Browsing by Subject Huntington's chorea

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Issue DateTitleAuthor(s)
30-Jun-2010A myriad of miRNA variants in control and Huntington's disease brain regions detected by massively parallel sequencingMartí Puig, Eulàlia; Pantano, Lorena; Bañez-Coronel, Mónica; Llorens Torres, Franc; Miñones Moyano, Elena; Porta, Sílvia; Sumoy, Lauro; Ferrer, Isidro (Ferrer Abizanda); Estivill, Xavier, 1955-
23-Feb-2012A pathogenic mechanism in Huntington"s disease involves small CAG-repeated RNAs with neurotoxic activityBañez-Coronel, Mónica; Porta, Sílvia; Kagerbauer, Birgit; Mateu Huertas, Elisabet; Pantano, Lorena; Ferrer, Isidro (Ferrer Abizanda); Guzmán, Manuel; Estivill, Xavier, 1955-; Martí Puig, Eulàlia
20-Jul-2017A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington's disease miceSuelves Caballol, Núria; Kirkham-McCarthy, Lucy; Lahue, Robert S.; Ginés Padrós, Silvia
Aug-2018A systematic linguistic profile of spontaneous narrative speech in pre-symptomatic and early stage Huntington's disease.Hinzen, Wolfram; Rosselló Ximenes, Joana; Morey, Caty; Camara Mancha, Estela; García-Gorro, Clara; Salvador, Raymond; Diego Balaguer, Ruth de
11-Jul-2022Altered m6A RNA methylation contributes to hippocampal memory deficits in Huntington's disease mice.Pupak, Anika; Singh, Ankita; Sancho Balsells, Anna; Alcalá Vida, Rafael; Espina, Marc; Giralt Coll, Albert; Martí Puig, Eulàlia; Vang Ørom, Ulf Andersson; Ginés Padrós, Silvia; Brito, Verónica
20-Oct-2004Biochemical, ultrastructural, and reversiblity studies on Huntingtin filaments isolated from mouse and human brainDíaz-Hernández, Miguel; Moreno-Herrero, Fernando; Gómez-Ramos, Pilar; Morán, María A.; Ferrer, Isidro (Ferrer Abizanda); Baró, Arturo M.; Avila, Jesús; Hernández, Félix; Lucas, José J.
18-Jun-2007Caracterización de efectores de diferenciación GABAérgica en células madre como herramienta terapéutica de enfermedades neurodegenerativas.Martín Ibáñez, Raquel
2-Dec-2019CD200 is up-regulated in R6/1 transgenic mouse model of Huntington's diseaseComella Bolla, Andrea; Valente, Tony; Miguez, Andrés; Brito, Verónica; Ginés Padrós, Silvia; Solà i Subirana, Carme; Straccia, Marco; Canals i Coll, Josep M.
22-Jul-2013Characterization of mechanisms underlying neuronal survival and plasticity in Huntington's diseaseAnglada Huguet, Marta
12-Jul-2012Characterization of the mechanisms underlying alterations in macroautophagy and survival signalling in Huntington’s diseaseRué Cabré, Laura
2012Cognitive dysfunction in Huntington¿s disease: Humans, mouse models and molecular mechanismsGiralt Torroella, Albert; Saavedra, Ana; Alberch i Vié, Jordi, 1959-; Pérez Navarro, Esther
22-Sep-2016COMT Val158Met Polymorphism Modulates Huntington's Disease ProgressionDiego Balaguer, Ruth de; Schramm, Catherine; Rebeix, Isabelle; Dupoux, Emmanuel; Dürr, Alexandra; Brice, Alexis; Charles, Perrine; Cleret de Langavant, Laurent; Youssov, Katia; Verny, Christophe; Damotte, Vincent; Azulay, Jean-Philippe; Goizet, Cyril; Tranchant, Christine; Maison, Patrick; Rialland, Amandine; Schmitz, David; Jacquemot, Charlotte; Fontaine, Bertrand; Bachoud-Lévi, Anne-Catherine; Simonin, Clémence; French Speaking Huntington Group
2011Conditional BDNF release under pathological conditions improves Huntington's disease pathology by delaying neuronal dysfunctionGiralt Torroella, Albert; Carreton, Olga; Lao-Peregrin, Cristina; Martín, Eduardo D.; Alberch i Vié, Jordi, 1959-
1-Aug-2019Cyclin-Dependent Kinase 5 Dysfunction Contributes to Depressive-like Behaviors in Huntington's Disease by Altering the DARPP-32 Phosphorylation Status in the Nucleus AccumbensBrito, Verónica; Giralt Torroella, Albert; Masana Nadal, Mercè; Royes, Aida; Espina, Marc; Sieiro, Esther; Alberch i Vié, Jordi, 1959-; Castañé, Anna; Girault, Jean-Antoine; Ginés Padrós, Silvia
2006Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminaseBorrell Pagès, Maria; Canals i Coll, Josep M.; Cordelières, Fabrice P.; Parker, J. Alex; Pineda Martí, José Ramón; Grange, Ghislaine; Bryson, Elzbieta A.; Guillermier, Martine; Hirsch, Etienne; Hantraye, Philippe; Cheetham, Michael E.; Néri, Christian; Alberch i Vié, Jordi, 1959-; Brouillet, Emmanuel; Saudou, Frédéric; Humbert, Sandrine
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.
23-Oct-2014Deep white matter in Huntington's diseasePhillips, Owen R.; Squitieri, Ferdinando; Sánchez Castañeda, Cristina; Elifani, Francesca; Caltagirone, Carlo; Sabatini, Umberto; Paola, Margherita di
28-May-2020Deficits in coordinated neuronal activity and network topology are striatal hallmarks in Huntington's disease.Fernández García, Sara; Orlandi, Javier G.; García-Díaz Barriga, Gerardo; Rodríguez Allué, Manuel José; Masana Nadal, Mercè; Soriano i Fradera, Jordi; Alberch i Vié, Jordi, 1959-
27-Nov-2014Description and Validation of New Therapeutical Targets to Prevent Neurodegenertlion and Cognitive Deficits in Huntington's DiseasePuigdellívol Cañadell, Maria del Mar
20-Mar-2017Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and micePardo Muñoz, Mònica; García-Díaz Barriga, Gerardo; Straccia, Marco; Sanders, Phil; Alberch i Vié, Jordi, 1959-; Canals i Coll, Josep M.; HD iPSC Consortium