Everything came together last year when Alexander Marson, Gurumurthy, and colleagues used Easi-CRISPR to reprogram the structure and function of human T cells without the need for viral vectors 6.

Researchers at Duke University and North Carolina State University have discovered a handful of new CRISPR-Cas systems that ...

What is the function of CRISPR gene-edited cell lines in research? In order to understand the role that different genes play in disease pathways, researchers need to be able to modify levels of ...

Researchers from Tel Aviv University utilized CRISPR to cut a single gene from cancer cells of head and neck tumors – and ...

A recent review published in the journal Engineering delves into the significant advancements and potential of CRISPR ...

Feb. 13, 2025 — A new study unravels the relationship between mitofusins (mitochondrial proteins) and autophagy. Using gene editing with CRISPR-Cas9, the team has been able to study these ...

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 ...

The San Francisco-based company housed a cell-specific in vivo gene editing platform that was designed to have a similar structure to an antibody-drug conjugate but with a CRISPR-Cas payload.