Enhanced Synaptic Activity and Epileptiform Events in the Embryonic KCC2 Deficient Hippocampus

by Khalilov, Ilgam, Chazal, Geneviève, Chudotvorova, Ilona, Pellegrino, Christophe, Corby, Séverine, Ferrand, Nadine, Gubkina, Olena, Nardou, Romain, Tyzio, Roman, Yamamoto, Sumii, Jentsch, Thomas J., Hübner, Christian A., Gaiarsa, Jean-Luc, Ben-Ari, Yehezkel, Medina, Igor
Published 2011

Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences

by Rieusset, Anne, Schaller, Fabienne, Unmehopa, Unga, Matarazzo, Valery, Watrin, Françoise, Linke, Matthias, Georges, Beatrice, Bischof, Jocelyn, Dijkstra, Femke, Bloemsma, Monique, Corby, Severine, Michel, François J., Wevrick, Rachel, Zechner, Ulrich, Swaab, Dick, Dudley, Keith, Bezin, Laurent, Muscatelli, Françoise
Published 2013