Cargando…
USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors
USP9X, is highly expressed in neural progenitors and, essential for neural development in mice. In humans, mutations in USP9X are associated with neurodevelopmental disorders. To understand USP9X’s role in neural progenitors, we studied the effects of altering its expression in both the human neural...
Autores principales: | Bridges, Caitlin R., Tan, Men-Chee, Premarathne, Susitha, Nanayakkara, Devathri, Bellette, Bernadette, Zencak, Dusan, Domingo, Deepti, Gecz, Jozef, Murtaza, Mariyam, Jolly, Lachlan A., Wood, Stephen A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427856/ https://www.ncbi.nlm.nih.gov/pubmed/28341829 http://dx.doi.org/10.1038/s41598-017-00149-0 |
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) -
La FAM fatale: USP9X in development and disease
por: Murtaza, Mariyam, et al.
Publicado: (2015) -
Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis
por: Stegeman, Shane, et al.
Publicado: (2013) -
Conditional Knockout of Raptor/mTORC1 Results in Dentin Malformation
por: Xie, Furong, et al.
Publicado: (2019) -
NLK phosphorylates Raptor to mediate stress-induced mTORC1 inhibition
por: Yuan, Hai-Xin, et al.
Publicado: (2015)