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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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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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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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include exceptionally rich cohorts with diverse omics, imaging, and molecular measurements. The Di Angelantonio-Ieva group is seeking to recruit up to two highly motivated Postdocs in Generative Machine
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single-element SNSPDs as well as kilopixel-scale imaging arrays which have high efficiency in the 2 – 16 µm wavelength range for applications in single-photon spectroscopy. The imaging arrays will be
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. The successful candidate will apply molecular, imaging, and electrophysiological methods to investigate the molecular mechanisms of somatic mechanotransduction. We use genetic mouse models and human cells to gain
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imaging, especially in vivo imaging Coding experience in Matlab, Python or R Record of first-author publications or preprints Success in competitive funding schemes/awards Experience with inflammatory
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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