Regional, layer, and cell-type-specific connectivity of the mouse default mode network.
CHD8 mutation leads to autistic-like behaviors and impaired striatal circuits.
CRISPR-CAS9 knockin mice for genome editing and cancer modeling.
Mice with Shank3 mutations associated with ASD and schizophrenia display both shared and distinct defects.
Homozygous loss of autism-risk gene CNTNAP2 results in reduced local and long-range prefrontal functional connectivity.
Can mouse imaging studies bring order to autism connectivity chaos?
Functional connectivity hubs of the mouse brain.
Autism-associated 16p11.2 microdeletion impairs prefrontal functional connectivity in mouse and human.
Deletion of autism risk gene Shank3 disrupts prefrontal connectivity.
Rbfox splicing factors promote neuronal maturation and axon initial segment assembly
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