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2003, Springer series in optical sciences, ISBN 9783540434931, Volume 87., xvii, 395
Book
Annual Review of Neuroscience, ISSN 0147-006X, 06/2009, Volume 32, Issue 1, pp. 435 - 506
Since the work of Golgi and Cajal, light microscopy has remained a key tool for neuroscientists to observe cellular properties. Ongoing advances have enabled... 
Super-resolution | Laser-scanning | Two-photon fluorescence | Fluorescence labeling | Transgenic mice | Fiber optics | laser-scanning | NEOCORTEX IN-VIVO | OPTICAL COHERENCE TOMOGRAPHY | PHOTOACTIVATED LOCALIZATION MICROSCOPY | super-resolution | MULTIFOCAL MULTIPHOTON MICROSCOPY | FIELD FLUORESCENCE MICROSCOPY | NEUROSCIENCES | STRUCTURED-ILLUMINATION MICROSCOPY | INDEPENDENT COMPONENT ANALYSIS | fiber optics | 2ND-HARMONIC GENERATION MICROSCOPY | two-photon fluorescence | transgenic mice | fluorescence labeling | STOKES-RAMAN SCATTERING | 2-PHOTON EXCITATION MICROSCOPY | Microscopy - methods | Image Cytometry - methods | Humans | Neurons - cytology | Molecular Biology - instrumentation | Molecular Biology - methods | Microscopy, Fluorescence - instrumentation | Microscopy - instrumentation | Neurons - physiology | Neurosciences - methods | Image Cytometry - instrumentation | Nervous System - cytology | Image Cytometry - trends | Mice, Transgenic | Microscopy - trends | Microscopy, Confocal - methods | Neurosciences - trends | Molecular Biology - trends | Animals | Microscopy, Fluorescence - methods | Microscopy, Fluorescence - trends | Mice | Microscopy, Confocal - trends | Microscopy, Confocal - instrumentation | Neurosciences - instrumentation | Evaluation | Usage | Neurosciences | Microscope and microscopy | Fluorescence | Research
Conference Proceeding
Journal Article
Journal of Microscopy, ISSN 0022-2720, 09/2011, Volume 243, Issue 3, pp. 221 - 226
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2013, Volume 110, Issue 32, pp. 13138 - 13143
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1763, pp. 129 - 136
Journal Article
Microscopy, ISSN 2050-5698, 08/2015, Volume 64, Issue 4, pp. 227 - 236
One of the most popular super-resolution microscopies that breaks the diffraction barrier is stimulated emission depletion (STED) microscopy. As the optical... 
Two-photon microscopy | Liquid crystal devices | Optical vortex | BREAKING | liquid crystal devices | FLUORESCENCE MICROSCOPY | optical vortex | FIELD | BARRIER | two-photon microscopy | LATERAL RESOLUTION | LIMIT | 2-PHOTON MICROSCOPY | LIQUID-CRYSTAL | MICROSCOPY
Journal Article