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Preferred start: from November 2025 Short description This project will (i) quantify global and regional deviations from typical ageing using brain-age models, (ii) disentangle prenatal vs. postnatal
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computational tools to evaluate models of biological and artificial vision, as part of the DFG-funded Collaborative Research Center (CRC) “Robust Vision” at the University of Tübingen. This is a unique
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state. The project will specifically investigate the role of endogenous retroelements in this context. Immune-functional consequences will be studied using in vivo mouse models, and in cell culture
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chemical–biological pathway. The advertised positions will support these efforts through research on advanced carbon capture methods, process modelling and optimization, and biological CO2 valorization in
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, longitudinal pattern mining, and explainable artificial intelligence for complex system analysis and understanding tightly collaborating with biologists and domain experts for iteratively refining models
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state. The project will specifically investigate the role of endogenous retroelements in this context. Immune-functional consequences will be studied using in vivo mouse models, and in cell culture
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of inflammation remains the role of hypoxia. In this 3-year CRC (DFG)-funded position, we will use novel genetic reporters and transgenic models to specifically address the role of hypoxia during these processes
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considered. The ideal candidate will have a background in immunology, tissue biology or cellular metabolism. Experience in working with animal models, cell isolations from tissues (lung, intestine), human