In this section

Weihang (Valerie) Chai

Weihang (Valerie) Chai, PhD

Director, Center for Genetic Diseases

weihang​.chai​@rosalindfranklin​.edu

 

  • Robert J. Bridges
    • Identification of potential drug candidates for the treatment of cystic fibrosis.
    • Probing human nasal epithelial cells for in vitropharmacogenomic studies for the treatment of cystic fibrosis.
  • Neil Bradbury
    • The regulation of membrane protein trafficking in cystic fibrosis.
    • Probing human nasal epithelial cells for in vitropharmacogenomic studies for the treatment of cystic fibrosis.
  • David M. Mueller
    • The structure and functional mechanism of the mitochondrial F1FO-ATPase. The structural basis for drugs and inhibitors that target the ATP synthase.
    • The structure and function of Cln3 - the gene defective in the juvenile form of Batten disease, a neurodegenerative disease of the brain.