(Q48948402)

17 February 2018

editorial

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title

3-D stimulated emission depletion microscopy with programmable aberration correction. (English)

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author

Daniel M. Davis

6

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Mark Neil

8

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author name string

Martin O Lenz

1

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Hugo G Sinclair

2

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Alexander Savell

3

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James H Clegg

4

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Alice C N Brown

5

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Chris Dunsby

7

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Paul M W French

9

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publication date

21 June 2013

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published in

Journal of Biophotonics

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volume

7

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issue

1-2

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page(s)

29-36

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Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy

cites work

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Properties of a 4Pi confocal fluorescence microscope

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

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Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission

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Ground-state-depletion fluorscence microscopy: A concept for breaking the diffraction resolution limit

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21 January 2018

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21 January 2018

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21 January 2018

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STED microscopy reveals that synaptotagmin remains clustered after synaptic vesicle exocytosis

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Investigation of the influence of the aberration induced by a plane interface on STED microscopy

21 January 2018

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Three-dimensional nanoscopy of colloidal crystals

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Macromolecular-scale resolution in biological fluorescence microscopy

21 January 2018

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Stimulated emission depletion microscopy with a supercontinuum source and fluorescence lifetime imaging.

21 January 2018

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Quantitative pupil analysis in stimulated emission depletion microscopy using phase retrieval.

21 January 2018

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Adaptive optics enables 3D STED microscopy in aberrating specimens

21 January 2018

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Double pass, common path method for arbitrary polarization control using a ferroelectric liquid crystal spatial light modulator

21 January 2018

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2,2′-Thiodiethanol: A new water soluble mounting medium for high resolution optical microscopy

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/JBIO.201300041

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17 February 2018

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17 February 2018