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Times Cited: 369
Times Cited: 369
Times Cited
Times Co-cited
Similarity
Damage-induced lncRNAs control the DNA damage response through interaction with DDRNAs at individual double-strand breaks.
Flavia Michelini, Sethuramasundaram Pitchiaya, Valerio Vitelli, Sheetal Sharma, Ubaldo Gioia, Fabio Pessina, Matteo Cabrini, Yejun Wang, Ilaria Capozzo, Fabio Iannelli,[...]. Nat Cell Biol 2017
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A role for small RNAs in DNA double-strand break repair.
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Drosha drives the formation of DNA:RNA hybrids around DNA break sites to facilitate DNA repair.
Wei-Ting Lu, Ben R Hawley, George L Skalka, Robert A Baldock, Ewan M Smith, Aldo S Bader, Michal Malewicz, Felicity Z Watts, Ania Wilczynska, Martin Bushell. Nat Commun 2018
Wei-Ting Lu, Ben R Hawley, George L Skalka, Robert A Baldock, Ewan M Smith, Aldo S Bader, Michal Malewicz, Felicity Z Watts, Ania Wilczynska, Martin Bushell. Nat Commun 2018
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Transient RNA-DNA Hybrids Are Required for Efficient Double-Strand Break Repair.
Corina Ohle, Rafael Tesorero, Géza Schermann, Nikolay Dobrev, Irmgard Sinning, Tamás Fischer. Cell 2016
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BRCA2 controls DNA:RNA hybrid level at DSBs by mediating RNase H2 recruitment.
Giuseppina D'Alessandro, Donna Rose Whelan, Sean Michael Howard, Valerio Vitelli, Xavier Renaudin, Marek Adamowicz, Fabio Iannelli, Corey Winston Jones-Weinert, MiYoung Lee, Valentina Matti,[...]. Nat Commun 2018
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Senataxin resolves RNA:DNA hybrids forming at DNA double-strand breaks to prevent translocations.
Sarah Cohen, Nadine Puget, Yea-Lih Lin, Thomas Clouaire, Marion Aguirrebengoa, Vincent Rocher, Philippe Pasero, Yvan Canitrot, Gaëlle Legube. Nat Commun 2018
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Functional transcription promoters at DNA double-strand breaks mediate RNA-driven phase separation of damage-response factors.
Fabio Pessina, Fabio Giavazzi, Yandong Yin, Ubaldo Gioia, Valerio Vitelli, Alessandro Galbiati, Sara Barozzi, Massimiliano Garre, Amanda Oldani, Andrew Flaus,[...]. Nat Cell Biol 2019
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DICER, DROSHA and DNA damage response RNAs are necessary for the secondary recruitment of DNA damage response factors.
Sofia Francia, Matteo Cabrini, Valentina Matti, Amanda Oldani, Fabrizio d'Adda di Fagagna. J Cell Sci 2016
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ATM-dependent chromatin changes silence transcription in cis to DNA double-strand breaks.
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Human Rad52 Promotes XPG-Mediated R-loop Processing to Initiate Transcription-Associated Homologous Recombination Repair.
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Ago2 facilitates Rad51 recruitment and DNA double-strand break repair by homologous recombination.
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Transcriptionally active chromatin recruits homologous recombination at DNA double-strand breaks.
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Transcript-RNA-templated DNA recombination and repair.
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Tyrosine kinase c-Abl couples RNA polymerase II transcription to DNA double-strand breaks.
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Next-generation sequencing reveals two populations of damage-induced small RNAs at endogenous DNA double-strand breaks.
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RNA polymerase III is required for the repair of DNA double-strand breaks by homologous recombination.
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BRCA1 recruitment to transcriptional pause sites is required for R-loop-driven DNA damage repair.
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DEAD Box 1 Facilitates Removal of RNA and Homologous Recombination at DNA Double-Strand Breaks.
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The DNA damage response: making it safe to play with knives.
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DNAPKcs-dependent arrest of RNA polymerase II transcription in the presence of DNA breaks.
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Nuclear phosphorylated Dicer processes double-stranded RNA in response to DNA damage.
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MRE11-RAD50-NBS1 Complex Is Sufficient to Promote Transcription by RNA Polymerase II at Double-Strand Breaks by Melting DNA Ends.
Sheetal Sharma, Roopesh Anand, Xuzhu Zhang, Sofia Francia, Flavia Michelini, Alessandro Galbiati, Hannah Williams, Daryl A Ronato, Jean-Yves Masson, Eli Rothenberg,[...]. Cell Rep 2021
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ATM, ATR, and DNA-PK: The Trinity at the Heart of the DNA Damage Response.
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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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EXOSC10 is required for RPA assembly and controlled DNA end resection at DNA double-strand breaks.
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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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Small RNAs Recruit Chromatin-Modifying Enzymes MMSET and Tip60 to Reconfigure Damaged DNA upon Double-Strand Break and Facilitate Repair.
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METTL3 and N6-Methyladenosine Promote Homologous Recombination-Mediated Repair of DSBs by Modulating DNA-RNA Hybrid Accumulation.
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RNF168 ubiquitinates K13-15 on H2A/H2AX to drive DNA damage signaling.
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BRCA2 prevents R-loop accumulation and associates with TREX-2 mRNA export factor PCID2.
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RNA-templated DNA repair.
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Single-molecule imaging of transcription at damaged chromatin.
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Human senataxin resolves RNA/DNA hybrids formed at transcriptional pause sites to promote Xrn2-dependent termination.
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DNA:RNA hybrids form at DNA double-strand breaks in transcriptionally active loci.
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A damaged genome's transcriptional landscape through multilayered expression profiling around in situ-mapped DNA double-strand breaks.
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The roles of RNA in DNA double-strand break repair.
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Phase separation of 53BP1 determines liquid-like behavior of DNA repair compartments.
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DNA damage during the G0/G1 phase triggers RNA-templated, Cockayne syndrome B-dependent homologous recombination.
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Comprehensive Mapping of Histone Modifications at DNA Double-Strand Breaks Deciphers Repair Pathway Chromatin Signatures.
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DNA double-strand break repair-pathway choice in somatic mammalian cells.
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Prevalent, Dynamic, and Conserved R-Loop Structures Associate with Specific Epigenomic Signatures in Mammals.
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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.