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Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma

Detalles Bibliográficos
Autores principales: Mata, Elena, Fernández, Sara, Astudillo, Aurora, Fernández, Rubén, García-Cosío, Mónica, Sánchez-Beato, Margarita, Provencio, Mariano, Estévez, Mónica, Montalbán, Carlos, Piris, Miguel A., García, Juan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411728/
https://www.ncbi.nlm.nih.gov/pubmed/30858359
http://dx.doi.org/10.1038/s41408-019-0195-7
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author Mata, Elena
Fernández, Sara
Astudillo, Aurora
Fernández, Rubén
García-Cosío, Mónica
Sánchez-Beato, Margarita
Provencio, Mariano
Estévez, Mónica
Montalbán, Carlos
Piris, Miguel A.
García, Juan F.
author_facet Mata, Elena
Fernández, Sara
Astudillo, Aurora
Fernández, Rubén
García-Cosío, Mónica
Sánchez-Beato, Margarita
Provencio, Mariano
Estévez, Mónica
Montalbán, Carlos
Piris, Miguel A.
García, Juan F.
author_sort Mata, Elena
collection PubMed
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spelling pubmed-64117282019-03-12 Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma Mata, Elena Fernández, Sara Astudillo, Aurora Fernández, Rubén García-Cosío, Mónica Sánchez-Beato, Margarita Provencio, Mariano Estévez, Mónica Montalbán, Carlos Piris, Miguel A. García, Juan F. Blood Cancer J Correspondence Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411728/ /pubmed/30858359 http://dx.doi.org/10.1038/s41408-019-0195-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Correspondence
Mata, Elena
Fernández, Sara
Astudillo, Aurora
Fernández, Rubén
García-Cosío, Mónica
Sánchez-Beato, Margarita
Provencio, Mariano
Estévez, Mónica
Montalbán, Carlos
Piris, Miguel A.
García, Juan F.
Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title_full Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title_fullStr Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title_full_unstemmed Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title_short Genomic analyses of microdissected Hodgkin and Reed-Sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic Hodgkin lymphoma
title_sort genomic analyses of microdissected hodgkin and reed-sternberg cells: mutations in epigenetic regulators and p53 are frequent in refractory classic hodgkin lymphoma
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411728/
https://www.ncbi.nlm.nih.gov/pubmed/30858359
http://dx.doi.org/10.1038/s41408-019-0195-7
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