The turbulent history of clinical trials in viral gene therapy has taught us important lessons about vector design and safety issues. Much effort was spent on analyzing genotoxicity after somatic integration of therapeutic DNA into the host genome. Based on these findings major improvements in vector design including the development of viral hybrid vectors for somatic integration have been achieved. This review provides a state-of-the-art overview of available hybrid vectors utilizing viruses for high transduction efficiencies in concert with various integration machineries for random and targeted integration patterns. It discusses advantages but also limitations of each vector system
<div><p>Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promi...
Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promising vec...
We recently developed adenovirus/transposase hybrid-vectors utilizing the previously described hyper...
The turbulent history of clinical trials in viral gene therapy has taught us important lessons about...
Gene therapy vectors based on the HIV-1 lentivirus are an attractive option for clinical applicatio...
We recently developed adenovirus/transposase hybrid-vectors utilizing the previously described hyper...
Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promising vec...
The concept of gene therapy was introduced with great promise and high expectations. However, what a...
The efficient delivery of therapeutic genes and appropriate gene expression are the crucial issues f...
In the last twenty-five years gene therapy has been used successfully to cure life-threatening monog...
Uncontrolled insertion of gene transfer vectors into the human genome is raising significant safety ...
Abstract: Several viruses have been engineered for gene therapy applications, and the specific prope...
Helper-dependent adenoviruses show great promise as gene delivery vectors. However, because they do ...
The use of viruses to transduce genes of interest into mammalian cells has been extremely revolution...
Gene transfer vectors derived from gamma-retroviruses or lentiviruses are currently used for the gen...
<div><p>Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promi...
Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promising vec...
We recently developed adenovirus/transposase hybrid-vectors utilizing the previously described hyper...
The turbulent history of clinical trials in viral gene therapy has taught us important lessons about...
Gene therapy vectors based on the HIV-1 lentivirus are an attractive option for clinical applicatio...
We recently developed adenovirus/transposase hybrid-vectors utilizing the previously described hyper...
Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promising vec...
The concept of gene therapy was introduced with great promise and high expectations. However, what a...
The efficient delivery of therapeutic genes and appropriate gene expression are the crucial issues f...
In the last twenty-five years gene therapy has been used successfully to cure life-threatening monog...
Uncontrolled insertion of gene transfer vectors into the human genome is raising significant safety ...
Abstract: Several viruses have been engineered for gene therapy applications, and the specific prope...
Helper-dependent adenoviruses show great promise as gene delivery vectors. However, because they do ...
The use of viruses to transduce genes of interest into mammalian cells has been extremely revolution...
Gene transfer vectors derived from gamma-retroviruses or lentiviruses are currently used for the gen...
<div><p>Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promi...
Recombinant adeno-associated viral (AAV) vectors have been shown to be one of the most promising vec...
We recently developed adenovirus/transposase hybrid-vectors utilizing the previously described hyper...