Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Juan A. G. Ranea"'
Autor:
Fernando Bonet, Oscar Campuzano, José Córdoba-Caballero, Mireia Alcalde, Georgia Sarquella-Brugada, Aitana Braza-Boïls, Ramon Brugada, Francisco Hernández-Torres, Maribel Quezada-Feijoo, Monica Ramos, Alipio Mangas, Juan A. G. Ranea, Rocío Toro
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1807 (2024)
Arrhythmogenic cardiomyopathy is an inherited entity characterized by irregular cell–cell adhesion, cardiomyocyte death and fibro-fatty replacement of ventricular myocytes, leading to malignant ventricular arrythmias, contractile dysfunction and su
Externí odkaz:
https://doaj.org/article/945d2dc181984d7480a2a40bb22752e5
Autor:
Ignacio Gómez-García, Maria L. Ladehesa-Pineda, Juan M. Diaz-Tocados, Clementina López-Medina, Maria C. Abalos-Aguilera, Desiree Ruiz-Vilches, Guillermo Paz-Lopez, Andres Gonzalez-Jimenez, Juan A. G. Ranea, Alejandro Escudero-Contreras, Isabel Moreno-Indias, Francisco J. Tinahones, Eduardo Collantes-Estévez, Patricia Ruiz-Limón
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionAxial spondyloarthritis (axSpA) is a heterogeneous disease that can be represented by radiographic axSpA (r-axSpA) and non-radiographic axSpA (nr-axSpA). This study aimed to evaluate the relationship between the markers of inflammation an
Externí odkaz:
https://doaj.org/article/3c1eb936666042a7ade15af5561ee4c3
Autor:
Helena Lucena-Padros, Nereida Bravo-Gil, Cristina Tous, Elena Rojano, Pedro Seoane-Zonjic, Raquel María Fernández, Juan A. G. Ranea, Guillermo Antiñolo, Salud Borrego
Publikováno v:
Biomolecules, Vol 14, Iss 2, p 164 (2024)
Hirschsprung’s disease (HSCR) is a rare developmental disorder in which enteric ganglia are missing along a portion of the intestine. HSCR has a complex inheritance, with RET as the major disease-causing gene. However, the pathogenesis of HSCR is s
Externí odkaz:
https://doaj.org/article/c974284fbc0d468180529d8232d8d2bc
Autor:
Elena Rojano, Fernando M. Jabato, James R. Perkins, José Córdoba-Caballero, Federico García-Criado, Ian Sillitoe, Christine Orengo, Juan A. G. Ranea, Pedro Seoane-Zonjic
Publikováno v:
BMC Bioinformatics, Vol 23, Iss 1, Pp 1-19 (2022)
Abstract Background Protein function prediction remains a key challenge. Domain composition affects protein function. Here we present DomFun, a Ruby gem that uses associations between protein domains and functions, calculated using multiple indices b
Externí odkaz:
https://doaj.org/article/04cbfecf2a7e4f32bcde7c8858ce38c0
Autor:
Antonio Vega-Rioja, Pedro Chacón, Lourdes Fernández-Delgado, Bouchra Doukkali, Alberto del Valle Rodríguez, James R. Perkins, Juan A. G. Ranea, Leticia Dominguez-Cereijo, Beatriz María Pérez-Machuca, Ricardo Palacios, David Rodríguez, Javier Monteseirín, David Ribas-Pérez
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundNeutrophils are involved in the pathophysiology of allergic asthma, where the Eosinophil Cationic Protein (ECP) is a critical inflammatory mediator. Although ECP production is attributed to eosinophils, we reported that ECP is also present
Externí odkaz:
https://doaj.org/article/a25f2bbc0e7e49e4ba31d6a0c37a21b5
Autor:
María José Sánchez-Quintero, Josué Delgado, Laura Martín Chaves, Dina Medina-Vera, Mora Murri, Víctor M. Becerra-Muñoz, Mario Estévez, María G. Crespo-Leiro, Guillermo Paz López, Andrés González-Jiménez, Juan A. G. Ranea, María Isabel Queipo-Ortuño, Isaac Plaza-Andrades, Jorge Rodríguez-Capitán, Francisco Javier Pavón-Morón, Manuel F. Jiménez-Navarro
Publikováno v:
Antioxidants, Vol 12, Iss 8, p 1643 (2023)
Essential oils sourced from herbs commonly used in the Mediterranean diet have demonstrated advantageous attributes as nutraceuticals and prebiotics within a model of severe cardiometabolic disorder. The primary objective of this study was to assess
Externí odkaz:
https://doaj.org/article/fcd87d92a4e44efbb6aa3f7e77fcbfd7
Autor:
Fernando M. Jabato, José Córdoba-Caballero, Elena Rojano, Carlos Romá-Mateo, Pascual Sanz, Belén Pérez, Diana Gallego, Pedro Seoane, Juan A. G. Ranea, James R. Perkins
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract High-throughput gene expression analysis is widely used. However, analysis is not straightforward. Multiple approaches should be applied and methods to combine their results implemented and investigated. We present methodology for the compre
Externí odkaz:
https://doaj.org/article/35510445a6824f5eb37caeaab2b029f1
Autor:
Elena Díaz-Santiago, M. Gonzalo Claros, Raquel Yahyaoui, Yolanda de Diego-Otero, Rocío Calvo, Janet Hoenicka, Francesc Palau, Juan A. G. Ranea, James R. Perkins
Publikováno v:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Neuromuscular disorders (NMDs) represent an important subset of rare diseases associated with elevated morbidity and mortality whose diagnosis can take years. Here we present a novel approach using systems biology to produce functionally-coherent phe
Externí odkaz:
https://doaj.org/article/0b1a57da523a479ebbf16cd47b3994b9
Publikováno v:
BMC Bioinformatics, Vol 18, Iss 1, Pp 1-2 (2017)
Externí odkaz:
https://doaj.org/article/5bf1d352b0e54f23bde2064fb61fe153
Autor:
Laura Castilla-Vallmanya, Mónica Centeno-Pla, Mercedes Serrano, Héctor Franco-Valls, Raúl Martínez-Cabrera, Aina Prat-Planas, Elena Rojano, Juan A G Ranea, Pedro Seoane, Clara Oliva, Abraham J Paredes-Fuentes, Gemma Marfany, Rafael Artuch, Daniel Grinberg, Raquel Rabionet, Susanna Balcells, Roser Urreizti
Publikováno v:
Journal of Medical Genetics. 60:406-415
BackgroundSchaaf-Yang syndrome (SYS) is caused by truncating mutations inMAGEL2, mapping to the Prader-Willi region (15q11-q13), with an observed phenotype partially overlapping that of Prader-Willi syndrome. MAGEL2 plays a role in retrograde transpo