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take approaches combining mouse developmental genetics, cell-type-specific viral tracing, ex vivo electrophysiology, opto/chemogenetics, in vivo imaging, single-nucleus RNA sequencing (snRNA-seq), and
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tracking analysis (NTA), NanoFlow cytometry, and advanced imaging techniques, as well as bioinformatic analysis of small RNAs and transcriptomic data. You will collaborate closely with partners working
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monitoring, control and predictive analysis during experimental operation. Both positions include reporting and publication of the results, and the opportunity to contribute to the supervision of PhD and MSc
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sciences. This includes the integration of various types of field-based and sensor-based data (soil, acoustic, images, and species data), as well as historical maps and satellite- and drone-based data. By
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. You will attend local and international scientific conferences. Your profile Applicants should hold a PhD in neurobiology, cell biology or related fields. You should be experienced in cellular
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qualifications at PhD level, in medical physics, physics, biomedical engineering or computer science. It is mandatory that your PhD degree is on a topic relevant for this specific position, i.e. in CT-imaging and
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related genome editing approaches to disrupt biological processes that support prostate cancer progression with a focus on metabolism, hormonal and stress response signaling. Preparing samples
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total scattering, WAXS and SAXS, imaging, and femtosecond X ray diffraction to probe structure and dynamics in real time under device relevant conditions. Target facilities include DESY, MAX IV, European
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of materials and devices during switching, combining methods such as laser pump and X ray probe total scattering, WAXS and SAXS, imaging, and femtosecond X ray diffraction to probe structure and dynamics in real
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this position, we seek to strengthen the platform by embedding/developing additional tools for data processing and analysis. The starting point for the developments will be our EasyNMR platform (see