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Early life oxytocin treatment improves thermo-sensory reactivity and maternal behavior in neonates lacking the autism-associated gene Magel2.
Da Prato LC, Zayan U, Abdallah D, Point V, Schaller F, Pallesi-Pocachard E, Montheil A, Canaan S, Gaiarsa JL, Muscatelli F, Matarazzo V. Da Prato LC, et al. Among authors: schaller f. Neuropsychopharmacology. 2022 Oct;47(11):1901-1912. doi: 10.1038/s41386-022-01313-5. Epub 2022 Apr 8. Neuropsychopharmacology. 2022. PMID: 35396500 Free PMC article.
Necdin protects embryonic motoneurons from programmed cell death.
Aebischer J, Sturny R, Andrieu D, Rieusset A, Schaller F, Geib S, Raoul C, Muscatelli F. Aebischer J, et al. Among authors: schaller f. PLoS One. 2011;6(9):e23764. doi: 10.1371/journal.pone.0023764. Epub 2011 Sep 2. PLoS One. 2011. PMID: 21912643 Free PMC article.
Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.
Rieusset A, Schaller F, Unmehopa U, Matarazzo V, Watrin F, Linke M, Georges B, Bischof J, Dijkstra F, Bloemsma M, Corby S, Michel FJ, Wevrick R, Zechner U, Swaab D, Dudley K, Bezin L, Muscatelli F. Rieusset A, et al. Among authors: schaller f. PLoS Genet. 2013;9(9):e1003752. doi: 10.1371/journal.pgen.1003752. Epub 2013 Sep 5. PLoS Genet. 2013. PMID: 24039599 Free PMC article.
An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.
Meziane H, Schaller F, Bauer S, Villard C, Matarazzo V, Riet F, Guillon G, Lafitte D, Desarmenien MG, Tauber M, Muscatelli F. Meziane H, et al. Among authors: schaller f. Biol Psychiatry. 2015 Jul 15;78(2):85-94. doi: 10.1016/j.biopsych.2014.11.010. Epub 2014 Nov 20. Biol Psychiatry. 2015. PMID: 25599930
Cytomegalovirus Infection of the Rat Developing Brain In Utero Prominently Targets Immune Cells and Promotes Early Microglial Activation.
Cloarec R, Bauer S, Luche H, Buhler E, Pallesi-Pocachard E, Salmi M, Courtens S, Massacrier A, Grenot P, Teissier N, Watrin F, Schaller F, Adle-Biassette H, Gressens P, Malissen M, Stamminger T, Streblow DN, Bruneau N, Szepetowski P. Cloarec R, et al. Among authors: schaller f. PLoS One. 2016 Jul 29;11(7):e0160176. doi: 10.1371/journal.pone.0160176. eCollection 2016. PLoS One. 2016. PMID: 27472761 Free PMC article.
A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.
Conti V, Carabalona A, Pallesi-Pocachard E, Leventer RJ, Schaller F, Parrini E, Deparis AA, Watrin F, Buhler E, Novara F, Lise S, Pagnamenta AT, Kini U, Taylor JC, Zuffardi O, Represa A, Keays DA, Guerrini R, Falace A, Cardoso C. Conti V, et al. Among authors: schaller f. J Vis Exp. 2017 Dec 1;(130):53570. doi: 10.3791/53570. J Vis Exp. 2017. PMID: 29286390 Free PMC article.
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