Effect of a rare genetic variant of TM7SF4 gene on osteoclasts of patients with Paget’s disease of bone

por Laurier, Emilie, Amiable, Nathalie, Gagnon, Edith, Brown, Jacques P., Michou, Laëtitia
Publicado 2017

Molecular effect of an OPTN common variant associated to Paget's disease of bone

por Silva, Iris A. L., Conceição, Natércia, Gagnon, Édith, Brown, Jacques P., Cancela, M. Leonor, Michou, Laëtitia
Publicado 2018

Attenuated clinical and osteoclastic phenotypes of Paget’s disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene

por Dessay, Mariam, Couture, Emile, Maaroufi, Halim, Fournier, Frédéric, Gagnon, Edith, Droit, Arnaud, Brown, Jacques P., Michou, Laëtitia
Publicado 2022

Detection of SQSTM1/P392L post-zygotic mutations in Paget’s disease of bone

por Guay-Bélanger, Sabrina, Picard, Sylvain, Gagnon, Edith, Morissette, Jean, Siris, Ethel S., Orcel, Philippe, Brown, Jacques P., Michou, Laëtitia
Publicado 2014

Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the SQSTM1 gene in Paget's disease of bone

por Dessay, Mariam, Jobin Gervais, François, Simonyan, David, Samson, Andréanne, Gleeton, Guylaine, Gagnon, Edith, Albert, Caroline, Brown, Jacques P., Michou, Laëtitia
Publicado 2020

Molecular test of Paget's disease of bone in families not linked to SQSTM1 gene mutations

por You, Yang, Simonyan, David, Bureau, Alexandre, Gagnon, Edith, Albert, Caroline, Guertin, Jason R., Tarride, Jean-Eric, Brown, Jacques P., Michou, Laëtitia
Publicado 2023

Novel Insights Regarding the Operational Characteristics and Teleological Purpose of the Renal Na(+)-K(+)-Cl(2) Cotransporter (NKCC2s) Splice Variants

por Brunet, Geneviève M., Gagnon, Edith, Simard, Charles F., Daigle, Nikolas D., Caron, Luc, Noël, Micheline, Lefoll, Marie-Hélène, Bergeron, Marc J., Isenring, Paul
Publicado 2005