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

Genome editing-based therapies typically aim to treat disease by correcting underlying genetic mutations in patient's cells.

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

Broken String Biosciences launched an early access program (EAP) through which select developers of gene edited therapeutics will be able to use Broken String’s INDUCE-seq ® technology in their own ...

A new method for safely inserting large chunks of DNA into genomes has now measured up in mice, potentially paving the way ...

INSTALL results showed successful and safe non-viral insertion of large genetic payloads in the livers of mice when delivered by lipid nanoparticles (LNPs). In contrast, mice experienced fatal immune ...