Stefan Henrich

Using 3D protein structures to derive 3D-QSARs.

Ting Wang, Rebecca C Wade, Stefan Henrich, 2004, Drug discovery today. Technologies.

Protein–protein interface-binding peptides inhibit the cancer therapy target human thymidylate synthase

Maria Paola Costi, Daniela Cardinale, Giambattista Guaitoli, 2011, Proceedings of the National Academy of Sciences.

Novel approaches for targeting thymidylate synthase to overcome the resistance and toxicity of anticancer drugs.

Maria Paola Costi, Rebecca C Wade, Divita Garg, 2010, Journal of medicinal chemistry.

Blue- and Green-Absorbing Visual Pigments ofDrosophila: Ectopic Expression and Physiological Characterization of the R8 Photoreceptor Cell-Specific Rh5 and Rh6 Rhodopsins

Armin Huber, Ernesto Salcedo, A. Huber, 1999, The Journal of Neuroscience.

On the use of PIPSA to Guide Target‐Selective Drug Design

Stefan Richter, Rebecca C Wade, R. Wade, 2008, ChemMedChem.

Comparative binding energy analysis for binding affinity and target selectivity prediction

Ting Wang, Niklas Blomberg, Rebecca C Wade, 2010, Proteins.

The 1.9-Å crystal structure of the noncollagenous (NC1) domain of human placenta collagen IV shows stabilization via a novel type of covalent Met-Lys cross-link

Robert Huber, Hans D. Bartunik, R. Huber, 2002, Proceedings of the National Academy of Sciences of the United States of America.

The crystal structure of the proprotein processing proteinase furin explains its stringent specificity

Robert Huber, Angus Cameron, R. Huber, 2003, Nature Structural Biology.