Zobrazeno 1 - 8
of 8
pro vyhledávání: '"José Luis Fernández‐Luna"'
Autor:
Andrea Fernández-Pérez, Olga Gutiérrez-Saiz, José Luis Fernández-Luna, Fernando Moreno, José María Saiz
Publikováno v:
Applied Sciences, Vol 9, Iss 14, p 2886 (2019)
Imaging polarimetry is a focus of increasing interest in diagnostic medicine because of its non-destructive nature and its potential to distinguish normal from tumor tissue. However, handling and understanding polarimetric images is not an easy task,
Externí odkaz:
https://doaj.org/article/9a912d67f6f8413fb27184d3569ebb34
Autor:
Carmelo Morales Angulo, Blanca Señaris, José Luis Fernández-Luna, Jaime Gallo-Terán, Rocío González-Aguado, Ana Fontalva
Publikováno v:
Acta Otorrinolaringológica Española. 62:83-86
Resumen Introduccion La mutacion A1555G del gen MTRNR1 del ADN mitocondrial es responsable de hipoacusia neurosensorial bilateral no sindromica que se ve exacerbada por la exposicion a aminoglucosidos. El objetivo de nuestro estudio fue determinar la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::509bc23eb177c3e72d63f354e3b69623
https://doi.org/10.1016/j.otorri.2010.08.003
https://doi.org/10.1016/j.otorri.2010.08.003
Autor:
Cristina Blázquez, Arkaitz Carracedo, Lucía Barrado, Pedro José Real, José Luis Fernández‐Luna, Guillermo Velasco, Marcos Malumbres, Manuel Guzmán
Publikováno v:
The FASEB Journal. 20:2633-2635
Melanoma causes the greatest number of skin cancer-related deaths worldwide. Despite intensive research, prevention and early detection are the only effective measures against melanoma, so new therapeutic strategies are necessary for the management o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c077b06b03b80ce4d16295d0fca4e39b
https://doi.org/10.1096/fj.06-6638fje
https://doi.org/10.1096/fj.06-6638fje
Autor:
José Luis Fernández-Luna, Blanca Señaris, Rocío González-Aguado, Carmelo Morales Angulo, Ana Fontalva, Jaime Gallo-Terán
Publikováno v:
Acta otorrinolaringologica espanola. 62(2)
Introduction The A1555G mitochondrial DNA (mtDNA) mutation is responsible for maternally inherited non-syndromic hearing loss that is increased by aminoglycoside exposure. The objective of this study was to ascertain the frequency of the A1555G mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c43dc4ae4669c11b72328047635c1f
https://pubmed.ncbi.nlm.nih.gov/21129708
https://pubmed.ncbi.nlm.nih.gov/21129708
Autor:
Xabier, Agirre, Ana, Fontalba, Enrique J, Andreu, Maria Dolores, Odero, María José, Larráyoz, Cristina, Montiel, María José, Calasanz, José Luis, Fernández-Luna, Felipe, Prósper
Publikováno v:
Haematologica. 88(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a85e13e68b9394bc439289e80bda2f20
https://pubmed.ncbi.nlm.nih.gov/14687999
https://pubmed.ncbi.nlm.nih.gov/14687999
Autor:
José Berciano, Javier Llorca, Onofre Combarros, Jon Infante, Cristina Sanz, José Luis Fernández-Luna
Publikováno v:
Journal of Neurology. 251:482-483
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a98eebcc31b032e7b3c66bee6312352
https://doi.org/10.1007/s00415-004-0375-6
https://doi.org/10.1007/s00415-004-0375-6
Autor:
Eloy F. Robles, Maria Mena-Varas, Laura Barrio, Sara V. Merino-Cortes, Péter Balogh, Ming-Qing Du, Takashi Akasaka, Anton Parker, Sergio Roa, Carlos Panizo, Idoia Martin-Guerrero, Reiner Siebert, Victor Segura, Xabier Agirre, Laura Macri-Pellizeri, Beatriz Aldaz, Amaia Vilas-Zornoza, Shaowei Zhang, Sarah Moody, Maria Jose Calasanz, Thomas Tousseyn, Cyril Broccardo, Pierre Brousset, Elena Campos-Sanchez, Cesar Cobaleda, Isidro Sanchez-Garcia, Jose Luis Fernandez-Luna, Ricardo Garcia-Muñoz, Esther Pena, Beatriz Bellosillo, Antonio Salar, Maria Joao Baptista, Jesús Maria Hernandez-Rivas, Marcos Gonzalez, Maria Jose Terol, Joan Climent, Antonio Ferrandez, Xavier Sagaert, Ari M. Melnick, Felipe Prosper, David G. Oscier, Yolanda R. Carrasco, Martin J. S. Dyer, Jose A. Martinez-Climent
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-16 (2016)
The homeobox NKX2 family of transcriptional factors has been shown to regulate fundamental developmental processes. Here, the authors show that NKX2-3 is a bona fideoncogenic driver in marginal-zone B-cell lymphoma and that it promotes lymphomagenesi
Externí odkaz:
https://doaj.org/article/8577d51efbf14e6384756140937ba872
Autor:
Orlando Serrano-Garrido, Carlos Peris-Torres, Silvia Redondo-García, Helena G. Asenjo, María del Carmen Plaza-Calonge, José Luis Fernandez-Luna, Juan Carlos Rodríguez-Manzaneque
Publikováno v:
Biomolecules, Vol 11, Iss 1, p 44 (2020)
Gliomas in general and the more advanced glioblastomas (GBM) in particular are the most usual tumors of the central nervous system with poor prognosis. GBM patients develop resistance to distinct therapies, in part due to the existence of tumor cell
Externí odkaz:
https://doaj.org/article/b4e28111ae9844eabb4c6c580b7210a4