Overview summary Although several viral vectors have been widely applied to the treatment of human disease, the development of nonviral vectors is still in their infancy. In this report, a novel cationic lipid, DMRIE/DOPE, has been incorporated into the DNA–liposome formulation that improves transfection efficiencies and allows up to 1,000-fold higher concentrations of DNA to be administered in vivo. In this paper, the safety and toxicity of this formulation is described in two species, mice and pigs, suggesting that it may prove useful for human gene therapy.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/63224/1/hum.1993.4.6-781.pd
International audiencePerformances of cationic lipid formulations for intravenous gene delivery to m...
AbstractCationic liposomes are useful to transfer genes into eukaryotic cells in vitro and in vivo. ...
Non–viral gene vectors exhibit several desirable properties, over their viral counterparts. This has...
Overview summary GAP-DLRIE/DOPE, a new cationic liposome preparation, is an efficient liposomal vect...
After a decade of clinical trials, gene therapy seems to have found its place between excessive ambi...
The clinical success of gene therapy is critically dependent on the development of efficient and saf...
AbstractWe characterized different cationic lipid-based gene delivery systems consisting of both lip...
AbstractStable complexes of cationic liposomes with plasmid DNA were prepared by (1) including a sma...
The clinical success of gene therapy is critically dependent on the development of efficient and saf...
Cellular delivery of DNA vectors for the expression of therapeutic proteins is a promising approach ...
International audienceOver the last several years, various gene delivery systems have been developed...
Gene therapy, as a promising therapeutics to treat genetic or acquired diseases, has achieved exciti...
Principle of gene therapy. Although the objectives and principles of gene therapy have been well-def...
Great expectations from the application of gene therapy approaches to human disease have been impair...
In the present study, we developed some novel gene delivery vectors, coated cationic complexes with ...
International audiencePerformances of cationic lipid formulations for intravenous gene delivery to m...
AbstractCationic liposomes are useful to transfer genes into eukaryotic cells in vitro and in vivo. ...
Non–viral gene vectors exhibit several desirable properties, over their viral counterparts. This has...
Overview summary GAP-DLRIE/DOPE, a new cationic liposome preparation, is an efficient liposomal vect...
After a decade of clinical trials, gene therapy seems to have found its place between excessive ambi...
The clinical success of gene therapy is critically dependent on the development of efficient and saf...
AbstractWe characterized different cationic lipid-based gene delivery systems consisting of both lip...
AbstractStable complexes of cationic liposomes with plasmid DNA were prepared by (1) including a sma...
The clinical success of gene therapy is critically dependent on the development of efficient and saf...
Cellular delivery of DNA vectors for the expression of therapeutic proteins is a promising approach ...
International audienceOver the last several years, various gene delivery systems have been developed...
Gene therapy, as a promising therapeutics to treat genetic or acquired diseases, has achieved exciti...
Principle of gene therapy. Although the objectives and principles of gene therapy have been well-def...
Great expectations from the application of gene therapy approaches to human disease have been impair...
In the present study, we developed some novel gene delivery vectors, coated cationic complexes with ...
International audiencePerformances of cationic lipid formulations for intravenous gene delivery to m...
AbstractCationic liposomes are useful to transfer genes into eukaryotic cells in vitro and in vivo. ...
Non–viral gene vectors exhibit several desirable properties, over their viral counterparts. This has...