Zhu Zhu, Woo-Hyun Chung, Eun Yong Shim, Sang Eun Lee, Grzegorz Ira. Cell 2008
Times Cited: 759
Times Cited: 759
Times Cited
Times Co-cited
Similarity
Sae2, Exo1 and Sgs1 collaborate in DNA double-strand break processing.
Eleni P Mimitou, Lorraine S Symington. Nature 2008
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DNA end resection by Dna2-Sgs1-RPA and its stimulation by Top3-Rmi1 and Mre11-Rad50-Xrs2.
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Human CtIP promotes DNA end resection.
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DNA double-strand break repair pathway choice is directed by distinct MRE11 nuclease activities.
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Physiological protein blocks direct the Mre11-Rad50-Xrs2 and Sae2 nuclease complex to initiate DNA end resection.
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Phosphorylated CtIP Functions as a Co-factor of the MRE11-RAD50-NBS1 Endonuclease in DNA End Resection.
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Saccharomyces Ku70, mre11/rad50 and RPA proteins regulate adaptation to G2/M arrest after DNA damage.
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The motor activity of DNA2 functions as an ssDNA translocase to promote DNA end resection.
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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.