The development over the past decade of methods for delivering genes to mammalian cells has stimulated great interest in the possibility of treating human disease by gene-based therapies. The major aim of gene therapy is to effectively deliver the genetic materials into cells, genetically modifying and repairing cell functions, which may induce therapeutic healing of disease conditions. This review provides a critical view of gene therapy with a major focus on advanced DNA nanoparticles technologies to control the in vivo location and function of administered genes.
No takes yet. Share an insight, caveat, or question.
Hossein Hosseinkhani (2006) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: