Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nuria García-Barberá"'
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)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24971cacfd2f92ed218d6758f4f9b7b2
https://doi.org/10.1080/09537104.2019.1696456
https://doi.org/10.1080/09537104.2019.1696456
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec547101d09c0b8a23888d2ab520a25d
http://link.springer.com/article/10.1038/s41598-019-40453-5
http://link.springer.com/article/10.1038/s41598-019-40453-5
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; Volume 12; Issue 7; Pages: 1185
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a51bdce66265fec6b797c14f5bb4f4f
https://doi.org/10.3390/jpm12071185
https://doi.org/10.3390/jpm12071185
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58c063c88c554f3957488ae80e35b748
Autor:
José Antonio Crespo-Matas, Vanessa Roldán, Nuria García-Barberá, Laura Zapata-Martínez, Rosa Cifuentes-Riquelme, Sonia Aguila, María Piedad Fernández-Pérez, Ascensión M de Los Reyes-García, Rocío González-Conejero, Constantino Martínez, Vicente Vicente, Francisco Marín, José Miguel Rivera-Caravaca, Laura Reguilón-Gallego, Raúl Teruel-Montoya
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 11
Journal of Clinical Medicine, Vol 9, Iss 3645, p 3645 (2020)
Volume 9
Issue 11
Journal of Clinical Medicine, Vol 9, Iss 3645, 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://explore.openaire.eu/search/publication?articleId=doi_dedup___::75b699dad9ab8066b1ae9b80bde2e8ba
https://pubmed.ncbi.nlm.nih.gov/33198388
https://pubmed.ncbi.nlm.nih.gov/33198388
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13d253c16f602e36e23449dc71670c6c
https://doi.org/10.1111/jth.13517
https://doi.org/10.1111/jth.13517
Autor:
Juan Carlos Espín, Nataliya Bohdan, Nuria García-Barberá, Vicente Vicente, Salvador Espín, Ginés Luengo-Gil, Constantino Martínez, Fernando Vallejo, Jose Yuste, Raúl Teruel-Montoya, Irene Martínez-Martínez
Publikováno v:
Thrombosis research. 183
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disease in which patients are at increased risk of thrombosis. The mechanisms underlying the associated thrombosis risk are still poorly understood, although it is known that Eculizumab, the drug of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b57fa7a5014153ee88417e97442c5ec
https://pubmed.ncbi.nlm.nih.gov/31671376
https://pubmed.ncbi.nlm.nih.gov/31671376