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Open AccessJournal Article

[Two-photon laser scanning fluorescence microscopy].

Katsumasa Fujita
- 01 Oct 2007 - 
- Vol. 52, pp 1778-1779
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This article is published in Tanpakushitsu kakusan koso. Protein nucleic acid enzyme.The article was published on 2007-10-01 and is currently open access. It has received 1480 citations till now. The article focuses on the topics: Scanning confocal electron microscopy & Microscopy.

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Simultaneous cellular-resolution optical perturbation and imaging of place cell firing fields.

TL;DR: An optical method for simultaneous cellular-resolution stimulation and large-scale recording of neuronal activity in behaving mice is developed and manipulated task-modulated activity in individual hippocampal CA1 place cells during spatial navigation in a virtual reality environment, mimicking natural place-field activity, or 'biasing', to reveal subthreshold dynamics.
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Major signal increase in fluorescence microscopy through dark-state relaxation

TL;DR: A substantial signal gain is reported in fluorescence microscopy by ensuring that transient molecular dark states with lifetimes >1 μs, such as the triplet state relax between two molecular absorption events.
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Optical sectioning microscopy with planar or structured illumination

TL;DR: This Review examines two techniques for optical sectioning based on planar illumination or structured illumination, particularly for applications involving high speeds, large fields of view or long-term imaging.
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Advances in Light Microscopy for Neuroscience

TL;DR: Progress in Mouse genetic approaches permit mosaic and inducible fluorescence-labeling strategies, whereas intrinsic contrast mechanisms allow in vivo imaging of animals and humans without use of exogenous markers.
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