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ACS Medicinal Chemistry Letters|March 18, 2026
Lead Optimization: Synthesis and Biological Evaluation of Griseofulvin Derivatives as Novel SIRT6 ActivatorsTilen Zorko, Jan Kogovšek, Luka Ciber, et al.
Molecules (Basel, Switzerland)|December 11, 2025
Synthesis of Bioconjugation Reagents for Use in Covalent Cross-Linking of Proteins by Azide-Alkyne CycloadditionNadja Suhorepec, Luka Ciber, Uroš Grošelj, et al.
The Journal of Biological Chemistry|January 18, 2007
Interaction between human cathepsins K, L, and S and elastins: mechanism of elastinolysis and inhibition by macromolecular inhibitorsMarko Novinec, Robert N Grass, Wendelin J Stark, et al.
IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control|May 16, 2025
Ultrasound-responsive mammalian cell synthetic biologyFilip Ivanovski, Vid Jazbec, Nina Varda, et al.
Biochimica Et Biophysica Acta. Proteins and Proteomics|February 12, 2017
The papain-like cysteine proteinases NbCysP6 and NbCysP7 are highly processive enzymes with substrate specificities complementary to Nicotiana benthamiana cathepsin BMelanie Paireder, Stefan Tholen, Andreas Porodko, et al.
International Journal of Molecular Sciences|December 11, 2025
Cooperativity in Escherichia coli L-Threonine Dehydrogenase and Its Inhibition by an Antibacterial N-Pyridylpyrazolone DerivativeAna Obaha, Nika Mikulič Vernik, Karmen Mlinar, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 9, 2022
Zinc pyrithione is a potent inhibitor of PLPro and cathepsin L enzymes with ex vivo inhibition of SARS-CoV-2 entry and replicationJerneja Kladnik, Ana Dolinar, Jakob Kljun, et al.
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