Cargando…
Risperidone Mitigates Enhanced Excitatory Neuronal Function and Repetitive Behavior Caused by an ASD-Associated Mutation of SIK1
Six mutations in the salt-inducible kinase 1 (SIK1)-coding gene have been identified in patients with early infantile epileptic encephalopathy (EIEE-30) accompanied by autistic symptoms. Two of the mutations are non-sense mutations that truncate the C-terminal region of SIK1. It has been shown that...
Autores principales: | Badawi, Moataz, Mori, Takuma, Kurihara, Taiga, Yoshizawa, Takahiro, Nohara, Katsuhiro, Kouyama-Suzuki, Emi, Yanagawa, Toru, Shirai, Yoshinori, Tabuchi, Katsuhiko |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289890/ https://www.ncbi.nlm.nih.gov/pubmed/34295222 http://dx.doi.org/10.3389/fnmol.2021.706494 |
Ejemplares similares
-
An Epilepsy-Associated Mutation of Salt-Inducible Kinase 1 Increases the Susceptibility to Epileptic Seizures and Interferes with Adrenocorticotropic Hormone Therapy for Infantile Spasms in Mice
por: Pang, Bo, et al.
Publicado: (2022) -
Correction: Deficiency of calcium/calmodulin-dependent serine protein kinase disrupts the excitatory-inhibitory balance of synapses by downregulating GluN2B
por: Mori, Takuma, et al.
Publicado: (2019) -
Deficiency of calcium/calmodulin-dependent serine protein kinase disrupts the excitatory-inhibitory balance of synapses by down-regulating GluN2B
por: Mori, Takuma, et al.
Publicado: (2019) -
IQSEC2 Deficiency Results in Abnormal Social Behaviors Relevant to Autism by Affecting Functions of Neural Circuits in the Medial Prefrontal Cortex
por: Mehta, Anuradha, et al.
Publicado: (2021) -
Structural Analysis Implicates CASK-Liprin-α2 Interaction in Cerebellar Granular Cell Death in MICPCH Syndrome
por: Guo, Qi, et al.
Publicado: (2023)