Researchers at the Yong Loo Lin School of Medicine, National University of Singapore (NUS Medicine) have developed a ...

The trajectory of base editing has been remarkable, progressing from the laboratory to patient care, treating debilitating or ...

Discover how CRISPR genome editing is revolutionizing medicine. Learn the science of Cas9, current clinical trials, and the ...

Researchers have engineered a new class of adenine base editors that reduce unwanted bystander mutations by two to three ...

What if gene editing could be designed as precisely as a race car tuned to a specific track?With new funding from Genome Canada and Ontario Genomics ...

Gene and cell therapy is moving fast – and in a clear direction. Programs are pushing toward more complex payloads, virus-free engineering, and manufacturing models that can scale from early research ...

Stanford Medicine researchers have built CRISPR-GPT, a large language model designed to automate the full arc of gene-editing ...

The researchers say that, to their knowledge, this is the first demonstration of programmable, site-specific integration of a ...

Researchers identified hundreds of anti-CRISPR proteins in human gut phages, including a new dual-function family that blocks ...

These ideas will be explored during the next event in the Equity Now Speaker Series, which will be held on April 3rd, 2026 at 11am (virtual). Public ...

Wikipedia faces scrutiny after Chavez page claims about DNA evidence appear to misstate New York Times reporting on paternity ...

Funding will expand the range of Dualase(R) genome editors for new high morbidity and mortality genetic disease targets. TORONTO, March 18, 2026 /PRNewswire/ - Specific Biologics Inc. ("Specific"), a ...