DNA holds the code for building life, but not all of it is useful. Some parts behave more like parasites, sticking around ...

created from that gene 1. The EST patent holder could withhold consent entirely or charge a fee. According to John Doll, Director of Biotechnology Examination at the USPTO, “The USPTO views this ...

Doctors announced this week that they have treated a newborn baby with a rare genetic disease using the world’s first personalized gene editing therapy. Geoff Bennett discussed the treatment and ...

A nine-month-old baby in the US, suffering from a rare genetic disorder, was successfully treated with personalised CRISPR gene editing therapy. According to a report from the Children’s Hospital of ...

A baby born with a rare genetic disease is "growing and thriving" after getting bespoke gene therapy. It's the first time anyone in the world has been given an experimental gene-editing treatment ...

Pittsburgh is bringing former manager Gene Lamont back to the organization to serve as a special advisor to newly tabbed manager Don Kelly. Triple-A manager Chris Truby is also being promoted to ...

When CRISPR was first introduced as a gene-editing tool in 2012, the world was in awe of all the possibilities it held — eventually earning its discoverers the Nobel Prize in Chemistry in 2020. Now, ...

A nine-month-old baby has become the first person ever to be successfully treated with personalized gene editing therapy. Researchers corrected a specific gene mutation in baby KJ Muldoon‘s ...

Former manager Gene Lamont is joining the Pirates as a special adviser to Kelly, and Triple-A Indianapolis manager Chris Truby has been added to the major-league coaching staff in an unspecified ...

An infant in Philadelphia has been successfully treated with a customized Crispr gene-editing therapy for a rare and deadly disease, doctors reported Thursday—a breakthrough in the futuristic ...

The goal is to reuse key parts of the treatment -- like the lipid nanoparticle and mRNA -- and simply swap in a custom set of instructions for each patient's specific gene mutation, Ahrens-Nicklas ...

They would use a technology known as CRISPR, a personalized gene-editing therapy, to find the one uniquely mutated gene out of 20,000 in his little body, and fix it. KJ subsequently received three ...