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Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt | Germany | 2 months ago
/m/x) - Transposable elements in the control of cell identity and reprogramming 102979 Full time 39 hrs./week Munich At Helmholtz Munich, we develop groundbreaking solutions for a healthier society in
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interface of stem-cell biology, neurovascular physiology and translational therapeutics. The postholder will benefit from the Cader Lab’s extensive expertise in iPSC modelling, neurovascular systems, and
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and research area: The ReHab project (“Re-habilitating: Power, Merit, and Social Mobility”) seeks to investigate the role of merit in medieval society. Drawing on two archival corpora—first, the letters
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in Metabolic Disease and Cell Signalling to carry out independent research, keeping with the aims of the laboratory and the Charles Perkins Centre (CPC). The successful candidate will contribute
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mouse/human cell lines, CRISPR-based gene editing, immunofluorescence, and confocal imaging. Prepare and publish research findings in peer-reviewed journals and present results at conferences. Assist in
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hold a high potential to be a sustainable option for several applications currently using lithium-ion batteries (LIB). In this project, Sodium-ion batteries for transport: from materials to cell
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our team as a Postdoctoral Researcher, focusing on cell line development for seafood. With the world’s population predicted to surpass nine billion by 2050, substantial challenges emerge regarding food
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at the Max Delbrück Center for Molecular Medicine (MDC) in Berlin. Our interdisciplinary team develops innovative computational approaches to reconstruct tissue trajectories from multimodal single-cell and
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and eager to contribute to the fast-developing field of cellular agriculture? We are seeking a mission-driven individual to join our team as a Postdoctoral Researcher, focusing on cell line development
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that is comprised of both wet-lab and computational scientists. Our group investigates the interplay between transcription factors and oncogenic drivers using large scale single-cell omics including single