New genomic research suggests our species descended from a deep fusion between two ancient lineages — one of them a mysterious “ghost.” ...

New @hopkinskimmel research finds extra copies of chromosome 1q may drive the earliest stages of pancreatic cancer. › ...

Learn how cats and humans can share key cancer mutations — and why those similarities could guide future treatment research.

International team uncovers gene mutations that cause rare and aggressive cancer in both cats and humans. Their findings could provide a path to treatments for both species.

A study introduces a scalable 2D human neuron platform to probe how brain-like rhythms emerge and how specific drugs reshape them, aiding epilepsy and autism research.

In humans, chronic high blood pressure forces the heart to work too hard. The muscle of the left ventricle thickens in defense, a condition called hypertrophy. Eventually, this leads to fibrosis, ...

KRAS is the most frequently mutated oncogene across all human cancers. Although different KRAS mutations have long been thought to exert the same cancer-driving effects, a new study led by UT ...

Fast functional testing of genetic variants, from newborn genomes to disease models like zebrafish, is transforming ambiguous DNA findings into confident, real‑time treatment decisions.

Seek Labs, a private TechBio company building a programmable disease response platform to detect, protect, and counter disease threats, has been awarded $2 million from the U.S. Department of ...

The Phase 1 study is a first-in-human, multicenter, open-label trial designed to evaluate the safety, tolerability, ...

Stanford and Princeton Researchers Debut MedOS, an AI-Robotics Co-Pilot to Reduce Error, Support Clinicians, and Bring AI Directly Into Surgical and Hospital Workflows PALO ALTO, CA - February 11, ...

Researchers at the University of North Carolina at Chapel Hill have uncovered how chronic inflammation disrupts the immune ...