Technique that inserts the genome of one bacterial species into the ‘dead’ cells of another could open doors for synthetic ...

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

Emerging antiviral defense systems are expanding the conceptual and practical boundaries of genome editing. Across bacteria, archaea, and eukaryotes, hosts ...

The name might sound like a Nordic god, but it is actually the molecular machinery that allows many different species to eat ...

Researchers have created the first living synthetic bacterium made from non-living parts by killing a bacterial cell and then ...

SAN FRANCISCO, 22nd March, 2026 (WAM) -- Scientists at the University of California have developed a new method to treat blood cancers by reprogramming immune cells directly inside the patient’s body, ...

His method of locating genes in human DNA allowed researchers to find disease-causing genes, and later to map the entire, ...

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

The current path to CAR-T cell therapy is, by any measure, a logistical ordeal. A patient’s immune cells must be drawn out of ...

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

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

A redacted correspondent, who sounds to be on the younger side of things, emails Jeffrey Epstein to thank him for their “fun” ...