Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Nuria García-Barberá"'
Autor:
Ascensión M. de los Reyes-García, José Miguel Rivera-Caravaca, Laura Zapata-Martínez, Sonia Águila, Andrea Véliz-Martínez, Nuria García-Barberá, Pablo Gil-Perez, Pedro J. Guijarro-Carrillo, Esteban Orenes-Piñero, Cecilia López-García, María L. Lozano, Francisco Marín, Constantino Martínez, Rocío González-Conejero
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 7, p 1185 (2022)
Studies on older patients have established notable conceptual changes in the etiopathogenesis of acute coronary syndrome (ACS), but little is known about this disease in young patients ( Q4 more frequently had a history of previous stroke (6.1% vs. 1
Externí odkaz:
https://doaj.org/article/2754d7baa79c4f6baf081116745a68c7
Autor:
María N. Barrachina, Irene Izquierdo, Lidia Hermida-Nogueira, Luis A. Morán, Amparo Pérez, Ana B. Arroyo, Nuria García-Barberá, Rocío González-Conejero, Sara Troitiño, Johannes A. Eble, José Rivera, Constantino Martínez, María I. Loza, Eduardo Domínguez, Ángel García
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 7, p 3304 (2021)
Background: Clinical management of ischemic events and prevention of vascular disease is based on antiplatelet drugs. Given the relevance of phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K) as a candidate target in thrombosis, the main goal of t
Externí odkaz:
https://doaj.org/article/0eca6e336cd14055bf7287d34d55e365
Autor:
José Miguel Rivera-Caravaca, Raúl Teruel-Montoya, Vanessa Roldán, Rosa Cifuentes-Riquelme, José Antonio Crespo-Matas, Ascensión María de los Reyes-García, Sonia Águila, María Piedad Fernández-Pérez, Laura Reguilón-Gallego, Laura Zapata-Martínez, Nuria García-Barberá, Vicente Vicente, Francisco Marín, Constantino Martínez, Rocío González-Conejero
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 11, p 3645 (2020)
Background. Atrial fibrillation (AF) increases the risk for stroke but also for non-stroke major adverse cardiovascular events (MACE). The 2MACE score was recently proposed to predict these events. Since the interest of microRNAs (miRNAs) in cardiova
Externí odkaz:
https://doaj.org/article/dca4be52824f4852bcf7b8d921fd8e46
Autor:
Alberto Del Monte, Ana B Arroyo, María J Andrés-Manzano, Nuria García-Barberá, María S Caleprico, Vicente Vicente, Vanessa Roldán, Rocío González-Conejero, Constantino Martínez, Vicente Andrés
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0198932 (2018)
BACKGROUND:Atherosclerosis involves activation of the IRAK1/TRAF6/NF-κB inflammatory cascade, which is negatively regulated by miR146a. Previous studies showed that the TT genotype of rs2431697, located near the miR-146a gene, drives lower miR-146a
Externí odkaz:
https://doaj.org/article/dc2a94d4793f46c0b129fd337ec7a1c5
Autor:
Salam Salloum-Asfar, Ana B Arroyo, Raúl Teruel-Montoya, Nuria García-Barberá, Vanessa Roldán, Vicente Vicente, Constantino Martínez, Rocío González-Conejero
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0154751 (2016)
MiRNAs have been reported as CIS-acting elements of several hemostatic factors, however, their mechanism as TRANS-acting elements mediated by a transcription factor is little known and could have important effects. HNF4α has a direct and important r
Externí odkaz:
https://doaj.org/article/32286c8ab41d428898982560f22bcb79
Autor:
Salam Salloum-Asfar, Raúl Teruel-Montoya, Ana B Arroyo, Nuria García-Barberá, Amarjit Chaudhry, Erin Schuetz, Ginés Luengo-Gil, Vicente Vicente, Rocío González-Conejero, Constantino Martínez
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111713 (2014)
High levels of factor XI (FXI) increase the risk of thromboembolic disease. However, the genetic and environmental factors regulating FXI expression are still largely unknown. The aim of our study was to evaluate the regulation of FXI by microRNAs (m
Externí odkaz:
https://doaj.org/article/08cfd42ff56648bda9188fdfefb454bf
Autor:
Nuria García-Barberá, María Piedad Fernández-Pérez, Constantino Martínez, Maria Luisa Lozano, Pedro Diaz-Lozano, Vicente Vicente, Lamya Garabet, Rocío González-Conejero, Sonia Aguila, Ascensión M de Los Reyes-García, Waleed Ghanima
Publikováno v:
Platelets. 31:906-912
No biological predictors for the increased risk of thrombosis in patients with immune thrombocytopenia (ITP) have been identified. The aim of the study was to investigate platelet and neutrophil activation as well neutrophil extracellular trap (NET)
Autor:
Nuria García-Barberá, Irene Martínez-Martínez, Juan Carlos Espín, Salvador Espín, Jose Yuste, Raúl Teruel-Montoya, Constantino Martínez, Fernando Vallejo, Nataliya Bohdan, Ginés Luengo-Gil, Vicente Vicente
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports
Scientific Reports
Paroxysmal Nocturnal Hemoglobinuria (PNH) is a clonal disease of blood cells caused by the lack of glycosyl phosphatidyl inositol anchored proteins bound to the cell membrane. In consequence, erythrocytes lead to intravascular hemolysis upon compleme
Autor:
Constantino Martínez, María N. Barrachina, José Rivera, Ángel García, Eduardo Domínguez, María Isabel Loza, Nuria García-Barberá, Sara Troitiño, Irene Izquierdo, Amparo Pérez, Lidia Hermida-Nogueira, Luis A. Morán, Rocío González-Conejero, Johannes A. Eble, Ana B. Arroyo
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 7
International Journal of Molecular Sciences, Vol 22, Iss 3304, p 3304 (2021)
Volume 22
Issue 7
International Journal of Molecular Sciences, Vol 22, Iss 3304, p 3304 (2021)
Background: Clinical management of ischemic events and prevention of vascular disease is based on antiplatelet drugs. Given the relevance of phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K) as a candidate target in thrombosis, the main goal of t
Autor:
Javier Corral, Vicente Vicente, M A Dasi, Juan Luis García, Nuria García-Barberá, S. Izquierdo, M.E. de la Morena-Barrio, Rocío González-Conejero, Jesús M. Hernández-Rivas, Jesus M Hernández-Sánchez, Bienvenida Argilés, José Padilla
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Essentials Vitamin K-dependent coagulant factor deficiency (VKCFD) is a rare autosomal recessive disorder. We describe a case of inherited VKCFD due to uniparental disomy. The homozygous mutation caused the absence of GGCX isoform 1 and overexpressio