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European Journal of Medicinal Chemistry|December 29, 2015
Design and synthesis of novel Y-shaped barbituric acid derivatives as PPARγ activatorsVaibhav A Dixit, Prakash Chandra Rathi, Shweta Bhagat, et al.Viruses|April 27, 2024
The ISG15-Protease USP18 Is a Pleiotropic Enhancer of HIV-1 ReplicationChaohui Lin, Edmund Osei Kuffour, Taolan Li, et al.Bioorganic & Medicinal Chemistry|September 11, 2019
Small-molecule inhibitors of nisin resistance protein NSR from the human pathogen Streptococcus agalactiaeNicola Porta, Julia Zaschke-Kriesche, Benedikt Frieg, et al.Colloids and Surfaces. B, Biointerfaces|July 13, 2024
Characterization of size-tuneable aescin-lipid nanoparticles as platform for stabilization of membrane proteinsFatima Escobedo, Mohanraj Gospalswamy, Pia Hägerbäumer, et al.Journal of Molecular Biology|October 13, 2025
Molecular Insights into CLD Domain Dynamics and Toxin Recruitment of the HlyA E. coli T1SSRocco Gentile, Stephan Schott-Verdugo, Sakshi Khosa, et al.Toxins|June 23, 2018
Interaction of Ochratoxin A and Its Thermal Degradation Product 2'R-Ochratoxin A with Human Serum AlbuminFranziska Sueck, Miklós Poór, Zelma Faisal, et al.Frontiers in Pharmacology|May 2, 2019
Novel 3,4-Dihydroisocoumarins Inhibit Human P-gp and BCRP in Multidrug Resistant Tumors and Demonstrate Substrate Inhibition of Yeast Pdr5Julia Sachs, Katja Döhl, Anja Weber, et al.Nature Methods|November 13, 2012
A toolkit and benchmark study for FRET-restrained high-precision structural modelingStanislav Kalinin, Thomas Peulen, Simon Sindbert, et al.Nature Communications|September 7, 2021
Structure and efflux mechanism of the yeast pleiotropic drug resistance transporter Pdr5Andrzej Harris, Manuel Wagner, Dijun Du, et al.Communications Biology|May 9, 2022
Functional and structural characterization of interactions between opposite subunits in HCN pacemaker channelsMahesh Kondapuram, Benedikt Frieg, Sezin Yüksel, et al.Pageof 28