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Times Cited: 125
Times Cited
Times Co-cited
Similarity
A role for small RNAs in DNA double-strand break repair.
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Site-specific DICER and DROSHA RNA products control the DNA-damage response.
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DICER, DROSHA and DNA damage response RNAs are necessary for the secondary recruitment of DNA damage response factors.
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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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BRCA2 controls DNA:RNA hybrid level at DSBs by mediating RNase H2 recruitment.
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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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ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
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