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methods of neural-microglia interactions, complementing already established multi-omics approaches: non-destructive fluorescence lifetime imaging microscopy (FLIM), mass spectrometry imaging and Raman
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Stimulation using advanced preclinical models for seizures and epilepsy. Analyze extensive datasets of neurophysiological signals, including local field potentials (LFP), unit activity and biosensor imaging
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recapitulating neural-microglia interactions, as well as establishing fluorescence lifetime imaging microscopy (FLIM) approaches and analysis pipelines to perform non-destructive monitoring of neuronal function
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