<div><p>The generation of specific mutant animal models is critical for functional analysis of human genes. The conventional gene targeting approach in embryonic stem cells (ESCs) by homologous recombination is however laborious, slow, expensive, and limited to species with functional ESCs. It is therefore a long-sought goal to develop an efficient and simple alternative gene targeting strategy. Here we demonstrate that, by combining an efficient ZFN pair and ssODN, a restriction site and a loxP site were successfully introduced into a specific genomic locus. A targeting efficiency up to 22.22% was achieved by coinciding the insertion site and the ZFN cleavage site isogenic and keeping the length of the homology arms equal and isogenic to t...
Gene engineering for generating targeted mouse mutants is a key technology for biomedical research. ...
Targeted gene mutation in the mouse is a primary strategy to understand gene function and relation t...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...
The generation of specific mutant animal models is critical for functional analysis of human genes. ...
The generation of specific mutant animal models is critical for functional analysis of human genes. ...
Gene targeting by homologous recombination in embryonic stem cells is extensively used to generate s...
<div><p>Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms an...
Gene knockout in murine embryonic stem cells (ESCs) has been an invaluable tool to study gene functi...
Single stranded oligodeoxynucleotide (ssODN) gene targeting may facilitate animal model creation and...
Single stranded oligodeoxynucleotide (ssODN) gene targeting may facilitate animal model creation and...
Gene knockout in murine embryonic stem cells (ESCs) has been an invaluable tool to study gene functi...
SummaryWe report here homologous recombination (HR)-mediated gene targeting of two different genes i...
The CRISPR/Cas9 system has rapidly advanced targeted genome editing technologies. However, its effic...
Targeted gene mutation in the mouse is a primary strategy to understand gene function and relation t...
The CRISPR/Cas9 system has rapidly advanced targeted genome editing technologies. However, its effic...
Gene engineering for generating targeted mouse mutants is a key technology for biomedical research. ...
Targeted gene mutation in the mouse is a primary strategy to understand gene function and relation t...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...
The generation of specific mutant animal models is critical for functional analysis of human genes. ...
The generation of specific mutant animal models is critical for functional analysis of human genes. ...
Gene targeting by homologous recombination in embryonic stem cells is extensively used to generate s...
<div><p>Zinc finger nucleases (ZFNs) enable precise genome modification in a variety of organisms an...
Gene knockout in murine embryonic stem cells (ESCs) has been an invaluable tool to study gene functi...
Single stranded oligodeoxynucleotide (ssODN) gene targeting may facilitate animal model creation and...
Single stranded oligodeoxynucleotide (ssODN) gene targeting may facilitate animal model creation and...
Gene knockout in murine embryonic stem cells (ESCs) has been an invaluable tool to study gene functi...
SummaryWe report here homologous recombination (HR)-mediated gene targeting of two different genes i...
The CRISPR/Cas9 system has rapidly advanced targeted genome editing technologies. However, its effic...
Targeted gene mutation in the mouse is a primary strategy to understand gene function and relation t...
The CRISPR/Cas9 system has rapidly advanced targeted genome editing technologies. However, its effic...
Gene engineering for generating targeted mouse mutants is a key technology for biomedical research. ...
Targeted gene mutation in the mouse is a primary strategy to understand gene function and relation t...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...