Peter Mac scientists have found a way to use the powerful gene editing tool CRISPR to silence cancer-causing gene mutations ...
is also a type of gene therapy. Its goal is to change how RNA interprets genetic instructions to control how proteins are made. In most recent advancements, RNA editing uses the CRISPR-Cas13 ...
The treatment for sickle cell disease and beta thalassemia is the first to be licensed using the gene-editing tool known as Crispr, for which its discoverers were awarded the Nobel prize in 2020.