Explore how adenovirus-delivered CRISPR/Cas9 gene editing technology is revolutionizing HIV treatment by targeting the CCR5 receptor.
Explore CRISPR-Cas9, the revolutionary gene-editing technology derived from bacterial defense systems that allows precise editing of DNA, its applications, and ethical implications.
Exploring CRISPR gene editing technology, its relationship to GMOs, and the profound ethical considerations surrounding genetic engineering.
Explore how CRISPR-Cas9, a revolutionary gene-editing tool derived from bacterial defense systems, is enabling precise genome editing with vast potential in medicine and biology.
How a simple cardboard box is bringing gene editing to classrooms and kitchens worldwide with a frugal CRISPR kit.
Exploring how CRISPR genome editing is revolutionizing silkworm research and sericulture through high-throughput genetic modifications.
How CRISPR gene editing and advanced gene therapies are transforming veterinary oncology by targeting cancer at its genetic roots.
In 2025, CRISPR graduated from theoretical marvel to clinical reality, curing infants of once-fatal diseases while igniting ethical debates that threaten to reshape human evolution.
Discover how CRISPR's NAG PAM breakthrough is expanding genome editing capabilities in rice, enabling precise modifications for disease resistance, drought tolerance, and improved nutrition.
Discover how scientists are using Barley stripe mosaic virus to deliver CRISPR gene editing tools directly into wheat, creating Fusarium head blight resistant plants without lengthy crossbreeding.