Cargando…
Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis
The deubiquitylating enzyme Usp9x is highly expressed in the developing mouse brain, and increased Usp9x expression enhances the self-renewal of neural progenitors in vitro. USP9X is a candidate gene for human neurodevelopmental disorders, including lissencephaly, epilepsy and X-linked intellectual...
Autores principales: | Stegeman, Shane, Jolly, Lachlan A., Premarathne, Susitha, Gecz, Jozef, Richards, Linda J., Mackay-Sim, Alan, Wood, Stephen A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702552/ https://www.ncbi.nlm.nih.gov/pubmed/23861879 http://dx.doi.org/10.1371/journal.pone.0068287 |
Ejemplares similares
-
Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors
por: Premarathne, Susitha, et al.
Publicado: (2017) -
USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors
por: Bridges, Caitlin R., et al.
Publicado: (2017) -
Usp9x-deficiency disrupts the morphological development of the postnatal hippocampal dentate gyrus
por: Oishi, Sabrina, et al.
Publicado: (2016) -
La FAM fatale: USP9X in development and disease
por: Murtaza, Mariyam, et al.
Publicado: (2015) -
Axotomy induces axonogenesis in hippocampal neurons through STAT3
por: Ohara, R, et al.
Publicado: (2011)