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at the IJM. This recently created team studies ancient genomes to better understand human evolution and its implications for biology and health. Where to apply Website https://emploi.cnrs.fr/Candidat/Offre
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molecules using site-specific conjugation strategies. - Development of DNA origami scaffolds to spatially organize and orient proteins for structural studies by single-particle Cryo-Electron Microscopy
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the framework of the ERC Synergy DynAMICs (Valérie Berthé, Florian Luca, and Joël Ouaknine). Topics of interest include, but are not limited to, the study of linear dynamic systems, symbolic dynamics, recurrent
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of publications, and dissemination of research. They will integrate into a team and work collaboratively. The postdoctoral researcher would integrate into the music cognition theme of the Laboratory for the Study
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world leading facility for studying magnetic and electronic properties of matter using advanced chiroptical techniques in the hard X-ray range. Combining element-selective X-ray circular dichroism with
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evaluation process etc please visit: ambercofund.eu Minimum requirements • PhD in structural biology/chemistry, with excellent knowledge of biochemistry and molecular biology, including experience in protein
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Researcher (R2) Positions PhD Positions Country France Application Deadline 5 Feb 2026 - 12:00 (Europe/Paris) Type of Contract Temporary Job Status Full-time Hours Per Week 35 Offer Starting Date 1 Sep 2026 Is
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hexafluorouranate NOUF6 and its derivatives - Writing of bibliographic report and publications following the results. The work will be carried out at the Clermont-Ferrand Institute of Chemistry (ICCF – UMR CNRS 6296
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Communauté d’universités et établissements de Toulouse | Toulouse, Midi Pyrenees | France | 2 months ago
dates Call opens: 3 November 2025 Deadline: 28 February 2026 Results: July 2026 Start date: since september 2026 Where to apply Website https://portail-tiris.univ-toulouse.fr/callforproject/475/proposal
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single molecule techniques to study tetraspanins (see references below), the project aims to understand how some proteins in the TSPANC8 family regulate the cleavage of substrates by the protease ADAM10, a