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, mathematical modelling, and stochastic molecular dynamics simulations to investigate the physical mechanism of how antibiotic treatments ultimately lead to bacterial cell death. The post-holder will join a
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there are currently no effective treatments, so this an area of significant unmet need. Redirected T cells offer the potential to specifically target pathogenic IgA1 producing cells. You will work closely with members
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expertise already in place. Improvement of cancer treatment remains a priority as 28% of UK deaths are still attributable to cancer. Neuroendocrine tumours (NETs), whilst rare, are the exemplar cancer type
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clinical and academic researchers to work independently and to support our PhD students and technical staff in the laboratory. An understanding of, or desire to learn single cell transcriptomics and the
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mechanism underlying the resensitisation to GC with the ultimate aim the development of a therapy which can override GC resistance at relapse and thus improve treatment response and outcomes. This project
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funded by the STFC Nuclear Security Science Network (‘NuSec’) https://www.nusec.uk/ You will be working as part of a team of PhD students and academic staff to deliver this project. The research may
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, Institute of Life Course and Medical Sciences (the University of Liverpool). The post is funded for 30-months, full-time. A PhD (or about to obtain) in extracellular matrix proteomics is required
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and help supervise DPhil students and other junior lab members. You will hold a PhD in molecular biology, genetics, or a related discipline, together with relevant experience. Experience in cell culture
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PhD in Engineering or Applied Physics, or a clearly related area. Experience of research in one or more of the following areas: mechanical engineering, electro-mechanical engineering, fluid dynamics
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apply Overview About the Role This is a fully funded project for 2 years including PhD fees for a doctor in training interested in a career in academic dermatology to undertake a PhD. A third year of