- Home
- Publications
- Publication Search
- Publication Details
Title
Persistent repair intermediates induce senescence
Authors
Keywords
-
Journal
Nature Communications
Volume 9, Issue 1, Pages -
Publisher
Springer Nature America, Inc
Online
2018-09-19
DOI
10.1038/s41467-018-06308-9
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- ATM, ATR, and DNA-PK: The Trinity at the Heart of the DNA Damage Response
- (2017) Andrew N. Blackford et al. MOLECULAR CELL
- Baculoviral delivery of CRISPR/Cas9 facilitates efficient genome editing in human cells
- (2017) Sanne Hindriksen et al. PLoS One
- Inhibition of Polo-like kinase 1 during the DNA damage response is mediated through loss of Aurora A recruitment by Bora
- (2016) W Bruinsma et al. ONCOGENE
- Hypersensitivity to DNA damage in antephase as a safeguard for genome stability
- (2016) Femke M. Feringa et al. Nature Communications
- The complexity of DNA double strand break is a crucial factor for activating ATR signaling pathway for G2/M checkpoint regulation regardless of ATM function
- (2015) Lian Xue et al. DNA REPAIR
- The same, only different - DNA damage checkpoints and their reversal throughout the cell cycle
- (2015) I. A. Shaltiel et al. JOURNAL OF CELL SCIENCE
- Nuclear translocation of Cyclin B1 marks the restriction point for terminal cell cycle exit in G2 phase
- (2014) Erik Müllers et al. CELL CYCLE
- Regulation of polo-like kinase 1 by DNA damage and PP2A/B55α
- (2014) Ling Wang et al. CELL CYCLE
- Transient Activation of p53 in G2 Phase Is Sufficient to Induce Senescence
- (2014) Lenno Krenning et al. MOLECULAR CELL
- Necessary and Sufficient Role for a Mitosis Skip in Senescence Induction
- (2014) Yoshikazu Johmura et al. MOLECULAR CELL
- Phosphorylation of EXO1 by CDKs 1 and 2 regulates DNA end resection and repair pathway choice
- (2014) Nozomi Tomimatsu et al. Nature Communications
- Gain-of-function mutations of PPM1D/Wip1 impair the p53-dependent G1 checkpoint
- (2013) Petra Kleiblova et al. JOURNAL OF CELL BIOLOGY
- DNA Damage Sensing by the ATM and ATR Kinases
- (2013) A. Marechal et al. Cold Spring Harbor Perspectives in Biology
- Controlling DNA-end resection: a new task for CDKs
- (2013) Lorenza P. Ferretti et al. Frontiers in Genetics
- Plk1 and CK2 Act in Concert to Regulate Rad51 during DNA Double Strand Break Repair
- (2012) Keiko Yata et al. MOLECULAR CELL
- The DNA Damage Response: Making It Safe to Play with Knives
- (2010) Alberto Ciccia et al. MOLECULAR CELL
- Purified human BRCA2 stimulates RAD51-mediated recombination
- (2010) Ryan B. Jensen et al. NATURE
- Wip1 confers G2 checkpoint recovery competence by counteracting p53-dependent transcriptional repression
- (2009) Arne Lindqvist et al. EMBO JOURNAL
- Distinct roles of ATR and DNA-PKcs in triggering DNA damage responses in ATM-deficient cells
- (2009) Nozomi Tomimatsu et al. EMBO REPORTS
- Single-Stranded DNA Orchestrates an ATM-to-ATR Switch at DNA Breaks
- (2009) Bunsyo Shiotani et al. MOLECULAR CELL
- The DNA-damage response in human biology and disease
- (2009) Stephen P. Jackson et al. NATURE
- ATR signaling can drive cells into senescence in the absence of DNA breaks
- (2008) L. I. Toledo et al. GENES & DEVELOPMENT
- PCNA-dependent regulation of p21 ubiquitylation and degradation via the CRL4Cdt2 ubiquitin ligase complex
- (2008) T. Abbas et al. GENES & DEVELOPMENT
- The CRL4Cdt2 ubiquitin ligase targets the degradation of p21Cip1 to control replication licensing
- (2008) Y. Kim et al. GENES & DEVELOPMENT
- CDK Inhibitor p21 Is Degraded by a Proliferating Cell Nuclear Antigen-coupled Cul4-DDB1Cdt2Pathway during S Phase and after UV Irradiation
- (2008) Hideo Nishitani et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- CDK targets Sae2 to control DNA-end resection and homologous recombination
- (2008) Pablo Huertas et al. NATURE
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search