The gene-editing technique is effective for treating some illnesses but it's been too expensive to consider it for rare ...

-Company announced that the U.S. Food and Drug Administration (FDA) granted Regenerative Medicine Advanced Therapy (RMAT) designation to CTX112 for the treatment of certain relapsed or refractory (R/R ...

Thanks to CRISPR, our medical specialists will soon have unprecedented control over how they treat and prevent some of our ...

US scientists have developed a new CRISPR toolkit to boost the treatment of genetic disorders. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a Nobel Prize-winning gene-editing ...

The gene-editing technique known as CRISPR is promising to revolutionize medicine. Some researchers are trying to help make it available for people with very rare genetic disorders.

Thanks to the revolutionary advancements in CRISPR technology, medical specialists are on the verge of transforming how we ...

Winners of the 2022 Nobel Prize in chemistry. From left to right, Carolyn R. Bertozzi, Morten Meldal, and K. Barry Sharpless. © Nobel Prize Outreach. Illustration by ...

In 2023, the US Food and Drug Administration approved the first gene therapy for Duchenne muscular dystrophy (DMD). But that therapy, Elevidys, can‘t replace the entire dystrophin gene ...

Premium Bonds holders will be frustrated to learn the prize fund rate in the monthly draw is dropping for a second time in January with fewer big prizes to win. The prize fund rate is already ...

Oleksandr Merezhko, a top MP from President Volodymyr Zelensky's party, has nominated U.S. President-elect Donald Trump for the 2025 Nobel Peace Prize, according to his letter to the Norwegian Nobel ...