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Showing results 1 to 13 of 13
RightsPreviewIssue DateTitleAuthor(s)Type
openAccessAlquezar_NBA_2012_33_2.pdf.jpgFeb-2012Alterations in cell cycle-related proteins in lymphoblasts from carries of the c.709-1G>A PGRN mutation associated with FTLD-TDP dementiaAlquézar, Carolina ; Esteras, Noemí ; Bartolomé Robledo, Fernando ; Merino, José J.; Alzualde, Ainhoa; López de Munain, Adolfo; Martín-Requero, Ángeles artículo
openAccessTREM2 Manuscript_Neurobiol Aging.pdf.jpg13-Sep-2013Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementiaRuiz, Agustín; Dols-Icardo, Oriol; Bullido, Mª Jesús; Pastor, Pau; Rodríguez-Rodríguez, Eloy; López de Munain, Adolfo; de Pancorbo, Marian M.; Pérez-Tur, Jordi  ; Álvarez, Victoria; Antonell, Anna; López-Arrieta, Jesús; Hernández, Isabel; Tárraga, Lluís; Boada, Mercè; Lleó, Alberto; Blesa, Rafael; Frank, Ana; Sastre, Isabel ; Razquin, Cristina; Ortega-Cubero, Sara; Lorenzo, Elena; Sánchez-Juan, Pascual; Combarros, Onofre; Moreno, Fermín; Gorostidi, Ana; Baquero, Miquel; Coto, Eliecer; Sánchez-Valle, Raquel; Clarimón, Jordiartículo
openAccesseditoroledisease.pdf.jpg2016Editorial: Role of stem cells in skeletal muscle development, regeneration, repair, aging and diseaseMuñoz-Cánoves, Pura; Carvajal, Jaime J. ; López de Munain, Adolfo; Izeta, Anderartículo
openAccessLRRK2 mutation.pdf.jpg2014Epitope mapping of antibodies to alpha-synuclein in LRRK2 mutation carriers, idiopathic Parkinson disease patients, and healthy controlsÁlvarez-Castelao, Beatriz; Gorostidi, Ana; Ruiz-Martínez, Javier; López de Munain, Adolfo; Castaño, José G.artículo
closedAccessaccesoRestringido.pdf.jpg2013Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patientsFernández-Costa, Juan M.; García López, A.; Zúñiga, Sheila; Fernández-Pedrosa, Victoria; Felipo-Benavent, Amelia ; Mata, Manuel de la; Jaka, Oihane; Aiastui, Ana; Hernández Torres, Francisco; Aguado, Begoña ; Pérez-Alonso, Manuel; Vilchez, Jesús J.; López de Munain, Adolfo; Artero, Rubénartículo
openAccessEpilepsy Research 2006-Ayerdi.pdf.jpg16-May-2006Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsyAyerdi Izquierdo, Ana; Stavrides, G.; Sellés-Martínez, J. J.; Larrea, L.; Bovo, G.; López de Munain, Adolfo; Bisulli, F.; Martí-Massó, J. F.; Michelucci, Roberto; Poza, J. J.; Tinuper, P.; Stephani, U.; Striano, P.; Staub, E.; Sarafidou, T.; Hinzmann, B.; Moschonas, N.; Siebert, R.; Deloukas, P.; Nobile, C.; Pérez-Tur, Jordi  artículo
openAccessidentificells.pdf.jpg2016Identification and characterization of the dermal Panniculus carnosus muscle stem cellsNaldaiz-Gastesi, Neia; López-Mayorga, Macarena ; Herrero, Diego; Bernad, Antonio; García-Verdugo, José M.; Carvajal, Jaime J. ; López de Munain, Adolfo; García-Parra, Patricia; Izeta, Anderartículo
openAccessPLOS_ONE 2012 Martín-Requero.pdf.jpg18-May-2012Inactivation of CDK6/pRb pathway normalizes survival pattern of lymphoblasts expressin the FTLD-TDP-Progranulin mutation c.709-1G>A.Alquézar, Carolina ; Esteras, Noemí ; Alzualde, Ainhoa; Moreno, Fermín; Sánchez Ayuso, Matilde ; López de Munain, Adolfo; Martín-Requero, Ángeles artículo
openAccessAudiol Neurootol 2008-Otaegui.pdf.jpg7-Apr-2008Molecular characterization of putative modulatory factors in two Spanish families with A1555G deafnessOtaegui, D.; Irizar, H.; Goicoechea, M.; Pérez-Tur, Jordi  ; Belar, M.; López de Munain, Adolfoartículo
openAccess2015 J Behav Brain Sci 5-101.pdf.jpg11-Mar-2015Parkin and LRRK2/Dardarin Mutations in Early Onset Parkinson’s Disease in the Basque Country (Spain)Martí Massó, J. F.; Ruiz-Martínez, Javier; Paisán-Ruiz, J.; Gorostidi, Ana; Bergareche, A.; López de Munain, Adolfo; Alzualde, A.; Pérez-Tur, Jordi  artículo
openAccess13024_2018_Article_235.pdf.jpg23-Jan-2018Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylationMadero-Pérez, Jesús; Fernández, Elena ; Fernández, Belén; Lara Ordóñez, Antonio J.; Blanca Ramírez, Marian; Gómez-Suaga, P.; Waschbüsch, Dieter; Lobbestael, Evy; Baekelandt, Veerle; Nairn, Angus C; Ruiz-Martínez, Javier; Aiastui, Ana; López de Munain, Adolfo; Lis, Pawel; Comptdaer, Thomas; Taymans, Jean-Marc; Chartier-Harlin, Marie-Christine; Beilina, Alexandria; Gonnelli, Adriano; Cookson, Mark R; Greggio, Elisa; Hilfiker, Sabineartículo
openAccessAlquezar_NBA_35_2014.pdf.jpg2014PGRN haploinsufficiency increased Wnt5a signaling in peripheral cells from frontotemporal lobar degeneration-progranulin mutation carriersAlquézar, Carolina ; Esteras, Noemí ; De la Encarnación, Ana; Alzualde, Ainhoa; Moreno, Fermín; López de Munain, Adolfo; Martín-Requero, Ángeles artículo
openAccess13024_2016_Article_102.pdf.jpg30-Apr-2016Targeting TDP-43 phosphorylation by Casein Kinase-1δ inhibitors: a novel strategy for the treatment of frontotemporal dementiaAlquézar, Carolina ; Salado, Irene G. ; De la Encarnación, Ana; Pérez, Daniel I.; Moreno, Fermín; Gil, Carmen  ; López de Munain, Adolfo; Martínez, Ana ; Martín-Requero, Ángeles artículo