Explore how CRISPR/Cas9 gene editing technology offers revolutionary therapeutic potential for treating Duchenne muscular dystrophy by correcting the underlying genetic mutations.
Discover how the innovative All-in-One exosome engineering strategy offers new hope for treating familial hypercholesterolemia through precise genetic therapy.
Discover how syncytins - ancient viral proteins - enable novel possibilities for transducing B cells and achieving well-tolerated in vivo gene transfer.
Discover how scientists engineered oxypurinol-responsive riboswitches from bacterial xanthine aptamers to control gene expression in mammalian cells.
Discover how scientists are using gene silencing technology to promote bone regeneration by targeting the Smurf1 protein, potentially revolutionizing fracture treatment.
Explore how gene therapy using DNA cleavage enzymes combined with mathematical modeling offers new hope for curing chronic Hepatitis B infection.
Breakthrough research in bone regeneration using gene-activated tissue engineering with PEI-condensed BMP-4 plasmid DNA