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Results 1-10 of 16 (Search time: 0.022 seconds).
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Issue DateTitleAuthor(s)
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
14-Oct-2021Isoform-Specific Reduction of the Basic Helix-Loop-Helix Transcription Factor TCF4 Levels in Huntington's DiseaseNurm, Kaja; Sepp, Mari; Castany Pladevall, Carla; Creus Muncunill, Jordi; Tuvikene, Jürgen; Sirp, Alex; Vihma, Hanna; Blake, Derek J.; Pérez Navarro, Esther; Timmusk, Tönis
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, Verónica; 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
30-Jul-2020Synaptic RTP801 contributes to motor-learning dysfunction in Huntington's diseaseMartín Flores, Núria; Pérez Sisqués, Leticia; Creus Muncunill, Jordi; Masana Nadal, Mercè; Ginés Padrós, Silvia; Alberch i Vié, Jordi, 1959-; Pérez Navarro, Esther; Malagelada Grau, Cristina
2012Cognitive dysfunction in Huntington¿s disease: Humans, mouse models and molecular mechanismsGiralt Torroella, Albert; Saavedra, Ana; Alberch i Vié, Jordi, 1959-; 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, 1959-; Ginés Padrós, Silvia; Pérez Navarro, Esther; Lucas, José J.
15-Feb-2012Don’t Take Away My P: Phosphatases as Therapeutic Targets in Huntington’s DiseaseSaavedra, Ana; Alberch i Vié, Jordi, 1959-; 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, 1959-; Pérez Otaño, Isabel; Malagelada Grau, Cristina; 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, 1959-