In 2025, baby KJ Muldoon became the first person to receive a personalized gene editing treatment, which likely saved his ...

The Oslo patient is the first person to be cured by a family member's bone marrow transplant. A 63-year-old man in Norway ...

After over a decade with HIV, a Norwegian man received a surprise through a stem cell donation from his sibling. The gifted ...

An HIV patient in Oslo has been in remission for the past five years following a stem cell transplant from his brother, who ...

Researchers say a new AI system can identify disease-causing mutations and explain their biological effects, potentially ...

Aortic aneurysms are characterized by abnormal enlargement of the aorta, the primary artery responsible for carrying blood ...

A newly identified gene mutation may help explain why schizophrenia patients struggle to update their understanding of ...

New research suggests that autoimmune diseases may be driven by DNA mutations in immune cells that remove the natural brakes ...

University of Virginia School of Medicine scientists have used a next-generation form of gene editing to fix the underlying cause of a severe form of epilepsy in lab mice.

PYNNACLE enrolled heavily pretreated TP53 Y220C–mutant ovarian cancer (median four prior lines), including platinum-resistant ...

The Scottish Medicines Consortium has approved osimertinib for adults with unresectable stage III EGFR-mutant NSCLC whose disease has not progressed after platinum-based chemoradiation.

Serially cloned mice hit a genetic “dead end” by generation 58, underscoring that sex evolved for variation, purging harmful ...