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describe and quantify the spatial characteristics and cellular interactions associated with colorectal response to neoadjuvant therapy.You will be jointly supervised by Professor Helen Byrne (Mathematical
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project goals are to develop and to deploy novel gene/cell-based therapeutics to restore cell-specific expressions of particular genes, at an appropriate time point, location, and in a relevant cell type
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establish routine cell surface proteome analysis using subcellular fractionation techniques, such as density gradient centrifugation and surface biotinylation followed by enrichment, to explore the surface
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Institute for Molecular and Computational Medicine (IMCM). You will test GSK assets and targets in established models of podocyte and mesangial cell pathology relevant to glomerular diseases. You will
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correlating findings with analysis of patient material. You will take a lead role in conducting wet lab experimentation, applying state-of-the-art single-cell multiomic approaches, including transcriptomic
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myeloproliferative neoplasms (MPNs). You will take a lead role in conducting wet lab experimentation, applying state-of-the-art single-cell multiomic approaches, including transcriptomic, genetic, and DNA methylation
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sources. The postdoctoral researcher will develop a chronic implantable system for characterizing the glucose-powered fuel cell. Your Specific Duties include: • Develop an electrochemical interface
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and leading a programme of numerical simulations relating to all aspects of our research on P-MoPAs; using particle-in-cell computer codes hosted on local and national high-performance computing
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biology, biochemistry, and cell biology techniques (e.g. molecular cloning, protein and RNA extraction, PCR, gel electrophoresis, western blotting, mammalian cell culture, genetic manipulation of cells
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of the project. Applicants should hold, or be close to completion of, PhD/DPhil in Biology or a related subject. You should have a high level of competence in cell biology and relevant experience demonstrated by