., Dutchak, Paul A., Sephton, Chantelle F.
Publicado 2021

Widespread alterations in microRNA biogenesis in human Huntington’s disease putamen

por Petry, Serena, Keraudren, Rémi, Nateghi, Behnaz, Loiselle, Andréanne, Pircs, Karolina, Jakobsson, Johan, Sephton, Chantelle, Langlois, Mélanie, St-Amour, Isabelle, Hébert, Sébastien S.
Publicado 2022

hnRNP A1B, a Splice Variant of HNRNPA1, Is Spatially and Temporally Regulated

por Gagné, Myriam, Deshaies, Jade-Emmanuelle, Sidibé, Hadjara, Benchaar, Yousri, Arbour, Danielle, Dubinski, Alicia, Litt, Gurleen, Peyrard, Sarah, Robitaille, Richard, Sephton, Chantelle F., Vande Velde, Christine
Publicado 2021

Neuronal dysfunction caused by FUSR521G promotes ALS-associated phenotypes that are attenuated by NF-κB inhibition

por Pelaez, Mari Carmen, Desmeules, Antoine, Gelon, Pauline A., Glasson, Bastien, Marcadet, Laetitia, Rodgers, Alicia, Phaneuf, Daniel, Pozzi, Silvia, Dutchak, Paul A., Julien, Jean-Pierre, Sephton, Chantelle F.
Publicado 2023

NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis

por Hui, Jeremy B., Silva, Jose Cesar Hernandez, Pelaez, Mari Carmen, Sévigny, Myriam, Venkatasubramani, Janani Priya, Plumereau, Quentin, Chahine, Mohamed, Proulx, Christophe D., Sephton, Chantelle F., Dutchak, Paul A.
Publicado 2022

Identification of Neuronal RNA Targets of TDP-43-containing Ribonucleoprotein Complexes

por Sephton, Chantelle F., Cenik, Can, Kucukural, Alper, Dammer, Eric B., Cenik, Basar, Han, YuHong, Dewey, Colleen M., Roth, Frederick P., Herz, Joachim, Peng, Junmin, Moore, Melissa J., Yu, Gang
Publicado 2011

Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLD

por Ward, Michael E., Taubes, Alice, Chen, Robert, Miller, Bruce L., Sephton, Chantelle F., Gelfand, Jeffrey M., Minami, Sakura, Boscardin, John, Martens, Lauren Herl, Seeley, William W., Yu, Gang, Herz, Joachim, Filiano, Anthony J., Arrant, Andrew E., Roberson, Erik D., Kraft, Timothy W., Farese, Robert V., Green, Ari, Gan, Li
Publicado 2014

A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics

por Nicolas, Gaël, Sévigny, Myriam, Lecoquierre, François, Marguet, Florent, Deschênes, Andréanne, del Pelaez, Maria Carment, Feuillette, Sébastien, Audebrand, Anaïs, Lecourtois, Magalie, Rousseau, Stéphane, Richard, Anne-Claire, Cassinari, Kévin, Deramecourt, Vincent, Duyckaerts, Charles, Boland, Anne, Deleuze, Jean-François, Meyer, Vincent, Clarimon Echavarria, Jordi, Gelpi, Ellen, Akiyama, Haruhiko, Hasegawa, Masato, Kawakami, Ito, Wong, Tsz H., Van Rooij, Jeroen G. J., Van Swieten, John C., Campion, Dominique, Dutchak, Paul A., Wallon, David, Lavoie-Cardinal, Flavie, Laquerrière, Annie, Rovelet-Lecrux, Anne, Sephton, Chantelle F.
Publicado 2022