Scientists study a molecular machine that moves jumping genes in DNA, paving the way for a new gene editing tool beyond ...

Genetic editing holds promise to treat incurable diseases, but the most popular method—CRISPR—sometimes does more harm than ...

More than a decade ago, scientists harnessed a bacterial molecular machine that identifies and cuts specific sections of DNA, ...

A genome-editing technique known as prime editing holds potential for treating many diseases by transforming faulty genes ...

CRISPRgenee is a new method that combines gene silencing and cutting to improve loss-of-function studies in human cells.

Researchers engineered and screened dozens of base editors to precisely target a single mutation without editing other portions of the DNA.

When scientists discovered how bacteria protect themselves against viral invaders, called phages, in the early 2000s, little did they know they'd stumbled upon a revolutionary tool researchers could ...

For years, the CRISPR-Cas9 genome technology has been reshaping genetic engineering, a precision tool to transform everything from agriculture to medicine. With its incredible efficiency, this ...

Scribe highlights latest data on Lp(a)-lowering therapy and novel AI platform for next-generation CRISPR-based therapeutics at two premier conferences ...

Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins are core components of fast-evolving therapeutic gene editing tools. Scientists have used CRISPR ...

UC and Broad have been involved in two interferences at the patent office. Interference No. 106,115 was the second interference between UC and Broad over patent rights to CRISPR-Cas9 technology in ...