Catalytically inactive CRISPR-associated 9 nuclease (dCas9) can be directed by short guide RNAs (gRNAs) to repress endogenous genes in bacteria and human cells. Here we show that a dCas9-VP64 transcriptional activation domain fusion protein can be directed by single or multiple gRNAs to increase expression of specific endogenous human genes. These results provide an important proof-of-principle that CRISPR-Cas systems can be used to target heterologous effector domains in human cells
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
While the catalog of mammalian transcripts and their expression levels in different cell types and d...
We develop an in vivo library-on-library methodology to simultaneously assess single guide RNA (sgRN...
Catalytically inactive CRISPR-associated 9 nuclease (dCas9) can be directed by short guide RNAs (gRN...
CRISPR RNA-guided endonucleases (RGENs) have rapidly emerged as a facile and efficient platform for ...
The Cas9 protein from the Streptococcus pyogenes CRISPR-Cas immune system has been adapted for both ...
Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) systems h...
CRISPR-Cas systems have been used with single-guide RNAs for accurate gene disruption and conversion...
The CRISPR/Cas9 system has been implemented in a variety of model organisms to mediate site-directed...
The bacteria-derived clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems a...
Gain-of-function studies often require the tedious cloning of transgene cDNA into vectors for overex...
CRISPR/Cas9 protein fused to transactivation domains can be used to control gene expression in human...
CRISPR/Cas9 protein fused to transactivation domains can be used to control gene expression in human...
SummaryThe genetic interrogation and reprogramming of cells requires methods for robust and precise ...
The bacteria-derived clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems a...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
While the catalog of mammalian transcripts and their expression levels in different cell types and d...
We develop an in vivo library-on-library methodology to simultaneously assess single guide RNA (sgRN...
Catalytically inactive CRISPR-associated 9 nuclease (dCas9) can be directed by short guide RNAs (gRN...
CRISPR RNA-guided endonucleases (RGENs) have rapidly emerged as a facile and efficient platform for ...
The Cas9 protein from the Streptococcus pyogenes CRISPR-Cas immune system has been adapted for both ...
Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) systems h...
CRISPR-Cas systems have been used with single-guide RNAs for accurate gene disruption and conversion...
The CRISPR/Cas9 system has been implemented in a variety of model organisms to mediate site-directed...
The bacteria-derived clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems a...
Gain-of-function studies often require the tedious cloning of transgene cDNA into vectors for overex...
CRISPR/Cas9 protein fused to transactivation domains can be used to control gene expression in human...
CRISPR/Cas9 protein fused to transactivation domains can be used to control gene expression in human...
SummaryThe genetic interrogation and reprogramming of cells requires methods for robust and precise ...
The bacteria-derived clustered regularly interspaced short palindromic repeat (CRISPR)-Cas systems a...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
While the catalog of mammalian transcripts and their expression levels in different cell types and d...
We develop an in vivo library-on-library methodology to simultaneously assess single guide RNA (sgRN...