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Pathology group. You will be part of a bigger EU-funded project which goal is to develop a safe and efficient cell therapy based on genome edited T cells for IgA nephropathy (IgAN). IgAN is the most common
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funded by BBSRC and is fixed-term for 24 months. This project is to develop simple cell (SimCell, non-dividing bacteria cell) based biocatalyst to transform waste from cultured meat process into essential
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-energy signals, characterizing background populations, improving event reconstruction, and understanding detector effects. They will contribute to LZ operations and performance optimization. This will
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project on the biophysical determinants of cell fate decisions in skin inflammatory diseases. Using a pioneering approach called spatial mechano-transcriptomics, recently developed by the Hallou Lab and
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in structural biology, cell biology and neurobiology, providing access to expertise and training in these areas. The successful candidate will focus on the structures and functions of adhesion
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this core-funded role you will lead the development of pipelines and tools for the analysis of data from cutting-edge single cell and spatial genomics platforms such as the 10x Chromium and Nanostring CosMx
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microscopy/live cell imaging. Please see the below 'Job Description' for further details on the project, responsibilities, and selection criteria, as well as further information about the university and how
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partnering academic or industrial institutions and present research findings in discussions with collaborators. To be successful in this role, you will hold a PhD/DPhil (or close to completion) in Cell Biology
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and how they contribute to cell heterogeneity. An important component of the studies will be to use advanced cell imaging, including confocal and super-resolution modalities. Projects will be
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of metals to hydrogen embrittlement, a phenomenon that is arguably the biggest threat to the deployment of a hydrogen energy infrastructure and the cause of numerous structural integrity problems in