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Deep two-photon brain imaging with a red-shifted fluorometric Ca(2+) indicator
In vivo Ca(2+) imaging of neuronal populations in deep cortical layers has remained a major challenge, as the recording depth of two-photon microscopy is limited because of the scattering and absorption of photons in brain tissue. A possible strategy to increase the imaging depth is the use of red-s...
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| Veröffentlicht in: | Proc Natl Acad Sci U S A |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4568712/ https://ncbi.nlm.nih.gov/pubmed/26305966 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1514209112 |
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