Research Articles
CRISPR and Muscular Dystrophy: Rewriting Genetic Code to Cure the Incurable
Explore how CRISPR gene editing technology is revolutionizing the treatment of muscular dystrophy, from genetic mechanisms to clinical trials.
CRISPR Gene Editing Fixes Muscular Dystrophy in Dogs
Groundbreaking CRISPR gene-editing treatment halts progression of Duchenne muscular dystrophy in dogs, signaling potential cure for children.
Nanomedicine for Muscular Dystrophy: Targeted Treatments on a Tiny Scale
Explore how nanomedicine is revolutionizing muscular dystrophy treatment through targeted nanoparticle delivery systems and recent scientific breakthroughs.