Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution.
By Mats Gustafsson. Proceedings of the National Academy of Sciences of the United States of America, 2005
2,198 citations recorded by the source corpus.
Subfields: Biomedical Engineering, Biophysics
View Paper: https://www.semanticscholar.org/paper/a35f8233952c1a7b16775ff7c09b05b40fdc2c02
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biomedical Engineering
- Stefan W. Hell
- X. Zhuang
- Bo Huang
- M. Bates
- Hanchuan Peng
- Alex Small
- Shane Stahlheber
- Rainer Heintzmann
In Biophysics
- Stefan W. Hell
- X. Zhuang
- Bo Huang
- M. Bates
- Hanchuan Peng
- Alex Small
- Shane Stahlheber
- Michael A. D. Taylor
Citations in the corpus
- Far-Field Optical Nanoscopy (2007, background): “In order to cover all directions, the array is rotated an adequate number of times [72].”
- Super-resolution Imaging of Chemical Synapses in the Brain (2010, positive): “These superresolution approaches include ensemble imaging methods, such as stimulated emission depletion (STED and related RESOLFT) microscopy (Hell, 2007; Klar and Hell, 1999) and saturated structured-illumination microscopy (SSIM) (Gustafsson, 2005), as well as single-molecule imaging methods, suc”
- What spatial light modulators can do for optical microscopy (2011, neutral): “based on saturation [135].”
- Optical Imaging and Spectroscopy (2009, background): “Particularly dramatic resolution is available in systems that combine nonlinear optical effects with structured illumination, as in stimulated emission depletion (STED) microscopy [116] and nonlinear structured illumination microscopy [107].”
- Fluorophore localization algorithms for super-resolution microscopy (2014, background): “…in overcoming this limit via several innovative super-resolution approaches, including localization of switchable fluorophores 2–5 , localization of fluorophores from sequential images of bleachable fluorophores 6,7 , saturation of upward transitions 8 and saturation of downward transitions 9,10 .”
- Biological Imaging Software Tools (2012, methodology): “Examples of developments enabled by software written in research laboratories include structured-illumination microscopy 2 , super-resolution microscopy 3–5 and Bessel-beam microscopy 6 .”
- Fluorescent probes for super-resolution imaging in living cells (2008, neutral): “, and saturated structured-illumination microscopy (SSIM”