Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11. 2 hemideletion
VJ Kumar, NM Grissom, SE McKee, H Schoch… - Translational …, 2018 - nature.com
Neurodevelopmental disorders, such as ASD and ADHD, affect males about three to four
times more often than females. 16p11. 2 hemideletion is a copy number variation that is …
times more often than females. 16p11. 2 hemideletion is a copy number variation that is …
Major vault protein, a candidate gene in 16p11. 2 microdeletion syndrome, is required for the homeostatic regulation of visual cortical plasticity
Microdeletion of a region in chromosome 16p11. 2 increases susceptibility to autism.
Although this region contains exons of 29 genes, disrupting only a small segment of the …
Although this region contains exons of 29 genes, disrupting only a small segment of the …
EGF regulates the interaction of Tks4 with Src through its SH2 and SH3 domains
The nonreceptor tyrosine kinase Src is a central component of the epidermal growth factor
(EGF) signaling pathway. Our group recently showed that the Frank-ter Haar syndrome …
(EGF) signaling pathway. Our group recently showed that the Frank-ter Haar syndrome …
Characterizing the hippocampal synaptic and sleep abnormalities of a mouse model of human chromosome 16P11. 2 Microdeletion
HC Lu - 2018 - search.proquest.com
The pathophysiology of neurodevelopmental disorders is often observed early in infancy
and toddlerhood. Mouse models of syndromic disorders have provided insight regarding …
and toddlerhood. Mouse models of syndromic disorders have provided insight regarding …