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pathways driving leukemic transformation during haematopoietic development. The successful candidate will use in vitro differentiation systems (ESC/iPSC) to model normal and malignant haematopoiesis
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) Cardiac development or disease. We are interested in applicants with strong interest in using the mouse as a model for human genetic diseases Research focus: Our lab investigates cell fate progression
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, and large language models (LLMs), for the analysis of high-throughput multi-omics datasets (especially single-cell and spatial omics) and large textual corpora (e.g., scientific literature). Our
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, lipid metabolism, and gene regulation. We investigate: Lipid metabolism of the nuclear envelope Nuclear pore complex architecture Chromatin-associated signaling pathways As one of our model systems, we
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medicine through our discoveries of today. At locations in Berlin-Buch, Berlin-Mitte, Heidelberg and Mannheim, our researchers harness interdisciplinary collaboration to decipher the complexities of disease
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researchers to support complex behavioral experiments. Qualifications: Experience in designing and building custom optical systems. Familiarity with Zemax and CAD software. Strong programming skills in C
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after damage. Methodologically, the project aims to develop novel organoid-on-a-chip models of kidney injury. The applied techniques will include mouse and human kidney organoids, tissue engineering
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understanding of geomagnetic field evolution across different timescales, including both stable and extreme periods. This will involve working with data-based models and numerical dynamo simulations
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(SDPs). You will design climate change mitigation scenarios that respect both climate targets and sustainable development goals using the REMIND model, one of the world’s leading integrated energy-economy
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). The aim is to use modern molecular biological methods and in vivo models to investigate the role of fibroblastic plasticity in cardiac remodeling and loss of function. Your role: Independent work on the