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support the development and implementation of assays to study neuronal resilience using CRISPR screening in human neuronal cell lines and human induced pluripotent stem cell-derived neurons. This is an
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vivo disease models. The postholder will have the opportunity to work with cutting edge single cell technologies including 10x mutli-omics, single cell genotyping, spatial transcriptomics, multiparameter
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conventional electronic structure modelling approaches. The work will be carried out in close collaboration with experimental groups in Oxford Materials and industrial partners working on energy-related
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and establish novel methods for protein-ligand affinity prediction that can offer significant speed gains but similar accuracy to absolute binding free energy (ABFE) calculations. This builds on a
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the propagation of systemic risks through global shipping networks, and how these networks may evolve in the future due to changing patterns in global trade, including those associated with the green energy
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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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-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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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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We are seeking an enthusiastic and highly motivated individual who is excited about the prospect of using B-cell genetics in an archetypal autoimmune disease to explore fundamental questions about