Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cristina Márquez-López"'
Autor:
Nieves García-Quintáns, Silvia Sacristán, Cristina Márquez-López, Cristina Sánchez-Ramos, Fernando Martinez-de-Benito, David Siniscalco, Andrés González-Guerra, Emilio Camafeita, Marta Roche-Molina, Mariya Lytvyn, David Morera, María I. Guillen, María A. Sanguino, David Sanz-Rosa, Daniel Martín-Pérez, Ricardo Garcia, Juan A. Bernal
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract The most prevalent genetic form of inherited arrhythmogenic cardiomyopathy (ACM) is caused by mutations in desmosomal plakophilin-2 (PKP2). By studying pathogenic deletion mutations in the desmosomal protein PKP2, here we identify a general
Externí odkaz:
https://doaj.org/article/10b925caee94464b82505e99e6d84978
Autor:
Mariya Lytvyn, Silvia Sacristán, Nieves García-Quintáns, Juan A. Bernal, Marta Roche-Molina, Andrés González-Guerra, David Siniscalco, Cristina Márquez-López, Ricardo Garcia, David Sanz-Rosa, Emilio Camafeita, Cristina Sánchez-Ramos, María I. Guillén, Daniel Martín-Pérez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Mutations in desmosomal Plakophilin-2 (PKP2) are the most prevalent drivers of arrhythmogenic cardiomyopathy (ACM) and a common cause of sudden cardiac death in young athletes. However, partner proteins that elucidate PKP2 cellular mechanism to under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92df7d65a84c543920adf6b50b922902
https://doi.org/10.1101/2020.09.14.296178
https://doi.org/10.1101/2020.09.14.296178
Autor:
Sandra Ríos Peces, Olga Genilloud, José Pérez del Palacio, Jose Prados, Consolación Melguizo, Francisca Vicente Pérez, Caridad Díaz Navarro, Cristina Jiménez-Luna, Octavio Caba, Cristina Márquez López
Publikováno v:
SLAS Discovery. 22:348-359
Pancreatic ductal adenocarcinoma is one of the most lethal tumors since it is usually detected at an advanced stage in which surgery and/or current chemotherapy have limited efficacy. The lack of sensitive and specific markers for diagnosis leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9144f2481f82c9cb2d4968a07778699f
https://doi.org/10.1177/1087057116671490
https://doi.org/10.1177/1087057116671490