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for applications within bloodsucking disease vectors as well as for conservation ecology in relation to windfarms. The field work comprises interdisciplinary collaboration with ecologists in the topics. Validation
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and Europe. The specific objectives are to: examine the main climatic and socioeconomic (e.g. age, income and gender) drivers of the spread of vector borne diseases using time series approaches. develop
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University of California Agriculture and Natural Resources | Davis, California | United States | 2 months ago
the Git version control system, or similar distributed VCS. Experience with Typescript, SASS, HTML5, and responsive design. Experience with SVG authoring for scalable vector graphics. Strong project
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Department's Website: https://engineering.uark.edu/ Summary of Job Duties: The Postdoctoral Research Associate - Biomedical Engineering will test commercially available membranes and develop novel membranes
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Job Purpose The School of Infection and Immunity (https://www.gla.ac.uk/schools/infectionimmunity/) MRC-University of Glasgow Centre for Virus Research (CVR) (http://www.cvr.ac.uk/) is seeking
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-cell suspensions and multi-parameter flow cytometry • Molecular cloning with focus on CRISPR-based approaches • Experience with viral vector systems (e.g., AAV production and purification) • Single-cell
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opportunity Hydrogen (H2) is widely recognised as a clean energy vector essential for decarbonising hard-to-abate sectors. Currently the large-scale deployment of hydrogen remains constrained by the limitations
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of the common attack vectors on the network layer Knowledge of operating system command-line tools and network tools to identify vulnerabilities Knowledge of operating systems and Database Concepts Knowledge
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editing platforms delivered by AAV vectors and lipid nanoparticles to treat Ornithine Transcarbamylase (OTC) deficiency in utero. This is an exciting opportunity to contribute to a field on the cusp
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team. The purpose of these projects is to develop adeno-associated viral vector (AAV) gene therapies for GNE myopathy, myotubular myopathy and Duchenne muscular dystrophy. AAV gene therapy for muscular