Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Lucía Recio"'
Autor:
Sven Schade, Rosa Arias, Fernando Vilariño, Héloïse Vilaseca, Diana Reinoso, Blanca Guasch, Sònia Roura, Lucía Recio, Sofia Bucca, A. Paula Rodriguez Müller, Dorte Riemenschneider
Publikováno v:
ARPHA Proceedings, Vol 6, Iss , Pp 179-184 (2024)
The European Commission has identified the role of Living Labs and Citizen Science as needed tools for the process of citizen-centric knowledge valorisation. Backed by the Memorandum of Understanding (MoU) between the European Citizen Science Associa
Externí odkaz:
https://doaj.org/article/ff92a43525674ce3a1806b0e704bb59c
Autor:
Laura Lorente-Herraiz, Angel M. Cuesta, Lucía Recio-Poveda, Luisa M. Botella, Virginia Albiñana
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 11, p 6163 (2024)
Pulmonary arteriovenous malformations (PAVMs) are vascular anomalies resulting in abnormal connections between pulmonary arteries and veins. In 80% of cases, PAVMs are present from birth, but clinical manifestations are rarely seen in childhood. Thes
Externí odkaz:
https://doaj.org/article/46b760980b3d4249acc0ee18550e8910
Autor:
Laura Lorente-Herraiz, Angel M. Cuesta, Jaime Granado, Lucía Recio-Poveda, Luisa-María Botella, Virginia Albiñana
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 7, p 3952 (2024)
Cerebral cavernous malformation (CCM) or familial cavernomatosis is a rare, autosomal dominant, inherited disease characterized by the presence of vascular malformations consisting of blood vessels with an abnormal structure in the form of clusters.
Externí odkaz:
https://doaj.org/article/fb9ef1dd16b245ee9c5d1227bef580e7
Autor:
Isabel de Rojas-P, Virginia Albiñana, Lucía Recio-Poveda, Amanda Rodriguez-Rufián, Ángel M. Cuesta, Luisa-María Botella
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-6 (2020)
Abstract Von Hippel-Lindau syndrome (VHL) is a rare disease of dominant inheritance that increases susceptibility to tumor development, with a complete penetrance at the age of 60. In this report, we present the unprecedented case of a VHL carrier wh
Externí odkaz:
https://doaj.org/article/383796de483f4052990caf2d77f6f9c3
Autor:
Angel M. Cuesta, Eunate Gallardo-Vara, Juan Casado-Vela, Lucía Recio-Poveda, Luisa-María Botella, Virginia Albiñana
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 8, p 4217 (2022)
Rare Diseases (RD) are defined by their prevalence in less than 5 in 10,000 of the general population. Considered individually, each RD may seem insignificant, but together they add up to more than 7000 different diseases. Research in RD is not attra
Externí odkaz:
https://doaj.org/article/37bf8baa0f37456ab8221b3d1bf57a19
Autor:
Virginia Albiñana, Lucía Recio-Poveda, Pilar González-Peramato, Luis Martinez-Piñeiro, Luisa María Botella, Angel M. Cuesta
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1325 (2022)
Von Hippel-Lindau (VHL) syndrome is a rare inherited cancer disease where the lack of VHL protein triggers the development of multisystemic tumors such us retinal hemangioblastomas (HBs), CNS-HBs, and clear cell renal cell carcinoma (ccRCC). Since st
Externí odkaz:
https://doaj.org/article/b7165d666e7d4946bf1eabf4014bea32
Autor:
Isabel de Rojas-P, Virginia Albiñana, Lyudmyla Taranets, Lucía Recio-Poveda, Angel M. Cuesta, Nikita Popov, Thales Kronenberger, Luisa M. Botella
Publikováno v:
Cells, Vol 10, Iss 9, p 2313 (2021)
Von Hippel–Lindau disease (VHL) is a rare hereditary disease characterized by the predisposal to develop different types of highly vascularized tumors. VHL patients carry a VHL mutation that causes partial lack of functional VHL protein (pVHL) in a
Externí odkaz:
https://doaj.org/article/babeceef9360404993b67bea04a5eba7
Autor:
Luisa Ojeda-Fernández, Lucía Recio-Poveda, Mikel Aristorena, Pedro Lastres, Francisco J Blanco, Francisco Sanz-Rodríguez, Eunate Gallardo-Vara, Mateo de las Casas-Engel, Ángel Corbí, Helen M Arthur, Carmelo Bernabeu, Luisa M Botella
Publikováno v:
PLoS Genetics, Vol 12, Iss 3, p e1005935 (2016)
Endoglin is an auxiliary receptor for members of the TGF-β superfamily and plays an important role in the homeostasis of the vessel wall. Mutations in endoglin gene (ENG) or in the closely related TGF-β receptor type I ACVRL1/ALK1 are responsible f
Externí odkaz:
https://doaj.org/article/63f0aca66e9c4e4a90b3922a52eccf65
Autor:
Virginia Albiñana, Eunate Gallardo-Vara, Juan Casado-Vela, Lucía Recio-Poveda, Luisa María Botella, Angel M Cuesta
Publikováno v:
Journal of clinical medicine. 11(15)
18 p.-4 fig.-1 tab.
Research on cancer therapies focuses on processes such as angiogenesis, cell signaling, stemness, metastasis, and drug resistance and inflammation, all of which are influenced by the cellular and molecular microenvironment of
Research on cancer therapies focuses on processes such as angiogenesis, cell signaling, stemness, metastasis, and drug resistance and inflammation, all of which are influenced by the cellular and molecular microenvironment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3e365082209838c0d4e125820a1f324
https://pubmed.ncbi.nlm.nih.gov/35956154
https://pubmed.ncbi.nlm.nih.gov/35956154
Autor:
Suriel, Errasti Díaz, Mercedes, Peñalva, Lucía, Recio-Poveda, Susana, Vilches, Juan, Casado-Vela, Julián, Pérez Pérez, Luisa María, Botella, Virginia, Albiñana, Angel M, Cuesta
Publikováno v:
Journal of clinical medicine. 11(11)
Hereditary Hemorrhagic Telangiectasia (HHT) is a rare disorder of vascular development. Common manifestations include epistaxis, telangiectasias and arteriovenous malformations in multiple organs. Different deletions or nonsense mutations have been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a6ad83735b6d72a84ef76935d53d64b
https://pubmed.ncbi.nlm.nih.gov/35683441
https://pubmed.ncbi.nlm.nih.gov/35683441