Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination.

By Mats Gustafsson, L. Shao, P. Carlton, C. R. Wang, I. Golubovskaya, W. Cande, D. Agard, J. Sedat. Biophysical Journal, 2008

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Super resolution fluorescence microscopy (2009, background): “Periodic illumination patterns can be created through the interference of multiple light sources in the axial direction (18), the lateral direction (19), or both (20).”
Extended-resolution structured illumination imaging of endocytic and cytoskeletal dynamics (2015, methodology): “However, rather than the triangle apodization A(k) = 1 – k/kmax normally used (53), we applied a g apodization A(k) = 1 – (k/kmax) , usually with g = 0.”
Lattice Light Sheet Microscopy: Imaging Molecules to Embryos at High Spatiotemporal Resolution (2014, positive): “These data were then used to reconstruct a 3D image (9) with resolution extended beyond the diffraction limit in x and z.”
Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure (2009, neutral): “IEEE J Sel Top Quant Electron 14(1):217–225.”
Frontiers in structured illumination microscopy (2016, background): “Current reviews consider SIM mainly as a wide-field technique that utilizes two-beam [13,28,29] or three-beam [30,31] interference to generate sinusoidal illumination patterns.”
Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination (2011, methodology): “A better alternative would be to use the algorithms of 3D superresolution S”