Optical sectioning microscopy

By J. Conchello, Jeff William Lichtman. Nature Methods, 2005

802 citations recorded by the source corpus.

Subfields: Biophysics, Radiology, Nuclear Medicine and Imaging

View Paper: https://www.semanticscholar.org/paper/2694ae872fa62ebc196884c20ff92d1f4798b629

How researchers see this paper

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In Biophysics

1. Joseph Huff
2. Lothar Schermelleh
3. Rainer Heintzmann
4. H. Leonhardt
5. Christos Davatzikos
6. K. Simons
7. M. Gerl

In Radiology, Nuclear Medicine and Imaging

1. Joseph Huff
2. Christos Davatzikos

Citations in the corpus

• The Airyscan detector from ZEISS: confocal imaging with improved signal-to-noise ratio and super-resolution (2015, background): “The increase in utilization of con focal imaging systems in basic biomedical research can be attributed to the ability of a confocal imaging system to produce optically sectioned images with high contrast while providing acquisition versatility to address many sample and application demands [1].”
• Advanced CLARITY for rapid and high-resolution imaging of intact tissues (2014, neutral): “(Conchello and Lichtman, 2005).”
• Review of spectral imaging technology in biomedical engineering: achievements and challenges (2013, background): “have summarized these techniques for optical imaging of thick tissues.(164,166) Some new optical sectioning techniques, such as planar illumination and structured illumination have been proposed in recent years.”
• Clarifying Tissue Clearing (2015, neutral): “…notably, commercial laser-scanning confocal microscopes, laser scanning two-photon microscopy, parallelized confocal (i.e., spinning disk), computational image deconvolution methods, and lightsheet approaches (reviewed in Conchello and Lichtman, 2005; Mertz, 2011; Reynaud et al., 2008).”
• A guide to super-resolution fluorescence microscopy (2010, background): “Using highly specific fluorescent labeling techniques such as immunocytochemistry, in situ hybridization, or fluorescent protein tags, the spatial distribution and dynamics of virtually every subcellular structure, protein, or genomic sequence of interest can be analyzed in chemically fixed or livin”