Browsing by author "Álvarez Puente, Diana"

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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)
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)
Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

Suárez Puente, Xosé Antón; Quesada Fernández, Víctor; García Osorio, Fernando; Cabanillas Farpón, Rubén; Cadiñanos Bañales, Juan; Martínez Fraile, Julia; Rodríguez Ordóñez, Gonzalo; Álvarez Puente, Diana; Fanjul Fernández, Miriam; Lévy, Nicolas; Pérez Freije, José María; López Otín, Carlos; Gutiérrez Fernández, Ana Yolanda (Elsevier, 2011)
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Quesada Fernández, Víctor; Conde del Campo, Laura; Villamor Casas, Neus; Rodríguez Ordóñez, Gonzalo; Ramsay, Andrew John; Álvarez Puente, Diana; Velasco Cotarelo, María Gloria; Pérez Freije, José María; Suárez Puente, Xosé Antón; López Otín, Carlos (2012)
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)
Non-coding recurrent mutations in chronic lymphocytic leukaemia

Suárez Puente, Xosé Antón; Beà, Silvia; Valdés Mas, Rafael María; Gutiérrez Abril, Jesús; Álvarez Puente, Diana; Quesada Fernández, Víctor; López Otín, Carlos (2015)
Novel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation

Soria Valles, Clara; Carrero Muñiz, Dido; Gabau, E.; Velasco Cotarelo, María Gloria; Quesada Fernández, Víctor; Bárcena Fernández, Clea; Moens, M.; Fieggen, K.; Möhrcken, S.; Owens, M.; Álvarez Puente, Diana; Asensio, O.; Loeys, B.; Pérez, Ana; Benoit, V.; Wuyts, W.; Lévy, Nicolas; Hennekam, R. C.; Sandre-Giovannoli, Annachiara de; López Otín, Carlos (2016)
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: Review of reported cases and recommendations for genetic testing and surveillance

Bellido, Fernando; Pineda, Marta; Aiza, Gemma; Valdés Mas, Rafael María; Álvarez Puente, Diana (2016)
Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes

Marqués, Patricia Isabel; Fonseca, Filipa; Carvalho, Ana Sofía; Álvarez Puente, Diana; Quesada Fernández, Víctor (2016)
Transplacental transfer of essential thrombocythemia in monozygotic twins

Valdés 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 (2016)
Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance

Ruiz de Garibay, Gorka; Mateo, Francesca; Stradella, Agostina; Álvarez Puente, Diana; Díaz Navarro, Ander; Suárez Puente, Xosé Antón (2018)
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia

Suárez Puente, Xosé Antón; Pinyol, Magda; Quesada Fernández, Víctor; Conde, Laura; Rodríguez Ordóñez, Gonzalo; Álvarez Puente, Diana; Pérez Freije, José María; Velasco Cotarelo, María Gloria (2011)

Browsing by author "Álvarez Puente, Diana"

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

Estimation of Copy Number Alterations from Exome Sequencing Data ﻿

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome ﻿

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia ﻿

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma ﻿

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

Non-coding recurrent mutations in chronic lymphocytic leukaemia ﻿

Novel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation ﻿

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: Review of reported cases and recommendations for genetic testing and surveillance ﻿

Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes ﻿

Transplacental transfer of essential thrombocythemia in monozygotic twins ﻿

Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance ﻿

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia ﻿

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

Estimation of Copy Number Alterations from Exome Sequencing Data

Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma

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

Non-coding recurrent mutations in chronic lymphocytic leukaemia

Novel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation

POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: Review of reported cases and recommendations for genetic testing and surveillance

Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes

Transplacental transfer of essential thrombocythemia in monozygotic twins

Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance

Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia