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                Bremen, a private, state-accredited, English-language research university. Our research group focuses on modeling dynamical processes in (bio)molecular systems using quantum and classical approaches 
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                latest technologies Flexible working hours, part-time models as well as home office A corporate culture of appreciation and promotion of equal opportunities Extensive training and continuing education 
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                groups in Mainz (Schweiger lab) and Basel (Keller Valsecchi lab) to investigate the molecular mechanisms controlling gene reactivation during development. Using human induced stem cell models with 
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                will closely cooperate with the PhD student at GFZ in order to link the interpretation of geodetic GNSS measurements with the modelling of glacial-isostatic adjustment (GIA). You will focus your work 
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                latest technologies Flexible working hours, part-time models as well as home office A corporate culture of appreciation and promotion of equal opportunities Extensive training and continuing education 
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                (extravascular coagulation signaling) in homeostatic condition as well as in aging mouse models. Identification of these interactions could provide new approaches to counteract or delay age associated exhaustion 
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                dynamic research environment with first-class laboratory facilities near Berlin and Potsdam a pleasant and appreciative working atmosphere flexible and family-friendly working time model and the possibility 
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                production, antibody binding assays, germ-free and gnotobiotic mouse models and human samples, bacterial transcriptomics, and single cell host transcriptomic analysis to obtain a detailed mechanistic 
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                significantly slows down the development of new desirable nanostructures. In this project, we will combine numerical models, experiments, and artificial intelligence (AI) to guide the design of specific DNA 
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                the Access-Repair-Restore model. Histones, an essential component of chromatin, are post-translationally modified via methylation, ubiquitination, and acetylation to regulate DDR-related chromatin functions