Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rosario Osta"'
Autor:
Rafael Gonzalo-Gobernado, Laura Moreno-Martínez, Paz González, Xose Manuel Dopazo, Ana Cristina Calvo, Isabel Pidal-Ladrón de Guevara, Elisa Seisdedos, Rodrigo Díaz-Muñoz, Britt Mellström, Rosario Osta, José Ramón Naranjo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 21, p 15783 (2023)
The interaction of the activating transcription factor 6 (ATF6), a key effector of the unfolded protein response (UPR) in the endoplasmic reticulum, with the neuronal calcium sensor Downstream Regulatory Element Antagonist Modulator (DREAM) is a pote
Externí odkaz:
https://doaj.org/article/79ba1bac1a3c4fa08312a5dc7b73ceca
Autor:
Anna Martínez-Muriana, Diego Pastor, Renzo Mancuso, Amaya Rando, Rosario Osta, Salvador Martínez, Rubèn López-Vales, Xavier Navarro
Publikováno v:
Stem Cell Research & Therapy, Vol 11, Iss 1, Pp 1-11 (2020)
Abstract 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 peri
Externí odkaz:
https://doaj.org/article/8d33161732da499ba5e50cfa37ffd723
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:
Anna, Martínez-Muriana, Diego, Pastor, Renzo, Mancuso, Amaya, Rando, Rosario, Osta, Salvador, Martínez, Rubèn, López-Vales, Xavier, Navarro
Publikováno v:
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 ne
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:
Mireia Herrando-Grabulosa, Rosario Osta, Caty Casas, Raquel Manzano, Renzo Mancuso, Xavier Navarro
Publikováno v:
Brain and behavior
Brain and Behavior
Europe PubMed Central
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Brain and Behavior
Europe PubMed Central
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Altres ajuts: Fundació La Marató de TV3 (110430/31/32), TERCEL and CIBERNED funds from the Fondo de Investigación Sanitaria of Spain. Sporadic and familiar amyotrophic lateral sclerosis (ALS) cases presented lower cholinergic activity than in heal
Autor:
F. J. Miana-Mena, Eduardo Piedrafita, Rosario Osta, Russel J. Reiter, Enrique Martínez-Ballarín, Cristina González-Mingot, Larrodé P, María Jesús Muñoz, Joaquin J. Garcia
Publikováno v:
Journal of Bioenergetics and Biomembranes. 43:181-186
A mutant form of the copper/zinc superoxide dismutase (SOD1) protein is found in some patients with amyotrophic lateral sclerosis (ALS). Alteration of the activity of this antioxidant enzyme leads to an oxidative stress imbalance, which damages the s
Autor:
Sara Oliván, F. J. Miana-Mena, Rosario Osta, Enrique Martínez-Ballarín, Russel J. Reiter, María Jesús Muñoz, Lorena Fuentes-Broto, Joaquin J. Garcia, Cristina González-Mingot, Larrodé P
Publikováno v:
Journal of Neurology. 258:762-769
A mutant form of the ubiquitous copper/zinc superoxide dismutase (SOD1) protein has been found in some patients with amyotrophic lateral sclerosis (ALS). We monitored oxidative stress in an animal model of ALS, the SOD(G93A) mouse, which develops a d
Autor:
Carmen Arnal, Joaquín C. Surra, Rosario Osta, Roberto Martínez-Beamonte, Ana C. Calvo, Sara Oliván, Jesús Osada, Raquel Manzano
Publikováno v:
The Journal of nutritional biochemistry. 25(8)
Amyotrophic lateral sclerosis is a neurodegenerative disease associated with mutations in antioxidant enzyme Cu/Zn-superoxide dismutase 1. Albeit there is no treatment for this disease, new insights related to an exacerbated lipid metabolism have bee
Autor:
Rosario Osta, Alberto García-Redondo, Ana C. Calvo, Janne M. Toivonen, Sara Oliván, María Moreno-Igoa, Raquel Manzano, María Jesús Muñoz, Pilar Zaragoza
Publikováno v:
Neuro-degenerative diseases. 8(5)
Background: In the superoxide dismutase 1 (SOD1)-G93A mouse model of amyotrophic lateral sclerosis (ALS), skeletal muscle is a key target of mutant SOD1 toxicity. However, the expression of factors that control the regenerative potential of the muscl