Jozsef Tozser

Potent new antiviral compound shows similar inhibition and structural interactions with drug resistant mutants and wild type HIV-1 protease.

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2007, Journal of medicinal chemistry.

Atomic resolution crystal structures of HIV‐1 protease and mutants V82A and I84V with saquinavir

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2007, Proteins.

Molecular basis for substrate recognition and drug resistance from 1.1 to 1.6 Å resolution crystal structures of HIV‐1 protease mutants with substrate analogs

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2005, The FEBS journal.

Tear fluid proteomics multimarkers for diabetic retinopathy screening

Adrienne Csutak, Andras Hajdu, Tunde Peto, 2013, BMC Ophthalmology.

Kinetic, stability, and structural changes in high-resolution crystal structures of HIV-1 protease with drug-resistant mutations L24I, I50V, and G73S.

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2005, Journal of molecular biology.

Crystal structures of HIV protease V82A and L90M mutants reveal changes in the indinavir-binding site.

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2004, European journal of biochemistry.

Combining mutations in HIV‐1 protease to understand mechanisms of resistance

Irene T Weber, Robert W Harrison, Yuan-Fang Wang, 2002, Proteins.