Significant progress has been made in the development of different types of nucleic acids, including plasmid DNA, siRNA and oligonucleotides with the potential to form the basis of new treatment options for genetic and acquired diseases. However, the lack of suitable vectors for efficient delivery of nucleic acids into target cells represents a major hurdle for the successful application of gene therapy.
CITATION STYLE
Faneca, H., Cardoso, A. L., Trabulo, S., Duarte, S., & de Lima, M. C. P. (2013). Cationic Liposome-Based Systems for Nucleic Acid Delivery: From the Formulation Development to Therapeutic Applications (pp. 153–184). https://doi.org/10.1007/978-94-007-6010-3_6
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