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pharmacological questions in large populations. The translational pharmacology group aims to understand variability in drug toxicity, drug metabolism and drug transport. Examples of this include cell-based models
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You will identify glycans in representative activated sludges and model biofilms You will assign biological functions to glycans in activated sludges and model biofilms You will oversee descriptions
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, you are expected to determine the molecular super-structure of TZ. You will monitor the gating mechanism of TZ in cellular models such as RPE1 or cultured dopaminergic neurons by immunofluorescence
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Lonza’s expertise and technology within peptide T cell immunogenicity, and the vast expertise within immunoinformatics and machine learning models at DTU to address this challenge. This will enable
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will benefit from Lonza’s expertise and technology within peptide T cell immunogenicity, and the vast expertise within immunoinformatics and machine learning models at DTU to address this challenge
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Job Description RISC-V open source and open standards as the nucleus for new platform models help to improve overall flexibility and productivity for a wide market access. Given the challenge
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characterization of photonic devices. Desired qualifications: Theoretical understanding of photonic integrated circuits. Experience with numerical modeling. Experience with Python programming. Additionally, we
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to integrate various structural biology data (NMR, SAXS, FRET, EPR) as well as computational models and simulations to create and interpret conformational ensembles of disordered protein regions, with the goal
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Two year postdoc position at Aarhus University for single molecule FRET based investigations of l...
in the target proteins. The postdoc will collect single molecule FRET data and by integration with existing atomic models establish trajectories for key conformational changes in the investigated
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to integrate various structural biology data (NMR, SAXS, FRET, EPR) as well as computational models and simulations to create and interpret conformational ensembles of disordered protein regions, with the goal