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microscopy imaging of neuronal activity in mutant mice, with a focus on mouse models of 22q11 and 3q29 deletion syndromes, high-risk genetic risks for developing psychiatric disorders, especially schizophrenia
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Postdoctoral Associate – Systems Neuroscience: In Vivo Imaging & Electrophysiology Location: Virginia Tech, Fralin Biomedical Research Institute at VTC (Roanoke, Virginia, USA) Lab: Shin Lab | Lab
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Are you interested in X-ray imaging and biomineralization and in contributing to an international interdisciplinary Human Frontier Science Program funded project on skeletal adaptations in
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We are seeking a highly motivated and skilled individual to join our neuroimaging laboratory, which specializes in multimodal image fusion, multiparametric modeling, and machine learning techniques
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To strengthen our team in the division “X-Ray Imaging” in Berlin-Steglitz, starting as soon as possible, we are looking for a Postdoctoral research assistant (m/f/d) in the field of physics
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investigate the connectivity of genetically defined populations of spinal interneurons using a diverse set of approaches, including expansion microscopy, tissue clearing and light-sheet imaging, as
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the fly brain based on electron-microscopic reconstruction; second, high-resolution live imaging data of the developmental transformations that encode information in biological neural networks
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Postdoc in Genetic Engineering of Green Microalga Chlamydomonas Reinhardtii with the Purpose of A...
Spectrometry Platform for Proteomics and Biomolecular Imaging’ (PLATO), which provides a highly international, collaborative, ambitious and innovative research environment in mass spectrometry-based proteomics
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and physicochemical characterization of novel materials (e.g. NMR, LC/MS, various separation technologies) · Proficiency in Immunology · Experience in animal handling, injections, and in vivo imaging
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Postdoctoral Research Associate - Human Organoid/Assembloid Models of Schizophrenia-associated Risks
imaging and electrophysiologic recordings of neuronal activity in human induced pluripotent stem cell (hiPSC)-derived organoids and assembloid models, with a focus on 22q11 and 3q29 deletion syndromes