Listar por autor "Suárez Puente, Xosé Antón"

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A practical guide for mutational signature analysis in hematological malignancies

Maura, F.; Degasperi, A.; Nadeu, F.; Leongamornlert, D.; Davies, H.; Moore, L.; Royo, R.; Ziccheddu, B.; Suárez Puente, Xosé Antón; Avet Loiseau, H.; Cambell, P. J.; Nik-Zainal, S.; Campo, E.; Munshi, N.; Bolli, N. (2019)
Absence or inhibition of matrix metalloproteinase-8 decreases ventilator-induced lung injury

Muñiz Albaiceta, Guillermo; Gutiérrez Fernández, Ana Yolanda; García Prieto, Emilio; Suárez Puente, Xosé Antón; Parra, Diego; Astudillo González, María Aurora; Campestre, Cristina; Cabrera Benítez, María Sandra; González López, Adrián; Fueyo Silva, Antonio Manuel; Taboada Costa, Francisco; López Otín, Carlos (2010)
Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants

Ruiz de Garibay, Gorka; Fernández García, Ignacio; Mazoyer, S.; Suárez Puente, Xosé Antón (2021)
An Epigenetic Mitotic Score Tracks the Proliferative History and Capacity of CLL Samples at Diagnosis and Is Associated with Clinical Outcome

Duran-Ferrer, Martí; Nadeu, Ferrán; Clot, Guillem; Suárez Puente, Xosé Antón; López Otín, Carlos (2018)
Análisis bioinformático y transcriptomico de genomas y degradomas: aplicación al estudio del cáncer y de la evolución

Rodríguez Ordóñez, Gonzalo (2010)
Aproximaciones bioinformáticas para la identificación de alteraciones en splicing en cáncer

Álvarez Eguiluz, Ángel (2015-07-21)
ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution

Royo, R.; Magnano, L.; Delgado, J.; Ruiz Gil, S.; Gelpí, J. L.; Heyn, H.; Taylor, M. A.; Stankovic, T.; Suárez Puente, Xosé Antón; Nadeu, F.; Campo, E. (2022)
Author correction: comparative and demographic analysis of orang-utan genomes (Nature (2011), 469, 7331, (529-533), 10.1038/nature09687)

Locke, D. P.; Hillier, L. D. W.; Warren, W. C.; Quesada Fernández, Víctor; Suárez Puente, Xosé Antón; Rodríguez Ordóñez, Gonzalo; López Otín, Carlos (2022)
Backtracking NOM1

Bousquets Muñoz, Pablo; Molina, O.; Varela, I.; Álvarez Eguiluz, Á.; Fernández Mateos, Javier; Gómez, A.; Sánchez, E. G.; Balbín, M.; Ruano, D.; Ramírez Orellana, M.; Suárez Puente, Xosé Antón; Menéndez, P.; Velasco Hernández, T. (2024)
Biología molecular, evolución y enfermedad en la Era Genómica

Rodríguez Ordóñez, Gonzalo; Quesada Fernández, Víctor; Suárez Puente, Xosé Antón; López Otín, Carlos (Universidad de Oviedo, Ediciones de la Universidad de Oviedo, 2013)
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)
Cell autonomous and systemic factors in progeria development

García Osorio, Fernando; Piñeiro Ugalde, Alejandro; Mariño García, Guillermo; Suárez Puente, Xosé Antón; Pérez Freije, José María; López Otín, Carlos (Portland Press, 2011)
Chromosome 12p amplification in triple-negative/BRCA1-mutated breast cancer associates with emergence of docetaxel resistance and carboplatin sensitivity

Gomez-Miragaya, J.; Díaz Navarro, Ander; Tonda, R.; Beltran, S.; Palomero, L.; Palafox, M.; Dobrolecki, L. E.; Huang, C.; Vasaikar, S.; Zhang, B.; Wulf, G. M.; Collado-Sole, A.; Trinidad, E. M.; Muñoz, P.; Pare, L.; Prat, A.; Bruna, A.; Caldas, C.; Arribas, J.; Soler-Monso, M.T.; Petit, A.; Balmaña, J.; Suárez Puente, Xosé Antón (2019)
Chronic lymphocytic leukemia and mantle cell lymphoma: Crossroads of genetic and microenvironment interactions

Suárez Puente, Xosé Antón; Jares, Pedro; Campo, Elías (2018)
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 tumour DNA from the cerebrospinal fluid allows the characterisation and monitoring of medulloblastoma

Escudero, L.; Llort, A.; Arias, A.; Díaz Navarro, Ander; Martínez Ricarte, F.; Rubio Pérez, C.; Mayor, R.; Caratù, G.; Martínez Sáez, E.; Vázquez Méndez, É.; Lesende Rodríguez, I.; Hladun, R.; Gros, L.; Ramón y Cajal, S.; Poca, M. A.; Suárez Puente, Xosé Antón (2020)
Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia

Nadeu, Ferrán; Delgado, Julio; Royo, Cristina; Suárez Puente, Xosé Antón; López Otín, Carlos (2016)
Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia

Nadeu, Ferrán; Clot, G.; Delgado, J.; Suárez Puente, Xosé Antón; López Otín, Carlos (2017)
Clinical Response to a Lapatinib-Based Therapy for a Li-Fraumeni Syndrome Patient with a Novel HER2(V659E) Mutation

Serra, Violeta; Vivancos, Ana; Suárez Puente, Xosé Antón; Felip, Enriqueta; Silberschmidt, Daniel; Caratù, Ginevra; Parra, Josep-Lluís; Mattos Arruda, Leticia de; Grueso, Judit; Hernández-Losa, Javier; Arribas, Joaquín; Prudkin, Ludmila; Nuciforo, Paolo; Scaltriti, Maurizio; Seoane Leston, Juan; Baselga, José (2013)
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)

Listar por autor "Suárez Puente, Xosé Antón"

A practical guide for mutational signature analysis in hematological malignancies ﻿

Absence or inhibition of matrix metalloproteinase-8 decreases ventilator-induced lung injury ﻿

Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants ﻿

An Epigenetic Mitotic Score Tracks the Proliferative History and Capacity of CLL Samples at Diagnosis and Is Associated with Clinical Outcome ﻿

Análisis bioinformático y transcriptomico de genomas y degradomas: aplicación al estudio del cáncer y de la evolución ﻿

Aproximaciones bioinformáticas para la identificación de alteraciones en splicing en cáncer ﻿

ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution ﻿

Author correction: comparative and demographic analysis of orang-utan genomes (Nature (2011), 469, 7331, (529-533), 10.1038/nature09687) ﻿

Backtracking NOM1 ﻿

Biología molecular, evolución y enfermedad en la Era Genómica ﻿

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

Cell autonomous and systemic factors in progeria development ﻿

Chromosome 12p amplification in triple-negative/BRCA1-mutated breast cancer associates with emergence of docetaxel resistance and carboplatin sensitivity ﻿

Chronic lymphocytic leukemia and mantle cell lymphoma: Crossroads of genetic and microenvironment interactions ﻿

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

Circulating tumour DNA from the cerebrospinal fluid allows the characterisation and monitoring of medulloblastoma ﻿

Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia ﻿

Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia ﻿

Clinical Response to a Lapatinib-Based Therapy for a Li-Fraumeni Syndrome Patient with a Novel HER2(V659E) Mutation ﻿

Common and rare variants of microRNA genes in autism spectrum disorders ﻿

A practical guide for mutational signature analysis in hematological malignancies

Absence or inhibition of matrix metalloproteinase-8 decreases ventilator-induced lung injury

Altered regulation of BRCA1 exon 11 splicing is associated with breast cancer risk in carriers of BRCA1 pathogenic variants

An Epigenetic Mitotic Score Tracks the Proliferative History and Capacity of CLL Samples at Diagnosis and Is Associated with Clinical Outcome

Análisis bioinformático y transcriptomico de genomas y degradomas: aplicación al estudio del cáncer y de la evolución

Aproximaciones bioinformáticas para la identificación de alteraciones en splicing en cáncer

ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution

Author correction: comparative and demographic analysis of orang-utan genomes (Nature (2011), 469, 7331, (529-533), 10.1038/nature09687)

Backtracking NOM1

Biología molecular, evolución y enfermedad en la Era Genómica

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

Cell autonomous and systemic factors in progeria development

Chromosome 12p amplification in triple-negative/BRCA1-mutated breast cancer associates with emergence of docetaxel resistance and carboplatin sensitivity

Chronic lymphocytic leukemia and mantle cell lymphoma: Crossroads of genetic and microenvironment interactions

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

Circulating tumour DNA from the cerebrospinal fluid allows the characterisation and monitoring of medulloblastoma

Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia

Clinical impact of the subclonal architecture and mutational complexity in chronic lymphocytic leukemia

Clinical Response to a Lapatinib-Based Therapy for a Li-Fraumeni Syndrome Patient with a Novel HER2(V659E) Mutation

Common and rare variants of microRNA genes in autism spectrum disorders