The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Replication protein A: directing traffic at the intersection of replication and repair
Open accessAbstract
Since the initial discovery of replication protein A (RPA) as a DNA replication factor, much progress has been made on elucidating critical roles for RPA in other DNA metabolic pathways. RPA has been shown to be required for DNA replication, DNA repair, DNA recombination, and the DNA damage response pathway with roles in checkpoint activation. This review summarizes the current understanding of RPA structure, phosphorylation and protein-protein interactions in mediating these DNA metabolic processes.
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Cites
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“This interaction is completely abolished with the mutant rfa-t11 protein indicating that RPA17 also binds to the N-terminus of RPA1 (98).”
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“Indeed, Mre11 and Rad9 interactions with RPA increase when RPA2 is phosphorylated (106, 107).”
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Cited by
Rad51-mediated replication fork reversal is a global response to genotoxic treatments in human cells
Zellweger, R., Dalcher, D., Mutreja, K., Berti, M., Schmid, J. A., Herrador, R., Vindigni, A., & Lopes, M. (2015) · Journal of Cell Biology · doi:10.1083/jcb.201406099 · Cited by 677
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Hsp90: A New Player in DNA Repair?
Pennisi, R., Ascenzi, P., & Di Masi, A. (2015) · Biomolecules · doi:10.3390/biom5042589 · Cited by 112
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Metadata
- Authors
- Oakley, G.
- Venue
- Frontiers in Bioscience
- Publisher
- IMR Press
- Published
- 2010
- Volume
- 15
- Issue
- 1
- Pages
- 883
- ISSN
- 1093-4715 (ISSN-L)
- 1093-9946
- DOI
- 10.2741/3652
- OpenAlex
- W1585519565
- Cited by
- 185
- References
- 18
- FWCI
- 4.49
- Type
- journal article
- Language
- en
- Open access
- bronze
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