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at adapting our blood-brain barrier model to predict the brain permeability of extracellular vesicles and therapeutic agents. It by the use of cell culture, automation, high content imaging, TEER and
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sequencing, high-resolution microscopy imaging, and data science methods. The second project focuses on providing service packages for single-cell and spatial omics research, as well as multimodal data
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reconstitution, cell biology, and fluorescence microscopy imaging tools, we aim to uncover how protein-membrane interactions promote membrane microdomain formation and how these structures respond to external
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