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- Institute of Bioorganic Chemistry Polish Academy of Sciences
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- International Institute of Molecular and Cell Biology in Warsaw
- Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences
- Maj Institute of Pharmacology Polish Academy of Sciences
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reference letters, but contact details instead). Where to apply Website https://jobrxiv.org/job/the-international-institute-of-molecular-mechanisms-277… Requirements Additional Information Work Location(s
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the interplay between iron homeostasis, ferroptosis, and protein aggregation using advanced cellular and animal models. Where to apply Website https://system.erecruiter.pl/FormTemplates/RecruitmentForm.aspx?WebID
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for Smart Economy 2021-2027 (FENG). Job description The Center for Quantum Digital Organic Memristors (CKCOM) project focuses on the development of a new generation of molecular memory and logic elements
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. To this end, we will employ advanced molecular, cellular, and systems biology methods and tools, as well as various research models—from standard cell lines to primary lines and several mouse models
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of this project is to investigate the role of reactive oxygen species and autophagy during Staphylococcus aureus infection. The postdoctoral researcher will employ animal infection models to dissect the cellular
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Jerzy Haber Institute of Catalysis and Surface Chemistry, Polish Academy of Sciences | Poland | 15 days ago
properties and a variety of potential applications. Application of the molecular dynamics methods combined with the approach based on the thermodynamic models of multicharged surfactant adsorption can provide
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of three-dimensional bone scaffold models, c. Design and fabrication (3D printing) of three-dimensional bone scaffold models, d. Preparation of samples for physicochemical and mechanical testing, e
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experiments in basic molecular biology, including cell culture in 2D and 3D models and their treatment with various factors; performing a wide range of cell-based assays; genetic engineering of cells; qPCR
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mechanistic details of these interactions remain unknown. So far, no atomic model has been identified for complexes between mutated transcripts and the aggregation-prone proteins bound to them. Due to the large
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/conditioning, 2D/3D models, implantation into the chorioallantoic membrane (CAM) model, and phenotypic/molecular analyses to study tumor heterogeneity, EMT-related traits, and drug response. The successful