Impaired regulation of KCC2 phosphorylation leads to neuronal network dysfunction and neurodevelopmental pathology.
Research Articles
Altered sleep architecture, rapid eye movement sleep, and neural oscillation in a mouse model of human chromosome 16p11.2 microdeletion.
Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency.
Developmental trajectories of infants with multiplex family risk for autism: A Baby Siblings Research Consortium study.
Engineering of human brain organoids with a functional vascular-like system.
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission.
Aberrant somatosensory processing and connectivity in mice lacking Engrailed-2.
The knockout of Synapsin II in mice impairs social behavior and functional connectivity generating an ASD-like phenotype.
A GluN2B mutation identified in autism prevents NMDA receptor trafficking and interferes with dendrite growth.
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