Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Serine Benachenhou"'
Autor:
Armita Abolghasemi, Maria Paulina Carullo, Ester Cisneros Aguilera, Asma Laroui, Rosalie Plantefeve, Daniela Rojas, Serine Benachenhou, María Victoria Ramírez, Mélodie Proteau-Lemieux, Jean-François Lepage, François Corbin, Mélanie Plourde, Mauricio Farez, Patricia Cogram, Artuela Çaku
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 18, p 10815 (2022)
Fragile X Syndrome (FXS) is the most prevalent monogenic cause of Autism Spectrum Disorders (ASDs). Despite a common genetic etiology, the affected individuals display heterogenous metabolic abnormalities including hypocholesterolemia. Although chang
Externí odkaz:
https://doaj.org/article/bbb934987c244f5abce6f71deafb8cff
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