Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Çaku A"'
Autor:
Sophie Bouhour, Rosalie Plantefève, Virginie Gillet, Armita Abolghasemi, Fatima Zahra Bouchouirab, Andrea A. Baccarelli, Larissa Takser, Artuela Çaku
Publikováno v:
Lipids in Health and Disease, Vol 23, Iss 1, Pp 1-11 (2024)
Abstract Background Dyslipidemias, including familial hypercholesterolemia (FH), are a significant risk factor for cardiovascular diseases. FH is a genetic disorder resulting in elevated levels of low-density lipoprotein cholesterol (LDL-C) and an in
Externí odkaz:
https://doaj.org/article/6f657c5d582f45c3948c85060ffba406
Publikováno v:
In Psychiatry Research July 2024 337
Autor:
Rojas, Daniela, Benachenhou, Sérine, Laroui, Asma, Aden, Amira Abdourahim, Abolghasemi, Armita, Galarneau, Luc, Irakoze, Taratibu Janvière, Plantefeve, Rosalie, Bouhour, Sophie, Toupin, Amanda, Corbin, François, Fink, Guy, Mallet, Pierre-Luc, Çaku, Artuela
Publikováno v:
In Journal of Steroid Biochemistry and Molecular Biology December 2023 235
Akademický článek
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Autor:
Asma Laroui, Luc Galarneau, Armita Abolghasemi, Sérine Benachenhou, Rosalie Plantefève, Fatima Zahra Bouchouirab, Jean François Lepage, François Corbin, Artuela Çaku
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract High plasma matrix metalloproteases-9 (MMP-9) levels have been reported in Fragile X Syndrome in a limited number of animal and human studies. Since the results obtained are method-dependent and not directly comparable, the clinical utility
Externí odkaz:
https://doaj.org/article/878db1aaaa1d4d2a896a7ab00e7cd7b0
Autor:
Amanda Toupin, Sérine Benachenhou, Armita Abolghasemi, Asma Laroui, Luc Galarneau, Thamàs Fülöp, François Corbin, Artuela Çaku
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Fragile X syndrome (FXS) is the most prevalent monogenic cause of intellectual disability and autism spectrum disorder (ASD). Affected individuals have a high prevalence of hypocholesterolemia, however, the underlying mechanisms and the clin
Externí odkaz:
https://doaj.org/article/6abfda0c56714ca1a5f284d18d851374
Autor:
Angelina Lacroix, Mélodie Proteau-Lemieux, Samantha Côté, Jamie Near, Steve C.N. Hui, Richard A.E. Edden, Sarah Lippé, Artuela Çaku, François Corbin, Jean-François Lepage
Publikováno v:
Neurobiology of Disease, Vol 174, Iss , Pp 105881- (2022)
Fragile-X syndrome (FXS) and Neurofibromatosis of type 1 (NF-1) are two monogenic disorders sharing neurobehavioral symptoms and pathophysiological mechanisms. Namely, preclinical models of both conditions show overactivity of the mTOR signaling path
Externí odkaz:
https://doaj.org/article/dd05ea7cf2774bfebae823359cf4e7d0
Autor:
Proteau-Lemieux, Mélodie, Lacroix, Angélina, Galarneau, Luc, Corbin, François, Lepage, Jean-François, Çaku, Artuela
Publikováno v:
In Progress in Neuropsychopharmacology & Biological Psychiatry 30 August 2021 110
Akademický článek
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Autor:
Camille Champigny, Florence Morin-Parent, Laurence Bellehumeur-Lefebvre, Artuela Çaku, Jean-François Lepage, François Corbin
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2022)
Background: Limited success of previous clinical trials for Fragile X syndrome (FXS) has led researchers to consider combining different drugs to correct the pleiotropic consequences caused by the absence of the Fragile X mental retardation protein (
Externí odkaz:
https://doaj.org/article/0cd73a9b493b43cc9b16929ae7ec6650