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- Università degli Studi di NApoli Federico II -Dipartimento di Medicina Molecolare e BiotecnologieMediche
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for research and employees from all over the world. We are looking for a Postdoctoral Fellow in Biochemistry-Proteomics (f/m/d) (Ref 01/2026) to join the group ‘Molecular Pharmacology & Cell Biology’ led by Prof
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: chmatallab.com , https://fgu.cas.cz/en/research-and-laboratories/research-departments/laboratory-of-cardiometabolism/ Key Responsibilities You will lead experimental research combining in vivo and in vitro models
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for boosting green and digital innovations”, Project ID 101186592, https://cordis.europa.eu/project/id/101186592 , running between February 2025 and January 2030 and funded by European Research Executive Agency
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signal transduction. · Significant experience in advanced molecular cloning, protein biochemistry, and single-cell approaches. · Experience in structural biology, proteomics-lipidomics, and
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Chemical Biological Centre (https://www.umu.se/en/kbc ) at Umeå University and is affiliated with the national Centre of Excellence – Umeå Centre for Microbial Research (UCMR) (https://www.umu.se/en/ucmr
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to core facilities including flow cytometry, FACS, confocal microscopy, high-throughput sequencing and proteomics. The selected candidate will be able to interact with a cross-disciplinary team of cell
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Università degli Studi di NApoli Federico II -Dipartimento di Medicina Molecolare e BiotecnologieMediche | Italy | 20 days ago
three-dimensional cultures and patient-derived organoids, and the analysis of data derived from “omics” techniques (such as RNA-seq, RIBO-seq, and proteomics). Where to apply Website https
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computational and wet bench scientists that utilize omics (e.g. genomic, epigenomic, fragmentomic, proteomic) approaches to profile tumor biopsies, circulating tumor DNA, and circulating tumor cells
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the Pereira laboratory: https://www.lsi.umich.edu/science/our-labs/filipa-pereira-lab Responsibilities* Experimental responsibilities will include: Perform genome engineering of Streptomyces strains
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initiation and progression. Using murine and humanized models, human patient samples, single-cell multiomics (CITE-seq), advanced flow cytometry, proteomics, and mechanistic studies, we aim to identify