Torthaí cuardaigh - Mertlíková-Kaiserová, Helena
- 1 - 9 toradh as 9 á dtaispeáint
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1
2′-deoxy-5,6-dihydro-5-azacytidine—a less toxic alternative of 2′-deoxy-5-azacytidine: A comparative study of hypomethylating potential de réir Matoušová, Marika, Votruba, Ivan, Otmar, Miroslav, Tloušťová, Eva, Günterová, Jana, Mertlíková-Kaiserová, Helena
Foilsithe / Cruthaithe 2011Téacs -
2
Amidate Prodrugs of 9-[2-(Phosphonomethoxy)Ethyl]Adenine as Inhibitors of Adenylate Cyclase Toxin from Bordetella pertussis de réir Šmídková, Markéta, Dvořáková, Alexandra, Tloušt'ová, Eva, Česnek, Michal, Janeba, Zlatko, Mertlíková-Kaiserová, Helena
Foilsithe / Cruthaithe 2014Téacs -
3
Halogen Dance-Based Synthesis of Phosphonomethoxyethyl (PME) Substituted 2-Aminothiazoles as Potent Inhibitors of Bacterial Adenylate Cyclases de réir Česnek, Michal, Šafránek, Michal, Dračínský, Martin, Tloušťová, Eva, Mertlíková-Kaiserová, Helena, Hayes, Michael P., Watts, Val J., Janeba, Zlatko
Foilsithe / Cruthaithe 2021Téacs -
4
Design and synthesis of fluorescent acyclic nucleoside phosphonates as potent inhibitors of bacterial adenylate cyclases de réir Břehová, Petra, Šmídková, Markéta, Skácel, Jan, Dračínský, Martin, Mertlíková-Kaiserová, Helena, Velasquez, Monica P. Soto, Watts, Val J., Janeba, Zlatko
Foilsithe / Cruthaithe 2016Téacs -
5
Nucleobase Modified Adefovir (PMEA) Analogues as Potent and Selective Inhibitors of Adenylate Cyclases from Bordetella pertussis and Bacillus anthracis de réir Česnek, Michal, Skácel, Jan, Jansa, Petr, Dračínský, Martin, Šmídková, Markéta, Mertlíková-Kaiserová, Helena, Soto-Velasquez, Monica P., Watts, Val J., Janeba, Zlatko
Foilsithe / Cruthaithe 2018Téacs -
6
Purine analogs as phosphatidylinositol 4-kinase IIIβ inhibitors de réir Šála, Michal, Kögler, Martin, Plačková, Pavla, Mejdrová, Ivana, Hřebabecký, Hubert, Procházková, Eliška, Strunin, Dmytro, Lee, Gary, Birkus, Gabriel, Weber, Jan, Mertlíková-Kaiserová, Helena, Nencka, Radim
Foilsithe / Cruthaithe 2016Téacs -
7
Acyclic nucleoside phosphonates with 2-aminothiazole base as inhibitors of bacterial and mammalian adenylate cyclases de réir Břehová, Petra, Chaloupecká, Ema, Česnek, Michal, Skácel, Jan, Dračínský, Martin, Tloušt’ová, Eva, Mertlíková-Kaiserová, Helena, Soto-Velasquez, Monica P., Watts, Val J., Janeba, Zlatko
Foilsithe / Cruthaithe 2021Téacs -
8
Druggable Hot Spots in the Schistosomiasis Cathepsin B1 Target Identified by Functional and Binding Mode Analysis of Potent Vinyl Sulfone Inhibitors de réir Jílková, Adéla, Rubešová, Petra, Fanfrlík, Jindřich, Fajtová, Pavla, Řezáčová, Pavlína, Brynda, Jiří, Lepšík, Martin, Mertlíková-Kaiserová, Helena, Emal, Cory D., Renslo, Adam R., Roush, William R., Horn, Martin, Caffrey, Conor R., Mareš, Michael
Foilsithe / Cruthaithe 2020Téacs -
9
Correction to “Synthesis and Cytotoxic and Antiviral Profiling of Pyrrolo- and Furo-Fused 7-Deazapurine Ribonucleosides” de réir Tokarenko, Anna, Lišková, Barbora, Smoleń, Sabina, Táborská, Natálie, Tichý, Michal, Gurská, Soňa, Perlíková, Pavla, Frydrych, Ivo, Tloušt’ová, Eva, Znojek, Pawel, Mertlíková-Kaiserová, Helena, Poštová Slavětínská, Lenka, Pohl, Radek, Klepetářová, Blanka, Khalid, Noor-Ul-Ain, Wenren, Yiqian, Laposa, Rebecca R., Džubák, Petr, Hajdúch, Marián, Hocek, Michal
Foilsithe / Cruthaithe 2019Téacs