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Stancho Stanchev

Showing results (21-30 of 27) with videos related to

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Journal of Molecular Histology|July 15, 2019
Cytoarchitecture of the dorsal claustrum of the cat: a quantitative Golgi studyDimka Hinova-Palova, Georgi Kotov, Boycho Landzhov, et al.
European Journal of Medicinal Chemistry|June 20, 2024
Extensive targeting of chemical space at the prime side of ketoamide inhibitors of rhomboid proteases by branched substituents empowers their selectivity and potencyKathrin Bach, Jan Dohnálek, Jana Škerlová, et al.
The Journal of Biological Chemistry|January 11, 2017
Sensitive Versatile Fluorogenic Transmembrane Peptide Substrates for Rhomboid Intramembrane ProteasesAnežka Tichá, Stancho Stanchev, Jan Škerle, et al.
The Journal of Biological Chemistry|December 15, 2024
The zymogenic form of SARS-CoV-2 main protease: A discrete target for drug discoveryPavel Novotný, Jana Humpolíčková, Veronika Nováková, et al.
Cell Chemical Biology|November 7, 2017
General and Modular Strategy for Designing Potent, Selective, and Pharmacologically Compliant Inhibitors of Rhomboid ProteasesAnežka Tichá, Stancho Stanchev, Kutti R Vinothkumar, et al.
The Journal of Biological Chemistry|February 8, 2025
An in vitro platform for the enzymatic characterization of the rhomboid protease RHBDL4Satarupa Bhaduri, Mac Kevin E Braza, Stancho Stanchev, et al.
Biorxiv : the Preprint Server for Biology|October 17, 2024
An <i>in vitro</i> platform for the enzymatic characterization of the rhomboid protease RHBDL4Satarupa Bhaduri, Mac Kevin E Braza, Stancho Stanchev, et al.
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Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Molecular Histology|July 15, 2019
Cytoarchitecture of the dorsal claustrum of the cat: a quantitative Golgi studyDimka Hinova-Palova, Georgi Kotov, Boycho Landzhov, et al.
European Journal of Medicinal Chemistry|June 20, 2024
Extensive targeting of chemical space at the prime side of ketoamide inhibitors of rhomboid proteases by branched substituents empowers their selectivity and potencyKathrin Bach, Jan Dohnálek, Jana Škerlová, et al.
The Journal of Biological Chemistry|January 11, 2017
Sensitive Versatile Fluorogenic Transmembrane Peptide Substrates for Rhomboid Intramembrane ProteasesAnežka Tichá, Stancho Stanchev, Jan Škerle, et al.
The Journal of Biological Chemistry|December 15, 2024
The zymogenic form of SARS-CoV-2 main protease: A discrete target for drug discoveryPavel Novotný, Jana Humpolíčková, Veronika Nováková, et al.
Cell Chemical Biology|November 7, 2017
General and Modular Strategy for Designing Potent, Selective, and Pharmacologically Compliant Inhibitors of Rhomboid ProteasesAnežka Tichá, Stancho Stanchev, Kutti R Vinothkumar, et al.
The Journal of Biological Chemistry|February 8, 2025
An in vitro platform for the enzymatic characterization of the rhomboid protease RHBDL4Satarupa Bhaduri, Mac Kevin E Braza, Stancho Stanchev, et al.
Biorxiv : the Preprint Server for Biology|October 17, 2024
An <i>in vitro</i> platform for the enzymatic characterization of the rhomboid protease RHBDL4Satarupa Bhaduri, Mac Kevin E Braza, Stancho Stanchev, et al.
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