Cargando…
Proteomic Analysis of Post-synaptic Density Fractions from Shank3 Mutant Mice Reveals Brain Region Specific Changes Relevant to Autism Spectrum Disorder
Disruption of the human SHANK3 gene can cause several neuropsychiatric disease entities including Phelan-McDermid syndrome, autism spectrum disorder (ASD), and intellectual disability. Although, a wide array of neurobiological studies strongly supports a major role for SHANK3 in organizing the post-...
Autores principales: | Reim, Dominik, Distler, Ute, Halbedl, Sonja, Verpelli, Chiara, Sala, Carlo, Bockmann, Juergen, Tenzer, Stefan, Boeckers, Tobias M., Schmeisser, Michael J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5306440/ https://www.ncbi.nlm.nih.gov/pubmed/28261056 http://dx.doi.org/10.3389/fnmol.2017.00026 |
Ejemplares similares
-
Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus
por: Heise, Christopher, et al.
Publicado: (2016) -
The Shank3 Interaction Partner ProSAPiP1 Regulates Postsynaptic SPAR Levels and the Maturation of Dendritic Spines in Hippocampal Neurons
por: Reim, Dominik, et al.
Publicado: (2016) -
Deletion of the Autism-Associated Protein SHANK3 Abolishes Structural Synaptic Plasticity after Brain Trauma
por: Urrutia-Ruiz, Carolina, et al.
Publicado: (2022) -
Shank2/3 double knockout-based screening of cortical subregions links the retrosplenial area to the loss of social memory in autism spectrum disorders
por: Garrido, Débora, et al.
Publicado: (2022) -
Pharmacological enhancement of mGlu5 receptors rescues behavioral
deficits in SHANK3 knock-out mice
por: Vicidomini, Cinzia, et al.
Publicado: (2016)