Rapid image deconvolution and multiview fusion for optical microscopy
The contrast and resolution of images obtained with optical microscopes can be improved
by deconvolution and computational fusion of multiple views of the same sample, but these …
by deconvolution and computational fusion of multiple views of the same sample, but these …
Advances in imaging plant cell dynamics
Advances in Imaging Plant Cell Dynamics | Plant Physiology | Oxford Academic Skip to Main
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Light sheet approaches for improved precision in 3D localization-based super-resolution imaging in mammalian cells
The development of imaging techniques beyond the diffraction limit has paved the way for
detailed studies of nanostructures and molecular mechanisms in biological systems …
detailed studies of nanostructures and molecular mechanisms in biological systems …
Multiview confocal super-resolution microscopy
Confocal microscopy remains a major workhorse in biomedical optical microscopy owing to
its reliability and flexibility in imaging various samples, but suffers from substantial point …
its reliability and flexibility in imaging various samples, but suffers from substantial point …
Simultaneous multiview capture and fusion improves spatial resolution in wide-field and light-sheet microscopy
Most fluorescence microscopes are inefficient, collecting only a small fraction of the emitted
light at any instant. Besides wasting valuable signal, this inefficiency also reduces spatial …
light at any instant. Besides wasting valuable signal, this inefficiency also reduces spatial …
Reflective imaging improves spatiotemporal resolution and collection efficiency in light sheet microscopy
Light-sheet fluorescence microscopy (LSFM) enables high-speed, high-resolution, and
gentle imaging of live specimens over extended periods. Here we describe a technique that …
gentle imaging of live specimens over extended periods. Here we describe a technique that …
Long-term intravital subcellular imaging with confocal scanning light-field microscopy
Long-term observation of subcellular dynamics in living organisms is limited by background
fluorescence originating from tissue scattering or dense labeling. Existing confocal …
fluorescence originating from tissue scattering or dense labeling. Existing confocal …
Visualizing calcium flux in freely moving nematode embryos
EL Ardiel, A Kumar, J Marbach, R Christensen… - Biophysical journal, 2017 - cell.com
The lack of physiological recordings from Caenorhabditis elegans embryos stands in stark
contrast to the comprehensive anatomical and gene expression datasets already available …
contrast to the comprehensive anatomical and gene expression datasets already available …
Fast fluorescence microscopy with light sheets
S Daetwyler, J Huisken - The Biological Bulletin, 2016 - journals.uchicago.edu
In light sheet microscopy, optical sectioning by selective fluorescence excitation with a sheet
of light is combined with fast full-frame acquisition. This illumination scheme provides …
of light is combined with fast full-frame acquisition. This illumination scheme provides …
A single-molecule localization microscopy method for tissues reveals nonrandom nuclear pore distribution in Drosophila
J Cheng, ES Allgeyer, JH Richens… - Journal of Cell …, 2021 - journals.biologists.com
Single-molecule localization microscopy (SMLM) can provide nanoscale resolution in thin
samples but has rarely been applied to tissues because of high background from out-of …
samples but has rarely been applied to tissues because of high background from out-of …