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SLM Microscopy: Scanless Two-Photon Imaging and Photostimulation with Spatial Light Modulators

Laser microscopy has generally poor temporal resolution, caused by the serial scanning of each pixel. This is a significant problem for imaging or optically manipulating neural circuits, since neuronal activity is fast. To help surmount this limitation, we have developed a “scanless” microscope that...

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Detalhes bibliográficos
Main Authors: Nikolenko, Volodymyr, Watson, Brendon O., Araya, Roberto, Woodruff, Alan, Peterka, Darcy S., Yuste, Rafael
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Research Foundation 2008
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2614319/
https://ncbi.nlm.nih.gov/pubmed/19129923
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/neuro.04.005.2008
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