Zobrazeno 1 - 10
of 110
pro vyhledávání: '"María Isidoro‐García"'
Autor:
Jacqueline Pérez-Pazos, Asunción García-Sánchez, Miguel Estravís, Emma Moreno-Jimenez, Natalia Morgado, Manuel Gómez-García, Jacinto Ramos-González, María Gil-Melcón, Cristina Martín-García, Francisco Muñoz-Bellido, Catalina Sanz, María Isidoro-García, Ignacio Dávila
Publikováno v:
ERJ Open Research, Vol 10, Iss 4 (2024)
Introduction Type 2 (T2) asthma is often associated with chronic rhinosinusitis with nasal polyposis (CRSwNP). Additionally, nonsteroidal anti-inflammatory drug (NSAID) intolerance leads to NSAID-exacerbated respiratory disease (N-ERD). Previous tran
Externí odkaz:
https://doaj.org/article/777f46a5cf5d4d5088e9fa04df5143f6
Autor:
Noemi Ferrito, Juan Báez-Flores, Mario Rodríguez-Martín, Julián Sastre-Rodríguez, Alessio Coppola, María Isidoro-García, Pablo Prieto-Matos, Jesus Lacal
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 16, p 8563 (2024)
RASopathies are a group of related genetic disorders caused by mutations in genes within the RAS/MAPK signaling pathway. This pathway is crucial for cell division, growth, and differentiation, and its disruption can lead to a variety of developmental
Externí odkaz:
https://doaj.org/article/77a15fd02540400c99f020faeb01582e
Autor:
Manuel Gómez-García, Emma Moreno-Jimenez, Natalia Morgado, Asunción García-Sánchez, María Gil-Melcón, Jacqueline Pérez-Pazos, Miguel Estravís, María Isidoro-García, Ignacio Dávila, Catalina Sanz
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8223 (2024)
In recent years, there has been growing interest in understanding the potential role of microbiota dysbiosis or alterations in the composition and function of human microbiota in the development of chronic rhinosinusitis with nasal polyposis (CRSwNP)
Externí odkaz:
https://doaj.org/article/dd016709675045e5b9d6bae544a29b31
Autor:
Mario Rodríguez-Martín, Juan Báez-Flores, Vanessa Ribes, María Isidoro-García, Jesus Lacal, Pablo Prieto-Matos
Publikováno v:
Biomedicines, Vol 12, Iss 4, p 841 (2024)
RASopathies, a group of neurodevelopmental congenital disorders stemming from mutations in the RAS/MAPK pathway, present a unique opportunity to delve into the intricacies of complex neurological disorders. Afflicting approximately one in a thousand
Externí odkaz:
https://doaj.org/article/4c8aa995b5554e85b9935a3d60f683db
Autor:
Aurora Gómez-Vecino, Roberto Corchado-Cobos, Adrián Blanco-Gómez, Natalia García-Sancha, Sonia Castillo-Lluva, Ana Martín-García, Marina Mendiburu-Eliçabe, Carlos Prieto, Sara Ruiz-Pinto, Guillermo Pita, Alejandro Velasco-Ruiz, Carmen Patino-Alonso, Purificación Galindo-Villardón, María Linarejos Vera-Pedrosa, José Jalife, Jian-Hua Mao, Guillermo Macías de Plasencia, Andrés Castellanos-Martín, María del Mar Sáez-Freire, Susana Fraile-Martín, Telmo Rodrigues-Teixeira, Carmen García-Macías, Julie Milena Galvis-Jiménez, Asunción García-Sánchez, María Isidoro-García, Manuel Fuentes, María Begoña García-Cenador, Francisco Javier García-Criado, Juan Luis García-Hernández, María Ángeles Hernández-García, Juan Jesús Cruz-Hernández, César Augusto Rodríguez-Sánchez, Alejandro Martín García-Sancho, Estefanía Pérez-López, Antonio Pérez-Martínez, Federico Gutiérrez-Larraya, Antonio J. Cartón, José Ángel García-Sáenz, Ana Patiño-García, Miguel Martín, Teresa Alonso-Gordoa, Christof Vulsteke, Lieselot Croes, Sigrid Hatse, Thomas Van Brussel, Diether Lambrechts, Hans Wildiers, Hang Chang, Marina Holgado-Madruga, Anna González-Neira, Pedro L. Sánchez, Jesús Pérez Losada
Publikováno v:
Cells, Vol 12, Iss 15, p 1956 (2023)
Cardiotoxicity due to anthracyclines (CDA) affects cancer patients, but we cannot predict who may suffer from this complication. CDA is a complex trait with a polygenic component that is mainly unidentified. We propose that levels of intermediate mol
Externí odkaz:
https://doaj.org/article/30117a66c9fb4e32901af4d0a0a24d13
Autor:
David Hansoe Heredero-Jung, Sandra Elena-Pérez, Asunción García-Sánchez, Miguel Estravís, María Isidoro-García, Catalina Sanz, Ignacio Dávila
Publikováno v:
Biomedicines, Vol 11, Iss 7, p 1966 (2023)
Chronic Rhinosinusitis with Nasal Polyposis (CRSwNP) affects the quality of life of patients suffering from it. The search for a suitable biomarker has been conducted over the last decades. Interleukin 5 receptor subunit alpha (IL-5Rα) involves the
Externí odkaz:
https://doaj.org/article/a9a291b7311347dbb989980e6357239d
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-17 (2021)
Abstract Background RASopathies are a group of syndromes showing clinical overlap caused by mutations in genes affecting the RAS-MAPK pathway. Consequent disruption on cellular signaling leads and is driven by phosphoproteome remodeling. However, we
Externí odkaz:
https://doaj.org/article/c12e4fcf2bed471a8c101c44342df7bf
Autor:
Elena Marcos-Vadillo, Lorena Carrascal-Laso, Ignacio Ramos-Gallego, Andrea Gaedigk, Belén García-Berrocal, Eduardo Mayor-Toranzo, Alfonso Sevillano-Jiménez, Almudena Sánchez, María Isidoro-García, Manuel Franco-Martín
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2022)
Precision medicine applied to psychiatry provides new insight into the promising field of precision psychiatry. Psychotic disorders are heterogeneous, complex, chronic, and severe mental disorders. Not only does the prognosis and the course of the di
Externí odkaz:
https://doaj.org/article/0d03a1010852463d8e7ab38816ad762a
Publikováno v:
Biomedicines, Vol 10, Iss 8, p 2044 (2022)
Neurofibromin is engaged in many cellular processes and when the proper protein functioning is impaired, it causes neurofibromatosis type 1 (NF1), one of the most common inherited neurological disorders. Recent advances in sequencing and screening of
Externí odkaz:
https://doaj.org/article/993d3950cbe54ae4801abac28388f791
Autor:
Leila Cardoso, Víctor Galán‐Gómez, María Dolores Corral‐Sánchez, Antonio Pérez‐Martínez, Susana Riesco, María Isidoro‐García, Adela Escudero
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract The clinical and laboratory criteria for hemophagocytic lymphohistiocytosis should be taken into account during the juvenile myelomonocytic leukemia diagnosis, specifically in CBL syndrome, to reveal the presence of primary rather than secon
Externí odkaz:
https://doaj.org/article/94997c2fc864407facdd73e69d1f416a