Gene transfer to the central nervous system (CNS) is complicated by the anatomic and physiologic isolation of the brain. Direct injection techniques circumvent this, and allow delivery of transgenes to specific areas of the CNS. Previously, direct transfection of cellular components of the CNS has been achieved using plasmid DNA. We report the use of cationic liposomes as a means of transfecting plasmids into adult mammalian brain. Using the gene for E. coli [beta]-galactosidase or the cDNA or human [beta]-glucuronidase as reporters, we demonstrate plasmid mediated gene transfer into the caudate putamen of adult mice with expression of the transgene for at least 21 days post-transfection.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/...
Currently in vivo gene delivery by synthetic vectors is hindered by the limited diffusibility of com...
International audienceIn vivo brain electroporation of DNA expression vectors is a widely used metho...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...
Abstract Background Chemical methods of transfection that have proven successful with cell lines oft...
International audienceBackground: Gene delivery within the central nervous system at postnatal age i...
Electroporation of non-viral plasmid DNA is a valuable tool to alter gene expression in the adult ce...
We investigated the ability of cationic liposomes composed of 1,5-dihexadecyl N-arginyl-L-glutamate ...
Neural stem cells may present an ideal route for gene therapy as well as offer new possibilities for...
AbstractThe intra-arterial injection of immortalized microglia transfected with the lacZ gene, resul...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
Genetic tools that permit functional or connectomic analysis of neuronal circuits are rapidly transf...
Cationic liposomes provide a means to introduce genes into cells both ex vivo and in vivo. In the pa...
Stable genetic modification of adult stem cells is fundamental for both developmental studies and th...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
Currently in vivo gene delivery by synthetic vectors is hindered by the limited diffusibility of com...
International audienceIn vivo brain electroporation of DNA expression vectors is a widely used metho...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...
Abstract Background Chemical methods of transfection that have proven successful with cell lines oft...
International audienceBackground: Gene delivery within the central nervous system at postnatal age i...
Electroporation of non-viral plasmid DNA is a valuable tool to alter gene expression in the adult ce...
We investigated the ability of cationic liposomes composed of 1,5-dihexadecyl N-arginyl-L-glutamate ...
Neural stem cells may present an ideal route for gene therapy as well as offer new possibilities for...
AbstractThe intra-arterial injection of immortalized microglia transfected with the lacZ gene, resul...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
Genetic tools that permit functional or connectomic analysis of neuronal circuits are rapidly transf...
Cationic liposomes provide a means to introduce genes into cells both ex vivo and in vivo. In the pa...
Stable genetic modification of adult stem cells is fundamental for both developmental studies and th...
The use of synthetic mRNA as an alternative gene delivery vector to traditional DNA-based constructs...
Currently in vivo gene delivery by synthetic vectors is hindered by the limited diffusibility of com...
International audienceIn vivo brain electroporation of DNA expression vectors is a widely used metho...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...