Ngā hua rapu - Mertlíková-Kaiserová, Helena

2′-deoxy-5,6-dihydro-5-azacytidine—a less toxic alternative of 2′-deoxy-5-azacytidine: A comparative study of hypomethylating potential mā Matoušová, Marika, Votruba, Ivan, Otmar, Miroslav, Tloušťová, Eva, Günterová, Jana, Mertlíková-Kaiserová, Helena

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Amidate Prodrugs of 9-[2-(Phosphonomethoxy)Ethyl]Adenine as Inhibitors of Adenylate Cyclase Toxin from Bordetella pertussis mā Šmídková, Markéta, Dvořáková, Alexandra, Tloušt'ová, Eva, Česnek, Michal, Janeba, Zlatko, Mertlíková-Kaiserová, Helena

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Halogen Dance-Based Synthesis of Phosphonomethoxyethyl (PME) Substituted 2-Aminothiazoles as Potent Inhibitors of Bacterial Adenylate Cyclases mā Česnek, Michal, Šafránek, Michal, Dračínský, Martin, Tloušťová, Eva, Mertlíková-Kaiserová, Helena, Hayes, Michael P., Watts, Val J., Janeba, Zlatko

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Design and synthesis of fluorescent acyclic nucleoside phosphonates as potent inhibitors of bacterial adenylate cyclases mā Břehová, Petra, Šmídková, Markéta, Skácel, Jan, Dračínský, Martin, Mertlíková-Kaiserová, Helena, Velasquez, Monica P. Soto, Watts, Val J., Janeba, Zlatko

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Nucleobase Modified Adefovir (PMEA) Analogues as Potent and Selective Inhibitors of Adenylate Cyclases from Bordetella pertussis and Bacillus anthracis mā Česnek, Michal, Skácel, Jan, Jansa, Petr, Dračínský, Martin, Šmídková, Markéta, Mertlíková-Kaiserová, Helena, Soto-Velasquez, Monica P., Watts, Val J., Janeba, Zlatko

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Purine analogs as phosphatidylinositol 4-kinase IIIβ inhibitors mā 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

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Acyclic nucleoside phosphonates with 2-aminothiazole base as inhibitors of bacterial and mammalian adenylate cyclases mā 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

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Druggable Hot Spots in the Schistosomiasis Cathepsin B1 Target Identified by Functional and Binding Mode Analysis of Potent Vinyl Sulfone Inhibitors mā 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

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Correction to “Synthesis and Cytotoxic and Antiviral Profiling of Pyrrolo- and Furo-Fused 7-Deazapurine Ribonucleosides” mā 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

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