Lara Bardtke

ORCID: 0000-0002-5302-9507
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About
Contact & Profiles
Research Areas
  • Malaria Research and Control
  • Trypanosoma species research and implications
  • Retinal Development and Disorders
  • Photoreceptor and optogenetics research
  • Photochromic and Fluorescence Chemistry
  • HIV/AIDS drug development and treatment
  • Aquaculture disease management and microbiota
  • Hemoglobinopathies and Related Disorders
  • Mosquito-borne diseases and control

Humboldt-Universität zu Berlin
2022-2025

Charité - Universitätsmedizin Berlin
2022-2025

Freie Universität Berlin
2022-2025

Australian National University
2022

German Center for Neurodegenerative Diseases
2021

Using retinal organoid systems, organ-like 3D tissues, relies implicitly on their robustness. However, essential key parameters, particularly growth and longer-term culture, are still insufficiently defined. Here, we hypothesize that a previously optimized protocol for high yield of evenly-sized mouse organoids with low variability facilitates assessment such parameters. We demonstrate these reliably complete retinogenesis, can be maintained at least up to 60 days in culture. During this...

10.3389/fcell.2021.645704 article EN cc-by Frontiers in Cell and Developmental Biology 2021-04-27

Artemisinin-based combination therapy (ACT) for the treatment of malaria is highly effective, well tolerated and safe. Episodes delayed haemolysis occur in up to 57.9% patients with severe treated intravenous artesunate, mainly caused by 'pitting' infected red blood cells spleen loss these once-infected RBCs (oiRBCs). Several reports indicate that post-treatment (PTH) also occurs uncomplicated oral ACT, calling systematic investigation.A prospective observational study identify incidence PTH...

10.1093/jtm/taad001 article EN cc-by-nc Journal of Travel Medicine 2023-01-05

After two consecutive AL treatment failures in a non-immune traveller returning from Uganda with Plasmodium falciparum malaria, the parasite showed artemisinin resistance ex vivo and vitro, but no associated genetic markers pfK13 or pfcoronin. In vitro evidence for increased lumefantrine tolerance was present, as were pfmdr1 alleles.

10.1093/jtm/taaf013 article EN other-oa Journal of Travel Medicine 2025-02-04
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