Topics

CRISPR gene editing enters mainstream medicine as Casgevy approval fuels a clinical trial pipeline for cancer, rare diseases, and autoimmune conditions with FDA cutting red tape.

MIT research shows how strategic gene arrangement on DNA can boost performance of engineered synthetic gene circuits.

New biosensors based on DNA origami nanotechnology might detect when to release drugs based on certain conditions inside the body.

Researchers have used AI to create DNA switches that control when and where genes in our body are turned on or off.

Scientists tweak mouse genes to mimic woolly mammoths, aiming to revive ancient species and boost ecosystems.

Researchers create a precise way to change DNA using artificial intelligence and gene tools, improving safety for modeling diseases and creating better therapies.

Researchers create a gentle tool to watch how cells fix damaged DNA without interfering, opening new ways to study diseases like cancer.

Artificial genes can construct complex structures inside cells by following a sequence similar to how IKEA furniture is assembled.

New technology from the University of Florida uses stable DNA guides to target RNA with greater precision and lower cost than traditional methods.

Cutting-edge AI and machine-learning algorithms can produce personalized patient predictions