Conserved sleep disturbances in FOXP1 syndrome originate from developmental dysregulation of peptidergic signaling

We have profiled gene expression from whole dissected brains of FoxP mutant Drosophila melanogaster. Overall design: Gene expression profiles in adult Drosophila brains were compared between FoxP mutants and their genetic background controls. 4 replicates per condition were used, each replicate was comprised of genetic material from 12 dissected fly brains.