Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cristina Egido-Turrión"'
Autor:
Cristina Egido-Turrión, Elisa Rossi, Claudia Ollauri-Ibáñez, María L. Pérez-García, María A. Sevilla, José María Bastida, José Ramón González-Porras, Alicia Rodríguez-Barbero, Carmelo Bernabeu, José M. Lopez-Novoa, Miguel Pericacho
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal-dominant genetic disorder involving defects in two predominant genes known as endoglin (ENG; HHT-1) and activin receptor-like kinase 1 (ACVRL1/ALK1; HHT-2). It is characterized by mucocutane
Externí odkaz:
https://doaj.org/article/d9857183e7e549468b77a46d55d5f672
Autor:
Alicia Rodríguez-Barbero, Laura Silva-Sousa, Miguel Pericacho, José M. López-Novoa, Elena Díaz-Rodríguez, Cristina Egido-Turrión, Claudia Ollauri-Ibáñez, Elena Núñez-Gómez
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Angiogenesis
instname
Angiogenesis
Endoglin (CD105) is an auxiliary receptor for members of the TFG-β superfamily. Whereas it has been demonstrated that the deficiency of endoglin leads to minor and defective angiogenesis, little is known about the effect of its increased expression,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02a37cedb6cda2139b45bf4388892b53
http://hdl.handle.net/10261/222759
http://hdl.handle.net/10261/222759
Autor:
Claudia Ollauri-Ibáñez, José M. López-Novoa, Miguel Pericacho, Cristina Egido-Turrión, Elena Núñez-Gómez, Laura Silva-Sousa, Alicia Rodríguez-Barbero
Angiogenesis is a complex process essential for tumor growth. For this reason, high levels of pro-angiogenic molecules, such as endoglin (CD105), are supposed to be related to greater tumor growth that lead to a poor cancer prognosis. However, we dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0873bc6ae9d4e2ff81e10a38733202e6
Autor:
Cristina Egido Turrión
Publikováno v:
GREDOS: Repositorio Institucional de la Universidad de Salamanca
Universidad de Salamanca (USAL)
GREDOS. Repositorio Institucional de la Universidad de Salamanca
instname
Universidad de Salamanca (USAL)
GREDOS. Repositorio Institucional de la Universidad de Salamanca
instname
[ES]La Telangiectasia Hemorrágica Hereditaria (HHT) es una enfermedad congénita, clasificada como enfermedad minoritaria. Las principales manifestaciones clínicas de esta enfermedad son la aparición de malformaciones vasculares y recurrentes even
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b237576345df1ca1c500ab4e9db2095
http://hdl.handle.net/10366/143750
http://hdl.handle.net/10366/143750