The genome-editing technology can be supercharged by artificial intelligence—and the results are already being felt.

The United States Food and Drug Administration has just approved the first-ever clinical trial that uses CRISPR-Cas13 RNA ...

Cell-to-cell communication through nanosized particles, working as messengers and carriers, can now be analyzed in a whole ...

CRISPR-Cas9 has long been likened to a kind ... as long as the target transcript that’s been recognized by the guide RNA is made early in the viral infection. But if the problematic snippet ...

Life Sciences Center (LSC) have discovered a unique way for cells to silence specific genes without cutting DNA. This ...

This protein can easily be programmed to find and bind to almost any desired target sequence, simply by giving it a piece of RNA to guide it in its search. When the CRISPR Cas9 protein is added to ...

CRISPR-Cas9 is a reprogrammable DNA cutting ... any sequence along the genome--by hitching it to a strand of guide RNA (green) whose sequence is complementary to that of the DNA target.

CRISPR-Cas9 has long been likened to a kind of genetic scissors ... or plasmid from a cell as long as the target transcript that’s been recognized by the guide RNA is made early in the viral infection ...

Yao. The success of RNA-targeting CRISPR tools depends on multiple factors, including the guide RNA sequence, the ...

With CRISPR-Cas9, the crRNA/tracrRNA sequence or an artificial guide RNA indicate where the DNA can be cut. It is relatively easy for scientists to produce different sequence variants from RNA ...