Here’s how it works. Scientists have transformed cancer cells into healthy muscle tissue in the lab using CRISPR gene-editing technology — and they hope new cancer treatments can be built on ...

In recent years, small extracellular vesicles (sEVs) have captured the attention of scientists due to their critical role in cell-to-cell communication and disease progression. These nanosized ...

The second tool is the CRISPR-Cas9 system, which allows easy and precise editing of any region of the genome. When it comes to traditional immortalized cell lines, such as HeLa or HEK293, cutting with ...