David Liu

Visitors are invited to explore galleries highlighting key discoveries and transformative insights in biomedicine.

Researchers have developed virus-like particles that deliver therapeutic levels of protein to animal models of disease.

A CRISPR-based gene editing technique called twin prime editing could be a new and safer approach to gene therapy.

Researchers have boosted the efficiency of prime editing, a highly versatile CRISPR-based gene editing technology, and used the improved system to correct disease mutations in cells.

Converting a pathogenic hemoglobin gene to a benign variant enables healthy blood cell production in an animal model of sickle cell disease.

By engineering proteins called proteases to find new targets with high selectivity, researchers mark a critical advance toward potential new treatments for a wide range of conditions

Correcting the mutation that causes progeria with base editing leads to strong symptom reduction and longer lifespan in an animal model

An engineered bacterial toxin is a key part of a gene editor that can make single-base changes in human mitochondria.