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will be hosted at LCPMR (Sorbonne Université, Paris), in a dynamic scientific environment internationally recognized for its expertise in attoscience, numerical methods, and modeling. The EPAD project
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and localization of a potential fault using the Matched Field Processing (MFP) method, based on the reconstruction of a response model of the inspected structure from the modal parameters predicted by
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postdoctoral researcher to study establishment of cell identities in human and mouse cerebral organoid models. - Study cell identities and lineages in physiological and pathological contexts - Develop protocols
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on solubility, dissolution kinetics, and microbial influences. Your work will refine global carbon cycle models, enhance CO₂ sequestration understanding, and position you at the forefront of ocean
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unknown in natural materials. Our approach is based on the use of self-assembly and physics of soft matter to design, manufacture and assemble colloidal resonators of sub-wavelength size, constituting
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research teams from different scientific cultures (ecology, physiology and ethology, chemistry and subatomic physics) develop very high level programs based on scientific instrumentation. The IPHC is
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from experimental data. Ultimately, the integration of incompatibility-based theory with continuum modelling of the wing disc will provide a mechanistic understanding of how residual stresses
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state of art of frequency-dependent model of winding in electrical machines • task 2: the aim of the second task is to propose simplified models, derived from the detailed models typically used
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and implemented in Fenics to: - Identify the mechanical properties of collagen hydrogels, depending on their manufacturing conditions, based on experimental data. - Improve these models to include
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cell tracking to identify the progenitors of these cells during regeneration. • Develop and apply a recombinase-based cell barcoding strategy to trace cell lineages during leg growth and regeneration