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dc.contributor.authorTrucco, Lucas-
dc.contributor.authorMundra, Piyushkumar-
dc.contributor.authorHogan, Kate-
dc.contributor.authorGarcia-Martinez, Pablo-
dc.contributor.authorViros, Amaya-
dc.contributor.authorMandal, Amit Kumar-
dc.contributor.authorMacagno, Nicolas-
dc.contributor.authorgaudy-marqueste, caroline-
dc.contributor.authorAllan, Donald-
dc.contributor.authorBaenke, Franziska-
dc.contributor.authorCook, Martin-
dc.contributor.authorMcManus, Clare-
dc.contributor.authorSanchez-Laorden, Berta-
dc.contributor.authorDhomen, Nathalie-
dc.contributor.authorMarais, Richard-
dc.date.accessioned2024-01-26T22:21:30Z-
dc.date.available2024-01-26T22:21:30Z-
dc.date.created2018-12-
dc.identifier.citationNature Medicine volume 25, pages221–224 (2019)es_ES
dc.identifier.issn1546-170X-
dc.identifier.issn1078-8956-
dc.identifier.urihttps://hdl.handle.net/11000/30787-
dc.description.abstractThe melanoma genome is dominated by ultraviolet radiation (UVR)-induced mutations. Their relevance in disease progression is unknown. Here we classify melanomas by mutation signatures and identify ten recurrently mutated UVR signature genes that predict patient survival. We validate these findings in primary human melanomas; in mice we show that this signature is imprinted by short-wavelength UVR and that four exposures to UVR are sufficient to accelerate melanomagenesis.es_ES
dc.formatapplication/pdfes_ES
dc.format.extent14es_ES
dc.language.isoenges_ES
dc.publisherNature Medicinees_ES
dc.rightsinfo:eu-repo/semantics/closedAccesses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleUltraviolet radiation–induced DNA damage is prognostic for outcome in melanomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.contributor.instituteInstitutos de la UMH::Instituto de Neurocienciases_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41591-018-0265-6es_ES
Aparece en las colecciones:
Instituto de Neurociencias


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