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PhD Student Brain multiregion singlecell transcriptomics of Myalgic Encephalomyelitis/CFSyndrome NIN
postmortem tissue, high-throughput sequencing, and translational neuroimmunology. You will be involved in identifying molecular targets and immune biomarkers for ME/CFS, potentially guiding future therapeutic
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aim to combine the best of both worlds, endowing passive networks with adaptability and spiking networks with memory and sequencing. We will explore the computational power of these systems and
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involve optimizing protocols to convert patient-derived skin cells into neurons (iNeurons). New AONs will be screened through reporter assays and RNA sequencing in iNeurons. Using advanced techniques
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, you will examine the economic impact of various policy measures on agricultural businesses, supply chains, or broader economic systems. There are opportunities across multiple teams, so we can explore
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. Perform protein interaction studies to unravel mechanisms by which viruses induce morphological changes in host cells. Use sequence specific fluorescent labeling to follow virus infection in a time resolved
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chains, or broader economic systems. There are opportunities across multiple teams, so we can explore together which projects best align with your interests. Do you enjoy calculating the effects of policy
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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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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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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