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structural technologies, this PhD position offers a unique opportunity. Join MET2ADAPT to engage with some of the most challenging and high-impact questions surrounding next-generation wind and wave energy
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, especially in the rapidly advancing fields of meta-materials, renewable energy systems, and intelligent structural technologies, this PhD position offers a unique opportunity. Join MET2ADAPT to engage with
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DTU Tenure Track Researcher on Nanoreactors for Operando Visualizations of Nanoparticle Catalysis...
ultrasensitive and quantitative methods for investigating gas-surface interactions on nanoparticles in nanoliter reaction volumes. Relating the three-dimensional surface structure, dynamics and catalytic functions
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drugs. To solve this problem, this project will investigate if allosteric inhibitors can be designed towards a number of transporters sharing the same protein structure folds (the LeuT-fold). The chosen
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Job Structure for Academic Staff at Universities (in Danish). Salary and terms of employment are in accordance with the collective agreement between the Danish Confederation of Professional Associations
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-Structures for Adaptable, Resilient and Sustainable Renewable Energy Power Plants), a prestigious Marie Skłodowska-Curie Doctoral Network funded by the European Union. As a Doctoral Candidate in MET2ADAPT, you
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is part of the MET2ADAPT Doctoral Network (Meta-Materials and Meta-Structures for Adaptable, Resilient and Sustainable Renewable Energy Power Plants), a prestigious Marie Skłodowska-Curie Doctoral
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, this PhD position might be the right fit for you! You will develop methodology for sustainability assessment of aggregate resource use in the construction sector applying a dissipation perspective on the
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of Professional Associations on Academics in the State (AC). The position is covered by the Protocol on Job Structure. Responsibilities and tasks in both PhD programmes Carry through an independent research project
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develop inhibitors as drugs. To solve this problem, this project will investigate if allosteric inhibitors can be designed towards a number of transporters sharing the same protein structure folds (the LeuT