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bind to protein ligands via sulphated residues that interact with positively charged regions within the protein ligand(s). The 3D organisation of these domains is therefore critical for their function
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-material capability with a suitable closure model; (2) improved strategy for interface tracking/capturing; (3) very high-speed scenarios with use of nonlinear Riemann-solvers. If time allows exploratory 3D
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cultures—a powerful 3D ex vivo model—this project will dissect the mechanistic links between mTOR signalling, reactive glial phenotypes, and complement activation. The project will also incorporate human
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student will take advantage of state-of-the-art soft polymer fabrication (3D/4D printing) and characterisation (i.e. electro-mechanical multi-axial testing rigs) equipment and the latest computational
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ligand(s). The 3D organisation of these domains is therefore critical for their function. The object of our studies is to gain a fundamental understanding of this incredible family of glycans, opening
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explore ways to control their motion in 3D space. Synthetic microswimmers have many potential biomedical applications, including targeted drug delivery and non-invasive medical treatments. The swimmers
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tools (e.g. Flow-3D), and keen to develop both technical and communication skills. Funding and Benefits The studentship includes: Full tuition fees A tax-free bursary of up to £25,000/year Access
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scenarios as typically encountered by UK mountain rescue teams and apply innovative biomechanical analysis using Bournemouth University ’s in-vivo 3D motion tracking technology to determine residual motion of
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will combine 2 and 3D cell culture systems, gastruloids development, FACS drug screening and next-generation sequencing with investigation of patient samples, to identify and characterise targetable
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fabricate (3D print) bespoke equipment tailored to the project's specific needs. Contribute to interdisciplinary research efforts, fostering collaboration between various research groups, and actively