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Issue DateTitleAuthor(s)
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
Jan-2016Down-regulation of BDNF in cell and animal models increases striatal-enriched protein tyrosine phosphatase 61 (STEP61) levelsXu, Jian; Kurup, Pradeep; Azkona, Garikoitz; Baguley, Tyler D.; Saavedra, Ana; Nairn, Angus C.; Ellman, Jonathan A.; Pérez Navarro, Esther; Lombroso, Paul J.
31-Jul-2019Teaching case 3-2019: Are nuclear clefts or invaginations the niche of intranuclear inclusions in FTLD-TDP?Molina Porcel, Laura; Pérez Navarro, Esther; Garcia-Forn, Marta; Westaway, David; Colom Cadena, Martí; Gelpi, Ellen
17-Dec-2020Lack of Annexin A6 exacerbates liver dysfunction and reduces lifespan of Niemann-Pick type C protein-deficient miceMeneses Salas, Elsa; Garcia-Forn, Marta; Castany Pladevall, Carla; Lu, Albert; Fajardo, Alba; Jose, Jaimy; Wahba, Mohamed; Bosch i Rodríguez, Marta; Pol i Sorolla, Albert; Tebar Ramon, Francesc; Klein, Andrés D.; Zanlungo, Silvana; Pérez Navarro, Esther; Grewal, Thomas; Enrich Bastús, Carles; Rentero Alfonso, Carles
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
1-Sep-2017The AMPA receptor positive allosteric modulator S 47445 rescues in vivo CA3-CA1 long-term potentiation and structural synaptic changes in old miceGiralt Torroella, Albert; Gómez Climent, María Ángeles; Alcalá Vida, Rafael; Bretin, Sylvie; Bertrand, Daniel; Delgado García, José M.; Pérez Navarro, Esther; Alberch i Vié, Jordi, 1959-; Gruart i Massó, Agnès
2012Cognitive dysfunction in Huntington¿s disease: Humans, mouse models and molecular mechanismsGiralt Torroella, Albert; Saavedra, Ana; Alberch i Vié, Jordi, 1959-; Pérez Navarro, Esther
Aug-2016BDNF Induces Striatal-Enriched Protein Tyrosine Phosphatase 61 Degradation Through the ProteasomeSaavedra, Ana; Puigdellívol Cañadell, Maria del Mar; Tyebji, Shiraz; Kurup, Pradeep; Xu, Jian; Ginés Padrós, Silvia; Alberch i Vié, Jordi, 1959-; Lombroso, Paul J.; 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
Nov-2022Increased Phospho-AKT in Blood Cells from LRRK2 G2019S Mutation CarriersGarrido, Alicia; Pérez Sisqués, Leticia; Simonet, Cristina; Campoy Campos, Genís; Solana Balaguer, Júlia; Martín Flores, Núria; Fernández, Manel; Soto, Marta; Obiang, Donina; Camara, Ana; Valldeoriola Serra, Francesc; Muñoz, Esteban; Compta, Yaroslau; Pérez Navarro, Esther; Alberch i Vié, Jordi, 1959-; Tolosa, Eduardo; Martí Domènech, Ma. Josep; Ezquerra, Mario; Malagelada Grau, Cristina; Fernández Santiago, Rubén