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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...
| Autores principales: | , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Research Foundation
2008
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| Materias: | |
| 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 |