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integrates CRISPR-based genome engineering, quantitative and live-cell microscopy, biochemistry, and computational analysis to dissect how cells sense and respond to replication-associated threats. Recent work
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on two types of phenomena: (i) Charge Density Wave (CDW) order in magnetic, lanthanide-based MOFs and (ii) electride-like, quasiatomic electron states that reside in the pores of certain MOFs. The aim
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production via at least one of the following techniques: magnetron sputtering, electrodeposition, wet chemical methods. The catalysts will be characterized via XPS, XRD, and electron microscopy and we will
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on two types of phenomena: (i) Charge Density Wave (CDW) order in magnetic, lanthanide-based MOFs and (ii) electride-like, quasiatomic electron states that reside in the pores of certain MOFs. The aim
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-FISH), expansion microscopy, confocal laser scanning microscopy, scanning or transmission electron microscopy, cryo-electron tomography (cryoTEM). Candidates who have prior experience with imaging
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for catalysis and electrocatalysis. You will develop a research activity within experimental characterization of electrocatalyst model catalysts using electrocatalysis workstations, scanning probe microscopy and
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insight Develop and use Python tools for EIS data processing and modeling Perform microstructural and compositional analysis (electron microscopy, XRD, Raman, EDS) Contribute to fabrication of SOE cells (3D
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interdisciplinary, collaborative project at the interface between nucleic-acid chemistry, DNA/RNA nanotechnology and cell biology. Your profile Applicants should hold a PhD in chemistry, molecular biology