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                the PhD trajectory (years 3 and 4) at the JRC in Ispra, Italy, where you will refine and test your models and methods in case studies of relevance for policy support. You will align your results and 
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                in scientific methodologies that have transformed the study of, and interest for bioarchaeological remains, makes the PhD project highly relevant across multiple academic domains. Although the botany 
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                morphological changes in host cells. - Use sequence specific fluorescent labeling to follow virus infection in a time resolved manner in different archaeal models. Organisation The University of Groningen is a 
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                throughout the horse breeding season (March–August). Your research will bridge basic biology and translational embryology. Using live imaging and single-cell sequencing approaches, you will investigate how 
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                , where you will refine and test your models and methods in case studies of relevance for policy support. You will align your results and proposed methods with the European Commission’s Environmental 
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                experts in other related research fields. You will lead the development of your own PhD research, aligning it with the research objectives and Work Packages (in particular WP2) of the project. You will 
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                how networks support cognition is one of the most exciting challenges in clinical neuroscience. For complex conditions such as multiple sclerosis and autism spectrum disorder, progress has been slowed 
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                expected to cover multiple cities in multiple countries in the majority world. The longitudinal approach covering multiple decades likely calls for the digital processing of archival, newspaper and policy 
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                enzyme engineering. The PhD project will involve bioinformatic selection of candidate enzymes, employing a combination of ‘off-the-shelf’ tools based on both sequence and structure. These enzymes will be 
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                of ‘off-the-shelf’ tools based on both sequence and structure. These enzymes will be produced, screened and the best variants subject to protein engineering campaigns. Once highly active variants