We describe a novel generation of lentiviral vectors that are particularly well suited for work with embryonic stem cells. The possibility of selecting cell lines with antibiotics and the rapid insertion of any combination of promoters and genes of interest makes them a powerful tool in the generation of transgenic ES cell lines. This vector can also greatly facilitate studies aimed at the improvement of neuronal engineering from ES cells, by making it possible to monitor the emergence and differentiation of neurons
Transplantation of neural cells engineered to produce growth factors or molecules with antitumor eff...
The identification of stem cells within a mixed population of cells is a major hurdle for stem cell ...
In this study, we have used a microRNA-regulated lentiviral reporter system to visualize and segrega...
We describe a novel generation of lentiviral vectors that are particularly well suited for work with...
The derivation of neural lineages from human embryonic stem cells (hESCs) in vitro is based largely ...
Generation of stable transgenic embryonic stem (ES) cell lines by classic transfection is still a di...
The implantation of genetically modified cells is considered for the chronic delivery of therapeutic...
Ce travail de thèse a été consacré à la transgenèse et la différenciation neuronale des cellules sou...
Lentiviral vectors are promising tools for the development of gene therapy since they can transduce ...
<div><p>The identification of stem cells within a mixed population of cells is a major hurdle for st...
Neural stem cells may present an ideal route for gene therapy as well as offer new possibilities for...
This report describes a technique for the generation of transgenic mice by in vivo manipulation of s...
The use of gene mutation/knock-out strategies in mouse embryonic stem (ES) cells has revolutionized ...
SummaryUnraveling the therapeutic potential of human embryonic stem cells (hESC) requires tools to m...
Transgenic manipulation of exogenous and endogenous gene expression in human embryonic stem cells (h...
Transplantation of neural cells engineered to produce growth factors or molecules with antitumor eff...
The identification of stem cells within a mixed population of cells is a major hurdle for stem cell ...
In this study, we have used a microRNA-regulated lentiviral reporter system to visualize and segrega...
We describe a novel generation of lentiviral vectors that are particularly well suited for work with...
The derivation of neural lineages from human embryonic stem cells (hESCs) in vitro is based largely ...
Generation of stable transgenic embryonic stem (ES) cell lines by classic transfection is still a di...
The implantation of genetically modified cells is considered for the chronic delivery of therapeutic...
Ce travail de thèse a été consacré à la transgenèse et la différenciation neuronale des cellules sou...
Lentiviral vectors are promising tools for the development of gene therapy since they can transduce ...
<div><p>The identification of stem cells within a mixed population of cells is a major hurdle for st...
Neural stem cells may present an ideal route for gene therapy as well as offer new possibilities for...
This report describes a technique for the generation of transgenic mice by in vivo manipulation of s...
The use of gene mutation/knock-out strategies in mouse embryonic stem (ES) cells has revolutionized ...
SummaryUnraveling the therapeutic potential of human embryonic stem cells (hESC) requires tools to m...
Transgenic manipulation of exogenous and endogenous gene expression in human embryonic stem cells (h...
Transplantation of neural cells engineered to produce growth factors or molecules with antitumor eff...
The identification of stem cells within a mixed population of cells is a major hurdle for stem cell ...
In this study, we have used a microRNA-regulated lentiviral reporter system to visualize and segrega...