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the extracellular space remains unclear. In this project, the interdisciplinary team will combine their expertise in bio-microfluidics (Thomas Pfohl, Physics Institute, University of Freiburg), bacterial ECM
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quantitative image analysis, numerical modeling, and explainable AI (XAI) with state-of-the-art biophysical methods. Using techniques such as traction force microscopy, microfluidics, 3D bioprinting, and
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to identify novel drugs for repurposing as ALS therapeutics. We also generated a microfluidic device enabling the study of axonal RNP granules as well as the functionality of neuromuscular junctions. Here, we
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for live-cell imaging of RNP granules, facilitating compound screening to identify novel drugs for repurposing as ALS therapeutics. We also generated a microfluidic device enabling the study of axonal RNP
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of microfluidic cultivation platforms for co-cultures Live-cell microscopy (including fluorescence, phase contrast and time-lapse) for the analysis of cell interactions. Conducting cultivation experiments with
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microfluidic techniques and 3D cell culture, you will grow human microvascular tissue on chip whose architecture self-organizes in response to vasoactive substances. Your work will lead the way to applications
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or microfluidics and ideally in quantitative data analysis. As a theoretical candidate, you have knowledge in quantitative biology, soft matter/complex systems physics or statistical physics. You enjoy working in
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or comparable degree in physics, biology, bioengineering, material engineering or a related discipline. You have experimental experience in cell/tissue culture, microfluidics, or a related discipline. You enjoy
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within the vents? You will grow two-dimensional hydrothermal vents on a microfluidic chip and quantify the vent geometry from your data. You will assess how geochemical mineral composition and inflow rate