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University of British Columbia | Northern British Columbia Fort Nelson, British Columbia | Canada | 8 days ago
migration through non-isotropic environments as well as through microfluidic devices. The goal is to develop artificial synthetic cells for biomedical and experimental research. As a by-product, we seek
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research in virology/immunology with potential for high-impact publications. The project will develop high-throughput microfluidic platforms for functional screening of antigen-specific T cells and
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for the parallelized monitoring of metabolites and environmental parameters to assess organoid- and assembloid formation Developing microfluidic chips that enable the multi parameter measurements of key molecular and
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cells and microfluidics to generate mature and functional vascular tissues. This work will be completed as part of our multidisciplinary team studying the interactions between cells and their
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. Experience with modelling and quantifying collective behavior and quantitative microscopy is essential. Experience with microfluidics will be favorably viewed. This project requires the tight integration
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of cancer evolution (Aitken 2025). We also repurpose technologies like microfluidics to better understand the molecular landscape of the earliest mitoses after mutagenesis (Ginno 2024). Your Tasks: We
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). The project will focus on CRISPR genome engineering of SVD-relevant mutations, differentiation of iPSCs into neurovascular cells, microfluidic 3D vascular tissue engineering, and identifying disease-relevant
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changes in microgravity conditions. d. Ability to perform cell culture and tissue models such as 3D tissue models and microfluidic systems to simulate microgravity. e. Understanding and experience with
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to innovative research projects focusing on precision medicine, microfluidic technologies, and immunotherapy. Qualifications: Knowledge of: Advanced immunology and cell biology principles. Microfluidic
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 2 months ago
intestinal mucosal immune response involved in the devastating intestinal disease affecting premature infants called necrotizing enterocolitis (NEC). We utilize a neonatal mouse model of NEC, microfluidic gut