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Title
Regulatory control of DNA end resection by Sae2 phosphorylation
Authors
Keywords
-
Journal
Nature Communications
Volume 9, Issue 1, Pages -
Publisher
Springer Nature America, Inc
Online
2018-09-25
DOI
10.1038/s41467-018-06417-5
References
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Related references
Note: Only part of the references are listed.- Main steps in DNA double-strand break repair: an introduction to homologous recombination and related processes
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- Plasticity of the Mre11–Rad50–Xrs2–Sae2 nuclease ensemble in the processing of DNA-bound obstacles
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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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- Xrs2 Dependent and Independent Functions of the Mre11-Rad50 Complex
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- Nbs1 Converts the Human Mre11/Rad50 Nuclease Complex into an Endo/Exonuclease Machine Specific for Protein-DNA Adducts
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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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- Regulation of Recombination and Genomic Maintenance
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- CDK targets Sae2 to control DNA-end resection and homologous recombination
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