Now showing items 261-280 of 708

  • Formation and differentiation of multiple mesenchymal lineages during lung development is regulated by {beta}-catenin signaling 

    De Langhe, S. P.; Carraro, G.; Tefft, D.; Li, Changgong; Xu, Xin; Chai, Y.; Minoo, P.; Hajihosseini, M. K.; Drouin, J.; Kaartinen, V.; Bellusci, S. (Public Library of Science, 2008)
    BACKGROUND: The role of ss-catenin signaling in mesodermal lineage formation and differentiation has been elusive. METHODOLOGY: To define the role of ss-catenin signaling in these processes, we used a Dermo1(Twist2)(Cre/+) line to target a floxed ...
  • Formation par concordance de script en orthophonie : récit de pratique en évaluation des troubles acquis de la communication 

    Using learning-by-concordance in speech-language pathology : pilot study in assessment of acquired neurogenic communication impairments
    Maftoul, Rebecca; Marcotte, Karine (EDP Sciences, 2023-07-13)
    Contexte : Le programme de maîtrise professionnelle en orthophonie de l’Université de Montréal a connu une refonte complète de programme en 2020, et s’inscrit maintenant dans une approche par compétence. La formation par concordance de script (FpC) a ...
  • Framing the care of injured workers : an empirical four-jurisdictional comparison of workers’ compensation boards’ healthcare policies 

    Hudon, Anne; MacEachen, Ellen; Lippel, Katherine (Springer, 2022-01-17)
    Purpose: The objective of this study was to explore how workers’ compensation policies related to healthcare provision for workers with musculoskeletal injuries can affect the delivery and trajectories of care for injured workers. The principal research ...
  • The French noun phrase in preschool children with SLI: morphosyntactic and error analyses 

    French noun phrase
    Royle, Phaedra; Stine, Isabelle (Cambridge University Press, 2013-11-13)
    We studied spontaneous speech noun-phrase production in eight French-speaking children with SLI (aged 5;0 to 5;11 months) and controls matched on age (4;10 to 5;11 months) or MLU (aged 3;2 to 4;1 months). Results showed that children with SLI ...
  • French translation and validation of the Synkinesis Assessment Questionnaire 

    French translation and validation of SAQ questionnaire
    Martineau, Sarah; Gascon, Laurence; Saltychev, Mikhail; Rahal, Akram; Marcotte, Karine; Moubayed, Sami (Cambridge University Press, 2020-09-22)
  • Frequency of Chromosome Healing and Interstitial Telomeres in 40 Cases of Constitutional Abnormalities 

    Fortin, Fléchère; Beaulieu Bergeron, Mélanie; Fetni, Raouf; Lemieux, Nicole (S. Karger AG, Basel, 2009-09-04)
    Human telomeres play a major role in stabilizing chromosome ends and preventing fusions. Chromosomes bearing a broken end are rescued by the acquisition of a new telomeric cap without any subtelomeric sequences being present at the breakpoint, a process ...
  • Functional characterization of CaVα2δ mutations associated with sudden cardiac death 

    Bourdin, Benoîte; Shakeri, Behzad; Tétreault, Marie-Philippe; Sauvé, Rémy; Lesage, Sylvie; Parent, Lucie (Elsevier, 2015-01-30)
    L-type Ca(2+) channels play a critical role in cardiac rhythmicity. These ion channels are oligomeric complexes formed by the pore-forming CaVα1 with the auxiliary CaVβ and CaVα2δ subunits. CaVα2δ increases the peak current density and improves the ...
  • Functional neuroimaging predictors of self-reported psychotic symptoms in adolescents 

    Bourque, Josiane; Spechler, Philip A.; Potvin, Stéphane; Whelan, Robert; Banaschewski, Tobias; Bokde, Arun W. L.; Bromberg, Uli; Büchel, Christian; Burke Quinlan, Erin; Conrod, Patricia (American Psychiatric Publishing, 2017-06-01)
    OBJECTIVE: This study investigated the neural correlates of psychotic-like experiences in youths during tasks involving inhibitory control, reward anticipation, and emotion processing. A secondary aim was to test whether these neurofunctional correlates ...
  • Further characterization and determination of the single amino acid change in the tsI138 reovirus thermosensitive mutant 

    Lemay, Guy; Bisaillon, Martin (NRC Research Press, 2012-05)
    Many temperature-sensitive mutants have been isolated in early studies of mammalian reovirus. However, the bio- logical properties and nature of the genetic alterations remain incompletely explored for most of these mutants. The mutation harbored by ...
  • Gait adaptations of individuals with cerebral palsy on irregular surfaces : a scoping review 

    Dussault-Picard, Cloé; Mohammadyari, S.G.; Arvisais, Denis; Robert, M.T.; Dixon, Philippe (Elsevier, 2022-05-10)
    Background Individuals with cerebral palsy (CP) have a reduced ability to perform motor tasks such as walking. During daily walking, they are confronted with environmental constraints such as irregular surfaces (e.g., relief and uneven surfaces) which ...
  • Gait-like vibration training improves gait abilities: a case report of a 62 year old person with a chronic incomplete spinal cord injury 

    Barthélémy, Agnès; Gagnon, Dany; Duclos, Cyril (Nature Publishing Group, 2016-07-21)
    The purpose of this single-subject case study was to quantify the effect of gait-like vibration training on gait abilities after an incomplete spinal cord injury. A 62 year old male with a chronic AIS D spinal cord injury at T11 completed nine sessions ...
  • Gambling Problems among Community Cocaine Users 

    Dufour, Magali; Nguyen, Noël; Bertrand, Karine; Perreault, Michel; Jutras-Aswad, Didier; Morvannou, Adèle; Bruneau, Julie; Berbiche, Djamal; Roy, Elise (Springer, 2016-09)
    Cocaine use is highly prevalent and a major public health problem. While some studies have reported frequent comorbidity problems among cocaine users, few studies have included evaluation of gambling problems. This study aimed to estimate the prevalence ...
  • GBA mutations are associated with Rapid eye movement sleep behavior disorder 

    Gan-Or, Ziv; Mirelman, Anat; Postuma, Ronald B.; Arnulf, Isabelle; Bar-Shira, Anat; Dauvilliers, Yves; Desautels, Alex; Gagnon, Jean-François; Leblond, Claire S.; Frauscher, Birgit; Alcalay, Roy N.; Saunders-Pullman, Rachel; Bressman, Susan B.; Marder, Karen; Monaca, Christelle; Högl, Birgit; Orr-Urtreger, Avi; Dion, Patrick A.; Montplaisir, Jacques-Yves; Giladi, Nir; Rouleau, Guy (Wiley, 2015-07-31)
    Rapid eye movement sleep behavior disorder and GBA mutations are both associated with Parkinson’s disease. The GBA gene was sequenced in idiopathic rapid eye movement sleep behavior disorder patients (n = 265), and compared to controls (n = 2240). Rapid ...
  • Gender and work in ergonomics : recent trends 

    Laberge, Marie; Lefrançois, Mélanie; Chadoin, Martin; Probst, Isabelle; Riel, Jessica; Casse, Christelle; Messing, Karen (Taylor and Francis, 2022-09-27)
    Since the establishment of the Gender and Work Technical Committee (TC) of the International Ergonomics Association (IEA) in 2006, many researchers have addressed the role of sex and gender in ergonomics, producing a great deal of new information. ...
  • A gender lens is needed in hepatitis C elimination research 

    Larney, Sarah; Madden, Annie; Marshall, Alison D.; Martin, Natasha K.; Treloar, Carla (Elsevier, 2022-03-17)
    The World Health Organisation has established a goal of eliminating the hepatitis C virus (HCV) as a public health threat by 2030. Considerable effort is being directed towards research to support and enhance HCV treatment uptake among people who inject ...
  • Gender-agreement errors on adjectives and determiners elicit different ERP patterns in French 

    Brucher, Ariane; Courteau, Émilie; Steinhauer, Karsten; Royle, Phaedra (2020-10)
  • Gender-Specific Situational Correlates of Syringe Sharing during a Single Injection Episode 

    Hottes, Travis S.; Bruneau, Julie; Daniel, Mark (2011-04)
  • Genetic markers of Restless Legs Syndrome in Parkinson disease 

    Gan-Or, Ziv; Alcalay, Roy N.; Bar-Shira, Anat; Leblond, Claire S.; Postuma, Ronald B.; Ben-Shachar, Shay; Waters, Cheryl; Johnson, Amelie; Levy, Oren; Mirelman, Anat; Gana-Weisz, Mali; Dupré, Nicolas; Montplaisir, Jacques-Yves; Giladi, Nir; Fahn, Stanley; Xiong, Lan; Dion, Patrick A.; Orr-Urtreger, Avi; Rouleau, Guy (Elsevier, 2015-06)
    INTRODUCTION: Several studies proposed that Restless Legs Syndrome (RLS) and Parkinson disease (PD) may be clinically and/or etiologically related. To examine this hypothesis, we aimed to determine whether the known RLS genetic markers may be associated ...
  • Genetically engineered E. coli Nissle attenuates hyperammonemia and prevents memory impairment in bile‐duct ligated rats 

    Ochoa‐Sanchez, Rafael; Oliveira, Mariana M.; Tremblay, Mélanie; Petrazzo, Grégory; Pant, Asha; Bosoi, Cristina R.; Perreault, Mylene; Querbes, William; Kurtz, Caroline B.; Rose, Christopher (Wiley, 2021-02-06)
    Hyperammonemia associated with chronic liver disease (CLD) is implicated in the pathogenesis of hepatic encephalopathy (HE). The gut is a major source of ammonia production that contributes to hyperammonemia in CLD and HE and remains the primary ...
  • La génétique inverse dans l'étude des réovirus: Progrès, obstacles et développements futurs 

    Lemay, Guy (John Libbey Eurotext, 2011-01)
    En génétique dite « classique », l’examen d’un phénotype conduit à l’étude des gènes impliqués dans son obtention. La génétique inverse est une méthode expérimentale très puissante dans laquelle, au contraire, le matériel génétique est modifié et utilisé ...