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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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Tapered diode-pumped continuous-wave alexandrite laser

TL;DR: In this article, a low-cost and efficient alexandrite (Cr:BeAl2O4) laser that is pumped by a high-brightness tapered diode laser (TDL) is described.
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Observing pure effects of counter-rotating terms without ultrastrong coupling: A single photon can simultaneously excite two qubits

TL;DR: In this article, a superconducting quantum circuit with two coupled flux qubits longitudinally interact with the same resonator is considered, and it is shown that the energy of a single photon can excite two qubits via higher-order transitions induced by the longitudinal couplings and the counter-rotating terms.
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Recent advancements in structured-illumination microscopy toward live-cell imaging.

TL;DR: Structured-illumination microscopy (SIM), a type of super-resolution microscopy, doubles the spatial resolution in all three dimensions by illuminating the sample with a patterned excitation light, followed by computer reconstruction.
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Fluorescence correlation spectroscopy: linking molecular dynamics to biological function in vitro and in situ

TL;DR: Fluorescence correlation spectroscopy is a minimally invasive real-time fluorescence technique capable of detecting single molecules in vitro and in situ and has become commonplace tools used to specifically unravel the spatio-temporal dynamics of macromolecular entities in living biological systems.
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Monomer sequence in PLGA microparticles: Effects on acidic microclimates and in vivo inflammatory response.

TL;DR: It is demonstrated that changing the monomer sequence in poly(lactic-co-glycolic acid)s (PLGAs) leads to dramatic differences in the rate of degradation and the internal acidic microclimate of microparticles degrading in vitro.
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