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mechanisms involving genetic, epigenetic and chromatin organisation factors governing the cell-type specific response to ARS mutations. Therefore, integrative genome-wide cis-regulatory network analysis
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cell cycle machinery. This project will combine live-cell imaging, phosphoproteomics, and metabolite profiling to unravel the complexity of phytohormonal regulation at the cellular level. Profile
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from established collaborations and access to centralized facilities with expertise in functional genomics and cell biology, proteomics, cutting-edge microscopy, immunology, technology development, and
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(genome sequencing), bioinformatics and single-cell (microscopy, microfluidics, FACS) analyses of E. coli bacteria and will be centred around the following themes: Pathways involved in robustness against de
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-research teams with a broad range of expertise, access to state-of-the-art technology and facilities ((epi-)genomics, transcriptomics, (single-cell) sequencing, bioinformatics, etc), institutional training
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of microbiology and laboratory automation. We are looking for a highly motivated PhD candidate with a strong engineering mindset and a keen interest in AI, automation and microbiology. Prior experience in
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mechanisms, with translational relevance for conditions such as chronic pain, bladder dysfunction, and other urinary tract disorders. The urinary bladder plays a vital role in storing and releasing urine
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candidate will work closely with experts in food allergy, neuroimmunology, gut physiology, and computational biology to characterize immune cell responses, construct spatial maps of inflammation along the gut
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mouse models with genetically engineered timing of synaptic development This work will contribute critical insight into how early brain development influences behavioral outcomes in ASD, and how