CRSP is a speculative buy for aggressive investors, driven by the commercial launch and multibillion-dollar potential of ...

Albino cane toads created using gene-editing technology reveal that albino animals face competitive disadvantages going far ...

For years, researchers have been trying to figure out how to treat inherited blood disorders like sickle cell disease without ...

CRISPR is a technology that can be used to edit genes and, as such, will likely change the world. The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell. After that ...

AI and machine learning are revolutionizing CRISPR technology, enhancing precision and efficiency in gene editing, paving the way for breakthroughs in genetic research and therapy.

A new generation of CRISPR technology developed at UNSW Sydney offers a safer path to treating genetic diseases like sickle ...

Shares of CRISPR Therapeutics CRSP have rallied 41.4% in the past three months, driven by encouraging data from a study of ...

A study has revealed that chemical tags once regarded as genetic clutter are in fact powerful gene silencers – and removing them could unlock safer treatments for inherited blood disorders.

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 ...

CRISPR/Cas9 works by having CRISPR (pieces of DNA sequences) guide Cas9 (an enzyme that can cut and edit DNA) to edit, alter, or repair genes. We think the company’s proprietary technology has ...

The ability to correct disease-causing genetic mistakes using genome editors holds great promise in medicine, but it is not ...