Microscopy and its focal switch
By Stefan W. Hell. Nature Methods, 2008
977 citations recorded by the source corpus.
Subfields: Biomedical Engineering, Biophysics, Electrical and Electronic Engineering
View Paper: https://www.semanticscholar.org/paper/33fdf2e01853e051985115c6f4435f8575607637
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
- X. Zhuang
- Stefan W. Hell
- Kok Hao Chen
- Debashish Chowdhury
- Giuseppe Vicidomini
- Markus Sauer
- M. Heilemann
- Patrizia Boccacci
In Biophysics
- Erik H. W. Meijering
- X. Zhuang
- Stefan W. Hell
- Kok Hao Chen
- Debashish Chowdhury
- Giuseppe Vicidomini
- Alistair N. Boettiger
- Markus Sauer
In Electrical and Electronic Engineering
- Debashish Chowdhury
- Giuseppe Vicidomini
- Patrizia Boccacci
- Mario Bertero
- Gabriele Desidera
- X. Zhuang
- Siyuan S Wang
- Alistair N. Boettiger
Citations in the corpus
- Tracking in cell and developmental biology. (2009, background): “On the hardware side, advances in optical systems design have taken light microscopy from widefield to (multiphoton) confocal and spinning disk microscopy [5] [6], and more recent efforts to break the diffraction barrier have further extended the palette [7] [8].”
- Stochastic mechano-chemical kinetics of molecular motors: A multidisciplinary enterprise from a physicist’s perspective (2012, background): “, switched ON (fluorescent) and OFF (non-fluorescent) with appropriately selected laser beams in a sequential manner [2129].”
- Direct stochastic optical reconstruction microscopy with standard fluorescent probes (2011, background): “Even though all concepts are very similar and excellent reviews have already been published highlighting the strengths and limitations of the different method”
- Brief update on endocytosis of nanomedicines (2019, background): “It is now possible to look deep inside cells past the previously restrictive diffraction limit of optical microscopes and into the realm of super resolution fluorescent microscopy [218,219].”
- Image deblurring with Poisson data: from cells to galaxies (2009, methodology): “In astronomy, it is a charged coupled device (CCD) camera while, in fluorescence microscopy, it can be also a photomultiplier tube (PMT) or an avalanche photo-diode (APD), as in the case of confocal, 4Pi, two-photon excitation and other microscopy techniques [48, 67].”
- Spatially resolved, highly multiplexed RNA profiling in single cells (2015, positive): “Last, theoretical predictions (17) indicate that the use of superresolution imaging (41, 42) could increase the resolvable density to ~10(5) molecules/mm(3), which should be ample to address the entire transcriptome, even in cell types with RNA densities substantially higher than that of IMR90.”