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Issue DateTitleAuthor(s)
1-Jun-2011Striatal-Enriched Protein Tyrosine Phosphatase Expression and Activity in Huntington's Disease: A STEP in the Resistance to ExcitotoxicitySaavedra, Ana; Giralt Torroella, Albert; Rué Cabré, Laura; Xifró i Collsamata, Xavier; Xu, Jian; Ortega, Zaira; Lucas, José J.; Lombroso, Paul J.; Alberch i Vié, Jordi; Pérez Navarro, Esther
5-Oct-2020M2 Cortex-Dorsolateral striatum stimulation reverses motor symptoms and synaptic deficits in Huntington's DiseaseFernández García, Sara; Conde-Berriozábal, Sara; García, Esther; Gort Paniello, Clara; Bernal Casas, David; García-Díaz Barriga, Gerardo; López Gil, Xavier; Muñoz-Moreno, Emma; Soria, Guadalupe; Campa, Leticia; Artigas Pérez, Francesc; Rodríguez Allué, Manuel José; Alberch i Vié, Jordi; Masana Nadal, Mercè
18-Jun-2020Reduced fractalkine levels lead to striatal synaptic plasticity deficits in Huntington's diseaseKim, Anya; García, Esther; Straccia, Marco; Comella Bolla, Andrea; Miguez, Andrés; Masana Nadal, Mercè; Alberch i Vié, Jordi; Canals i Coll, Josep M.; Rodríguez Allué, Manuel José
15-Mar-2012Long-term memory deficits in Huntington's disease are associated with reduced CBP histone acetylase activityGiralt Torroella, Albert; Puigdellívol Cañadell, Maria del Mar; Carreton, Olga; Paoletti Rubia, Paola; Valero, J.; Parra-Damas, A.; Saura Antolín, Carlos A. (Carlos Alberto); Alberch i Vié, Jordi; Ginés Padrós, Silvia
11-May-2021RTP801 regulates motor cortex synaptic transmission and learningPérez Sisqués, Leticia; Martín Flores, Núria; Masana Nadal, Mercè; Solana Balaguer, Júlia; Llobet, Arnau; Romaní Aumedes, Joan; Canal de la Iglesia, Mercè; Campoy Campos, Genís; García, Esther; Sánchez Fernández, Núria; Fernández García, Sara; Gilbert, James P.; Rodríguez Allué, Manuel José; Man, Heng-Ye; Feinstein, Elena; Williamson, David L.; Soto del Cerro, David; Gasull Casanova, Xavier; Alberch i Vié, Jordi; Malagelada Grau, Cristina
5-Feb-2021Neuron type-specific increase in lamin B1 contributes to nuclear dysfunction in Huntington's diseaseAlcalá Vida, Rafael; Garcia-Forn, Marta; Castany Pladevall, Carla; Creus Muncunill, Jordi; Ito, Yoko; Blanco, Enrique; Golbano, Arantxa; Crespí-Vázquez, Kilian; Parry, Aled; Slater, Guy; Samarajiwa, Shamith; Peiró, Sandra; Croce, Luciano Di; Narita, Masashi; Pérez Navarro, Esther
Apr-2021Huntington's disease brain-derived small RNAs recapitulate associated neuropathology in wild-type miceCreus Muncunill, Jordi; Guisado Corcoll, Anna; Venturi, Veronica; Pantano, Lorena; Escaramís Babiano, Geòrgia; Gardia de Herreros, Marta; Solanguren-Beascoa, Maria; Gámez Valero, Ana; Navarrete, Cristina; Masana Nadal, Mercè; Llorens Torres, Franc; Diaz-Lucena, Daniela; Pérez Navarro, Esther; Martí Puig, Eulàlia
1-Aug-2013Suppressing aberrant GluN3A expression rescues synaptic and behavioral impairments in Huntington's disease modelsMarco, Sonia; Giralt Torroella, Albert; Petrovic, Milos; Pouladi, Mahmoud A.; Martínez Turrillas, Rebeca; Martínez Hernández, Jose; Kaltenbach, Linda S.; Torres Peraza, Jesús Fernando; Graham, Rona K.; Watanabe, Masahiko; Luján, Rafael; Nakanishi, Nobuki; Lipton, Stuart A.; Lo, Donald C.; Hayden, Michael R.; Alberch i Vié, Jordi; Wesseling, John F.; Pérez Otaño, Isabel
2012Cognitive dysfunction in Huntington¿s disease: Humans, mouse models and molecular mechanismsGiralt Torroella, Albert; Saavedra, Ana; Alberch i Vié, Jordi; Pérez Navarro, Esther