Cargando…
Progress toward therapeutic potential for AFQ056 in Fragile X syndrome
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the leading single-gene cause of autism. It is caused by the lack of production of the Fragile X mental retardation protein (FMRP), resulting in cognitive deficits, hyperactivity, and autistic behaviors. Breakt...
Autores principales: | Sourial, Mary, Cheng, Connie, Doering, Laurie C |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4863540/ https://www.ncbi.nlm.nih.gov/pubmed/27186135 http://dx.doi.org/10.2147/JEP.S27044 |
Ejemplares similares
-
Astrocytes and Developmental Plasticity in Fragile X
por: Cheng, Connie, et al.
Publicado: (2012) -
Mavoglurant (AFQ056) for the treatment of levodopa-induced dyskinesia in patients with Parkinson’s disease: a meta-analysis
por: Negida, Ahmed, et al.
Publicado: (2021) -
Astrocyte-Secreted Factors Selectively Alter Neural Stem and Progenitor Cell Proliferation in the Fragile X Mouse
por: Sourial, Mary, et al.
Publicado: (2016) -
The mGluR5 antagonist AFQ056 does not affect methylation and transcription of the mutant FMR1 gene in vitro
por: Tabolacci, Elisabetta, et al.
Publicado: (2012) -
Astrocyte-secreted thrombospondin-1 modulates synapse and spine defects in the fragile X mouse model
por: Cheng, Connie, et al.
Publicado: (2016)