Mechanism of homologous recombination: mediators and helicases take on regulatory functions
By P. Sung, H. Klein. Nature reviews. Molecular cell biology, 2006
726 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/f29b524295e3e08cbaf469fb3d8c96abf612d3b6
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
In Oncology
Citations in the corpus
- Overexpressed of RAD51 suppresses recombination defects: a possible mechanism to reverse genomic instability (2010, background): “The proteins directly involved in the displacement of RPA are named ‘recombination mediators’ (Table 1) (10,11) (here sometimes referred to as just ‘mediators’).”
- Maintaining genome stability at the replication fork (2010, background): “These proteins do not affect FANCD2 ubiquitylation, but contribute to HR repai”
- Regulation of DNA repair throughout the cell cycle (2008, background): “Studies in budding yeast have established that HR is carried out by the products of the conserved RAD52 epistasis group of gene”
- How the fanconi anemia pathway guards the genome. (2009, background): “FANCD1, better known as BRCA2, is a recombination mediator that facilitates the formation of Rad51 nucleofilaments (134, 161).”