Listar por autor "Valdés Mas, Rafael María"

Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia

Bretones Sánchez, Gabriel

; García Álvarez, Miguel

; Rodríguez Arango, Javier

; Rodríguez Martínez, David

; Valdés Mas, Rafael María

; Quesada Fernández, Víctor

; López Otín, Carlos

(2018)

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

Bellido, Fernando; Sowada, N.; Mur, P.; Valdés Mas, Rafael María

; Balbín Felechosa, Milagros

; Blay Albors, Pilar

(2018)

CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D1(-) mantle cell lymphoma

Martín García, David; Navarro, Alba; Valdés Mas, Rafael María

; Gutiérrez Abril, Jesús

; López Otín, Carlos

; Suárez Puente, Xosé Antón

(2019)

Chronic lymphocytic leukemia: Looking into the dark side of the genome

Valdés Mas, Rafael María

; Gutiérrez Abril, Jesús

; Suárez Puente, Xosé Antón

; López Otín, Carlos

(2016)

Circulating Tumor Cells (CTCs) for Comprehensive and Multiregional Non-Invasive Genetic Characterization of Multiple Myeloma (MM)

José Garcés, Juan; Bretones Sánchez, Gabriel

; Burgos, Leire; Valdés Mas, Rafael María

; Alignani, Diego; Álvarez Puente, Diana

; Goicoechea, Ibai; García Álvarez, Miguel

; Garate, Sonia; Rodríguez, Idoia; López Otín, Carlos

(2019)

Common and rare variants of microRNA genes in autism spectrum disorders

Toma, Claudio; Torrico, Bárbara; Hervas, Amaia; Valdés Mas, Rafael María

; Suárez Puente, Xosé Antón

(2015)

Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine

Castellsague, Joan; Gel, Bernat; Fernández Rodríguez, Juana; Valdés Mas, Rafael María

; Suárez Puente, Xosé Antón

(2015)

Cryptic insertions of the immunoglobulin light chain enhancer regions activate CCND3 and CCND2 in cyclin D1-negative mantle cell lymphomas

Martín García, D.; Navarro, A.; Clot, G.; Gutiérrez Abril, Jesús

; Valdés Mas, Rafael María

; López Otín, Carlos

; Suárez Puente, Xosé Antón

(2017)

Determinación de alteraciones en el número de copia a partir de datos de secuenciación de exomas tumorales

Valdés Mas, Rafael María

(2012-06-14)

Estimation of Copy Number Alterations from Exome Sequencing Data

Valdés Mas, Rafael María

; Beà, Silvia; Álvarez Puente, Diana

; López Otín, Carlos

; Suárez Puente, Xosé Antón

(2012)

Estrategia de secuenciación y análisis bioinformático para el estudio del cáncer y de las enfermedades hereditarias

Valdés Mas, Rafael María

(Servicio de Medios Audiovisuales, 2017)

Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype

Seguí, 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 (2014)

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

Toma, 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. (2014)

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Seguí, Nuria; Mina, L. B.; Lázaro, Conxi; Valdés Mas, Rafael María

; Balbín Felechosa, Milagros

; Blay Albors, Pilar

; Suárez Puente, Xosé Antón

(2015)

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis

Mur, Pilar; de Voer, Richarda M.; Olivera Salguero, Rubén; Valdés Mas, Rafael María

; Suárez Puente, Xosé Antón

(2018)

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis

Mur, P.; Jemth, A. S.; Bevc, L.; Valdés Mas, Rafael María

; Suárez Puente, Xosé Antón

(2018)

Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice

Bárcena 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

(2019)

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma

Beà, Silvia; Valdés Mas, Rafael María

; Navarro, Alba; Salaverria, Itziar; Martín-García, David; Jares, Pedro; Giné, Eva; Pinyol, Magda; Royo, Cristina; Nadeu, Ferrán; Conde, Laura; Juan, Manel; Clot, Guillem; Vizán, Pedro; Di Croce, Luciano; Álvarez Puente, Diana

; López Guerra, Mónica; López Otín, Carlos

; Suárez Puente, Xosé Antón

(2013)

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Valdés 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

(2014)

Natural history and cell of origin of TCF3-ZNF384 and PTPN11 mutations in monozygotic twins with concordant BCP-ALL

Bueno, C.; Tejedor Vaquero, Juan Ramón

; Bashford Rogers, R.; González Silva, L.; Valdés Mas, Rafael María

; Agraz Doblás, A.; De La Guardia, R. D.; Ribera, J.; Zamora, L.; Bilhou-Nabera, C.; Abermil, N.; Guermouche, H.; Gouache, E.; Leverger, G.; Fernández Fraga, Mario

; Fernández Fernández, Agustín

; Ballerini, P.; Varela, I.; Menéndez, P. (2019)

Listar por autor "Valdés Mas, Rafael María"

Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia ﻿

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer ﻿

CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D1(-) mantle cell lymphoma ﻿

Chronic lymphocytic leukemia: Looking into the dark side of the genome ﻿

Circulating Tumor Cells (CTCs) for Comprehensive and Multiregional Non-Invasive Genetic Characterization of Multiple Myeloma (MM) ﻿

Common and rare variants of microRNA genes in autism spectrum disorders ﻿

Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine ﻿

Cryptic insertions of the immunoglobulin light chain enhancer regions activate CCND3 and CCND2 in cyclin D1-negative mantle cell lymphomas ﻿

Determinación de alteraciones en el número de copia a partir de datos de secuenciación de exomas tumorales ﻿

Estimation of Copy Number Alterations from Exome Sequencing Data ﻿

Estrategia de secuenciación y análisis bioinformático para el estudio del cáncer y de las enfermedades hereditarias ﻿

Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype ﻿

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations ﻿

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair ﻿

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis ﻿

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis ﻿

Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice ﻿

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma ﻿

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy ﻿

Natural history and cell of origin of TCF3-ZNF384 and PTPN11 mutations in monozygotic twins with concordant BCP-ALL ﻿

Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia

Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer

CCND2 and CCND3 hijack immunoglobulin light-chain enhancers in cyclin D1(-) mantle cell lymphoma

Chronic lymphocytic leukemia: Looking into the dark side of the genome

Circulating Tumor Cells (CTCs) for Comprehensive and Multiregional Non-Invasive Genetic Characterization of Multiple Myeloma (MM)

Common and rare variants of microRNA genes in autism spectrum disorders

Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine

Cryptic insertions of the immunoglobulin light chain enhancer regions activate CCND3 and CCND2 in cyclin D1-negative mantle cell lymphomas

Determinación de alteraciones en el número de copia a partir de datos de secuenciación de exomas tumorales

Estimation of Copy Number Alterations from Exome Sequencing Data

Estrategia de secuenciación y análisis bioinformático para el estudio del cáncer y de las enfermedades hereditarias

Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis

Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis

Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Natural history and cell of origin of TCF3-ZNF384 and PTPN11 mutations in monozygotic twins with concordant BCP-ALL