Uses of viral vectors have thus far eclipsed uses of non-viral vectors for gene therapy delivery in the clinic. Viral vectors, however, have certain issues involving genome integration, the inability to be delivered repeatedly, and possible host rejection. Fortunately, development of non-viral DNA vectors has progressed steadily, especially in plasmid vector length reduction, now allowing these tools to fill in specifically where viral or other non-viral vectors may not be the best options. In this review, we examine the improvements made to non-viral DNA gene therapy vectors, highlight opportunities for their further development, address therapeutic needs for which their use is the logical choice, and discuss their future expansion into t...
Gene therapy is the transfer of genetic material to cure a disease or at least to improve the clinic...
www.tcrt.org Gene therapy as part of modern molecular medicine holds great promise for the treatment...
Adverse events in using viral-based vectors to deliver and integrate therapeutic DNA into patients i...
Uses of viral vectors have thus far eclipsed uses of non-viral vectors for gene therapy delivery in ...
Efficient delivery of genetic material into cells is a critical process to translate gene therapy in...
Gene therapy and its promise for treating human diseases has been around for over two decades, yet a...
Medical research continues to illuminate the origins of many human diseases. Gene therapy has been w...
Although the development of effective viral vectors put gene therapy on the road to commercializatio...
International audienceGene therapy offers important perspectives in current and future medicine but ...
Introduction: This review presents recent developments in the use of nonviral vectors and transfer t...
Cancers are generally treated by radiotherapy, chemotherapy and radical surgery alone, or combinatio...
Gene therapy requires efficient vectors for delivering therapeutic genes. Advances in developments o...
The many platform and poster presentations at the last annual meeting of the American Society for Ge...
The research and development of non-viral gene therapy has been extensive over the past decade and h...
Abstract: Several viruses have been engineered for gene therapy applications, and the specific prope...
Gene therapy is the transfer of genetic material to cure a disease or at least to improve the clinic...
www.tcrt.org Gene therapy as part of modern molecular medicine holds great promise for the treatment...
Adverse events in using viral-based vectors to deliver and integrate therapeutic DNA into patients i...
Uses of viral vectors have thus far eclipsed uses of non-viral vectors for gene therapy delivery in ...
Efficient delivery of genetic material into cells is a critical process to translate gene therapy in...
Gene therapy and its promise for treating human diseases has been around for over two decades, yet a...
Medical research continues to illuminate the origins of many human diseases. Gene therapy has been w...
Although the development of effective viral vectors put gene therapy on the road to commercializatio...
International audienceGene therapy offers important perspectives in current and future medicine but ...
Introduction: This review presents recent developments in the use of nonviral vectors and transfer t...
Cancers are generally treated by radiotherapy, chemotherapy and radical surgery alone, or combinatio...
Gene therapy requires efficient vectors for delivering therapeutic genes. Advances in developments o...
The many platform and poster presentations at the last annual meeting of the American Society for Ge...
The research and development of non-viral gene therapy has been extensive over the past decade and h...
Abstract: Several viruses have been engineered for gene therapy applications, and the specific prope...
Gene therapy is the transfer of genetic material to cure a disease or at least to improve the clinic...
www.tcrt.org Gene therapy as part of modern molecular medicine holds great promise for the treatment...
Adverse events in using viral-based vectors to deliver and integrate therapeutic DNA into patients i...