Impaired perceptual learning in a mouse model of fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.
Research Articles
Biallelic variants in VARS in a family with two siblings with intellectual disability and microcephaly: Case report and review of the literature.
CLIP and massively parallel functional analysis of CELF6 reveal a role in destabilizing synaptic gene mRNAs through interaction with 3′ UTR elements.
Altered neocortical gene expression, brain overgrowth and functional over-connectivity in Chd8 haploinsufficient mice.
Adult Ube3a gene reinstatement restores the electrophysiological deficits of prefrontal cortex layer 5 neurons in a mouse model of Angelman syndrome.
Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk.
5-hydroxymethylcytosine alterations in the human postmortem brains of autism spectrum disorder.
Altered dendritic spine function and integration in a mouse model of fragile X syndrome.
The microglial innate immune receptor TREM2 is required for synapse elimination and normal brain connectivity.
5-HT release in nucleus accumbens rescues social deficits in mouse autism model.
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