Targeted delivery of biological agents to atherosclerotic plaques may provide a novel treatment and/or useful tool for imaging of atherosclerosis in vivo. However, there are no known viral vectors ...

Cancer gene therapy is often carried out by the introduction of specific genes into cancer host cells that destroy cancer or that will enhance the immune response against cancer cells. Viruses are ...

A new variation of the CRISPR-Cas9 gene editing system makes it easier to re-engineer massive quantities of cells for therapeutic applications. The approach, developed at Gladstone Institutes and UC ...