Understanding information processing in the brain requires monitoring neuronal activity at high spatiotemporal resolution. Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser scanning, we imaged neuronal activity in vivo at up to 3,000 frames per second and submicrometer spatial resolution. This imaging method enabled monitoring of both supra- and subthreshold electrical activity down to 345 μm below the brain surface in head-fixed awake mice.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199528 | PMC |
| http://dx.doi.org/10.1038/s41592-020-0762-7 | DOI Listing |
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