Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

77 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule.
Hébert B, Pietropaolo S, Même S, Laudier B, Laugeray A, Doisne N, Quartier A, Lefeuvre S, Got L, Cahard D, Laumonnier F, Crusio WE, Pichon J, Menuet A, Perche O, Briault S. Hébert B, et al. Among authors: briault s. Orphanet J Rare Dis. 2014 Aug 1;9:124. doi: 10.1186/s13023-014-0124-6. Orphanet J Rare Dis. 2014. PMID: 25079250 Free PMC article.
Pre- and postnatal exposure to low dose glufosinate ammonium induces autism-like phenotypes in mice.
Laugeray A, Herzine A, Perche O, Hébert B, Aguillon-Naury M, Richard O, Menuet A, Mazaud-Guittot S, Lesné L, Briault S, Jegou B, Pichon J, Montécot-Dubourg C, Mortaud S. Laugeray A, et al. Among authors: briault s. Front Behav Neurosci. 2014 Nov 20;8:390. doi: 10.3389/fnbeh.2014.00390. eCollection 2014. Front Behav Neurosci. 2014. PMID: 25477793 Free PMC article.
Early Retinal Defects in Fmr1-/y Mice: Toward a Critical Role of Visual Dys-Sensitivity in the Fragile X Syndrome Phenotype?
Perche O, Felgerolle C, Ardourel M, Bazinet A, Pâris A, Rossignol R, Meyer-Dilhet G, Mausset-Bonnefont AL, Hébert B, Laurenceau D, Montécot-Dubourg C, Menuet A, Bizot JC, Pichon J, Ranchon-Cole I, Briault S. Perche O, et al. Among authors: briault s. Front Cell Neurosci. 2018 Apr 6;12:96. doi: 10.3389/fncel.2018.00096. eCollection 2018. Front Cell Neurosci. 2018. PMID: 29681800 Free PMC article.
Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation.
Laumonnier F, Roger S, Guérin P, Molinari F, M'rad R, Cahard D, Belhadj A, Halayem M, Persico AM, Elia M, Romano V, Holbert S, Andres C, Chaabouni H, Colleaux L, Constant J, Le Guennec JY, Briault S. Laumonnier F, et al. Among authors: briault s. Am J Psychiatry. 2006 Sep;163(9):1622-9. doi: 10.1176/ajp.2006.163.9.1622. Am J Psychiatry. 2006. PMID: 16946189
FG syndrome: the FGS2 locus revisited.
Perche O, Laudier B, Menuet A, Odent S, Laumonnier F, Briault S. Perche O, et al. Among authors: briault s. Am J Med Genet A. 2012 Jun;158A(6):1489-92. doi: 10.1002/ajmg.a.35322. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528511 No abstract available.
Dysregulation of FOXG1 pathway in a 14q12 microdeletion case.
Perche O, Haddad G, Menuet A, Callier P, Marcos M, Briault S, Laudier B. Perche O, et al. Among authors: briault s. Am J Med Genet A. 2013 Dec;161A(12):3072-7. doi: 10.1002/ajmg.a.36170. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 23956198
77 results