Abstract : Two-photon microscopy is the most effective approach for deep-tissue fluorescence cellular imaging; however, its application to high-throughput or high-content imaging is often hampered by low pixel rates, challenging multicolor excitation and potential cumulative photodamage. To overcome these limitations, we extended our prior work and combined two-photon scanned light-sheet...
https://hal-polytechnique.archives-ouvertes.fr/hal-01048680
Contributor : Denis Roura
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Submitted on : Wednesday, November 19, 2014 - 9:50:49 AM
Last modification on : Wednesday, April 17, 2019 - 2:30:04 PM
Long-term archiving on : Friday, February 20, 2015 - 10:15:49 AM
