29 evolution "https:" "https:" "https:" "https:" "https:" "https:" "Aix Marseille Université " scholarships at Newcastle University
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at https://blogs.ncl.ac.uk/astrophds/ Number Of Awards 1 Start Date 1st October 2026 Award Duration 3.5 years Application Closing Date 6th March 2026 Sponsor Science and Technology Facilities Council (STFC
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stakeholders. Ultimately, the findings will provide strategic evidence for the development of long-term adaptation pathways that will help to navigate severe socio-economic disruption from drought events
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-generation into medical device software development processes. You will be trained to carry out research that combines software engineering, formal methods, and safety assurance. You are not expected to have
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PhD Studentship: Development of a robust hydrological modelling framework for drought risk assessments Award Summary This studentship provides a tax-free annual living allowance of £25,726 plus a
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development of wide bandgap device-based integrated motor drives, advanced control techniques for next-generation drives, and innovative approaches to reducing passive components in electric drive systems. Your
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: (a) security, (b) reliability, (c) selectivity, (d) speed, and (e) robustness. https://www.spenergynetworks.co.uk/pages/d_suite_project.aspx Number Of Awards 1 Start Date October 2026 Award Duration 4
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models, in-house laboratory tests in a wind-wave-current flume (https://research.ncl.ac.uk/amh/ ) and numerical methodology to quantify biofouling impacts on flow-induced vibration phenomena, structural
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to enhance both accuracy and computational efficiency, enabling near real time water quality forecasting. This development will provide a more reliable, science-based foundation for environmental decision
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project costs will also be provided. Overview In vitro models of cardiac tissue are synthetic tissues produced in the lab which allow for the development of organs and the treatment of diseases to be
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element modelling techniques and scripting. Osteogenesis imperfect (OI), also known as ‘brittle bone disease’ is a genetic condition which affects the development of type I collagen. Patients with OI have