Browsing by Author Sáez, Mauricio A.
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) |
|---|---|---|
| 8-May-2018 | Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice | Jorge Torres, Olga C.; Szczesna, Karolina; Roa, Laura; Casal, Carmen; Gonzalez Somermeyer, Louisa; Soler, Marta; Velasco, Cecilia D.; Martinez San Segundo, Pablo; Petazzi, Paolo; Sáez, Mauricio A.; Delgado Morales, Raul; Fourcade, Stéphane; Pujol Onofre, Aurora; Huertas, Dori; Llobet Berenguer, Artur, 1972-; Guil, Sonia; Esteller, Manel |
| Apr-2016 | Mutations in JMJD1C are involved in Rett syndrome and intellectual disability | Sáez, Mauricio A.; Fernández Rodríguez, Juana; Moutinho, Cátia; Sanchez-Mut, Jose Vicente; Gómez, Antonio; Vidal, Enrique; Petazzi, Paolo; Szczesna, Karolina; López Serra, Paula; Lucariello, Mario; Lorden, Patricia; Delgado-Morales, Raul; Caridad, Olga J. de la; Huertas, Dori; Gelpí Buchaca, Josep Lluís; Orozco López, Modesto; López Dóriga Guerra, Adriana; Milà i Recasens, Montserrat; Pérez Jurado, Luis A.; Pineda, Mercedes; Armstrong i Morón, Judith; Lázaro García, Conxi; Esteller, Manel |
| Dec-2016 | Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype | Lucariello, Mario; Vidal, Enrique; Vidal, Silvia; Sáez, Mauricio A.; Roa, Laura; Huertas, Dori; Pineda Marfà, Mercè; Dalfó Capella, Esther; Dopazo, Joaquín; Jurado, Paola; Armstrong i Morón, Judith; Esteller, Manel |