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Mariusz Milik

Showing results (1-10 of 10) with videos related to

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Protein Engineering|September 12, 2003
Common Structural Cliques: a tool for protein structure and function analysisMariusz Milik, Sándor Szalma, Krzysztof A Olszewski
Current Medicinal Chemistry|February 7, 2017
Mitogen-activated Protein Kinase (MAPK) Interacting Kinases 1 and 2 (MNK1 and MNK2) as Targets for Cancer Therapy: Recent Progress in the Development of MNK InhibitorsAgnieszka Dreas, Maciej Mikulski, Mariusz Milik, et al.
Journal of Structural Biology|May 24, 2026
Crystal structure, thermostability and temperature-dependent enzymatic activity of an exo-β-d-glucosaminidase from Pyrococcus chitonophagusKatarzyna Biniek-Antosiak, Daniel Baranowski, Joanna Śliwiak, et al.
Journal of Molecular Modeling|January 24, 2019
How to design potent and selective DYRK1B inhibitors? Molecular modeling studyAgnieszka Szamborska-Gbur, Ewelina Rutkowska, Agnieszka Dreas, et al.
Journal of Medicinal Chemistry|March 25, 2008
"Virtual fragment linking": an approach to identify potent binders from low affinity fragment hitsThomas J Crisman, Andreas Bender, Mariusz Milik, et al.
Journal of Medicinal Chemistry|April 22, 2009
Mapping adverse drug reactions in chemical spaceJosef Scheiber, Jeremy L Jenkins, Sai Chetan K Sukuru, et al.
Journal of Chemical Information and Modeling|May 13, 2009
Gaining insight into off-target mediated effects of drug candidates with a comprehensive systems chemical biology analysisJosef Scheiber, Bin Chen, Mariusz Milik, et al.
International Journal of Molecular Sciences|February 11, 2023
Design and Synthesis of New Quinazolin-4-one Derivatives with Negative mGlu<sub>7</sub> Receptor Modulation Activity and Antipsychotic-Like PropertiesKatarzyna Kaczorowska, Anna Stankiewicz, Ryszard Bugno, et al.
European Journal of Medicinal Chemistry|December 11, 2020
Discovery of indazole-pyridinone derivatives as a novel class of potent and selective MNK1/2 kinase inhibitors that protecting against endotoxin-induced septic shockAgnieszka Dreas, Katarzyna Kucwaj-Brysz, Karolina Pyziak, et al.
Bioorganic & Medicinal Chemistry Letters|January 11, 2019
5-Keto-3-cyano-2,4-diaminothiophenes as selective maternal embryonic leucine zipper kinase inhibitorsNicolas Boutard, Aleksandra Sabiniarz, Klaudia Czerwińska, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Protein Engineering|September 12, 2003
Common Structural Cliques: a tool for protein structure and function analysisMariusz Milik, Sándor Szalma, Krzysztof A Olszewski
Current Medicinal Chemistry|February 7, 2017
Mitogen-activated Protein Kinase (MAPK) Interacting Kinases 1 and 2 (MNK1 and MNK2) as Targets for Cancer Therapy: Recent Progress in the Development of MNK InhibitorsAgnieszka Dreas, Maciej Mikulski, Mariusz Milik, et al.
Journal of Structural Biology|May 24, 2026
Crystal structure, thermostability and temperature-dependent enzymatic activity of an exo-β-d-glucosaminidase from Pyrococcus chitonophagusKatarzyna Biniek-Antosiak, Daniel Baranowski, Joanna Śliwiak, et al.
Journal of Molecular Modeling|January 24, 2019
How to design potent and selective DYRK1B inhibitors? Molecular modeling studyAgnieszka Szamborska-Gbur, Ewelina Rutkowska, Agnieszka Dreas, et al.
Journal of Medicinal Chemistry|March 25, 2008
"Virtual fragment linking": an approach to identify potent binders from low affinity fragment hitsThomas J Crisman, Andreas Bender, Mariusz Milik, et al.
Journal of Medicinal Chemistry|April 22, 2009
Mapping adverse drug reactions in chemical spaceJosef Scheiber, Jeremy L Jenkins, Sai Chetan K Sukuru, et al.
Journal of Chemical Information and Modeling|May 13, 2009
Gaining insight into off-target mediated effects of drug candidates with a comprehensive systems chemical biology analysisJosef Scheiber, Bin Chen, Mariusz Milik, et al.
International Journal of Molecular Sciences|February 11, 2023
Design and Synthesis of New Quinazolin-4-one Derivatives with Negative mGlu<sub>7</sub> Receptor Modulation Activity and Antipsychotic-Like PropertiesKatarzyna Kaczorowska, Anna Stankiewicz, Ryszard Bugno, et al.
European Journal of Medicinal Chemistry|December 11, 2020
Discovery of indazole-pyridinone derivatives as a novel class of potent and selective MNK1/2 kinase inhibitors that protecting against endotoxin-induced septic shockAgnieszka Dreas, Katarzyna Kucwaj-Brysz, Karolina Pyziak, et al.
Bioorganic & Medicinal Chemistry Letters|January 11, 2019
5-Keto-3-cyano-2,4-diaminothiophenes as selective maternal embryonic leucine zipper kinase inhibitorsNicolas Boutard, Aleksandra Sabiniarz, Klaudia Czerwińska, et al.
Pageof 1