Synthetic gene delivery vehicles have made significant progress in the past decade in demonstrating strong potential for targeted delivery to specific cells, low toxicity and immunogenicity, and large carrying capacity. However, significant advances must still be made to increase the efficiency of both polymer and lipid vehicles. Furthermore, techniques to generate more effective targeting moieties for a variety of cell types, as well as means to consistently assemble vectors containing these targeting ligands, are areas for further improvement. This review focuses on significant recent advances in generating a number of novel targeted vectors, and discusses progress in the development of new genetic and chemical systems to enhance the targ...
International audienceOver the last several years, various gene delivery systems have been developed...
Gene therapy, because of its aim to eradicate the causes rather than the symptoms of diseases, is be...
Gene delivery is the science of transferring genetic material into cells by means of a vector to alt...
Gene therapy is emerging as a revolutionary alternative to conventional therapeutic approaches. Howe...
Abstract Background Gene delivery systems are essentially necessary for the gene therapy of human ge...
© 2016, Human Stem Cell Institute. All rights reserved.For effective transfection of the eukaryotic ...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
International audienceNucleic acid delivery constitutes an emerging therapeutic strategy to cure var...
Gene therapy has the potential to treat both acquired and inherited genetic diseases. Generally, two...
Nonviral vectors which offer a safer and versatile alternative to viral vectors have been developed ...
Three recent approvals and over 100 ongoing clinical trials make adeno‐associated virus (AAV)‐based ...
Genetic vaccines offer a treatment opportunity based upon successful gene delivery to specific immun...
Non–viral gene vectors exhibit several desirable properties, over their viral counterparts. This has...
International audienceInitially, gene therapy was viewed as an approach for treating hereditary dise...
Lack of selectivity together with severe side effects in conventional cancer treatment have afforded...
International audienceOver the last several years, various gene delivery systems have been developed...
Gene therapy, because of its aim to eradicate the causes rather than the symptoms of diseases, is be...
Gene delivery is the science of transferring genetic material into cells by means of a vector to alt...
Gene therapy is emerging as a revolutionary alternative to conventional therapeutic approaches. Howe...
Abstract Background Gene delivery systems are essentially necessary for the gene therapy of human ge...
© 2016, Human Stem Cell Institute. All rights reserved.For effective transfection of the eukaryotic ...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
International audienceNucleic acid delivery constitutes an emerging therapeutic strategy to cure var...
Gene therapy has the potential to treat both acquired and inherited genetic diseases. Generally, two...
Nonviral vectors which offer a safer and versatile alternative to viral vectors have been developed ...
Three recent approvals and over 100 ongoing clinical trials make adeno‐associated virus (AAV)‐based ...
Genetic vaccines offer a treatment opportunity based upon successful gene delivery to specific immun...
Non–viral gene vectors exhibit several desirable properties, over their viral counterparts. This has...
International audienceInitially, gene therapy was viewed as an approach for treating hereditary dise...
Lack of selectivity together with severe side effects in conventional cancer treatment have afforded...
International audienceOver the last several years, various gene delivery systems have been developed...
Gene therapy, because of its aim to eradicate the causes rather than the symptoms of diseases, is be...
Gene delivery is the science of transferring genetic material into cells by means of a vector to alt...