Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Félix-Antoine Bérubé"'
Autor:
André Do, Vanessa Michaud, Jean-François Stephan, Miltiadis Moreau, Élise Benoît, Félix-Antoine Bérubé, Antoine Bibaud-De Serres, Alain Taillefer, Philippe Vincent
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
Psilocybin has reemerged as a promising treatment for difficult-to-treat depression (DTD). Although there is limited evidence regarding interactions between psilocybin and other psychotropic drugs, clinical trials require that patients discontinue th
Externí odkaz:
https://doaj.org/article/75e06e668ae34ac8a8c9e366dd91ba07
Autor:
Christophe Tav, Éric Fournier, Michèle Fournier, Fatemeh Khadangi, Audrey Baguette, Maxime C. Côté, Maruhen A. D. Silveira, Félix-Antoine Bérubé-Simard, Guillaume Bourque, Arnaud Droit, Steve Bilodeau
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Transcription-factor binding to cis-regulatory regions regulates the gene expression program of a cell, but occupancy is often a poor predictor of the gene response. Here, we show that glucocorticoid stimulation led to the reorganization of transcrip
Externí odkaz:
https://doaj.org/article/46a0e08edf1d4f4bbd95e182c99dc81e
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e93989 (2014)
The Hox gene family encodes homeodomain-containing transcriptional regulators that confer positional information to axial and paraxial tissues in the developing embryo. The dynamic Hox gene expression pattern requires mechanisms that differentially c
Externí odkaz:
https://doaj.org/article/2cdcac8a52d64c12a50b40ec2536ba48
Autor:
Yan Coulombe, Margot Lemieux, Julie Moreau, Josée Aubin, Milan Joksimovic, Félix-Antoine Bérubé-Simard, Sébastien Tabariès, Olivier Boucherat, François Guillou, Christian Larochelle, Christopher K Tuggle, Lucie Jeannotte
Publikováno v:
PLoS ONE, Vol 5, Iss 5, p e10600 (2010)
The genomic organization of Hox clusters is fundamental for the precise spatio-temporal regulation and the function of each Hox gene, and hence for correct embryo patterning. Multiple overlapping transcriptional units exist at the Hoxa5 locus reflect
Externí odkaz:
https://doaj.org/article/2de42b3a8c4f485fb907223a1c72b138
Autor:
Laurence Roy, Amal Abdel‐Baki, Félix‐Antoine Bérubé, Anne Crocker, Luigi de Benedictis, Mathieu Dostie, Eric Latimer, Marc‐André Roy
Publikováno v:
Early Intervention in Psychiatry. 17:495-501
Autor:
Sephora Sallis, Félix-Antoine Bérubé-Simard, Benoit Grondin, Elizabeth Leduc, Fatiha Azouz, Catherine Bélanger, Nicolas Pilon
Publikováno v:
Life Science Alliance. 6:e202302133
CHARGE syndrome is a neural crest-related disorder mainly caused by mutation of the chromatin remodeler-coding geneCHD7. Alternative causes include mutation of other chromatin and/or splicing factors. One of these additional players is the poorly cha
Autor:
Lionel Cailhol, Félix-Antoine Bérubé, Hélène Busque, Pierre David, Ali Jaber, Noémie Noiseux-Lescop, Frédéric Pérusse
Publikováno v:
L'Évolution Psychiatrique. 86:67-76
Resume Objectif Le trouble de la personnalite limite (TPL) est caracterise par une importante impulsivite ainsi qu’une instabilite de l’image de soi, des emotions et des relations. Les proches d’individus TPL sont souvent consideres comme des v
Publikováno v:
Personality and mental healthREFERENCES.
Individuals with personality disorders have a decreased life expectancy compared to the general population in part due to physical illnesses. Many hypotheses have been suggested to explain those physical illnesses such as hormone imbalance, medicatio
Publikováno v:
Sante mentale au Quebec. 46(2)
Objectives Comorbidities that are less well known than substance use disorders may occur in individuals experiencing a first-episode psychosis (FEP). This article reviews the importance of these comorbidities through a synthesis of the literature, in
Autor:
Sephora Sallis, Félix-Antoine Bérubé-Simard, Benoit Grondin, Elizabeth Leduc, Fatiha Azouz, Catherine Bélanger, Nicolas Pilon
The poorly characterized protein FAM172A is mutated in some individuals affected by a disorder of neural crest development called CHARGE syndrome. We also know that FAM172A can interact with the main CHARGE syndrome-associated protein CHD7 and the sm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5ed5b8f12a323886cf0f119b970dd10
https://doi.org/10.1101/2022.03.04.482948
https://doi.org/10.1101/2022.03.04.482948