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

Australian researchers have demonstrated that the use of a new, less toxic drug combination after stem cell transplants for ...

Brain Tumours, particularly malignant types such as glioblastoma multiforme (GBM), continue to pose a significant clinical ...

By uncovering RNA’s previously unknown function to repair DNA damage, our findings show how RNA may directly contribute to the stability and evolution of the genome. It’s not merely a passive ...

Human–animal chimaeras are an exciting yet challenging area of research. Human cells are coaxed to grow in animal embryos, allowing researchers to study human tissue development. But the long-term ...

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

Turning a $10,000 investment into $1 million represents a financial dream for many — a 100x return that would require an ...

Gene therapy is revolutionizing how they're treated, and the Fred Hutch Cancer Center in Seattle is at the center of it all. ...

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

Koby Baranes, PhD, head of science at Clock Bio, cautions, “Aging is not yet fully understood and existing models often fail ...

Crispr Therapeutics AG leverages CASGEVY's rollout, a robust pipeline in cardiovascular, oncology, & partnerships to large ...

Many countries lack blood donors. The quest to create an artificial, lab-made blood type that could make up for supply ...