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an innovative academic education to more than 20000 students, conduct pioneering scientific research and play an important service-providing role in society. We are one of the largest, most international and most
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an innovative academic education to more than 20000 students, conduct pioneering scientific research and play an important service-providing role in society. We are one of the largest, most international and most
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an innovative academic education to more than 20000 students, conduct pioneering scientific research and play an important service-providing role in society. We are one of the largest, most international and most
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scientist to study the human-specific genetic mechanisms of development and function of cortical neurons. Join us to undertake a highly interdisciplinary project focusing on a long-standing and fascinating
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scientist to study the human-specific genetic mechanisms of development and function of cortical neurons. Join us to undertake a highly interdisciplinary project focusing on a long-standing and fascinating
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, Reliability and Trust (SnT) at the University of Luxembourg is a leading international research and innovation centre in secure, reliable and trustworthy ICT systems and services. We play an instrumental role
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methods (e.g., PCA, PLS-DA, clustering, neural networks) to enable automated, polymer-specific classification. Optimize workflows for high-throughput imaging and real-world sample variability, minimizing
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optimization and validation and in addition, we aim to discover novel VHHs capable of crossing the blood-CSF barrier and delivering therapeutic cargoes to the brain. You will become an integral member of a
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will focus on the development, optimization and application of multi-modal analysis strategies and pipelines for sequencing data generated on nucleic acids isolated from biofluids (genomics, epigenomics
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electrophysiology to translational models, including animal studies and analyses of human tissue samples. This full-stack methodology enables us to directly link molecular channel function with disease phenotypes