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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.
FMR protein: Evidence of an emerging role in retinal aging?
Ardourel M, Ranchon-Cole I, Pâris A, Felgerolle C, Acar N, Lesne F, Briault S, Perche O. Ardourel M, et al. Among authors: briault s. Exp Eye Res. 2022 Dec;225:109282. doi: 10.1016/j.exer.2022.109282. Epub 2022 Oct 17. Exp Eye Res. 2022. PMID: 36265576 Free article.
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.
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.
78 results