The ability of nonviral gene delivery systems to overcome extracellular and intracellular barriers is a critical issue for future clinical applications. In recent years, several efforts were focused on the elucidation of the gene transfer mechanisms and on the development of multicomponent systems in order to improve both targeted gene delivery and transfection efficiency. The transport of the therapeutic DNA from the cytoplasm into the nucleus is an inefficient process and is considered as the major limiting step in nondividing cells. One of the strategies to improve nuclear uptake of DNA is taking advantage of the cellular nuclear import machinery. Synthetic peptides containing a nuclear localization signal (NLS) are bound to the DNA so t...
The major intracellular barriers associated with DNA delivery using nonviral vectors are inefficient...
Gene therapy provides a great hope for the treatment of many acquired and inherited life-threatening...
An interest in nuclear proteins as possible gene vectors arose as early as 1988. Nuclear proteins po...
AbstractThe cellular delivery of therapeutic agents and their localization within cells is currently...
A series of NLS sequence peptides were synthesized with a fluorescein tag and their propensities to ...
Nuclear translocation of plasmid DNA from cytoplasm is a bottleneck for efficient nonviral transfect...
The ultimate destination for most gene therapy vectors is the nucleus and nuclear import of potentia...
The generation of cell lines stably expressing recombinant material is a lengthy process and there h...
The design of non-viral vectors that efficiently deliver genetic materials into cells, in particular...
UnrestrictedNuclear transport of cell-penetrating peptides is commonly believed to be facilitated by...
AbstractThe nuclear localization signal (NLS) of the SV40 large T antigen efficiently induces nuclea...
Polylysine (pLy) has been used successfully as a DNA carrier in receptor-mediated gene transfer, enh...
Abstract Background For improved uptake of oligonucleotide-based therapy, the oligonucleotides often...
In order for peptide nucleic acids (PNAs) to be effective as therapeutic agents, methods for cellula...
AbstractUsing an in vivo assay system, nuclear import ability in individual cells was determined by ...
The major intracellular barriers associated with DNA delivery using nonviral vectors are inefficient...
Gene therapy provides a great hope for the treatment of many acquired and inherited life-threatening...
An interest in nuclear proteins as possible gene vectors arose as early as 1988. Nuclear proteins po...
AbstractThe cellular delivery of therapeutic agents and their localization within cells is currently...
A series of NLS sequence peptides were synthesized with a fluorescein tag and their propensities to ...
Nuclear translocation of plasmid DNA from cytoplasm is a bottleneck for efficient nonviral transfect...
The ultimate destination for most gene therapy vectors is the nucleus and nuclear import of potentia...
The generation of cell lines stably expressing recombinant material is a lengthy process and there h...
The design of non-viral vectors that efficiently deliver genetic materials into cells, in particular...
UnrestrictedNuclear transport of cell-penetrating peptides is commonly believed to be facilitated by...
AbstractThe nuclear localization signal (NLS) of the SV40 large T antigen efficiently induces nuclea...
Polylysine (pLy) has been used successfully as a DNA carrier in receptor-mediated gene transfer, enh...
Abstract Background For improved uptake of oligonucleotide-based therapy, the oligonucleotides often...
In order for peptide nucleic acids (PNAs) to be effective as therapeutic agents, methods for cellula...
AbstractUsing an in vivo assay system, nuclear import ability in individual cells was determined by ...
The major intracellular barriers associated with DNA delivery using nonviral vectors are inefficient...
Gene therapy provides a great hope for the treatment of many acquired and inherited life-threatening...
An interest in nuclear proteins as possible gene vectors arose as early as 1988. Nuclear proteins po...