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Using two-photon microscopy, we imaged the spontaneous activity in a known neuronal circuit in vivo.
Using live-cell laser scanning microscopy, we imaged capsid and tegument protein transport in axons within the microgrooves of the chamber during viral egress.
Using in vivo two-photon laser-scanning microscopy, we imaged calcium activity in response to airflow presentations from the calyx, the input region of the MB, and the vertical and horizontal lobes, the output regions of the MB.
Using FRET-based microscopy, we imaged cells from single time points to visualize heterogeneity in c-di-GMP levels.
To further illustrate the heat sinking properties of glass in photothermal microscopy, we imaged a solution of 60 nm gold NPs at a concentration of 1∙10 NPs/mL contained within a PDMS (polydimethylsiloxane) microchannel.
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Using refractive index matching and confocal microscopy, we have imaged many interesting features within wild-type, mutant, and engineered biofilms, including cellular phenotypes that vary with position, the effect of growth conditions, and gene expression through reporter constructs.
With a video-rate third harmonic generation (THG) microscopy system, we imaged the micro-circulation beneath the human skin without labeling.
Using time-lapse microscopy we recorded images of embryos every 5 minutes for 10 hours.
By using a combination of bright field and fluorescent microscopy, we could image the RBCs, channel walls and WBCs simultaneously (Figure 2A and Video S1).
Using time-lapse microscopy, we acquired images of pre-labeled N3F-derived ECMs before and after plating OVCAR5 and OVCAR10 cells.
Using size exclusion chromatography and atomic force microscopy, we isolated and imaged microfibrils from both healthy and diabetic aortas.
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