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dc.creatorGómez González, Belénes
dc.creatorSessa, Gaetanaes
dc.creatorCarreira, Auraes
dc.creatorAguilera López, Andréses
dc.date.accessioned2021-09-02T13:50:29Z
dc.date.available2021-09-02T13:50:29Z
dc.date.issued2021
dc.identifier.citationGómez González, B., Sessa, G., Carreira, A. y Aguilera López, A. (2021). A new interaction between BRCA2 and DDX5 promotes the repair of DNA breaks at transcribed chromatin. Molecular and Cellular Oncology, 8 (3), 1910474.
dc.identifier.issn2372-3556es
dc.identifier.urihttps://hdl.handle.net/11441/125296
dc.description.abstractIn a recent report, we have revealed a new interaction between the BRCA2 DNA repair associated protein (BRCA2) and the DEAD-box helicase 5 (DDX5) at DNA breaks that promotes unwinding DNA-RNA hybrids within transcribed chromatin and favors repair. Interestingly, BRCA2–DDX5 interaction is impaired in cells expressing the BRCA2T207A missense variant found in breast cancer patients.es
dc.formatapplication/pdfes
dc.format.extent6 p.es
dc.language.isoenges
dc.publisherTaylor & Francises
dc.relation.ispartofMolecular and Cellular Oncology, 8 (3), 1910474.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectBRCA2es
dc.subjectBreast canceres
dc.subjectDDX5es
dc.subjectDNA-RNA hybrides
dc.subjectDouble-strand breakes
dc.subjectDSB repaires
dc.subjectHomologous recombinationes
dc.titleA new interaction between BRCA2 and DDX5 promotes the repair of DNA breaks at transcribed chromatines
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/submittedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Genéticaes
dc.relation.publisherversionhttps://doi.org/10.1080/23723556.2021.1910474es
dc.identifier.doi10.1080/23723556.2021.1910474es
dc.journaltitleMolecular and Cellular Oncologyes
dc.publication.volumen8es
dc.publication.issue3es
dc.publication.initialPage1910474es

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