Two-Photon STED Microscopy for Nanoscale Imaging of Neural Morphology In Vivo

The advent of super-resolution microscopy offers to bridge the gap between electron and light microscopy. It has opened up the possibility of visualizing cellular structures and dynamic signaling events on the "mesoscale" well below the classic diffraction barrier of light microscopy (10-2...

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Vydané v:	Methods in molecular biology (Clifton, N.J.) Ročník 1663; s. 45
Hlavní autori:	Ter Veer, Mirelle J T, Pfeiffer, Thomas, Nägerl, U Valentin
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	United States 01.01.2017
Predmet:	Animals Dendritic Spines Mice Microglia - cytology Microscopy, Fluorescence - instrumentation Microscopy, Fluorescence - methods Nanotechnology Neurons - cytology Cranial window Nanoscale neural morphology Dendritic spines Microglia-synapse interactions Microglial processes Acute brain slice s Two-photon microscopy Mouse cortex STED microscopy Super-resolution imaging in vivo
ISSN:	1940-6029, 1940-6029
On-line prístup:	Zistit podrobnosti o prístupe
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