Researchers from Carnegie Mellon University have discovered a way to target RNA that could lead to new treatment options for ...
Endoxifen program into rare pediatric neuromuscular disease along with previously received Rare Pediatric Disease Designation ...
The Star Press on MSN
Accessible van giveaway helps Hoosiers like Kim Ball
Kim Ball received an accessible van from the Muscular Dystrophy Family Foundation. Applications for the next giveaway are ...
Parent Project Muscular Dystrophy (PPMD), the largest U.S. non-profit leading Duchenne and Becker muscular dystrophy care, research, and advocacy efforts, celebrated a powerful and inspiring Walt ...
Precision BioSciences, Inc. (Nasdaq: DTIL), a clinical stage gene editing company utilizing its novel proprietary ARCUS® ...
Indiana residents with muscular dystrophy can apply for a free accessible van through the Muscular Dystrophy Family Foundation's annual giveaway program. The foundation awards accessible vans to one ...
HONG KONG, Jan. 5, 2026 /PRNewswire/ -- GenEditBio Limited ("GenEditBio"), a clinical-stage biotechnology startup focusing on genome-editing therapeutic solutions, today announced that the U.S. Food ...
If your forearms won’t grow, it’s not genetics — it’s the way you train. These 5 proven forearm exercises build grip strength, wrist stability, and real muscle. From Zottman curls to wrist curls, this ...
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