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: Conduct cutting-edge research in gene therapy, including gene editing, the use of viral vectors, and emerging technologies such as CRISPR. Develop and validate preclinical models (in vitro and in vivo
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screening (e.g., CRISPR-based or related screening approaches), viral infection models, and insect or arthropod cell culture systems. The successful candidate will work with Norbert Perrimon to develop and
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mouse models. Key responsibilities include CRISPR/Cas9-mediated generation of global and cell-specific gene knockout mice, mouse colony management, and molecular validation. Perform immunological and
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proteins identified from this screen will be validated using siRNA-mediated knockdown and CRISPR knockout in bacterial adherence assays to determine which specific cell surface proteins mediate interactions
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the University of Vienna: https://doschem.univie.ac.at/ The standard employment contract is for three years . Initially limited to 1.5 years, the employment relationship is automatically extended to three years
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single photon counting, nucleoproteins, CRISPR/CAS9, riboswitches, high pressure The ability to “see” single biomolecules with laser microscopy has led to a revolution in research opportunities
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editing strategies (CRISPR/Cas and other emerging tools) in bacteria, fungi, and yeasts. Conduct metabolic engineering approaches to enhance the production of high value‑added compounds. Develop and
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disease. They are also conducting advanced CRISPR screens to interrogate the complex genetic basis of these disorders. The lab has been supported by the ERC for the past 15 years. Now we are seeking a
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itself as a regional center of excellence in CRISPR genome editing, with a focus on advancing opportunity crops tailored to the marginal regions of Africa. These areas, defined by arid and saline
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well as outside the organization. The work will include: Designing and conducting experiments related to starch biosynthesis and granule morphogenesis in potato Application of genome editing approaches (e.g. CRISPR