Cargando…
In vivo synaptic transmission and morphology in mouse models of Tuberous sclerosis, Fragile X syndrome, Neurofibromatosis type 1, and Costello syndrome
Defects in the rat sarcoma viral oncogene homolog (Ras)/extracellular-signal-regulated kinase and the phosphatidylinositol 3-kinase-mammalian target of rapamycin (mTOR) signaling pathways are responsible for several neurodevelopmental disorders. These disorders are an important cause for intellectua...
Autores principales: | Wang, Tiantian, de Kok, Laura, Willemsen, Rob, Elgersma, Ype, Borst, J. Gerard G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4490249/ https://www.ncbi.nlm.nih.gov/pubmed/26190969 http://dx.doi.org/10.3389/fncel.2015.00234 |
Ejemplares similares
-
Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome
por: Wang, Tiantian, et al.
Publicado: (2018) -
Mechanisms underlying cognitive deficits in a mouse model for Costello Syndrome are distinct from other RASopathy mouse models
por: Schreiber, Jadwiga, et al.
Publicado: (2017) -
Autism Symptoms in Children and Young Adults With Fragile X Syndrome, Angelman Syndrome, Tuberous Sclerosis Complex, and Neurofibromatosis Type 1: A Cross-Syndrome Comparison
por: Lubbers, Kyra, et al.
Publicado: (2022) -
Anterior lenticular opacities in Costello Syndrome
por: Thakur, Anchal, et al.
Publicado: (2021) -
Rare association of Turner syndrome with neurofibromatosis type 1 and tuberous sclerosis complex
por: Suttur, Malini S., et al.
Publicado: (2009)