Cargando…
Analysis of the Xenopus Werner syndrome protein in DNA double-strand break repair
Werner syndrome is associated with premature aging and increased risk of cancer. Werner syndrome protein (WRN) is a RecQ-type DNA helicase, which seems to participate in DNA replication, double-strand break (DSB) repair, and telomere maintenance; however, its exact function remains elusive. Using Xe...
Autores principales: | Yan, Hong, McCane, Jill, Toczylowski, Thomas, Chen, Chinyi |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2171202/ https://www.ncbi.nlm.nih.gov/pubmed/16247024 http://dx.doi.org/10.1083/jcb.200502077 |
Ejemplares similares
-
Replication protein A promotes 5′→3′ end processing during homology-dependent DNA double-strand break repair
por: Yan, Hong, et al.
Publicado: (2011) -
Mechanistic analysis of Xenopus EXO1's function in 5′-strand resection at DNA double-strand breaks
por: Liao, Shuren, et al.
Publicado: (2011) -
The N-terminus of RPA large subunit and its spatial position are important for the 5′->3′ resection of DNA double-strand breaks
por: Tammaro, Margaret, et al.
Publicado: (2015) -
CDK2 phosphorylation of Werner protein (WRN) contributes to WRN’s DNA double‐strand break repair pathway choice
por: Lee, Jong‐Hyuk, et al.
Publicado: (2021) -
Analysis of MRE11's function in the 5′→3′ processing of DNA double-strand breaks
por: Liao, Shuren, et al.
Publicado: (2012)