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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| closedAccess |  | 2014 | Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers | Zugazagoitia, Jon; Vega, Ana; González-Sarmiento, Rogelio CSIC ORCID ; Cruz, Juan Jesús CSIC ORCID; Hoya, Miguel de la | artículo |
| closedAccess |  | 2011 | Long-Range Epigenetic Silencing Associates with Deregulation of Ikaros Targets in Colorectal Cancer Cells | Javierre, Biola M.; González-Sarmiento, Rogelio CSIC ORCID | artículo |
| openAccess |  | 18-ago-2020 | Matrix Metalloproteinases in Age-Related Macular Degeneration (AMD) | García-Onrubia, Luis; Valentín-Bravo, F. Javier; Coco-Martin, Rosa M.; González-Sarmiento, Rogelio CSIC ORCID ; Pastor, José Carlos; Usategui-Martín, Ricardo; Pastor-Idoate, Salvador | artículo |
| openAccess |  | 7-mar-2019 | Meta-analysis of the rs243865 MMP-2 polymorphism and age-related macular degeneration risk | Usategui-Martín, Ricardo; Pastor-Idoate, Salvador; Chamorro, Antonio J.; Fernández, Itziar; Fernández-Bueno, Iván; Marcos-Martín, Miguel; González-Sarmiento, Rogelio CSIC ORCID ; Pastor, José Carlos | actas de congreso |
| openAccess |  | 2021 | Methoxy and bromo scans on N-(5-methoxyphenyl) methoxybenzenesulphonamides reveal potent cytotoxic compounds, especially against the human breast adenocarcinoma MCF7 cell line | González, Myriam; Ovejero-Sánchez, María; Vicente-Blázquez, Alba CSIC; Medarde, Manuel; González-Sarmiento, Rogelio CSIC ORCID ; Peláez, Rafael | artículo |
| openAccess |  | 2021 | Microtubule Destabilizing Sulfonamides as an Alternative to Taxane-Based Chemotherapy | González, Myriam; Ovejero-Sánchez, María; Vicente-Blázquez, Alba CSIC; Álvarez, Raquel; Herrero, Ana B. CSIC ORCID; Medarde, Manuel; González-Sarmiento, Rogelio CSIC ORCID ; Peláez, Rafael | artículo |
| openAccess |  | 24-ago-2010 | Molecular analysis of ex-vivo CD133+ GBM cells revealed a common invasive and angiogenic profile but different proliferative signatures among high grade gliomas | García, Juan L. CSIC ORCID CVN ; Pérez-Caro, M. CSIC; Hernández, Jesús M. CSIC ORCID ; González-Sarmiento, Rogelio CSIC ORCID ; Sánchez-Martín, M. | artículo |
| closedAccess |  | 15-sep-2018 | Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism | Siffo, Sofia; Adrover, Ezequiela; Citterio, Cintia E.; Miras, Mirta B.; Balbi, Viviana A.; Chiesa, Ana; Weill, Jacques; Sobrero, Gabriela; González, Verónica G.; Papendieck, Patricia; Bueno-Martínez, Elena CSIC ORCID CVN; González-Sarmiento, Rogelio CSIC ORCID ; Rivolta, Carina M.; Targovnik, Héctor M. | artículo |
| closedAccess |  | 2013 | Molecular evidence of type 2 mosaicism in Gorlin syndrome | Torrelo, Antonio; Hernández-Martín, Angela; González-Sarmiento, Rogelio CSIC ORCID | artículo |
| closedAccess |  | 2020 | Multiple familial trichoepitheliomas: Ultrasonographic findings | Capusan, Tania M.; Noguera-Morel, Lucero; Bueno, Elena; Colmenero, Isabel; Torrelo, Antonio; González-Sarmiento, Rogelio CSIC ORCID ; Hernández-Martín, Angela | carta al director |
| closedAccess |  | 2022 | Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis | Molina, Maricel F.; Papendieck, Patricia; Sobrero, Gabriela; Balbi, Viviana A.; Belforte, Fiorella S.; Bueno, Elena; Adrover, Ezequiela; Olcese, María C.; Chiesa, Ana; Miras, Mirta B.; González, Verónica G.; Gomes Pio, Mauricio; González-Sarmiento, Rogelio CSIC ORCID ; Targovnik, Héctor M.; Rivolta, Carina M. | artículo |
| openAccess |  | ene-2020 | Neurofilament-lysosomal genetic intersections in the cortical network of stuttering | Benito-Aragón, Claudia; González-Sarmiento, Rogelio CSIC ORCID ; Liddell, Thomas; Díez, Ibai; d'Oleire Uquillas, Federico; Ortiz-Terán, Laura; Bueichekú, Elisenda; Ming Chow, Ho; Chang, Soo-Eun; Sepulcre, Jorge | artículo |
| closedAccess |  | 2013 | New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism | Citterio, Cintia E.; González-Sarmiento, Rogelio CSIC ORCID ; Targovnik, Héctor M. | artículo |
| openAccess |  | 2017 | NOMO-1 gene is deleted in early-onset colorectal cancer | Perea, José; García, Juan L. CSIC ORCID CVN ; Pérez García, Jessica; Rueda, Daniel; Arriba, María; Rodríguez, Yolanda; Urioste, Miguel; González-Sarmiento, Rogelio CSIC ORCID | artículo |
| closedAccess |  | 2018 | Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome | Alonso, Natalia; Cañueto, Javier; Ciria, S.; Bueno, Elena; Palacios-Álvarez, Irene; Alegre, M.; Badenas, C.; Barreiro, A.; Peña, Laura; Maldonado, C.; Nespeira-Jato, M. V.; Peña-Penabad, C.; Azon, A.; Gavrilova, M.; Ferrer, I.; Sanmartin, O.; Robles, L.; Hernández-Martín, Angela; Urioste, Miguel; Puig, S.; Puig, L.; González-Sarmiento, Rogelio CSIC ORCID | artículo |
| openAccess |  | 23-jun-2020 | Novel dominant KCNQ2 exon 7 partial in-frame duplication in a complex epileptic and neurodevelopmental delay syndrome | Lazo, Pedro A. CSIC ORCID ; García, Juan L. CSIC ORCID CVN ; Gómez-Puertas, Paulino CSIC ORCID ; Marcos-Alcalde, Íñigo CSIC ORCID; Arjona, César; Villarroel, Álvaro CSIC ORCID; González-Sarmiento, Rogelio CSIC ORCID ; Fons, Carmen | artículo |
| openAccess |  | 23-jun-2020 | Novel Dominant KCNQ2 Exon 7 Partial In-Frame Duplication in a Complex Epileptic and Neurodevelopmental Delay Syndrome | Lazo, Pedro A. CSIC ORCID ; García, Juan L. CSIC ORCID CVN ; Gómez-Puertas, Paulino CSIC ORCID ; Marcos-Alcalde, Íñigo CSIC ORCID; Arjona, César; Vallarroel, Alvaro; González-Sarmiento, Rogelio CSIC ORCID ; Fons, Carmen | artículo |
| closedAccess |  | 2014 | Novel mutation pA64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene # | Sklate, R. T.; González-Sarmiento, Rogelio CSIC ORCID ; Targovnik, Héctor M.; Rivolta, Carina M. | artículo |
| closedAccess |  | 2013 | Novel mutational mechanism in the thyroglobulin gene: Imperfect DNA inversion as a cause for hereditary hypothyroidism | Citterio, Cintia E.; González-Sarmiento, Rogelio CSIC ORCID ; Targovnik, Héctor M. | artículo |
| openAccess |  | 2020 | Oncogenic driver mutations predict outcome in a cohort of head and neck squamous cell carcinoma (HNSCC) patients within a clinical trial | Fernández-Mateos, Javier; Pérez-García, Jessica; Seijas-Tamayo, Raquel; Mesía, Ricard; Rubió‑Casadevall, Jordi; García‑Girón, Carlos; Iglesias, Lara; Carral Maseda, Alberto; Adansa Klain, Juan Carlos; Taberna, Miren; Vazquez, Silvia; Gómez, María Asunción; Barco,Edel del; Ocaña, Alberto; González-Sarmiento, Rogelio CSIC ORCID ; Cruz, Juan Jesús CSIC ORCID | artículo |
