Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Gabriel Olmos"'
Autor:
Aina Medina-Dols, Guillem Cañellas, Toni Capó, Montse Solé, Marina Mola-Caminal, Natalia Cullell, Marina Jaume, Laura Nadal-Salas, Jaume Llinàs, Lluis Gómez, Silvia Tur, Carmen Jiménez, Rosa M. Díaz, Caty Carrera, Elena Muiño, Cristina Gallego-Fabrega, Carolina Soriano-Tárraga, Laura Ruiz-Guerra, Josep Pol-Fuster, Víctor Asensio, Josep Muncunill, Aarne Fleischer, Amanda Iglesias, Eva Giralt-Steinhauer, Uxue Lazcano, Isabel Fernández-Pérez, Joan Jiménez-Balado, Marina Gabriel-Salazar, Miguel Garcia-Gabilondo, Ting Lei, Nuria-Paz Torres-Aguila, Jara Cárcel-Márquez, Jerònia Lladó, Gabriel Olmos, Anna Rosell, Joan Montaner, Anna M. Planas, Raquel Rabionet, Mar Hernández-Guillamon, Jordi Jiménez-Conde, Israel Fernández-Cadenas, Cristòfol Vives-Bauzá
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-13 (2024)
Abstract Through GWAS studies we identified PATJ associated with functional outcome after ischemic stroke (IS). The aim of this study was to determine PATJ role in brain endothelial cells (ECs) in the context of stroke outcome. PATJ expression analys
Externí odkaz:
https://doaj.org/article/a3a6afd055e1410284b6f07d9b5f4bf3
Autor:
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Bernat Ortega-Vila, Jaume Llinàs, Jessica Hernandez-Rodriguez, Jerònia Lladó, Gabriel Olmos, Konstantin Strauch, Damià Heine-Suñer, Cristòfol Vives-Bauzà, Antònia Flaquer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract We investigated the genetic causes of major mental disorders (MMDs) including schizophrenia, bipolar disorder I, major depressive disorder and attention deficit hyperactive disorder, in a large family pedigree from Alpujarras, South of Spain
Externí odkaz:
https://doaj.org/article/604aa068781048feb2bfa2c3f746e73d
Autor:
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor Asensio, Bernat Ortega-Vila, Diego Marzese, Carme Vidal, Carmen Santos, Jerònia Lladó, Gabriel Olmos, Damià Heine-Suñer, Konstantin Strauch, Antònia Flaquer, Cristòfol Vives-Bauzà
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Psychosis is a highly heritable and heterogeneous psychiatric condition. Its genetic architecture is thought to be the result of the joint effect of common and rare variants. Families with high prevalence are an interesting approach to shed light on
Externí odkaz:
https://doaj.org/article/20ce0e6571ce4dd9a2d2f3bdcbba9097
Autor:
Gabriel Olmos, Lucía Tabares, Jerònia Lladó, Rosa M. Soler, Laura Torres-Benito, Andrea Cardona-Rossinyol, Ana Garcera, Víctor Caraballo-Miralles
Publikováno v:
International Journal of Molecular Sciences, Vol 14, Iss 6, Pp 11424-11437 (2013)
Spinal muscular atrophy (SMA) is a neurodegenerative disease produced by low levels of Survival Motor Neuron (SMN) protein that affects alpha motoneurons in the spinal cord. Notch signaling is a cell-cell communication system well known as a master r
Externí odkaz:
https://doaj.org/article/f2dd2ee0bb304419b52efba1f4ec8880
Autor:
Gabriel Olmos, Jerònia Lladó
Publikováno v:
Mediators of Inflammation, Vol 2014 (2014)
Tumor necrosis factor alpha (TNF-α) is a proinflammatory cytokine that exerts both homeostatic and pathophysiological roles in the central nervous system. In pathological conditions, microglia release large amounts of TNF-α; this de novo production
Externí odkaz:
https://doaj.org/article/e6bfd0bc6c7440d2b812fbf95b484254
Publikováno v:
Journal of the American College of Cardiology. 79:1278
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fcdada534b23c7494fd4495e3278bb2
https://doi.org/10.1016/s0735-1097(22)02269-0
https://doi.org/10.1016/s0735-1097(22)02269-0
Autor:
Josep, Pol-Fuster, Francesca, Cañellas, Laura, Ruiz-Guerra, Aina, Medina-Dols, Bàrbara, Bisbal-Carrió, Víctor, Asensio, Bernat, Ortega-Vila, Diego, Marzese, Carme, Vidal, Carmen, Santos, Jerònia, Lladó, Gabriel, Olmos, Damià, Heine-Suñer, Konstantin, Strauch, Antònia, Flaquer, Cristòfol, Vives-Bauzà
Publikováno v:
Frontiers in Genetics
Psychosis is a highly heritable and heterogeneous psychiatric condition. Its genetic architecture is thought to be the result of the joint effect of common and rare variants. Families with high prevalence are an interesting approach to shed light on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0e964d084320cbf1069b8ef9c116216
https://pubmed.ncbi.nlm.nih.gov/33897758
https://pubmed.ncbi.nlm.nih.gov/33897758
Autor:
Sonia Lazcano-Bautista, Sergio Gabriel Olmos-Temois, Norma Balderrabano-Saucedo, Oscar Ulises Preciado-Gutierrez, Andrés Preciado-Anaya, Nestor Rafael Leyva Reyes, Fabiola Zarate-Ordoñez, Dan Hu, Humberto Castro-Villacorta, Hector Barajas-Martinez
Publikováno v:
Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology. 28(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::601e34387550a89ae5055d2d59e3d572
https://pubmed.ncbi.nlm.nih.gov/31897995
https://pubmed.ncbi.nlm.nih.gov/31897995
Akademický článek
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Autor:
Estefania Pinero-Martos, Josep Pol-Fuster, Damian Heine-Suñer, Laura Ruiz-Guerra, Eugenia Cisneros-Barroso, Aina Medina-Dols, Jerònia Lladó, Gabriel Olmos, Bernardo Ortega-Vila, Cristofol Vives-Bauza
Publikováno v:
Human Molecular Genetics. 25:4157-4169
Disrupted in Schizophrenia-1 (DISC1) has been associated with a broad spectrum of mental disorders. DISC1 is a multi-compartmentalized protein found in the cytoplasm, centrosome, nuclei and mostly enriched in mitochondria. In order to shed light on D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::607d3c9c681cb9ade6308f4d0337370a
https://doi.org/10.1093/hmg/ddw250
https://doi.org/10.1093/hmg/ddw250