Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission.

By Thomas A. Klar, S. Jakobs, M. Dyba, A. Egner, Stefan W. Hell. Proceedings of the National Academy of Sciences of the United States of America, 2000

1,787 citations recorded by the source corpus.

Subfields: Biomedical Engineering, Biophysics, Physical and Theoretical Chemistry

View Paper: https://www.semanticscholar.org/paper/c454765df18e80decd17b69582e42c7851023ccc

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

1. A. Ting
2. Marta Fernandez-Suarez
3. Miles J. Padgett
4. Andrew Forbes
5. M. Gather
6. Ebrahim Karimi
7. S. Yun
8. Stefan W. Hell

In Biophysics

1. Stefan W. Hell
2. A. Ting
3. Marta Fernandez-Suarez
4. M. Gather
5. S. Yun
6. Jennifer Lippincott-Schwartz
7. Samuel T. Hess
8. M. Ritsch-Marte

In Physical and Theoretical Chemistry

1. C. Rosales-Guzmán
2. Stefan W. Hell
3. M. Gather

Citations in the corpus

• Foundations of Confocal Scanned Imaging in Light Microscopy (2006, background): “Thus, the volume of region actually fluorescing is carved smaller than the standard two-photon excitation volume, and, in fact, Hell and Wichmann (1994) report having reduced the height of the point-spread function (PSF) by as much as a factor of five (see also Klar et al., 2000, Chapter 31, this ”
• Studying protein dynamics in living cells (2001, methodology): “Moreover, light microscopes with improved resolution are available, including the 4-PI and the STIMULATED EMISSION MICROSCOPES”
• Roadmap on structured light (2016, background): “An application that already exists but which will undoubtedly be developed further occurs in stimulated emission depletion (STED) super-resolution microscopy [10].”
• Single-cell biological lasers (2011, methodology): “Stimulated emission is an emerging scheme to improve the resolution and sensitivity of microscopic imaging in biomedical scienc”
• Ultra-high resolution imaging by fluorescence photoactivation localization microscopy. (2006, methodology): “FPALM does not require scanning either the beam or the sample, as is necessary in RESOLFT (including STED), 4Pi, and standard confocal microscopy (6,13,15).”
• Fluorescent probes for super-resolution imaging in living cells (2008, methodology): “STED was the first far-field super-resolution imaging technique to be applied to cell imagin”