Ultra-high resolution imaging by fluorescence photoactivation localization microscopy.

3,478 citations recorded by the source corpus.

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

SINGLE-PARTICLE TRACKING (2009, background): “Subdiffraction images can be formed by building up a final image from many repeated images, each with a concentration of active labels so low that the labels are at least a Rayleigh length apart [122–129].”
Super-resolution Imaging of Chemical Synapses in the Brain (2010, neutral): “Iterating this procedure to obtain the localizations of many fluorophores then allows the reconstruction of a sub-diffraction-limit image from these localization points (Betzig et al., 2006; Hess et al., 2006; Rust et al., 2006).”
Fast, background-free, 3D super-resolution optical fluctuation imaging (SOFI) (2009, methodology): “Stochastic techniques using photoswitchable probes have also been developed such as photo-activated localization microscopy (fPALM) (7), stochastic optical reconstruction microscopy (STORM) (8), PALM (9), and variants thereof (10, 11).”
Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure (2009, background): “The multiphase interferometric microscopy (the i in iPALM) recovers the z–axis position, and simultaneously PALM (6, 22, 23) recovers the x–y coordinates on high densities of FP-fusion molecules that occur in cellular structures.”