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
Contributeur : Denis Roura
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Soumis le : mercredi 19 novembre 2014 - 09:50:49
Dernière modification le : jeudi 10 mai 2018 - 02:08:19
Document(s) archivé(s) le : vendredi 20 février 2015 - 10:15:49
