“…The virus-mediated insertion of foreign DNA into a target cell ultimately creates chimeric products which are able to perform a tailored interaction with their targets therefore fulfilling the therapeutic action. Although viral transduction techniques have been the most frequently employed gene carriers, plasmid transfection techniques involving liposome nanoparticle-mediated delivery of circular DNA, have also been recently reported [137, 138, 139, 140]. Gene modification technologies have been widely employed in hematology [141, 142, 143], oncology [14, 144, 145, 146], and more recently in neurology, as well [147, 148, 149].…”