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

por 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
Publicado 2011

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

por 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
Publicado 2013