Loss of p21 promoted tumorigenesis in the background of telomere dysfunctions induced by TRF2 and Wrn deficiency

Werner syndrome (WS) is a rare autosomal recessive progeria disease with genetic instability/cancer predisposition, thus a good model in understanding aging related carcinogenesis. Telomere dysfunction induced cellular senescence is essential in the manifestation of the WS phenotype. Our previous da...

Descripción completa

Detalles Bibliográficos
Autores principales: Si, Xiaoyu, Shao, Chihao, Li, Jing, Jia, Shuting, Tang, Wenru, Zhang, Jihong, Yang, Julun, Wu, Xiaoming, Luo, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821038/
https://www.ncbi.nlm.nih.gov/pubmed/29483835
http://dx.doi.org/10.7150/ijbs.23477

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821038/
https://www.ncbi.nlm.nih.gov/pubmed/29483835
http://dx.doi.org/10.7150/ijbs.23477

Ejemplares similares