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dc.contributor.authorVågbø, Cathrine Broberg
dc.contributor.authorSlupphaug, Geir
dc.date.accessioned2021-04-28T07:58:24Z
dc.date.available2021-04-28T07:58:24Z
dc.date.created2020-12-06T17:06:24Z
dc.date.issued2020
dc.identifier.citationDNA Repair. 2020, 95 1-11.en_US
dc.identifier.issn1568-7864
dc.identifier.urihttps://hdl.handle.net/11250/2740057
dc.description.abstractOur genome is constantly subject to damage from exogenous and endogenous sources, and cells respond to such damage by initiating a DNA damage response (DDR). Failure to induce an adequate DDR can result in increased mutation load, chromosomal aberrations and a variety of human diseases, including cancer. A rapidly growing body of evidence suggests that a large number of RNA binding proteins are involved in the DDR, and several canonical DNA repair factors have moonlighting functions in RNA metabolism. RNA polymerases and RNA itself have been implicated at various stages of the DDR, including damage sensing, recruitment of DNA repair factors and tethering of broken DNA ends. RNA may even serve as a template for DNA repair under certain conditions. Given the vast number of non-coding RNAs in cells, we have barely started to decipher their potential involvement in genomic maintenance and future research on the interrelationship between RNA and DNA repair may open entirely new treatment options for human disease.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleRNA in DNA repairen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-11en_US
dc.source.volume95en_US
dc.source.journalDNA Repairen_US
dc.identifier.doi10.1016/j.dnarep.2020.102927
dc.identifier.cristin1856628
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal