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Field
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. Solid knowledge in cell and structural biology, as well as expertise in sample preparation and 3D electron microscopy image analysis, are required. Holder of a PhD in biology or biophysics, you have
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of wildtype and Bdf1-mutant C. albicans strains. The project will also involve developing high-resolution 3D X-ray imaging approaches to investigate morphotype-dependent changes in the nuclear and subcellular
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with 3D cell culture, organoids or tissue engineering will be considered a strong advantage. Experience with image analysis software (ImageJ/Fiji) and scientific computing tools (Python, R or equivalent
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breakdown or electromigration). Compared to other imaging modalities such as electron microscopy, X-ray microscopy is non-destructive and hence ideally suited for in-situ and operando 3D imaging. However, at
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breakdown or electromigration). Compared to other imaging modalities such as electron microscopy, X-ray microscopy is non-destructive and hence ideally suited for in-situ and operando 3D imaging. However, at
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-disciplinary team. Our research sits at the cutting edge of regenerative medicine and neurobiology, utilizing state-of-the-art human induced pluripotent stem cell (hiPSC) models, 3D tissue engineering, and
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transfer at the liquid-solid interface. To connect materials to devices, you will prototype booster-bed reactors from mL to L scale by 3D printing and support the transfer of promising formulations toward
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. Experience with quantitative image analysis and deep learning tools for segmentation and classification (e.g., Cellpose, napari, scikit-image, PyTorch). Experience with 3D culture systems, organoids
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culture, including 3D culture, co-culture, organoid culture, or matrix-embedded cell systems. Experience with fluorescence microscopy and quantitative image analysis. Proficiency in standard molecular
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to 3D transistor architectures and stacked, hybrid-bonded devices, non-destructive, high-resolution 3D imaging is becoming a necessity. Unfortunately, current 3D X-ray nanoimaging methods