Phacilitate’s annual event dawns as cell and gene therapies reach a new tipping point: the science has hit new heights just ...

SAYRE, PA, UNITED STATES, January 13, 2026 /EINPresswire.com/ -- Bookspert is excited to announce the launch of Lawless ...

US biotech start-up Aurora Therapeutics has launched with $16 million in seed funding from Menlo Ventures, aiming to turn one-off CRISPR gene-editing successes into a scalable model for rare diseases.

For the first time in history, doctors have successfully used a personalized gene-editing therapy to treat a rare genetic disorder. The patient, a baby named KJ, was born with a condition called CPS1 ...

KJ Muldoon, the first infant to undergo gene-editing therapy, has accomplished another first as a 1-year-old — his first steps KJ is walking at home ahead of Christmas after being hospitalized last ...

KJ Muldoon, who was born with a rare genetic disorder call CPS1 Deficiency, became the first patient in the world to receive a personalized CRISPR gene editing therapy. Jack Smith tells lawmakers his ...

From reproductive rights to climate change to Big Tech, The Independent is on the ground when the story is developing. Whether it's investigating the financials of Elon Musk's pro-Trump PAC or ...

The FDA has introduced a new “plausible mechanism pathway” aimed at expediting approval of personalized therapies for rare diseases. The approach, detailed in a Nov. 12 article in The New England ...

Add Yahoo as a preferred source to see more of our stories on Google. Late last year, dozens of researchers spanning thousands of miles banded together in a race to save one baby boy’s life. The ...

Late last year, dozens of researchers spanning thousands of miles banded together in a race to save one baby boy’s life. The result was a world first: a cutting-edge, gene-editing therapy fashioned ...