University of Southampton
doi: 10.13039/501100005765 , 10.13039/501100005765 , 10.13039/501100013990 , 10.13039/501100000739 , 10.13039/501100013990
RRID: RRID:SCR_008086 , RRID:nlx_56990
Wikidata: Q76473
ISNI: 0000000419369297 , 0000000121551272 , 0000000121814263
FundRef: 501100000739
doi: 10.13039/501100005765 , 10.13039/501100005765 , 10.13039/501100013990 , 10.13039/501100000739 , 10.13039/501100013990
RRID: RRID:SCR_008086 , RRID:nlx_56990
Wikidata: Q76473
ISNI: 0000000419369297 , 0000000121551272 , 0000000121814263
FundRef: 501100000739
University of Southampton
Funder
4,144 Projects, page 1 of 829
assignment_turned_in Project2018 - 2020Partners:University of SouthamptonUniversity of SouthamptonFunder: UK Research and Innovation Project Code: EP/S515589/1Funder Contribution: 244,180 GBPDoctoral Training Partnerships: a range of postgraduate training is funded by the Research Councils. For information on current funding routes, see the common terminology at https://www.ukri.org/apply-for-funding/how-we-fund-studentships/. Training grants may be to one organisation or to a consortia of research organisations. This portal will show the lead organisation only.
All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=ukri________::a2dee1d778b8abdf8efe502e7cd29180&type=result"></script>'); --> </script>
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For further information contact us at helpdesk@openaire.euOpen Access Mandate for Publications assignment_turned_in Project2016 - 2018Partners:University of SouthamptonUniversity of SouthamptonFunder: European Commission Project Code: 703530Overall Budget: 195,455 EURFunder Contribution: 195,455 EURDynOMIS aims to elucidate the antigen selection mechanisms of the adaptive immune system at the molecular level in the highly complex cellular environment. Major histocompatibility complex class I molecules (MHC-I) is a key mediator of adaptive immunity, the cell’s arsenal against infectious pathogens and malignant transformations. MHC-I present antigenic peptides to cytotoxic T lymphocytes at the cell surface, which in turn unleash their cytotoxic apparatus only when peptides from non-healthy proteins are recognized. This process is the result of an equally important peptide selecting function in the early secretory pathway, a mechanism that has not been clearly understood in spite of its fundamental role in vaccination. Deep understanding of the exact mechanisms that drive peptide selection by MHC-I will help to predict immunoprotective epitopes in infections and cancer, which will in turn pave the way for the development of more effective T cell-targeting vaccines and biomarkers to stratify patients’ suitability for immunotherapy. DynOMIS will employ a sophisticated, interdisciplinary approach that integrates quantitative computational systems modelling to identify molecular mechanism from cellular biochemical information, experimental investigation of the structure and dynamics of peptide-bound MHC-I over a large range of timescales, and state-of-the-art molecular dynamics simulations and free energy calculations to elucidate the thermodynamic basis of the peptide selection mechanism in the context of their interactions with cellular cofactors. To this end, DynOMIS will be carried out by an experienced researcher at a world-leading interdisciplinary group comprising molecular immunologists, structural biologists, computational chemists, and industrial partners with a strong focus on clinically relevant immunological research.
All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=corda__h2020::1b8dc1c7b4ac32aac6fe607beb0a90e2&type=result"></script>'); --> </script>
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For further information contact us at helpdesk@openaire.euassignment_turned_in Project2020 - 2024Partners:University of SouthamptonUniversity of SouthamptonFunder: UK Research and Innovation Project Code: 2488257The student will conduct research training through the UKRI MINDS Centre for Doctoral Training, a four-year integrated PhD programme, with a focus on the Embedded Artificial Intelligence theme. The research conducted in this theme will investigate how to efficiently and reliably embed algorithmic techniques such as deep learning, Bayesian inference and optimisation in low-power devices. This may address challenges around low-shot and transfer learning, and managing performance/efficiency trade-offs.
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For further information contact us at helpdesk@openaire.eumore_vert All Research productsarrow_drop_down <script type="text/javascript"> <!-- document.write('<div id="oa_widget"></div>'); document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=ukri________::10e7a860cce15e9ca5c8b434f66de376&type=result"></script>'); --> </script>
For further information contact us at helpdesk@openaire.euOpen Access Mandate for Publications and Research data assignment_turned_in Project2025 - 2027Partners:University of SouthamptonUniversity of SouthamptonFunder: European Commission Project Code: 101208028Funder Contribution: 276,188 EURArchitecturally heterogeneous multi-material multi-principal element alloy (MPEA) composites represent a unique class of heterostructured materials with great potential to evade the strength–ductility trade-off dilemma. However, most conventional processing routes involving high temperatures (e.g., casting, additive manufacturing, and powder metallurgy) suffer from various metallurgical issues such as excessive elemental diffusion, segregation, hard intermetallic phase formation, cracking, and poor densification. To mitigate these challenges, the project suggests prefabricating various MPEA powders into billets using cold spraying (CS) and then employing solid-state friction stir processing (FSP) to achieve microstructural densification. This approach will initiate various dynamic recrystallizations in different compositional domains, allowing us to engineer architecturally heterogeneous multi-material MPEA composites. In general, this project will be implemented in phases, including optimizing process, controlling the heterostructure, evaluating mechanical performances from ambient to cryogenic temperatures, and elucidating deformation mechanisms. The results can be expected to build up the “processing–microstructure–mechanical behavior” correlations of the newly developed multi-material MPEA composites in a quantitative manner. This will facilitate the design and fabrication of similar heterostructured composites, thereby impacting a wide range of industrial sectors, e.g., transport, defense, nuclear, and manufacturing.
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For further information contact us at helpdesk@openaire.euassignment_turned_in Project2017 - 2021Partners:University of SouthamptonUniversity of SouthamptonFunder: UK Research and Innovation Project Code: 1948507The technical objectives of the project are: 1) enhance and extend an integrated aircraft design process building on an existing framework; introduce into the design process a range of disciplinary models of varying fidelity that will allow for an accurate yet rapid engineering design; 2) develop and implement passive and active control technologies that take advantage of wing elasticity in order to reshape the wing for optimal aerodynamic performance and minimal structural loads per flight condition; and limit the peak loads to improve passenger comfort/reduce the load factor, reduce the structural weight and to improve the fatigue resistance.
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