Investigators have developed STITCHR, a new gene editing tool that can insert therapeutic genes into specific locations without causing unwanted mutations. The system can be formulated completely as ...

While de-extinction projects capture headlines with dreams of resurrecting mammoths, the same technologies at play — especially CRISPR — are quietly transforming something even more profound: human ...

CRISPR-Cas9 gene editing technology has emerged as one of the most transformative advancements in medicine and biotechnology.

The potential for cell and gene therapies is growing, offering groundbreaking treatments for rare genetic disorders and ...

Thalassemia and Sickle Cell Anaemia are common genetic disorders, with options for treatment and prevention available.

Groundbreaking gene-editing treatment exa-cel is now available for NHS patients with sickle cell disease, offering a ...

New precision genome editing technologies are transforming the therapeutic landscape for patients with certain cancers and ...

The Breakthrough Prize Foundation today announced the winners of the 2025 Breakthrough Prizes, honoring scientists driving ...

Collaborative research defines a novel approach to understanding how certain proteins called transcription factors determine which genetic programs will drive cell growth and maturation. The method, ...

The pilot project is being taken up in three districts of East and West Singhbhum and Seraikela-Kharsawan districts where ...

Scientists at the Centre for Cellular and Molecular Biology (CCMB), working under the National Sickle Cell Anaemia Elimination Mission (NSCAEM), have partnered with the Tata Steel Foundation (TSF) and ...