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Scientific Reports|June 12, 2020
Association of Alk1 and Endoglin Polymorphisms with Cardiovascular DamageMercedes Garzon-Martinez, Nuria Perretta-Tejedor, Luis Garcia-Ortiz, et al.
Cancer Letters|May 7, 2005
BRCA1-2 mutations in breast cancer: identification of nine new variants of BRCA1-2 genes in a population from central Western SpainRaquel Salazar, Juan Jesús Cruz-Hernandez, Enrique Sanchez-Valdivieso, et al.
BMJ Open|April 5, 2014
Relationship between target organ damage and blood pressure, retinal vessel calibre, oxidative stress and polymorphisms in VAV-2 and VAV-3 genes in patients with hypertension: a case-control study protocol (LOD-Hipertension)Manuel A Gomez-Marcos, Rogelio Gonzalez-Sarmiento, José I Recio-Rodríguez, et al.
BMC Cancer|August 26, 2010
Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomasJuan L Garcia, Maria Perez-Caro, Juan A Gomez-Moreta, et al.
Molecular and Cellular Probes|March 10, 2009
Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor beta geneCarina M Rivolta, María C Olcese, Fiorella S Belforte, et al.
BMJ Open|June 9, 2016
Association between different risk factors and vascular accelerated ageing (EVA study): study protocol for a cross-sectional, descriptive observational studyManuel A Gomez-Marcos, Carlos Martinez-Salgado, Rogelio Gonzalez-Sarmiento, et al.
The Journal of Experimental Medicine|March 2, 2011
The human Tp53 Arg72Pro polymorphism explains different functional prognosis in strokeJose C Gomez-Sanchez, Maria Delgado-Esteban, Irene Rodriguez-Hernandez, et al.
Journal of Cell Science|July 25, 2007
Combinatorial effects of splice variants modulate function of AiolosRosalia Caballero, Fernando Setien, Lidia Lopez-Serra, et al.
Journal of Medical Genetics|April 12, 2012
Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic casesBeatriz Martinez-Delgado, Kira Yanowsky, Lucia Inglada-Perez, et al.
Molecular and Cellular Endocrinology|December 25, 2017
Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidismSofia Siffo, Ezequiela Adrover, Cintia E Citterio, et al.
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