In a world first, a child diagnosed with a rare metabolic disorder has been successfully treated with a customized CRISPR ...

This is the first gene editor to use a CRISPR-associated transposase to make targeted edits at therapeutically useful levels in humans.

Genome editing is a relatively new technology, and we've had a breakthrough with the development of two novel varieties using ...

The CRISPR-Cas9 patent landscape remains complex and unsettled. The Federal Circuit’s latest decision in University of California v.

ISTANBUL, TURKEY, May 19, 2025 /EINPresswire / -- Delegates from more than 70 countries have gathered in Istanbul for the largest seed industry event in the world, the World Seed Congress 2025 , amid ...

And when a ribosome reads from this mRNA to make the protein, it reads inosine as though it was guanine. Thus, A-to-I mRNA ...

US infant KJ Muldoon makes history as first patient treated with personalized gene-editing, offering hope for rare illnesses.

Every year, up to 50 million people contract an infection that often seems like a mild stomach bug. Most recover with only ...

In a major breakthrough, a patient has been treated with a personalized CRISPR therapeutic that aims to cure their rare genetic disease... | Genetics And Genomics ...

Entamoeba histolytica infects nearly 50 million people each year and kills around 70,000. It’s a shape-shifting parasite that ...

Biden was seen by doctors last week after urinary symptoms and a prostate nodule were found. He was diagnosed with prostate ...