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Multi-modal registration for correlative microscopy using image analogies [PDF]

Medical Image Analysis, 2014
Correlative microscopy is a methodology combining the functionality of light microscopy with the high resolution of electron microscopy and other microscopy technologies for the same biological specimen.
Tian Cao, Kirk J Czymmek, Shannon Modla
exaly   +2 more sources

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Membrane Architecture in the Spotlight of Correlative Microscopy

Trends in Cell Biology, 2020
Cellular membranes differ in their molecular organisation, shape, and dynamics. Knowing how these properties of membrane architecture relate to the presence and function of specific membrane components is fundamental for understanding membrane-associated cellular processes.
Wanda Kukulski, Iva Ganeva
exaly   +4 more sources

Correlative Microscopy

2013
Correlative microscopy is a method when for the analysis of the very same cell or tissue area several different methods of light or electron microscopy are used. Usually these methods of analysis are separated by the period of additional preparation. Traditionally, LM and EM observations are carried out in different populations of cells/tissues.
Alexander A, Mironov, Galina V, Beznoussenko   +1 more
openaire   +2 more sources

Correlation plenoptic microscopy

Photonics for Quantum, 2021
We present a new technique for performing three-dimensional optical microscopy based on correlation plenoptic imaging. This approach, named Correlation Plenoptic Microscopy (CPM), exploits correlations between intensity fluctuations of pseudo-thermal light to retrieve plenoptic information about the sample, i. e.
Davide Giannella, Gianlorenzo Massaro, Francesco Di Lena, Francesco Scattarella, Alessio Scagliola, Francesco V. Pepe, Milena D'Angelo   +6 more
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Confocal microscopy by aperture correlation

Optics Letters, 1996
Most confocal microscopes do not produce images in real time with nonlaser light sources. The tandem scanning confocal microscope does produce such images but, because the pinhole apertures of the Nipkov disk must be placed far apart to reduce cross talk between neighboring pinholes, only 1% or less of the light available for imaging is used.
T, Wilson, R, Juskaitis, M A, Neil, M, Kozubek   +3 more
openaire   +2 more sources

Correlated Light Microscopy and Electron Microscopy

2012
Understanding where, when, and how biomolecules (inter)act is crucial to uncover fundamental mechanisms in cell biology. Recent developments in fluorescence light microscopy (FLM) allow protein imaging in living cells and at the near molecular level. However, fluorescence microscopy only reveals selected biomolecules or organelles but not the (ultra ...
Sjollema, Klaas A., Schnell, Ulrike, Kuipers, Jeroen, Kalicharan, Ruby, Giepmans, Ben N. G.   +4 more
openaire   +3 more sources

High-precision correlative fluorescence and electron cryo microscopy using two independent alignment markers

Ultramicroscopy, 2014
Correlative light and electron microscopy (CLEM) is an emerging technique which combines functional information provided by fluorescence microscopy (FM) with the high-resolution structural information of electron microscopy (EM). So far, correlative cryo
Rainer Kaufmann, Harald Wodrich, Kay Grünewald   +2 more
exaly   +2 more sources

Correlative Light And Electron Microscopy

2008
Mc 2009. Microscopy Conference, Graz, Austria. 30 August - 4 September 2009. First Joint Meeting Of Dreiländertagung And Multinational Congress On Microscopy.
Schwarz, H., Humbel, B.M.
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Structured illumination microscopy and correlative microscopy to study autophagy

Methods, 2015
Autophagy is a predominant eukaryotic mechanism for the engulfment of "portions" of cytoplasm allowing their degradation to recycle metabolites. The autophagy is ubiquitous among the life kingdom revealing the importance of this pathway that appears more complex than previously thought. Several reviews have already addressed how to monitor this pathway
Laure-Anne, Ligeon, Nicolas, Barois, Elisabeth, Werkmeister, Antonino, Bongiovanni, Frank, Lafont   +4 more
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Correlative SIM-STORM Microscopy

2017
The ability to specifically label subcellular structures or even proteins of interest in combination with the ability to look at live specimens turned fluorescence light microscopy into an invaluable tool. However, conventional light microscopy is diffraction limited, which restricts the lateral resolution to around 200 nm laterally and 600-800 nm ...
Burri O, Laroche T, Guiet R, Seitz A
openaire   +3 more sources