BANF1 and Dravet syndrome: Further, global transcriptomic analysis of late-phase human DS cells revealed widespread differences concerning isogenic euploid cells with increased expression of genes that encourage entry into and maintenance of cells in the S-phase, upregulation of the Notch, Wnt, and Interferon pathways, and upregulation of REST. In contrast, there was downregulation of the expression of genes whose products are involved in chromatin remodeling, including components of the BAF complex.