Artificial Self-Assembling Systems for Gene

Discusses recent advances in artificial self-assembling systems, including retrotransposon vectors, hairpin ribozymes, triple-helix-forming oligonucleotides, liposome-mediated transfection, and photonic nanostructures. Addresses developing efficient synthetic vectors such as modular self-assembling systems mimicking important features of viral vectors. Presents new developments in synthetic self-assembling gene delivery systems, including innovations in nonviral systems, targeting nucleic acids, ligand-polylysine mediated transfer, dendrimer-mediated transfection, cationic liposomes, and polylysine DNA complexes.

Synthetic Retrotransposon Vectors and Gene Targeting
A New Retroviral Vector and a New Method To Target Homologous Recombination in Mammalian Cells
Development of the Hairpin Ribozyme as aGene Therapy Approach to Human Immunodeficiency Virus Type-1 Infection
Replicating Plasmid Vectors for Cancer Gene Therapy
Gene Targeting Using Triple-Helix-Forming Oligonucleotides
Effects of Lipololysaccahrideson Liposome-Mediated Transfection and the Consequence for DNA Preparation for Gene Therapy
The Application of Electronic Pulse Delivery in Gene Therapy
Progressand Perspectives
Self-Assembling DNA Photonic Nanostructures
Controllable Gene Therapy Using Nonviral Systems
Progress in Targeting Nucleic Acids to the Liver
Advances in Receptor-Mediated Gene Transfer into Cells In Vitro and In Vivo
Ligand-Polylysine Mediated Gene Transfer
Efficient Transfer of Genetic Material into Mammalian Cells Using Polyamidoamine Dendrimers as Synthetic Vectors
Dendrimer-Mediated Transfection
The Proton Sponge
A Trick the Viruses Did Not Exploit
Biomaterials for Gene Transfer
Self-Assembling Nanostructured Aquasomes
Gene Transfer by Liposome-Entrapped Polycation-Condensed DNA
LPDI and LPDIIR
Gene Transfer into Mammalian Cells Using Synthetic Cationic Lipids
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Artificial Self-Assembling Systems for Gene Delivery

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