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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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Optical control and study of biological processes at the single-cell level in a live organism.

TL;DR: A non-exhaustive list of examples of cellular interactions and developmental pathways that could benefit from new approaches to optogenetics, including the use of photo-sensitive DNA-encoded proteins as sensitive reporters and efficient actuators to perturb and monitor physiological processes.
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Two-photon microscopy with dynamic focusing objective using a liquid lens

TL;DR: In this article, the authors investigate the use of a liquid lens embedded in an aberration-corrected custom microscope for z-dimensional scanning in 3D resolved two-photon microscopy.
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Spectroscopic studies of the mechanism of reversible photodegradation of 1-substituted aminoanthraquinone-doped polymers

TL;DR: In this article, the mechanism of reversible photodegradation of 1-substituted aminoanthraquinones doped into poly(methyl methacrylate) and polystyrene was investigated.
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Arbitrary-scan imaging for two-photon microscopy

TL;DR: In this paper, a two-photon fluorescence microscope with a nearisotropic scan rate of 400 Hz was used to image dendritic processes that follow non-linear paths in 3D space.
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In vivo imaging of hematopoietic stem cell development in the zebrafish

TL;DR: Recent studies related to the non-invasive in vivo imaging of HSC transgenics are summarized to show that zebrafish transgenic lines are powerful tools for developmental biology and disease.
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