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Field
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. fluorescence microscopy, flow cytometry, image analysis or CRISPR/Cas9). Experience with mitochondrial biology, tumour–stromal interactions, extracellular vesicles, intercellular communication or therapy
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electron microscopy. PhD candidate 2 will use this fundamental understanding to extrapolate towards more complex textures, including entire lattices and guided by state-of-the-art nano-lithographies, in
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biology / Immunology laboratory experience, such as: Flow cytometry and FACS, immunofluorescence microscopy/imaging, cell culture, tumour cell killing assays, tissue processing, etc. Molecular biology
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. eLife (2019). PMID: 31042147 Wang G, Moffitt JR, Zhuang X. Multiplexed imaging of high-density libraries of RNAs with MERFISH and expansion microscopy. Sci Rep 8, 4847 (2018). PMID: 29555914 Moffitt JR
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or more of the following would be advantageous but is not essential: mammalian cell culture, molecular biology, microscopy, genetic manipulation, chromatin or epigenetic assays, and cancer or ageing model
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the University of Basel. Experience in the following areas are of special interest: Mammalian cell culture and analysis (Microscopy, qRT-PCR) Hydrogel formulations and characterisation (Rheometry, Atomic Force
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. The dynamics of head eversion will be characterized by combining confocal and electron microscopy. These approaches will allow us to quantify changes in tissue shape, curvature, and thickness during
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for high-aspect-ratio vertical interconnects characterise the results (SEM, AFM, XCT, optical microscopy) for geometric accuracy, durability and interfacial strength -validate scalability and
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interconnects characterise the results (SEM, AFM, XCT, optical microscopy) for geometric accuracy, durability and interfacial strength -validate scalability and sustainability: less material waste, better energy
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enhanced electrochemical sensing, field-responsive coatings, and energy-harvesting architectures. The candidate will use advanced fabrication, microscopy, and spectroscopy techniques, and work within an