(A) Scheme of DNA elements tested indicating the location of the STAT binding sites. The sna-rg R2 reporter comprises the cis-regulatory sequence deleted in the CRISPR-Cas9 snaΔrgR2 mutation. Expression at st11 of the full sna-rg-GFP (B), sna-rg R1-GFP (C), sna-rg R2-GFP (D), and sna-rg R2P2-GFP (E) constructs. (F) Scheme showing the fragment deleted in the snaΔrgR2 mutation indicating the sequence of the sgRNAs used and the sequences flanking the deletion. (TIF)</p
Summary: Cas9 nucleases can be programmed with single guide RNAs (sgRNAs) to mediate gene editing. H...
International audienceAnalysis of CRISPR-SaCas9 Off-Targets In order to verify whether SaCas9 and sg...
<p>(A) Schematic of the strategy for the <i>ssnA</i> gene deletion in the SS2 GD01 strain via double...
(A) Representation of the minimal sna-rg R2P2 subfragments indicating the location of the putative S...
Loss-of-function experiments are essential for the functional investigation of cis-regulatory elemen...
A schematic of the snai2 gene displays where the three guide RNAs (gRNAs) were designed for CRISPR/C...
<p>(<b>A</b>) Schematic illustration of the CRISPR/Cas system. The guide RNA (gRNA) binds to the 20-...
<p>The number of times a particular nt was found to be deleted upon sequence analysis is represented...
A major goal since the completion of the Human Genome Project is the functional characterization of ...
<p>(A) Schematic illustrating the <i>GmFEI2</i>-SP2 target sequence (blue) and corresponding PAM (re...
<p>Sequence of sgRNAs and primers used for CRISPR/Cas9 knockout cell generation and evaluation.</p
<p><b>A)</b> Primary human monocyte DNase- and ChIP-Seq (H3K4me3 and K3K27me3) coverages at the tran...
<p>(A) The <i>Snai3</i> WT genomic DNA region contains the <i>Rnf166</i> gene 5 kb upstream and the ...
<p>(A) Schematic illustrating the target sequence (blue) and corresponding PAM (red). PCR amplificat...
Massively parallel sequencing technologies have made it possible to generate large quantities of seq...
Summary: Cas9 nucleases can be programmed with single guide RNAs (sgRNAs) to mediate gene editing. H...
International audienceAnalysis of CRISPR-SaCas9 Off-Targets In order to verify whether SaCas9 and sg...
<p>(A) Schematic of the strategy for the <i>ssnA</i> gene deletion in the SS2 GD01 strain via double...
(A) Representation of the minimal sna-rg R2P2 subfragments indicating the location of the putative S...
Loss-of-function experiments are essential for the functional investigation of cis-regulatory elemen...
A schematic of the snai2 gene displays where the three guide RNAs (gRNAs) were designed for CRISPR/C...
<p>(<b>A</b>) Schematic illustration of the CRISPR/Cas system. The guide RNA (gRNA) binds to the 20-...
<p>The number of times a particular nt was found to be deleted upon sequence analysis is represented...
A major goal since the completion of the Human Genome Project is the functional characterization of ...
<p>(A) Schematic illustrating the <i>GmFEI2</i>-SP2 target sequence (blue) and corresponding PAM (re...
<p>Sequence of sgRNAs and primers used for CRISPR/Cas9 knockout cell generation and evaluation.</p
<p><b>A)</b> Primary human monocyte DNase- and ChIP-Seq (H3K4me3 and K3K27me3) coverages at the tran...
<p>(A) The <i>Snai3</i> WT genomic DNA region contains the <i>Rnf166</i> gene 5 kb upstream and the ...
<p>(A) Schematic illustrating the target sequence (blue) and corresponding PAM (red). PCR amplificat...
Massively parallel sequencing technologies have made it possible to generate large quantities of seq...
Summary: Cas9 nucleases can be programmed with single guide RNAs (sgRNAs) to mediate gene editing. H...
International audienceAnalysis of CRISPR-SaCas9 Off-Targets In order to verify whether SaCas9 and sg...
<p>(A) Schematic of the strategy for the <i>ssnA</i> gene deletion in the SS2 GD01 strain via double...