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Times Cited: 327
Times Cited: 327
Times Cited
Times Co-cited
Similarity
A role for small RNAs in DNA double-strand break repair.
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Damage-induced lncRNAs control the DNA damage response through interaction with DDRNAs at individual double-strand breaks.
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Drosha drives the formation of DNA:RNA hybrids around DNA break sites to facilitate DNA repair.
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BRCA2 controls DNA:RNA hybrid level at DSBs by mediating RNase H2 recruitment.
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Transient RNA-DNA Hybrids Are Required for Efficient Double-Strand Break Repair.
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Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations.
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Functional transcription promoters at DNA double-strand breaks mediate RNA-driven phase separation of damage-response factors.
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Tyrosine kinase c-Abl couples RNA polymerase II transcription to DNA double-strand breaks.
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Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes.
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Small RNAs Recruit Chromatin-Modifying Enzymes MMSET and Tip60 to Reconfigure Damaged DNA upon Double-Strand Break and Facilitate Repair.
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Genome-wide Map of R-Loop-Induced Damage Reveals How a Subset of R-Loops Contributes to Genomic Instability.
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DNA damage triggers SAF-A and RNA biogenesis factors exclusion from chromatin coupled to R-loops removal.
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The roles of RNA in DNA double-strand break repair.
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From "Cellular" RNA to "Smart" RNA: Multiple Roles of RNA in Genome Stability and Beyond.
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53BP1 exchanges slowly at the sites of DNA damage and appears to require RNA for its association with chromatin.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.