Uli kazmaier
Affiliations: | saarland university |
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Junk L, Schmiedel VM, Guha S, et al. (2024) Homo-BacPROTAC-induced degradation of ClpC1 as a strategy against drug-resistant mycobacteria. Nature Communications. 15: 2005 |
Hoi DM, Junker S, Junk L, et al. (2023) Clp-targeting BacPROTACs impair mycobacterial proteostasis and survival. Cell. 186: 2176-2192.e22 |
Greve J, Mogk A, Kazmaier U. (2022) Total Synthesis and Biological Evaluation of Modified Ilamycin Derivatives. Marine Drugs. 20 |
Morreale FE, Kleine S, Leodolter J, et al. (2022) BacPROTACs mediate targeted protein degradation in bacteria. Cell |
Kazmaier U, Junk L. (2021) Recent Developments on the Synthesis and Bioactivity of Ilamycins/Rufomycins and Cyclomarins, Marine Cyclopeptides That Demonstrate Anti-Malaria and Anti-Tuberculosis Activity. Marine Drugs. 19 |
Kiefer A, Bader CD, Held J, et al. (2019) Synthesis of New Cyclomarin Derivatives and Their Biological Evaluation towards Mycobacterium Tuberculosis and Plasmodium Falciparum. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Koczian F, Nagło O, Vomacka J, et al. (2019) Targeting the endoplasmic reticulum-mitochondria interface sensitizes leukemia cells to cytostatics. Haematologica. 104: 546-555 |
Truebenbach I, Gorges J, Kuhn J, et al. (2017) Sequence-Defined Oligoamide Drug Conjugates of Pretubulysin and Methotrexate for Folate Receptor Targeted Cancer Therapy. Macromolecular Bioscience |
Barbie P, Kazmaier U. (2016) Total synthesis of cyclomarins A, C and D, marine cyclic peptides with interesting anti-tuberculosis and anti-malaria activities. Organic & Biomolecular Chemistry. 14: 6036-54 |
Eirich J, Braig S, Schyschka L, et al. (2014) A small molecule inhibits protein disulfide isomerase and triggers the chemosensitization of cancer cells. Angewandte Chemie (International Ed. in English). 53: 12960-5 |