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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Detalles Bibliográficos
Autores principales: Nikolenko, Volodymyr, Watson, Brendon O., Araya, Roberto, Woodruff, Alan, Peterka, Darcy S., Yuste, Rafael
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2008
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614319/
https://www.ncbi.nlm.nih.gov/pubmed/19129923
http://dx.doi.org/10.3389/neuro.04.005.2008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614319/
https://www.ncbi.nlm.nih.gov/pubmed/19129923
http://dx.doi.org/10.3389/neuro.04.005.2008

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