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and signal processing methods using machine learning techniques to enhance the resilience, efficiency, and security of cell-free massive MIMO systems, which are expected to play a key role in next
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both sites. The project sits at the interface of cell line engineering, protein science and machine learning and you will receive advanced training in these areas while developing methods to accelerate
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at Birmingham (UAB) for a Researcher V focused on stem cell and gene editing research. The Zhao Lab investigates the biology of stem cells and their applications in modeling and treating human diseases, with
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to early phase clinical trials. We collaborate with investigators intramurally (Duke Pharmacology & Cancer Biology, Cell Biology, Biomedical Engineering), and extramurally nationally and internationally
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, cell biology, biomedicine, molecular medicine, human biology, or biochemistry for a PhD thesis. This project is embedded within the DZIF-German Center for Infection Research, thematic translational unit
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degree in Biology, Biochemistry or Chemistry Experience in protein biochemistry, molecular biology and/or cell biology Willingness to learn new methods and technologies in an international and
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, focusing on purpose-driven topology design (optimizing cell and module arrangement for performance) and vertical integration (seamless integration into vehicle architecture). You will create automated
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transcriptomics (PubMed ID 40849297). This embeds with the focus of the group of applying single cell / spatial transcriptomics to better understand human neurological diseases on a wider scale (see e.g. PubMed IDs
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PhD Studentship - EASTBIO - Functional Genomics of Host Determinants in Viral Entry and Transmission
work will include mammalian cell culture, CRISPR-based gene editing, and infection models using pseudotyped and replication competent viruses. The student will learn to perform and interpret high-content
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modulators of P2X7 (facilitating ion channel opening) can engage with the protein and alter downstream cell signalling pathways. We will use a newly developed method from our group called on-cell saturation