Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David Sánchez-Ortiz"'
Autor:
Javier Segovia-Cubero, Lorena Ruiz-Bautista, Luis Maiz-Carro, Rosa M. Girón-Moreno, M. Concepción Prados-Sánchez, M. Teresa Martínez-Martínez, Montserrat González-Estecha, Susana Mingo-Santos, Manuel Gómez-Bueno, Clara Salas-Antón, Miguel A. Cavero-Gibanel, Miguel Pastrana-Ledesma, Pablo García-Pavía, Rosalía Laporta-Hernández, David Sánchez-Ortiz, Luis Alonso-Pulpón
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
IntroductionWe conducted a study to determine the prevalence of structural heart disease in patients with CF, the characteristics of a cardiomyopathy not previously described in this population, and its possible relationship with nutritional deficien
Externí odkaz:
https://doaj.org/article/48992d6432c54ed2998117dc08b6846f
Autor:
Paula Vela Martín, Andrea Matutano Muñoz, David Sánchez Ortiz, Fernando Domínguez, Ana Royuela, Marta Cobo Marcos
Publikováno v:
Revista Española de Cardiología (English Edition). 76:477-480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cc6d08f55e5f66b9a4310fd2d313349
https://doi.org/10.1016/j.rec.2022.11.007
https://doi.org/10.1016/j.rec.2022.11.007
Autor:
Paula Vela Martín, Andrea Matutano Muñoz, David Sánchez Ortiz, Fernando Domínguez, Ana Royuela, Marta Cobo Marcos
Publikováno v:
Revista Española de Cardiología. 76:477-480
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::797915490d5e1fc0c2a3b91e5300252a
https://doi.org/10.1016/j.recesp.2022.11.009
https://doi.org/10.1016/j.recesp.2022.11.009
Autor:
Laura Sen-Martín, Ángel Fernández-Trasancos, Miguel Lopez-Unzu, David Sánchez-Ortiz, María Rosaria Pricolo, Jorge Alegre-Cebollada
Publikováno v:
Circulation Research. 131
Background: Familial cardiomyopathies are caused by inherited genetic mutations resulting in anatomical and/or mechanical alterations that compromise cardiac function. The missense variant R502W in cardiac myosin-binding protein C (cMyBP-C) is the mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44c73c2f205c1664a4f0d60c7392dd4c
https://doi.org/10.1161/res.131.suppl_1.ec105
https://doi.org/10.1161/res.131.suppl_1.ec105
Autor:
Inés Carmen Rodríguez García, María del Pilar Carrera González, Vanesa Cantón Habas, Mercedes López-Pardo Martínez, José Hernández Ascanio, Carlos José Pérula de Torres, Juan Crisóstomo Vacas Pérez, Manuel Toledano Estepa, Sergio David Sánchez Ortiz, Manuel Rich Ruiz, Pilar María Lora López
Publikováno v:
Revista de Innovación y Buenas Prácticas Docentes. 9:53-60
espanolEl avance tecnologico y la consecuente incorporacion de las TICs en el ambito docente ha conllevado la aparicion de nuevas herramientas para facilitar a los docentes el proceso de seguimiento y evaluacion del alumnado. De igual forma, dicho av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01ea9eb063c2c13d20d3e061079185ae
https://doi.org/10.21071/ripadoc.v9i1.12609
https://doi.org/10.21071/ripadoc.v9i1.12609
Autor:
Diana Velázquez-Carreras, Kathleen M. Ruppel, Fernando Domínguez, Divya Pathak, David Sánchez-Ortiz, Neha Nandwani, Jorge Alegre-Cebollada, Carmen Suay-Corredera, Silvia Vilches, Pablo García-Pavía, Lorenzo Monserrat, James A. Spudich, David De Sancho, Maria Rosaria Pricolo, Carolina Pimenta-Lopes, Giulia Frisso, Elías Herrero-Galán, Iñigo Urrutia-Irazabal
Publikováno v:
ACS Nano
Hypertrophic cardiomyopathy (HCM) is a disease of the myocardium caused by mutations in sarcomeric proteins with mechanical roles, such as the molecular motor myosin. Around half of the HCM-causing genetic variants target contraction modulator cardia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e9cc259c3ef4838a36f57718dceb2e0
https://europepmc.org/articles/PMC8514129/
https://europepmc.org/articles/PMC8514129/
Autor:
Helena García-Cebollada, Juan J. Galano-Frutos, Diego García-Giustiniani, Silvia Vilches, Jorge Alegre-Cebollada, Carmen Suay-Corredera, Fernando Dominguez, Javier Sancho, David Sánchez-Ortiz, Luis Serrano, Lorenzo Monserrat, Maria Sabater Molina, Elías Herrero-Galán, Giulia Frisso, Pablo García-Pavía, Maria Rosaria Pricolo, Roberto Barriales-Villa, Javier Delgado, Diana Velázquez-Carreras
Publikováno v:
The Journal of Biological Chemistry
RUC. Repositorio da Universidade da Coruña
instname
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Digital.CSIC. Repositorio Institucional del CSIC
RUC. Repositorio da Universidade da Coruña
instname
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Digital.CSIC. Repositorio Institucional del CSIC
14 pags. 5 figs., 2 tabs.
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. Variants in MYBPC3, the gene encoding cardiac myosin-binding protein C (cMyBP-C), are the leading cause of HCM. However, the pathogenicity
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. Variants in MYBPC3, the gene encoding cardiac myosin-binding protein C (cMyBP-C), are the leading cause of HCM. However, the pathogenicity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb1d1118094c79afb658819aeb46079a
http://hdl.handle.net/11588/854009
http://hdl.handle.net/11588/854009
Autor:
Silvia Vilches, Iñigo Urrutia-Irazabal, Carolina Pimenta-Lopes, Jorge Alegre-Cebollada, Pablo García-Pavía, Carmen Suay-Corredera, David Sánchez-Ortiz, Maria Rosaria Pricolo, Fernando Domínguez, Elías Herrero-Galán, Giulia Frisso, Diana Velázquez-Carreras, Lorenzo Monserrat
Hypertrophic cardiomyopathy (HCM) is a disease of the myocardium caused by mutations in sarcomeric proteins with mechanical roles, such as the molecular motor myosin. Around half of the HCM-causing genetic variants target contraction modulator cardia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81b2156bd590fbc8677094962649ba38
https://doi.org/10.1101/2020.09.19.304618
https://doi.org/10.1101/2020.09.19.304618
Autor:
Diana Velázquez-Carreras, Lorenzo Monserrat, Javier Sancho, Fernando Domínguez, Javier Delgado, Diego García-Giustiniani, Carmen Suay-Corredera, Luis Serrano, Giulia Frisso, Roberto Barriales-Villa, David Sánchez-Ortiz, Jorge Alegre-Cebollada, Helena García-Cebollada, Juan J. Galano-Frutos, Silvia Vilches, Pablo García-Pavía, Maria Rosaria Pricolo, Elías Herrero-Galán, Maria Sabater Molina
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. Mutations inMYBPC3, the gene encoding cardiac myosin-binding protein C (cMyBP-C), are a leading cause of HCM. However, it remains challenging to define whether specific g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a55694e246756b5c9a74aba9f710dba8
Autor:
Carmen Suay-Corredera, Luis Serrano, David Sánchez-Ortiz, Diego García-Giustiniani, Roberto Barriales-Villa, Fernando Domínguez, Lorenzo Monserrat, Diana Velázquez-Carreras, Javier Delgado, Pablo García-Pavía, Maria Rosaria Pricolo, Silvia Vilches, Jorge Alegre-Cebollada, Elías Herrero-Galán, Giulia Frisso
Publikováno v:
Circulation Research. 125
Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. Mutations in cardiac myosin-binding protein C (cMyBP-C) are a leading cause of HCM. However, as for many other genetic diseases, it remains challenging to define whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbdc274c356d73c0e15a6741baa1ef00
https://doi.org/10.1161/res.125.suppl_1.471
https://doi.org/10.1161/res.125.suppl_1.471