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Issue DateTitleAuthor(s)
5-Sep-2013Regulation of Hippocampal cGMP Levels as a Candidate to Treat Cognitive Deficits in Huntington's DiseaseSaavedra, Ana; Giralt Torroella, Albert; Arumí, Helena; Alberch i Vié, Jordi; Pérez Navarro, Esther
31-Oct-2011Increased 90-kDa ribosomal S6 kinase (Rsk) activity is protective against mutant huntingtin toxicityXifró i Collsamata, Xavier; Anglada Huguet, Marta; Rué Cabré, Laura; Saavedra, Ana; Pérez Navarro, Esther; Alberch i Vié, Jordi
1-Nov-2016Targeting CAG repeat RNAs reduces Huntington's disease phenotype independently of huntingtin levelsRué Cabré, Laura; Bañez-Coronel, Mónica; Creus Muncunill, Jordi; Giralt Torroella, Albert; Alcalá Vida, Rafael; Mentxaka, Gartze; Kagerbauer, Birgit; Zomeño Abellán, M. Teresa; Aranda, Zeus; Venturi, Verónica; Pérez Navarro, Esther; Estivill, Xavier, 1955-; Martí Puig, Eulàlia
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
1-Sep-2015Decreased glycogen synthase kinase-3 levels and activity contribute to Huntington's diseaseFernández-Nogales, Marta; Hernández, Félix; Miguez, Andrés; Alberch i Vié, Jordi; Ginés Padrós, Silvia; Pérez Navarro, Esther; Lucas, José J.
Dec-2018Pharmacogenetic Modulation of STEP improves motor and cognitive function in a mouse model of Huntington's disease.Garcia-Forn, Marta; Martínez Torres, Sara; García-Díaz Barriga, Gerardo; Alberch i Vié, Jordi; Milà i Recasens, Montserrat; Azkona, Garikoitz; Pérez Navarro, Esther
Oct-2018Increased levels of rictor prevent mutant huntingtin-induced neuronal degenerationCreus Muncunill, Jordi; Rué Cabré, Laura; Alcalá Vida, Rafael; Badillos Rodríguez, Raquel; Romaní Aumedes, Joan; Marco, Sonia; Alberch i Vié, Jordi; Pérez Otaño, Isabel; Malagelada Grau, Cristina; Pérez Navarro, Esther
2012Cognitive dysfunction in Huntington¿s disease: Humans, mouse models and molecular mechanismsGiralt Torroella, Albert; Saavedra, Ana; Alberch i Vié, Jordi; Pérez Navarro, Esther