Gene editing enables researchers to correct mutation in muscle stem cells in DMD model: Correction of mutation in muscle stem cells with CRISPR editing may pave the way for lifelong treatments for muscular dystrophy

Duchenne muscular dystrophy (DMD) is a rare but devastating genetic

Viruses found to use intricate ‘treadmill’ to move cargo across bacterial cells: State-of-the-art technologies reveal bacterial cells organized like human cells, offering insights for new phage therapies on untreatable infections

Countless textbooks have characterized bacteria as simple, disorganized blobs of