Werner syndrome protein positively regulates XRCC4-like factor transcription

XRCC4-like factor (XLF) is involved in non-homologous end joining-mediated repair of DNA double-strand breaks (DSBs). Mutations in the WRN gene results in the development of Werner syndrome (WS), a rare autosomal recessive disorder characterized by premature ageing and genome instability. In the pre...

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Detalles Bibliográficos
Autores principales: LIU, DONGYUN, DENG, XIAOLI, YUAN, CHONGZHEN, CHEN, LIN, CONG, YUSHENG, XU, XINGZHI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020486/
https://www.ncbi.nlm.nih.gov/pubmed/24626809
http://dx.doi.org/10.3892/mmr.2014.2030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020486/
https://www.ncbi.nlm.nih.gov/pubmed/24626809
http://dx.doi.org/10.3892/mmr.2014.2030

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