Forecasts in biotech market indicate that by 2030, gene therapy will become more accessible, potentially generating hundreds ...

A research team led by scientists from the Helmholtz Institute for RNA-based Infection Research (HIRI) has introduced a new ...

CRISPR — short for clustered regularly interspaced short palindromic repeats — is a method of genetic editing that uses RNA ...

A genome-editing technique known as prime editing holds potential for treating many diseases by transforming faulty genes into functional ones. However, the process carries a small chance of inserting ...

A study, published in the journal Frontiers in Genome Editing, outlines a method for editing single plant cells from sterile ...

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

Multisystemic smooth muscle dysfunction syndrome (MSMDS) is a rare condition associated with stroke, aortic dissection (tearing) and death in childhood. Currently, there is no effective treatment or ...

They look like ordinary horses, with their honey brown coats and white patches. But these 10-month-old foals in Argentina are ...

A newly developed tool utilises AI to predict how cells repair their DNA after it is cut by gene editing tools such as CRISPR ...

Researchers have unveiled a new type of nanostructure that dramatically improves CRISPR delivery. Called lipid nanoparticle ...

Northwestern scientists have developed a new nanostructure that supercharges CRISPR’s ability to safely and efficiently enter cells, potentially unlocking its full power to treat genetic diseases. By ...