The ability to control gene expression across a wide range is crucial for many fields, including bioengineering, disease ...

Recent breakthroughs and regulatory shifts in gene editing might be the key to moving from treating the symptoms of diseases ...

Scientists are exploring gene editing as a way to correct trisomy at the cellular level. Using CRISPR-Cas9, researchers ...

The future of medicine with CRISPR and CAR-T therapy, exploring ethical, societal, and accessibility challenges in healthcare ...

Receptors on B and T cells hint at what the immune system is targeting. An AI approach called Mal-ID developed increases diagnostic accuracy, particularly for autoimmune diseases.

The Aviram Lab investigates the molecular mechanisms that protect microorganisms from their own pathogenic invaders.

Scientists at the Garvan Institute of Medical Research have discovered that certain gene variations linked to leukemia can ...

With ready-to-use, immune-cloaked CD34+ and CD4+ T-cell derived ... Innovation enabled by proprietary STAR-CRISPR™ gene editing technology The Allo Chassis™ cell lines are immediately ...

By Balambal Suryanarayanan CRISPR-Cas9 is a repurposed gene editing tool that allows scientists to cut, replace, and insert pieces of DNA in precise regions along the strand. Courtesy of NIH Image ...