Gene editing of patients’ blood stem cells can potentially cure many blood disorders. But introducing targeted edits into these cells has been challenging, and the edits aren’t always stable once the cells engraft in the bone marrow. Researchers now report a CRISPR approach that overcomes these technical challenges.
Related Posts
Order Antibiotics online
June 8, 2024Buying antibiotics online
June 8, 2024How do antibiotics work?
June 8, 2024Flagyl: a beacon of hope in the fight against trichomoniasis
February 17, 2024Metronidazole for bacterial infection
February 1, 2023