Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams–Beuren Syndrome

بواسطة Borralleras, Cristina, Sahun, Ignasi, Pérez-Jurado, Luis A, Campuzano, Victoria
الحاوية / القاعدة Mol Ther (2015)

Targeting Dyrk1A with AAVshRNA Attenuates Motor Alterations in TgDyrk1A, a Mouse Model of Down Syndrome

بواسطة Ortiz-Abalia, Jon, Sahún, Ignasi, Altafaj, Xavier, Andreu, Núria, Estivill, Xavier, Dierssen, Mara, Fillat, Cristina
منشور في 2008

Dissociation between CA3–CA1 Synaptic Plasticity and Associative Learning in TgNTRK3 Transgenic Mice

بواسطة Sahún, Ignasi, Delgado-García, José María, Amador-Arjona, Alejandro, Giralt, Albert, Alberch, Jordi, Dierssen, Mara, Gruart, Agnès
الحاوية / القاعدة J Neurosci (2007)

Cognition and Hippocampal Plasticity in the Mouse Is Altered by Monosomy of a Genomic Region Implicated in Down Syndrome

بواسطة Sahún, Ignasi, Marechal, Damien, Pereira, Patricia Lopes, Nalesso, Valérie, Gruart, Agnes, Garcia, José Maria Delgado, Antonarakis, Stylianos E., Dierssen, Mara, Herault, Yann
منشور في 2014

Overexpression of Reelin Prevents the Manifestation of Behavioral Phenotypes Related to Schizophrenia and Bipolar Disorder

بواسطة Teixeira, Cátia M, Martín, Eduardo D, Sahún, Ignasi, Masachs, Nuria, Pujadas, Lluís, Corvelo, André, Bosch, Carles, Rossi, Daniela, Martinez, Albert, Maldonado, Rafael, Dierssen, Mara, Soriano, Eduardo
منشور في 2011

Ceramide Levels Regulated by Carnitine Palmitoyltransferase 1C Control Dendritic Spine Maturation and Cognition

بواسطة Carrasco, Patricia, Sahún, Ignasi, McDonald, Jerome, Ramírez, Sara, Jacas, Jordi, Gratacós, Esther, Sierra, Adriana Y., Serra, Dolors, Herrero, Laura, Acker-Palmer, Amparo, Hegardt, Fausto G., Dierssen, Mara, Casals, Núria
منشور في 2012

Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region

بواسطة Brault, Véronique, Duchon, Arnaud, Romestaing, Caroline, Sahun, Ignasi, Pothion, Stéphanie, Karout, Mona, Borel, Christelle, Dembele, Doulaye, Bizot, Jean-Charles, Messaddeq, Nadia, Sharp, Andrew J., Roussel, Damien, Antonarakis, Stylianos E, Dierssen, Mara, Hérault, Yann
الحاوية / القاعدة PLoS Genet (2015)

Reduced Mid1 Expression and Delayed Neuromotor Development in daDREAM Transgenic Mice

بواسطة Dierssen, Mara, Fedrizzi, Laura, Gomez-Villafuertes, Rosa, de Lagran, María Martinez, Gutierrez-Adan, Alfonso, Sahún, Ignasi, Pintado, Belen, Oliveros, Juan C., Dopazo, Xose M., Gonzalez, Paz, Brini, Marisa, Mellström, Britt, Carafoli, Ernesto, Naranjo, Jose R.
منشور في 2012

A new mouse model for the trisomy of the Abcg1–U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome

بواسطة Pereira, Patricia Lopes, Magnol, Laetitia, Sahún, Ignasi, Brault, Véronique, Duchon, Arnaud, Prandini, Paola, Gruart, Agnès, Bizot, Jean-Charles, Chadefaux-Vekemans, Bernadette, Deutsch, Samuel, Trovero, Fabrice, Delgado-García, José María, Antonarakis, Stylianos E., Dierssen, Mara, Herault, Yann
منشور في 2009

Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome

بواسطة Arranz, Juan, Balducci, Elisa, Arató, Krisztina, Sánchez-Elexpuru, Gentzane, Najas, Sònia, Parras, Alberto, Rebollo, Elena, Pijuan, Isabel, Erb, lonas, Verde, Gaetano, Sahun, Ignasi, Barallobre, Maria J., Lucas, José J., Sánchez, Marina P., de la Luna, Susana, Arbonés, Maria L.
الحاوية / القاعدة Neurobiol Dis (2019)

Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss

بواسطة Espino Guarch, Meritxell, Font-Llitjós, Mariona, Murillo-Cuesta, Silvia, Errasti- Murugarren, Ekaitz, Celaya, Adelaida M, Girotto, Giorgia, Vuckovic, Dragana, Mezzavilla, Massimo, Vilches, Clara, Bodoy, Susanna, Sahún, Ignasi, González, Laura, Prat, Esther, Zorzano, Antonio, Dierssen, Mara, Varela-Nieto, Isabel, Gasparini, Paolo, Palacín, Manuel, Nunes, Virginia
الحاوية / القاعدة eLife (2018)

DREAM Controls the On/Off Switch of Specific Activity-Dependent Transcription Pathways

بواسطة Mellström, Britt, Sahún, Ignasi, Ruiz-Nuño, Ana, Murtra, Patricia, Gomez-Villafuertes, Rosa, Savignac, Magali, Oliveros, Juan C., Gonzalez, Paz, Kastanauskaite, Asta, Knafo, Shira, Zhuo, Min, Higuera-Matas, Alejandro, Errington, Michael L., Maldonado, Rafael, DeFelipe, Javier, Jefferys, John G. R., Bliss, Tim V. P., Dierssen, Mara, Naranjo, Jose R.
منشور في 2014