muscles
| 1 min read
Researchers are using CRISPR gene editing to restore function of the mutant protein that causes Duchenne muscular dystrophy, a genetic disease that causes muscle degeneration.
Page 1 of 1 - 1 Total Items
Subscribe to our eNewsletters
Stay connected with all of the latest from Drug Discovery News.
SubscribeSponsored
From primer design to sample preparation, explore comprehensive strategies to optimize PCR throughput and reproducibility.
DNA-based testing is emerging as a sensitive way to uncover and control a hidden threat in biomanufacturing.
Learn how molecular dynamics, AI-aided design, and structural insights combine to reshape how therapeutic proteins are created, validated, and optimized.
