Loss of MECP2 Leads to Activation of P53 and Neuronal Senescence

To determine the role for mutations of MECP2 in Rett syndrome, we generated isogenic lines of human induced pluripotent stem cells, neural progenitor cells, and neurons from patient fibroblasts with and without MECP2 expression in an attempt to recapitulate disease phenotypes in vitro. Molecular pro...

Descripción completa

Detalles Bibliográficos
Autores principales: Ohashi, Minori, Korsakova, Elena, Allen, Denise, Lee, Peiyee, Fu, Kai, Vargas, Benni S., Cinkornpumin, Jessica, Salas, Carlos, Park, Jenny C., Germanguz, Igal, Langerman, Justin, Chronis, Contantinos, Kuoy, Edward, Tran, Stephen, Xiao, Xinshu, Pellegrini, Matteo, Plath, Kathrin, Lowry, William E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995366/
https://www.ncbi.nlm.nih.gov/pubmed/29742391
http://dx.doi.org/10.1016/j.stemcr.2018.04.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995366/
https://www.ncbi.nlm.nih.gov/pubmed/29742391
http://dx.doi.org/10.1016/j.stemcr.2018.04.001

Ejemplares similares