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Results 31-40 of 47 (Search time: 0.02 seconds).
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Issue DateTitleAuthor(s)
2-Sep-2014Neurotrophin receptor p75NTR mediates Huntington's disease-associated synaptic and memory dysfunctionBrito, Verónica; Giralt Torroella, Albert; Enriquez-Barreto, Lilian; Puigdellívol Cañadell, Maria del Mar; Suelves Caballol, Núria; Zamora-Moratalla, Alfonsa; Ballesteros, Jesús J.; Martín, Eduardo D.; Dominguez-Iturza, Nuria; Morales, Miguel; Alberch i Vié, Jordi, 1959-; Ginés Padrós, Silvia
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, 1959-; Masana Nadal, Mercè
3-May-2023M2 Cortex Circuitry and Sensory-Induced Behavioral Alterations in Huntington's Disease: Role of Superior ColliculusConde-Berriozábal, Sara; García Gilabert, Lia; García García, Esther; Sitjà Roqueta, Laia; López Gil, Xavier; Muñoz-Moreno, Emma; Boutagouga Boudjadja, Mehdi; Soria, Guadalupe; Rodríguez Allué, Manuel José; Alberch i Vié, Jordi, 1959-; Masana Nadal, Mercè
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, 1959-; Ginés Padrós, Silvia
28-Jan-2022Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) Protects Striatal Cells and Improves Motor Function in Huntington's Disease Models: Role of PAC1 Receptor.Solés Tarrés, Irene; Cabezas Llobet, Núria; Lefranc, Benjamin; Leprince, Jérôme; Alberch i Vié, Jordi, 1959-; Vaudry, David; Xifró i Collsamata, Xavier
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, 1959-; Milà i Recasens, Montserrat; Azkona, Garikoitz; Pérez Navarro, Esther
6-Dec-2006Mutant huntingtin impairs the post-Golgi trafficking of brain-derived neurotrophic factor but not its Val66Met polymorphism.Toro, Daniel del; Canals i Coll, Josep M.; Ginés Padrós, Silvia; Kojima, Masami; Egea Guri, Gustavo; Alberch i Vié, Jordi, 1959-
30-May-2017Pyk2 modulates hippocampal excitatory synapses and contributes to cognitive deficits in a Huntington's disease model.Giralt Torroella, Albert; Brito, Verónica; Chevy, Quentin; Simonnet, Clémence; Otsu, Yo; Cifuentes Díaz, Carmen; Pins, Benoit de; Coura, Renata; Alberch i Vié, Jordi, 1959-; Ginés Padrós, Silvia; Poncer, Jean Christophe; Girault, Jean-Antoine
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, 1959-; Canals i Coll, Josep M.; Rodríguez Allué, Manuel José
24-Sep-2022Postnatal Foxp2 regulates early psychiatric-like phenotypes and associated molecular alterations in the R6/1 transgenic mouse model of Huntington's diseaseRodríguez Urgellés, Ened; Rodríguez Navarro, Irene; Ballasch, Ivan; Del Toro, Daniel; Del Castillo, Ignacio; Brito, Verónica; Alberch i Vié, Jordi, 1959-; Giralt Torroella, Albert