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, and fluorescent microscopy. Experience in studying skin, hair follicle, skin cancer, or epithelial-mesenchymal interaction, and genetically engineered mouse models is a plus. The ideal candidate should
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advanced biochemical methods (e.g., SPR, BLI, ELISA, fluorescence-based assays) Has experience with yeast display Has strong documentation of peer-reviewed publications Demonstrates the ability to work
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-molecule metabolite signatures. Design and optimisation of fluorescent probes, high-throughput biochemical assays, and chromatographic and mass spectrometry-based platforms for quantitative biomarker
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for mitochondrial mRNA levels and degradation using a fluorescent microscopy-based approach. The proteins identified in this screening will be further characterized through various molecular, biochemical, and
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qualifications An M.D., Ph.D. or M.D./Ph.D. is required Preferred qualifications Candidates with a background in vascular biology, cell and developmental biology, mouse genetics, fluorescence microscopy and/or
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-stranded architecture for cotranscriptional folding of RNA nanostructures. Science (2014). https://doi.org/10.1126/science.1253920 [2] An RNA origami robot that traps and releases a fluorescent aptamer
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://doi.org/10.1126/science.1253920 [2] An RNA origami robot that traps and releases a fluorescent aptamer. Science Advances (2024). https://doi.org/10.1126/sciadv.adk1250 Your qualifications: Required
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://doi.org/10.1126/science.1253920 [2] An RNA origami robot that traps and releases a fluorescent aptamer. Science Advances (2024). https://doi.org/10.1126/sciadv.adk1250 Your qualifications: Required
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force microscopy (AFM), advanced fluorescence and confocal microscopy, and quantitative biophysics. The project aims to elucidate how mechanical properties and forces emerge from molecular and structural
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experiments group (You+Supervisor+support by lab). These collaborations enable practically relevant and breakthrough results. This team goal requires initially videomicroscopy of X-Y fluorescently labeled sperm