Research Interest
Our lab is dedicated to developing innovative gene therapies for currently incurable diseases. We design Adeno-Associated Virus (AAV) vectors that deliver genes more efficiently and precisely to target tissues, and we build advanced mouse models that more faithfully recapitulate human biology. In parallel, we are pioneering gene therapy strategies to repair the liver, with the ultimate goal of creating transformative treatments.
Major Areas of Research
1. Development of novel AAV capsids with improved tissue targeting
2. Generation of humanized mouse models for AAV capsid screening
3. Mechanisms and therapeutic strategies for treating liver diseases