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Biomolecules|February 25, 2022
Robust Recombinant Expression of Human Placental Ribonuclease Inhibitor in Insect CellsBeáta Flachner, Krisztina Dobi, Anett Benedek, et al.
Bioorganic & Medicinal Chemistry Letters|August 13, 2018
Inhibition of the LOX enzyme family members with old and new ligands. Selectivity analysis revisitedIstván Hajdú, József Kardos, Balázs Major, et al.
Industrial & Engineering Chemistry Research|August 12, 2024
Development of Continuous Additive-Controlled MSMPR Crystallization by DoE-Based Batch ExperimentsGyörgy Nimród Stoffán, Zsolt Lőrincz, Éva Pusztai, et al.
Molecules (Basel, Switzerland)|September 28, 2021
Rapid Identification of Potential Drug Candidates from Multi-Million Compounds' Repositories. Combination of 2D Similarity Search with 3D Ligand/Structure Based Methods and In Vitro ScreeningKatalin Szilágyi, Beáta Flachner, István Hajdú, et al.
Journal of Chemical Information and Modeling|January 14, 2016
Structure-Based Consensus Scoring Scheme for Selecting Class A Aminergic GPCR FragmentsÁdám A Kelemen, Róbert Kiss, György G Ferenczy, et al.
International Journal of Pharmaceutics|July 27, 2025
Complex investigation of the effect mechanism of polyvinylpyrrolidone in the additive-assisted crystallization of famotidineGyörgy Nimród Stoffán, Tibor Höltzl, Zsolt Lőrincz, et al.
Immunology Letters|February 18, 2014
Monoclonal antibody proteomics: use of antibody mimotope displaying phages and the relevant synthetic peptides for mAb scoutingIstván Hajdú, Beáta Flachner, Melinda Bognár, et al.
International Journal of Cell Biology|November 9, 2023
RuX: A Novel, Flexible, and Sensitive Mifepristone-Induced Transcriptional Regulation SystemAnne Meinzinger, Áron Zsigmond, Péter Horváth, et al.
Molecular Diversity|January 11, 2017
Identification of potential glutaminyl cyclase inhibitors from lead-like libraries by in silico and in vitro fragment-based screeningMária Szaszkó, István Hajdú, Beáta Flachner, et al.
Molecules (Basel, Switzerland)|June 1, 2014
Combination of 2D/3D ligand-based similarity search in rapid virtual screening from multimillion compound repositories. Selection and biological evaluation of potential PDE4 and PDE5 inhibitorsKrisztina Dobi, István Hajdú, Beáta Flachner, et al.
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