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mechanisms by which co-inhibitory receptors, including PD-1, BTLA, TIGIT, and CD200R, regulate T cell function in autoimmune settings. Despite sharing common downstream signalling components such as SHP1 and
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process, leading to more resilient development. An important second aim of the project is in working with networks of institutes in central Asia to strengthen capacity, and to develop further efforts in
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great place to work. Application Process Applications for this vacancy are to be made online via www.recruit.ox.ac.uk and Vacancy ID 181852 . You will be required to upload your curriculum vitae and a
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project that leverages disparate expertise across the consortium to attempt to deliver real-world impact. Candidates who have submitted their final PhD thesis at the point of interview and are awaiting
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career to biological research are particularly welcome to apply. Candidates who have submitted their final PhD thesis at the point of interview and are awaiting final examination are eligible to apply
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groups. With a strong focus on human tissue use we are looking for this post holder to become one of the deputy human tissue point of contact for the department. This will be an advisory role guiding
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the AM fungus, R. irregularis. The project focuses on obtaining a mechanistic understanding of EV biogenesis, cargo loading and signals that regulate EV release during the interaction. The post-doc will
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analysis of EVs isolated during the interaction of M. truncatula and the AM fungus, R. irregularis. The project focuses on obtaining a mechanistic understanding of EV biogenesis, cargo loading and signals
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(e.g. phonetic, typological, geo-historical, topographical, and sociolinguistic) variably promote or inhibit prosodic convergence between languages in contact, and map findings on a digital multi-modal
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into real-world settings. You will be responsible for developing machine learning and AI algorithms for a range of data and applications (e.g. natural language processing, multivariate time-series data