Using the CRISPR/Cas9 genome-editing system to mutate the gene regions encoding particular protein domains could result in a new and more efficient method to screen for druggable protein targets ...

and sticking on a fluorescent protein to allow for visual tracking. A guide RNA, along with the addition of an oligonucleotide sequence, sent the Cas9 RNA-ward. “Just as CRISPR-Cas9 is making genetic ...

The Cas9 protein ... use of CRISPR. It’s called genome editing – or gene editing – but usually the results are not as precise as that term implies. CRISPR can also be used to make precise ...

Cas9, scientists reconstitute live African swine fever virus from synthetic genomes, accelerating vaccine development for ...

Gene editing technologies allow scientists to use enzymes -- in this case, Cas9 (CRISPR-associated protein 9 ... offer a valuable tool to researchers creating new therapies for a host of ...

CRISPR-Cas9 genome editing exploits the CRISPR-Cas ... Gene-edited mouse models are crucial for disease research but remain challenging to create. Here, authors introduce the CRISPR-VIM, using ...

The CRISPR-Cas (Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR) and its associated protein (Cas9 ... potential of CRISPR-Cas9. 1 Furthermore, it could create doubts about ...

Advances in the gene-editing technology known as CRISPR-Cas9 over the past 15 years have yielded important ... This advance, he said, will offer a valuable tool to researchers creating new therapies ...