Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Rosario Osta"'
Autor:
Laura Moreno-Martínez, Rosario Osta, Christian Lunetta, Ana C. Calvo, Pilar Zaragoza, Claudia Tarlarini, Leticia Moreno-García, Miriam de la Torre, F. J. Miana-Mena
Publikováno v:
International Journal of Molecular Sciences
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Volume 22
Issue 5
International Journal of Molecular Sciences, Vol 22, Iss 2523, p 2523 (2021)
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Volume 22
Issue 5
International Journal of Molecular Sciences, Vol 22, Iss 2523, p 2523 (2021)
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Since NLRP3 inflammasome plays a pivotal role in several neurodegenerative disorders, we hypothesized that levels of inflammasome components could help in diagnosis or prognosis of amyotrophic lateral sclerosis (ALS). Gene and protein expression was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a90509c8664bc15d0786d62dd77fab7e
http://zaguan.unizar.es/record/102175
http://zaguan.unizar.es/record/102175
Autor:
Amaya Rando, Salvador Martinez, Diego Pastor, Xavier Navarro, Anna Martínez-Muriana, Rubèn López-Vales, Renzo Mancuso, Rosario Osta
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-11 (2020)
Stem cell research & therapy
Universitat Autònoma de Barcelona
Digital.CSIC. Repositorio Institucional del CSIC
instname
Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-11 (2020)
Stem cell research & therapy
[Background]: The simultaneous contribution of several etiopathogenic disturbances makes amyotrophic lateral sclerosis (ALS) a fatal and challenging disease. Here, we studied two different cell therapy protocols to protect both central and peripheral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67648091af0f83113d4d6f68a26d045a
https://ddd.uab.cat/record/226251
https://ddd.uab.cat/record/226251
Autor:
Jesús Esteban-Pérez, Ana C. Calvo, Pilar Cordero-vázquez, Raquel Manzano, Sara Oliván, Alberto García-Redondo, María Jesús Muñoz, Rosario Osta, Pilar Zaragoza, Gabriela Atencia-Cibreiro
Publikováno v:
PLoS ONE
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
PLoS ONE, Vol 7, Iss 3, p e32632 (2012)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
PLoS ONE, Vol 7, Iss 3, p e32632 (2012)
The pathophysiological mechanisms of both familial and sporadic Amyotrophic Lateral Sclerosis (ALS) are unknown, although growing evidence suggests that skeletal muscle tissue is a primary target of ALS toxicity. Skeletal muscle biopsies were perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b423b421f16464ffdc1c25f82d30e34d
http://zaguan.unizar.es/record/70699
http://zaguan.unizar.es/record/70699
Publikováno v:
Muscle & Nerve. 50:943-949
Introduction: We assessed the predictive value of electrophysiological tests as a marker of clinical disease onset and survival in superoxide-dismutase 1 (SOD1)G93A mice. Methods: We evaluated the accuracy of electrophysiological tests in differentia
Autor:
José Luis Muñoz-Blanco, Adrián Galiana, Pilar Zaragoza, Laura Moreno, Lucía Galán, Marina Mora, Claudia Tarlarini, Paz Torre Merino, Miguel A. Martín, Juan M. Cano, Silvana Penco, Larrodé P, Pilar Cordero Vázquez, Juan F. Roy, Alexandra Juárez Rufián, Elena Pegoraro, María Jesús Muñoz, Gianni Sorarù, Jesús Mora, Gabriela Atencia Cibreiro, Ana C. Calvo, Christian Lunetta, Rosario Osta, Alberto Garcia Redondo, Jesús Esteban
Publikováno v:
Aging and Disease
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
The identification of more reliable diagnostic or prognostic biomarkers in age-related neurodegenerative diseases, such as Amyotrophic Lateral Sclerosis (ALS), is urgently needed. The objective in this study was to identify more reliable prognostic b
Autor:
Pilar Zaragoza, Rosario Osta, Samanta Gasco, Ana C. Calvo, Alberto García-Redondo, Amaya Rando
Publikováno v:
American journal of physiology. Cell physiology. 311(6)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a difficult diagnosis and prognosis. In this regard, new and more reliable biomarkers for the disease are needed. We propose peripheral blood, and, more specifically, the h
Publikováno v:
Neurotherapeutics
Amyotrophic lateral sclerosis is a neurodegenerative disorder characterized by progressive weakness, muscle atrophy, and paralysis due to the loss of upper and lower motoneurons (MNs). Sigma-1 receptor (sigma-1R) activation promotes neuroprotection a
Autor:
Clementina Rodellar, Didier Montarras, Rosario Osta, Raquel Manzano, Pilar Zaragoza, Ana C. Calvo, Janne M. Toivonen, Sara Oliván
Publikováno v:
Neurodegenerative Diseases. 11:153-164
Background: Amyotrophic lateral sclerosis (ALS) is the most common adult-onset neurodegenerative disease characterized by ascending muscle weakness, atrophy and paralysis. Early muscle abnormalities that precede motor neuron loss in ALS may destabili
Autor:
Xavier Navarro, Isaac Francos-Quijorna, Adrian Olmos-Alonso, Rosario Osta, Diego Gomez-Nicola, Rubèn López-Vales, V. Hugh Perry, Anna Martínez-Muriana, Renzo Mancuso
Publikováno v:
Scientific Reports
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientific reports
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientific reports
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Inflammation is a common neuropathological feature in several neurological disorders, including amyotrophic lateral sclerosis (ALS). We have studied the contribution of CSF1R signalling to inflammation in ALS, as a pathway previously reported to cont
Publikováno v:
Brain research
Amyotrophic lateral sclerosis GALS) is a neurodegenerative disorder characterized by the loss of upper and lower motoneurons. Clinically, it is manifested by weakness, muscle atrophy and progressive paralysis and ends up with patients' death 2-5 year