Conditional inactivation of individual genes in mice using site-specific recombinases is an extremely powerful method for determining the complex roles of mammalian genes in developmental and tissue-specific contexts, a major goal of post-genomic research. However, the process of generating mice with recombinase recognition sequences placed at specific locations within a gene, while maintaining a functional allele, is time consuming, expensive and technically challenging. We describe a system that combines gene trap and site-specific DNA inversion to generate mouse embryonic stem (ES) cell clones for the rapid production of conditional knockout mice, and the use of this system in an initial gene trap screen. Gene trapping should allow the s...
Because of shared physiological, anatomical and metabolical features with humans, mice have served f...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...
Gene trapping is a method of generating murine embryonic stem (ES) cell lines containing insertional...
A type of retroviral gene trap vectors has been developed that can induce conditional mutations in m...
A type of retroviral gene trap vectors has been developed that can induce conditional mutations in m...
AbstractWe have developed anin vitrogene trap screen for novel murine genes that allows one to deter...
A major challenge of the postgenomic era is the functional characterization of every single gene wi...
As little as a decade ago, generation of a single knockout mouse line was an expensive and time-cons...
A major challenge of the postgenomic era is the functional characterization of every single gene wit...
Gene targeting in ES cells is extensively used to generate designed mouse mutants and to study gene ...
Conditional gene targeting allows spatial and temporal control of genetic modifications and is used ...
AbstractThe gene trap methodology is a powerful tool to characterize novel genes and analyze their i...
Gene targeting in ES cells is extensively used to generate designed mouse mutants and to study gene ...
Gene targeting in mouse embryonic stem (ES) cells can be used to generate single gene mutations or d...
Analysis of genetically engineered mice is crucial for our understanding of the in vivo function of ...
Because of shared physiological, anatomical and metabolical features with humans, mice have served f...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...
Gene trapping is a method of generating murine embryonic stem (ES) cell lines containing insertional...
A type of retroviral gene trap vectors has been developed that can induce conditional mutations in m...
A type of retroviral gene trap vectors has been developed that can induce conditional mutations in m...
AbstractWe have developed anin vitrogene trap screen for novel murine genes that allows one to deter...
A major challenge of the postgenomic era is the functional characterization of every single gene wi...
As little as a decade ago, generation of a single knockout mouse line was an expensive and time-cons...
A major challenge of the postgenomic era is the functional characterization of every single gene wit...
Gene targeting in ES cells is extensively used to generate designed mouse mutants and to study gene ...
Conditional gene targeting allows spatial and temporal control of genetic modifications and is used ...
AbstractThe gene trap methodology is a powerful tool to characterize novel genes and analyze their i...
Gene targeting in ES cells is extensively used to generate designed mouse mutants and to study gene ...
Gene targeting in mouse embryonic stem (ES) cells can be used to generate single gene mutations or d...
Analysis of genetically engineered mice is crucial for our understanding of the in vivo function of ...
Because of shared physiological, anatomical and metabolical features with humans, mice have served f...
SummaryInduction of double-strand DNA breaks (DSBs) by engineered nucleases, such as CRISPR/Cas9 or ...
Gene trapping is a method of generating murine embryonic stem (ES) cell lines containing insertional...