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Instituto de Investigação e Inovação em Saúde da Universidade do Porto (i3S) | Portugal | about 2 months ago
out research duties within the project “FibroRevert - Modeling and targeting cell-extracellular matrix communication to revert tissue fibrosis”, GA 101221669, funded by the European Research Council
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of Ferris State University with a major in Forensic Biology, Biotechnology, Biochemistry Essential Duties/Responsibilities: Design and revise laboratory protocols In hand cell based assay development Lab note
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host–fungus interactions. Skilled in designing and performing in vitro antifungal assays, cell culture techniques, and molecular biology methods. Skilled in conducting and interpreting in vivo animal
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applications. By tracking ^89Zr-labelled cells over extended periods of up to one month, you will investigate immune cell homing and trafficking, generating new insights into disease mechanisms and the potential
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multidisciplinary network of researchers within the departments of Molecular Cell Biology & Immunology and Pathology at Amsterdam UMC. Would you like to know more about the different phases within the PhD trajectory
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-on-brain.eu/ ). You will employ techniques such as organoid cultures (pluripotent stem cell and tissue-derived), transcriptomic analyses, CRISPR-Cas engineering, and other state-of-the-art tools. Your
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to develop and utilize innovative, interpretable data-driven analysis methods to significantly advance our understanding of immune cell inter-relations within the cancer microenvironment. We will apply
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molecular complexes during cellular transitions. Your project will apply cutting-edge proteomics, polysome profiling and imaging technologies such as cryo-EM, cryo-ET to study changes occurring in plant
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), University of Tübingen (Germany). The starting date in flexible within 2027. Research Our newly established group studies the structural basis of the changes occurring in molecular complexes during cellular
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Your position Despite the success of EBV-specific T-cell therapies in selected malignancies, therapeutic efficacy remains limited in tumors expressing only a restricted repertoire of viral antigens