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Browsing by Uniovi Authors Valdés Mas, Rafael María

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Showing results 1 to 20 of 23
Issue DateTitleAuthor(s)
2019CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D1(-) mantle cell lymphomaMartín García, David; Navarro, Alba; Valdés Mas, Rafael María; Gutiérrez Abril, Jesús; López Otín, Carlos; Suárez Puente, Xosé Antón
2019Healthspan and lifespan extension by fecal microbiota transplantation into progeroid miceBárcena Fernández, Clea; Valdés Mas, Rafael María; Mayoral García, Pablo; Garabaya Fernández, Cecilia; Durand, S.; Rodríguez Fíaz, Francisco José; Fernández García, María Teresa; Salazar, Nuria; Nogacka, A. M.; Garatachea, N.; Bossut, N.; Aprahamian, F.; Lucia, A.; Kroemer, Guido; Pérez Freije, José María; Moral Quirós, Pedro; López Otín, Carlos
2018Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposisMur, Pilar; de Voer, Richarda M.; Olivera Salguero, Rubén; Valdés Mas, Rafael María; Suárez Puente, Xosé Antón
2018Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemiaBretones Sánchez, Gabriel; García Álvarez, Miguel; Rodríguez Arango, Javier; Rodríguez Martínez, David; Valdés Mas, Rafael María; Quesada Fernández, Víctor; López Otín, Carlos
2018Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal CancerBellido, Fernando; Sowada, N.; Mur, P.; Valdés Mas, Rafael María; Balbín Felechosa, Milagros; Blay Albors, Pilar
2018Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposisMur, P.; Jemth, A. S.; Bevc, L.; Valdés Mas, Rafael María; Suárez Puente, Xosé Antón
2017Estrategia de secuenciación y análisis bioinformático para el estudio del cáncer y de las enfermedades hereditariasValdés Mas, Rafael María
23-Dec-2016Sequencing strategies and bioinformatic tools for the study of cancer and heredaty diseasesValdés Mas, Rafael María
2016Transplacental transfer of essential thrombocythemia in monozygotic twinsValdés Mas, Rafael María; Gutiérrez Abril, Jesús; Sánchez Pitiot, Ana Gloria; Santamaría Ruiz de Azúa, Íñigo; Álvarez Puente, Diana; Muñiz Lobato, Sara; Balbín Felechosa, Milagros; Suárez Puente, Xosé Antón
2016Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposisMur, Pilar; Sánchez-Cuartielles, Elena; Aussó, Susanna; Aiza, Gemma; Valdés Mas, Rafael María; Pineda, Marta; Navarro, Matilde; Brunet, Joan; Urioste, Miguel; Lázaro, Conxi; Moreno, Víctor; Capellá, Gabriel; Puente, Xosé S.; Valle, Laura
2016Chronic lymphocytic leukemia: Looking into the dark side of the genomeValdés Mas, Rafael María; Gutiérrez Abril, Jesús; Suárez Puente, Xosé Antón; López Otín, Carlos
2016POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: Review of reported cases and recommendations for genetic testing and surveillanceBellido, Fernando; Pineda, Marta; Aiza, Gemma; Valdés Mas, Rafael María; Álvarez Puente, Diana
2015Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA RepairSeguí, Nuria; Mina, L. B.; Lázaro, Conxi; Valdés Mas, Rafael María; Balbín Felechosa, Milagros; Blay Albors, Pilar; Suárez Puente, Xosé Antón
2015Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicineCastellsague, Joan; Gel, Bernat; Fernández Rodríguez, Juana; Valdés Mas, Rafael María; Suárez Puente, Xosé Antón
2015Common and rare variants of microRNA genes in autism spectrum disordersToma, Claudio; Torrico, Bárbara; Hervas, Amaia; Valdés Mas, Rafael María; Suárez Puente, Xosé Antón
2015Non-coding recurrent mutations in chronic lymphocytic leukaemiaSuárez Puente, Xosé Antón; Beà, Silvia; Valdés Mas, Rafael María; Gutiérrez Abril, Jesús; Álvarez Puente, Diana; Quesada Fernández, Víctor; López Otín, Carlos
2014Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathyValdés Mas, Rafael María; Gutiérrez Fernández, Ana Yolanda; Gómez de Oña, Juan; Coto García, Eliecer; Astudillo González, María Aurora; Álvarez Puente, Diana; Rodríguez Reguero, José Julián
2014Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotypeSeguí, Nuria; Navarro, Matilde; Pineda, Marta; Kogër, Nicole; Bellido, Fernando; González, Sara; Campos, Olga; Iglesias, Silvia; Valdés Mas, Rafael María; López-Dóriga, Adriana; Gut, Marta; Blanco, Ignacio; Lázaro, Conxi; Capellá, Gabriel; Suárez Puente, Xosé Antón; Plotz, Guido; Valle, Laura
2014Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutationsToma, Claudio; Torrico, Bárbara; Hervas, Amaia; Valdés Mas, Rafael María; Tristan-Noguero, A.; Padillo, V.; Maristany, M.; Salgado, Marta; Arenas, C.; Suárez Puente, Xosé Antón; Bayés, Mónica; Cormand, B.
2013Signatures of mutational processes in human cancerAlexandrov, Ludmil B.; Nik-Zainal, Serena; Wedge, David C.; López Otín, Carlos; Suárez Puente, Xosé Antón; Valdés Mas, Rafael María
Showing results 1 to 20 of 23

 

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