Applied computational biology discoveries vastly expand the range of CRISPR’s access to DNA sequences.

New CRISPR-based research tool delivers results in an hour; researchers share protocol and kits to advance research and move toward clinical validation.

Neuroscientists identify genes that modulate the disease’s toxic effects.

Researchers find master regulator needed for Toxoplasma gondii parasite to chronically infect host; promising step toward infection treatment, prevention.

Smart materials change properties in response to specific DNA sequences; could be used in a variety of devices.

Engineers program human and bacterial cells to keep a record of complex molecular events.

Whitehead Institute team finds drugs that activate a key brain gene; initial tests in cells and mice show promise for rare, untreatable neurodevelopmental disorder.

The new system, dubbed RESCUE, allows RNA edits to be made that were not previously possible.

By introducing a gene variant associated with autism into monkeys, researchers hope to study treatment options for severe neurodevelopmental disorders.

Researchers identify and develop new CRISPR-associated transposase system for targeted integration of DNA, adding key capabilities to gene-editing technology.