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Journal of Biomolecular Screening|September 29, 2004
Comparison of the usefulness of the MTT, ATP, and calcein assays to predict the potency of cytotoxic agents in various human cancer cell linesHenrik Mueller, Matthias U Kassack, Michael WieseChemmedchem|September 22, 2009
Combined pharmacophore modeling, docking, and 3D QSAR studies of ABCB1 and ABCC1 transporter inhibitorsIlza K Pajeva, Christoph Globisch, Michael WieseJournal of Medicinal Chemistry|April 30, 2004
Structure-function relationships of multidrug resistance P-glycoproteinIlza K Pajeva, Christoph Globisch, Michael WieseThe FEBS Journal|November 3, 2009
Comparison of the inward- and outward-open homology models and ligand binding of human P-glycoproteinIlza K Pajeva, Christoph Globisch, Michael WieseEuropean Journal of Medicinal Chemistry|August 26, 2017
Synthesis and biological investigation of 2,4-substituted quinazolines as highly potent inhibitors of breast cancer resistance protein (ABCG2)Michael K Krapf, Jennifer Gallus, Michael WieseBiochimica Et Biophysica Acta. Biomembranes|November 5, 2016
Pyrrolopyrimidine derivatives and purine analogs as novel activators of Multidrug Resistance-associated Protein 1 (MRP1, ABCC1)Sven Marcel Schmitt, Katja Stefan, Michael WieseJournal of Medicinal Chemistry|March 5, 2016
Pyrrolopyrimidine Derivatives as Novel Inhibitors of Multidrug Resistance-Associated Protein 1 (MRP1, ABCC1)Sven Marcel Schmitt, Katja Stefan, Michael WieseChemmedchem|January 5, 2008
Identification of putative binding sites of P-glycoprotein based on its homology modelChristoph Globisch, Ilza K Pajeva, Michael WieseBioorganic & Medicinal Chemistry|November 25, 2011
Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance proteinKapil Juvale, Veronika F S Pape, Michael WieseChemmedchem|March 5, 2015
Scaffold identification of a new class of potent and selective BCRP inhibitorsFederico Marighetti, Kerstin Steggemann, Maria Karbaum, et al.Pageof 31