The Canadian Path from Discovery to Implementation of Personalized Medicine Approaches

por Richer, Étienne, Syme, Rachel, Robbins, Stephen M., Lasko, Paul
Publicado 2017

Core elements of participant consent documents for Canadian human genomics research and the National Human Genome Library: guidance for policy

por Longstaff, Holly, Flamenbaum, Jaime, Richer, Etienne, Egar, Jeanne, McMaster, Christopher R., Zawati, Ma’n H.
Publicado 2022

Éléments fondamentaux des documents de consentement à participer à la recherche sur le génome humain au Canada et de la Bibliothèque génomique humaine pancanadienne : orientation p...

por Longstaff, Holly, Flamenbaum, Jaime, Richer, Etienne, Egar, Jeanne, McMaster, Christopher R., Zawati, Ma’n H.
Publicado 2022

Burden of acute gastroenteritis among children younger than 5 years of age – a survey among parents in the United Arab Emirates

por Howidi, Mohammad, Al Kaabi, Nawal, El Khoury, Antoine C, Brandtmüller, Agnes, Nagy, Laszlo, Richer, Etienne, Haddadin, Wissam, Miqdady, Mohamad S
Publicado 2012

Iron- and Hepcidin-Independent Downregulation of the Iron Exporter Ferroportin in Macrophages during Salmonella Infection

por Willemetz, Alexandra, Beatty, Sean, Richer, Etienne, Rubio, Aude, Auriac, Anne, Milkereit, Ruth J., Thibaudeau, Olivier, Vaulont, Sophie, Malo, Danielle, Canonne-Hergaux, François
Publicado 2017

Suppression of Hepcidin Expression and Iron Overload Mediate Salmonella Susceptibility in Ankyrin 1 ENU-Induced Mutant

por Yuki, Kyoko E., Eva, Megan M., Richer, Etienne, Chung, Dudley, Paquet, Marilène, Cellier, Mathieu, Canonne-Hergaux, François, Vaulont, Sophie, Vidal, Silvia M., Malo, Danielle
Publicado 2013

Digitalisation and COVID-19: The Perfect Storm

por Horgan, Denis, Hackett, Joanne, Westphalen, C. Benedikt, Kalra, Dipak, Richer, Etienne, Romao, Mario, Andreu, Antonio L., Lal, Jonathan A., Bernini, Chiara, Tumiene, Birute, Boccia, Stefania, Montserrat, Antoni
Publicado 2020

Contribution of increased ISG15, ISGylation and deregulated Type I IFN signaling in Usp18 mutant mice during the course of bacterial infections

por Dauphinee, Shauna M., Richer, Etienne, Eva, Megan M., McIntosh, Fiona, Paquet, Marilène, Dangoor, David, Burkart, Christoph, Zhang, Dong-Er, Gruenheid, Samantha, Gros, Philippe, Behr, Marcel, Malo, Danielle
Publicado 2014

Rare diseases and space health: optimizing synergies from scientific questions to care

por Puscas, Maria, Martineau, Gabrielle, Bhella, Gurjot, Bonnen, Penelope E., Carr, Phil, Lim, Robyn, Mitchell, John, Osmond, Matthew, Urquieta, Emmanuel, Flamenbaum, Jaime, Iaria, Giuseppe, Joly, Yann, Richer, Étienne, Saary, Joan, Saint-Jacques, David, Buckley, Nicole, Low-Decarie, Etienne
Publicado 2022

Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations

por D'Angelo, Carla S., Hermes, Azure, McMaster, Christopher R., Prichep, Elissa, Richer, Étienne, van der Westhuizen, Francois H., Repetto, Gabriela M., Mengchun, Gong, Malherbe, Helen, Reichardt, Juergen K. V., Arbour, Laura, Hudson, Maui, du Plessis, Kelly, Haendel, Melissa, Wilcox, Phillip, Lynch, Sally Ann, Rind, Shamir, Easteal, Simon, Estivill, Xavier, Thomas, Yarlalu, Baynam, Gareth
Publicado 2020