Molecular views of recombination proteins and their control
By S. West. Nature reviews. Molecular cell biology, 2003
1,019 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/d7e1d590524b942124349a5acf073f3bd09faa06
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Citations in the corpus
- RAD51 and Breast Cancer Susceptibility: No Evidence for Rare Variant Association in the Breast Cancer Family Registry Study (2012, background): “4) is the central protein of homologous recombination, playing the critical role of catalyzing the strand transfer between a broken sequence and its undamaged homologue in order to re-synthesize the damaged region [16].”
- Synthetic lethal targeting of PTEN mutant cells with PARP inhibitors (2009, positive): “Extending this observation, we demonstrated that PTEN mutant tumour cells also had a reduced capacity to form nuclear RAD51 foci in response to DNA damage, a surrogate marker of HR activity (West, 2003) (Fig 1B, Figs S1B and S2 of Supporting Information).”
- Concerted Loading of Mcm2-7 Double Hexamers Around DNA during DNA Replication Origin Licensing (2009, background): “This is analogous to the bacterial RuvAB Holliday junction branch migrating enzyme in which two RuvB hexamers pump double-stranded DNA through a tetramer of RuvA, which coordinates the separation and reannealing of strands (West, 2003).”
- The role of double-strand break repair — insights from human genetics (2006, methodology): “DNA synthesis using the sister strand as a template is followed by branch migration and subsequent resolution of the heteroduplex (see Ref”
- The roles of BRCA1 and BRCA2 and associated proteins in the maintenance of genomic stability (2006, background): “Other proteins implicated in assisting this process include RAD54, the RAD51 paralogues and BRCA2 (van Gent et al., 2001; West, 2003).”
- Alternative-NHEJ Is a Mechanistically Distinct Pathway of Mammalian Chromosome Break Repair (2008, background): “RAD52 can function in vitro to directly promote homologous strand annealing, and also to mediate RAD51 function during strand exchange [28].”
- RIF1 Is Essential for 53BP1-Dependent Nonhomologous End Joining and Suppression of DNA Double-Strand Break Resection (2013, background): “In contrast, HR is a largely error-free mechanism of DSB repair that is primarily active in S and G2 cell cycle phases, which requires an intact homologous duplex sequence as a repair template (West, 2003).”
- Regulation of homologous recombination in eukaryotes (2010, background): “Finally, in postsynapsis, the three subpathways of HR are distinguished (Figure 1), each with specific enzymatic requirements that have been only partially defined (69, 91, 129, 161).”