Mgr. Denisa VESELÁ, Ph.D.

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585634914

Katedra experimentální biologie

Přírodovědecká fakulta

Šlechtitelů 27 A (hlavní budova)

3.22

věd. prac. ob. biologických

ČLÁNEK
Delgado T., Veselá D., Dostálová H., Kryštof V., Vojáčková V., Jorda R., Strnad M., Salas CO. New Inhibitors of Bcr-Abl Based on 2,6,9-Trisubstituted Purine Scaffold Elicit Cytotoxicity in Chronic Myeloid Leukemia-Derived Cell Lines Sensitive and Resistant to TKIs. Pharmaceutics. 2024.
Parisis N., Dans PD., Jbara M., Veselá D. Histone H3 serine-57 is a CHK1 substrate whose phosphorylation affects DNA repair. Nature Communications. 2023.
Hendrychová D., Jorda R., Kryštof V. How selective are clinical CDK4/6 inhibitors? MEDICINAL RESEARCH REVIEWS. 2021.
Jorda R., Magar P., Hendrychová D., Kryštof V. Novel modified leucine and phenylalanine dipeptides modulate viability and attachment of cancer cells. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY. 2020.
Salas CO., Zarate AM., Kryštof V., Hendrychová D., Jorda R. Promising 2,6,9-Trisubstituted Purine Derivatives for Anticancer Compounds: Synthesis, 3D-QSAR, and Preliminary Biological Assays. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2020.
Xavier NM., Goncalves-Pereira R., Jorda R., Hendrychová D., Oliveira MC. Novel dodecyl-containing azido and glucuronamide-based nucleosides exhibiting anticancer potential. PURE AND APPLIED CHEMISTRY. 2019.
Krajčovičová S., Jorda R., Hendrychová D., Kryštof V., Soural M. Solid-phase synthesis for thalidomide-based proteolysis-targeting chimeras (PROTAC). CHEMICAL COMMUNICATIONS. 2019.
Jorda R., Hendrychová D., Voller J., Řezníčková E., Gucký T., Kryštof V. How Selective Are Pharmacological Inhibitors of Cell-Cycle-Regulating Cyclin-Dependent Kinases? JOURNAL OF MEDICINAL CHEMISTRY. 2018.
Krajčovičová S., Gucký T., Hendrychová D., Kryštof V., Soural M. A Stepwise Approach for the Synthesis of Folic Acid Conjugates with Protein Kinases Inhibitors. Journal of Organic Chemistry. 2017.

Uživatel nepovolil zobrazení dat v Portále UP.

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