Plasmidsaurus, the company that sequences while you sleep, today announced the launch of a new product update that delivers full-length AAV genome sequences, including subgenomic variants, in just ...

A new review in Genes and Diseases explores the central role of MYC, a master regulatory protein, in the development and ...

A baby born with a rare and dangerous genetic disease is thriving after getting an experimental gene editing treatment made ...

A new review in Genes and Diseases explores the central role of MYC, a master regulatory protein, in the development and progression of cancer, spotlighting its potential as a multidimensional ...

The researchers described the unprecedented speed of the oversight steps as being "through alternative procedures." In month ...

The technique used on a 9½-month-old boy with a rare condition has the potential to help people with thousands of other ...

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 ...

Scientists present current evidence for a new gene therapy for Duchenne muscular dystrophy called delandistrogene moxeparvovec.

You can reach Jason on Signal at JasonMast.05. NEW ORLEANS — The mood at the annual meeting of the American Society of Cell and Gene Therapy isn’t amazing. The biotech market has been bad for ...

A baby born with a rare and dangerous genetic disease is growing and thriving after getting an experimental gene editing treatment made just for him. Researchers described the case in a new study ...