To improve the nuclear-targeted delivery of non-viral vectors, extensive effort has been carried out on the development of smart vectors which could overcome multiple barriers. The nuclear envelope presents a major barrier to transgene delivery. Viruses are capable of crossing the nuclear envelope to efficiently deliver their genome into the nucleus through the specialized protein components. However, non-viral vectors are preferred over viral ones because of the safety concerns associated with the latter. Non-viral delivery systems have been designed to include various types of components to enable nuclear translocation at the periphery of the nucleus. This review summarizes the progress of research regarding nuclear transport mechanisms. ...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
Several advances in non-viral gene transfer technology have been reported over the past year. Cation...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
To improve the nuclear-targeted delivery of non-viral vectors, extensive effort has been carried out...
Non-viral gene therapy vectors have not yet achieved the gene transfer efficiency of viral vectors b...
Gene therapy, the expression in cells of genetic material that has therapeutic activity, holds great...
Gene delivery vectors must deliver their cargoes into the cytosol or the nucleus, where DNA or siRNA...
Gene therapy utilizes genetic material in order to cure patients either by DNA vaccines or by replac...
Gene delivery is the science of transferring genetic material into cells by means of a vector to alt...
The aim of gene therapy is to treat, cure or prevent a disease by replacing defective genes, introdu...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
Nucleus, as the machinery for genome transcription, play prominent roles to support the fundamental ...
Delivery of genes, including plasmid DNAs, short interfering RNAs (siRNAs), and messenger RNAs (mRNA...
Delivery of transgenic DNA into mammalian cells is critical to realizing the potential of synthetic ...
The promise of cancer gene therapeutics is hampered by difficulties in the in vivo delivery to the t...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
Several advances in non-viral gene transfer technology have been reported over the past year. Cation...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
To improve the nuclear-targeted delivery of non-viral vectors, extensive effort has been carried out...
Non-viral gene therapy vectors have not yet achieved the gene transfer efficiency of viral vectors b...
Gene therapy, the expression in cells of genetic material that has therapeutic activity, holds great...
Gene delivery vectors must deliver their cargoes into the cytosol or the nucleus, where DNA or siRNA...
Gene therapy utilizes genetic material in order to cure patients either by DNA vaccines or by replac...
Gene delivery is the science of transferring genetic material into cells by means of a vector to alt...
The aim of gene therapy is to treat, cure or prevent a disease by replacing defective genes, introdu...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
Nucleus, as the machinery for genome transcription, play prominent roles to support the fundamental ...
Delivery of genes, including plasmid DNAs, short interfering RNAs (siRNAs), and messenger RNAs (mRNA...
Delivery of transgenic DNA into mammalian cells is critical to realizing the potential of synthetic ...
The promise of cancer gene therapeutics is hampered by difficulties in the in vivo delivery to the t...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...
Several advances in non-viral gene transfer technology have been reported over the past year. Cation...
Gene delivery is the transfer of genetic material into recipient cells to alter some functions. As t...