Embark on a journey into the world of CRISPR gene editing, a groundbreaking technology that allows scientists to modify genes with precision and potential far-reaching implications. CRISPR gene ...

2023 was an important year for patients with sickle cell disease. The FDA approved Vertex’s “Casgevy,” a CRISPR-based therapy for the treatment of sickle cell disease marking it as the first ...

The CRISPR gene editing technique, for instance, allows scientists to pinpoint an exact sequence of DNA within a gene, excise it using the Cas9 enzyme, and paste in a new segment of DNA in place ...

Scientists have developed a novel gene editing tool that could have vast implications for research and therapeutics. This technology is called STITCHR (site-specific target-primed insertion through ...

CRISPR gene editing reveals biological mechanism behind common blood disorder Date: April 8, 2022 Source: University of New South Wales Summary: Researchers have used CRISPR gene editing -- a type ...

Researchers have developed a new method which makes CRISPR gene editing more precise than conventional methods. The method selects the molecules best suited for helping the CRISPR-Cas9 protein ...

NtRON Bio announced today, following its recent U.S. patent application related to colorectal cancer using the IMPA™ phage engineering technology, it has now completed the filing of two patents for a ...

In contrast to previous human-embryo editing studies, Mitalipov’s team reported a high success rate at correcting a disease-causing mutation in a gene. The team claimed that the CRISPR–Cas9 ...