Regulation of DNA double-strand break repair pathway choice
By M. Shrivastav, L. D. Haro, J. Nickoloff. Cell Research, 2008
1,279 citations recorded by the source corpus.
Subfields: Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/ecbff8209c36265fdbafff4292740950066fc5ce
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cell Biology
- Michael J Bozzella
- Vera Gorbunova
- Z. Mao
- Alberto Ciccia
- Andrei Seluanov
- Stephen J. Elledge
- A. Bowie
- S. Paludan
In Molecular Biology
- Jennifer A. Doudna
- Steven Lin
- Alberto Ciccia
- Michael J Bozzella
- Vera Gorbunova
- Z. Mao
- Andrei Seluanov
- Stephen J. Elledge
Citations in the corpus
- 53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks (2010, neutral): “Our data are consistent with the idea that these two DSB repair pathways compete for repair of replication-associated chromatid breaks (Saberi et al., 2007; Shrivastav et al., 2008; Sonoda et al., 2006).”
- Comparison of nonhomologous end joining and homologous recombination in human cells (2008, background): “Both DSB repair pathways play important roles in mammalian DSB repair [4,5].”
- Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery (2014, background): “Although chemical or genetic interruption of the NHEJ pathway can favor HDR (Shrivastav et al., 2008), such manipulations can be difficult to employ, harmful to cells or both.”
- The DNA Damage Response: Making it safe to play with knives (2010, background): “Interestingly, ABCDE phosphorylation, which can also be induced by ATM, has been shown to facilitate the access of DNA ends to DSB resecting enzymes in order to promote HR whenNHEJ fails (Shrivastav et al., 2008).”