F. Liang

Discovery of Clinically Approved Agents That Promote Suppression of Cystic Fibrosis Transmembrane Conductance Regulator Nonsense Mutations.

D. Bedwell, K. Keeling, S. Rowe, 2016, American journal of respiratory and critical care medicine.

Nonsense Mediated RNA Decay Pathway Inhibition Restores Expression and Function of W1282X CFTR.

Shuling Guo, B. Monia, H. Bihler, 2019, American journal of respiratory cell and molecular biology.

A small molecule that induces translational readthrough of CFTR nonsense mutations by eRF1 depletion

R. Green, E. Mendenhall, R. Bostwick, 2021, Nature Communications.

Isogenic cell models of cystic fibrosis-causing variants in natively expressing pulmonary epithelial cells.

A. Sivachenko, P. Thomas, H. Bihler, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

High-Throughput Screening for Readthrough Modulators of CFTR PTC Mutations

H. Bihler, J. Mahiou, M. Mense, 2017, SLAS technology.