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Csaba Magyar

Showing results (21-30 of 29) with videos related to

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Journal of Chemical Information and Computer Sciences|March 23, 2004
Noncovalent cross-links in context with other structural and functional elements of proteinsEva Tüdos, András Fiser, Agnes Simon, et al.
Journal of Cheminformatics|January 12, 2021
Identifying new topoisomerase II poison scaffolds by combining publicly available toxicity data and 2D/3D-based virtual screeningAnna Lovrics, Veronika F S Pape, Dániel Szisz, et al.
Biochemical Pharmacology|September 29, 2020
Synergistic transport of a fluorescent coumarin probe marks coumarins as pharmacological modulators of Organic anion-transporting polypeptide, OATP3A1Éva Bakos, Gábor E Tusnády, Orsolya Német, et al.
Nucleic Acids Research|November 11, 2024
MFIB 2.0: a major update of the database of protein complexes formed by mutual folding of the constituting protein chainsErzsébet Fichó, Rita Pancsa, Csaba Magyar, et al.
Protein Science : a Publication of the Protein Society|April 29, 2025
To be, or not to be cleaved: Directed evolution of a canonical serine protease inhibitor against active and inactive protease pair identifies binding loop residue critical for prevention of proteolytic cleavageZsombor Köller, Bálint Zoltán Németh, Bence Kiss, 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.
Chemical Biology & Drug Design|April 1, 2015
Combination of Pharmacophore Matching, 2D Similarity Search, and In Vitro Biological Assays in the Selection of Potential 5-HT6 Antagonists from Large Commercial RepositoriesKrisztina Dobi, Beáta Flachner, Mária Pukáncsik, et al.
Molecular Cancer|October 28, 2025
Safe delivery of a highly toxic anthracycline derivative through liposomal nanoformulation achieves complete cancer regressionAndrás Füredi, Szilárd Tóth, Kristóf Hegedüs, et al.
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Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Chemical Information and Computer Sciences|March 23, 2004
Noncovalent cross-links in context with other structural and functional elements of proteinsEva Tüdos, András Fiser, Agnes Simon, et al.
Journal of Cheminformatics|January 12, 2021
Identifying new topoisomerase II poison scaffolds by combining publicly available toxicity data and 2D/3D-based virtual screeningAnna Lovrics, Veronika F S Pape, Dániel Szisz, et al.
Biochemical Pharmacology|September 29, 2020
Synergistic transport of a fluorescent coumarin probe marks coumarins as pharmacological modulators of Organic anion-transporting polypeptide, OATP3A1Éva Bakos, Gábor E Tusnády, Orsolya Német, et al.
Nucleic Acids Research|November 11, 2024
MFIB 2.0: a major update of the database of protein complexes formed by mutual folding of the constituting protein chainsErzsébet Fichó, Rita Pancsa, Csaba Magyar, et al.
Protein Science : a Publication of the Protein Society|April 29, 2025
To be, or not to be cleaved: Directed evolution of a canonical serine protease inhibitor against active and inactive protease pair identifies binding loop residue critical for prevention of proteolytic cleavageZsombor Köller, Bálint Zoltán Németh, Bence Kiss, 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.
Chemical Biology & Drug Design|April 1, 2015
Combination of Pharmacophore Matching, 2D Similarity Search, and In Vitro Biological Assays in the Selection of Potential 5-HT6 Antagonists from Large Commercial RepositoriesKrisztina Dobi, Beáta Flachner, Mária Pukáncsik, et al.
Molecular Cancer|October 28, 2025
Safe delivery of a highly toxic anthracycline derivative through liposomal nanoformulation achieves complete cancer regressionAndrás Füredi, Szilárd Tóth, Kristóf Hegedüs, et al.
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