CRISPR Gene editing therapy is used for the first time in living humans with amazing results.

For decades, researchers have wondered why some people with risky gene variants go on to develop Parkinson’s disease, while ...

A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...

Japanese researchers have successfully eliminated the extra chromosome responsible for Down syndrome using CRISPR gene ...

The 12-month price targets, analyzed by analysts, offer insights with an average target of $33.11, a high estimate of $68.00, ...

Here comes the anti-CRISPR protein AcrVIB1, a promising inhibitor whose precise role has not yet been determined. In cooperation with the Helmholtz Centre for Infection Research (HZI) in ...

RNA gene scissors (CRISPR-Cas13) are gaining significant attention as a next-generation gene therapy with fewer side effects.

Cells are constantly subjected to DNA damage from a range of internal and environmental sources. It is estimated that cells ...

A team at Kobe University has created a game-changing resource for autism research: 63 mouse embryonic stem cell lines, each ...

Researchers have created a standardized mouse stem cell library containing 63 genetic variants strongly linked to autism ...

Delve into what the new CRISPR tool, CAST, has to offer. CRISPR-associated transposases are already gaining traction in ...