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structural health monitoring of structures immersed in heavy fluids, by continuing to develop the “Modal Strain Energy” and “Matched Field Processing” methods for detecting and locating a potential defect in
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of these communities to ecological and biogeochemical processes. This work will feed into wider project goals to understand the role of dormancy as a regulator of biogeochemical cycles, and to link dormancy
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Process: designing, preparing, shaping and characterizing materials in order to discover, control and optimize specific functions. The ICMCB carries out fundamental research on model materials and/or
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of proteins by applying a simple electrical potential in solution. This electro-bioconjugation reaction occurs within minutes, providing a fast and biocompatible process for the functionalization of viral
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. This will be made on different Cu-FR4-Cu laminate test-structures with a FR4 thickness ranging between 35 to 100 μm. A preliminary assembly process optimization will be performed (e.g., temperature
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conjugates into fluorescent nanostructures, which growth results from a combination of dynamic covalent and supramolecular processes, moving from solution studies to model lipid membranes, then live cells
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of the variability and uncertainty of simulated outputs • an explicit quantification of prediction error • an interpretable and controllable structure (e.g., Gaussian processes, …) 2. Model industrial system
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investigate the molecular mechanisms that underlie the regenerative capacity of injured neurons. Our research focuses on gene regulation processes, particularly the translational control of mRNAs into proteins
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cellular biophysics -Backround in microfluidics -Background in image processing Website for additional job details https://emploi.cnrs.fr/Offres/CDD/UMR5588-CHAMIS-012/Default.aspx Work Location(s) Number
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criteria Level I animal experimentation, expertise in animal surgery, skills in pharmacokinetic analysis. Website for additional job details https://emploi.cnrs.fr/Offres/CDD/UMR7275-HELMAR-006/Default.aspx