An experimental gene therapy seems to slow the progression of Huntington’s disease by about 75 per cent, and researchers are ...
An Illinois family pushed for both boys to receive the potentially life changing medical treatment after one was approved and ...
The UAE has become the second country worldwide to approve Itvisma, a groundbreaking gene therapy for spinal muscular atrophy ...
X-linked retinoschisis gene replacement therapy, aiming to improve retinal architecture and visual function in young male ...
Explore 2025's groundbreaking scientific discoveries: the MoM-z14 galaxy, personalised CRISPR therapy, regenerative medicine, ...
A small group of volunteers will receive multiple injections of the experimental treatments next month, says Unlimited Bio.
Kids like David with SMA Type 1 typically don’t survive past the age of two. He may be the first to have gene therapy as ...
The first infant to undergo gene-editing therapy has accomplished another first — his first steps. KJ Muldoon is walking and ...
Talk about a Christmas miracle!A medical breakthrough came just in time and changed one baby’s life — and gave his family a ...
TOMI Environmental Solutions, Inc.® ('TOMI”) (NASDAQ: TOMZ), a global leader in disinfection and decontamination solutions, ...
Taysha Gene Therapies (TSHA) is back in focus after its Rett syndrome program hit several milestones at once, including FDA Breakthrough Therapy Designation for TSHA-102 and encouraging REVEAL study ...
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Confirming the effectiveness of targeted therapy for gene mutation that causes hearing loss...Up to ...
A treatment that is effective against hearing loss caused by the 'MPZL2 gene' mutation has been developed. A research team ...
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