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Open AccessJournal ArticleDOI

Advances in multiphoton microscopy technology

Erich Hoover, +1 more
- 01 Feb 2013 - 
- Vol. 7, Iss: 2, pp 93-101
TLDR
The basic architecture of a multiphoton microscope capable of real-time analysis of cellular structure and function is discussed and the state-of-the-art technologies for the quantitative imaging of biological phenomena are summarized.
Abstract
The ability to dynamically image features deep within living organisms, permitting real-time analysis of cellular structure and function, is important for biological science. This Review article discusses multiphoton microscopy capable of such analysis, along with technologies that are pushing the limits of phenomena that can be quantitatively imaged.

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Citations
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Two-Photon-Pumped Perovskite Semiconductor Nanocrystal Lasers.

TL;DR: Stable two-photon-pumped lasing is demonstrated at a remarkable low threshold by coupling CsPbBr3 nanocrystals with microtubule resonators and these findings suggest perovskite nanocry crystals can be used as excellent gain medium for high-performance frequency-up-conversion lasers toward practical applications.
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3D cell culture systems modeling tumor growth determinants in cancer target discovery

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Recent advances in fibre lasers for nonlinear microscopy

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References
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Journal ArticleDOI

Two-Photon Laser Scanning Fluorescence Microscopy

TL;DR: The fluorescence emission increased quadratically with the excitation intensity so that fluorescence and photo-bleaching were confined to the vicinity of the focal plane as expected for cooperative two-photon excitation.
Journal ArticleDOI

Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
Journal ArticleDOI

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: A new type of scanning fluorescence microscope capable of resolving 35 nm in the far field is proposed, overcome the diffraction resolution limit by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point-spread function.
Journal Article

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: In this paper, the authors proposed a new type of scanning fluorescence microscope capable of resolving 35 nm in the far field by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point spread function.
Journal ArticleDOI

Deep tissue two-photon microscopy

TL;DR: Fundamental concepts of nonlinear microscopy are reviewed and conditions relevant for achieving large imaging depths in intact tissue are discussed.
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