revolutionizing genome editing beyond traditional CRISPR

CRISPR-Cas9 has reshaped what’s possible in genetic engineering. By giving scientists a precise way to cut DNA, it opened the door to targeted gene therapies, disease modeling, and even the prospect of correcting inherited disorders at the source.

But CRISPR isn’t perfect. Its mechanism, making double-strand breaks in DNA, relies on the cell’s own repair system,…