Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/92052/files/pdf
Reference75 articles.
1. Modeling Autism by SHANK Gene Mutations in Mice
2. Proline-Rich Synapse-Associated Proteins ProSAP1 and ProSAP2 Interact with Synaptic Proteins of the SAPAP/GKAP Family
3. SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism
4. Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation
5. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
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1. Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions;Nature Communications;2024-08-09
2. Probing cognitive flexibility in Shank2-deficient mice: Effects of D-cycloserine and NMDAR signaling hub dynamics;Progress in Neuro-Psychopharmacology and Biological Psychiatry;2024-08
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