[1] BETZIG E, TRAUTMAN J K, HARRIS T D, et al. Breaking the diffraction barrier: optical microscopy on a nanometric scale[J]. Science, 251, 1468-1470(1991).

[2] AXELROD D. Total internal reflection fluorescence microscopy in cell biology[J]. Traffic, 2, 764-774(2001).

[3] HELL S W. Toward fluorescence nanoscopy[J]. Nature Biotechnology, 21, 1347-1355(2003).

[4] EGGELING C, RINGEMANN C, MEDDA R, et al. Direct observation of the nanoscale dynamics of membrane lipids in a living cell[J]. Nature, 457, 1159-1162(2009).

[5] BETZIG E, PATTERSON G H, SOUGRAT R, et al. Imaging intracellular fluorescent proteins at nanometer resolution[J]. Science, 313, 1642-1645(2006).

[6] RUST M J, BATES M, ZHUANG X W. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)[J]. Nature Methods, 3, 793-796(2006).

[7] THOMPSON R E, LARSON D R, WEBB W W. Precise nanometer localization analysis for individual fluorescent probes[J]. Biophysical Journal, 82, 2775-2783(2002).

[8] GUSTAFSSON M G L. Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy[J]. Journal of Microscopy, 198, 82-87(2000).

[9] WU Y, SHROFF H. Faster, sharper, and deeper: structured illumination microscopy for biological imaging[J]. Nature Methods, 15, 1011-1019(2018).

[10] GUSTAFSSON M G L, SHAO L, CARLTON P M, et al. Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination[J]. Biophysical Journal, 94, 4957-4970(2008).

[11] SHROFF S A, FIENUP J R, WILLIAMS D R. Phase-shift estimation in sinusoidally illuminated images for lateral superresolution[J]. Journal of the Optical Society of America A, 26, 413-424(2009).

[12] WICKER K, MANDULA O, BEST G, et al. Phase optimisation for structured illumination microscopy[J]. Optics Express, 21, 2032-2049(2013).

[13] ZHOU X, LEI M, DAN D, et al. Image recombination transform algorithm for superresolution structured illumination microscopy[J]. Journal of Biomedical Optics, 21, 096009(2016).

[14] CHU K Q, MCMILLAN P J, SMITH Z J, et al. Image reconstruction for structured-illumination microscopy with low signal level[J]. Optics Express, 22, 8687-8702(2014).

[15] HUANG X SH, FAN J CH, LI L J, et al. Fast, long-term, super-resolution imaging with Hessian structured illumination microscopy[J]. Nature Biotechnology, 36, 451-459(2018).

[16] ZHOU B, HUANG X SH, FAN J CH, et al. sCMOS noise-corrected superresolution reconstruction algorithm for structured illumination microscopy[J]. Photonics, 9, 172(2022).

[17] WEN G, LI S M, WANG L B, et al. High-fidelity structured illumination microscopy by point-spread-function engineering[J]. Light:Science & Applications, 10, 70(2021).

[18] PEREZ V, CHANG B J, STELZER E H K. Optimal 2D-SIM reconstruction by two filtering steps with Richardson-Lucy deconvolution[J]. Scientific Reports, 6, 37149(2016).

[19] SMITH C S, SLOTMAN J A, SCHERMELLEH L, et al. Structured illumination microscopy with noise-controlled image reconstructions[J]. Nature Methods, 18, 821-828(2021).

[20] WANG H D, RIVENSON Y, JIN Y Y, et al. Deep learning enables cross-modality super-resolution in fluorescence microscopy[J]. Nature Methods, 16, 103-110(2019).

[21] JIN L H, LIU B, ZHAO F Q, et al. Deep learning enables structured illumination microscopy with low light levels and enhanced speed[J]. Nature Communications, 11, 1934(2020).

[22] [22] ZHANG Y L, LI K P, LI K, et al. . Image superresolution using very deep residual channel attention wks[C]. Proceedings of the 15th European Conference on Computer Vision, Springer, 2018: 294310.

[23] CHEN J J, SASAKI H, LAI H, et al. Three-dimensional residual channel attention networks denoise and sharpen fluorescence microscopy image volumes[J]. Nature Methods, 18, 678-687(2021).

[24] QIAO CH, LI D, GUO Y T, LIU CH, et al. Evaluation and development of deep neural networks for image super-resolution in optical microscopy[J]. Nature Methods, 18, 194-202(2021).

[25] SCHULZ O, PIEPER C, CLEVER M, et al. Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy[J]. Proceedings of the National Academy of Sciences of the United States of America, 110, 21000-21005(2013).

[26] ZHAO W S, ZHAO SH Q, LI L J, et al. Sparse deconvolution improves the resolution of live-cell super-resolution fluorescence microscopy[J]. Nature Biotechnology, 40, 606-617(2022).

[27] NIEUWENHUIZEN R P J, LIDKE K A, BATES M, et al. Measuring image resolution in optical nanoscopy[J]. Nature Methods, 10, 557-562(2013).

[28] BANTERLE N, BUI K H, LEMKE E A, et al. Fourier ring correlation as a resolution criterion for super-resolution microscopy[J]. Journal of Structural Biology, 183, 363-367(2013).

[29] ROSENTHAL P B, HENDERSON R. Optimal determination of particle orientation, absolute hand, and contrast loss in single-particle electron cryomicroscopy[J]. Journal of Molecular Biology, 333, 721-745(2003).

[30] SAXTON W O, BAUMEISTER W. The correlation averaging of a regularly arranged bacterial cell envelope protein[J]. Journal of Microscopy, 127, 127-138(1982).

[31] DESCLOUX A, GRUßMAYER K S, RADENOVIC A. Parameter-free image resolution estimation based on decorrelation analysis[J]. Nature Methods, 16, 918-924(2019).

[32] CULLEY S, ALBRECHT D, JACOBS C, et al. Quantitative mapping and minimization of super-resolution optical imaging artifacts[J]. Nature Methods, 15, 263-266(2018).

[33] [33] BALL G, DEMMERLE J, KAUFMANN R, et al. . SIMcheck: a toolbox f successful superresolution structured illumination microscopy[J]. Scientific Repts, 2015, 5: 15915.

[34] FIOLKA R, BECK M, STEMMER A. Structured illumination in total internal reflection fluorescence microscopy using a spatial light modulator[J]. Optics Letters, 33, 1629-1631(2008).

[35] KNER P, CHHUN B B, GRIFFIS E R, et al. Super-resolution video microscopy of live cells by structured illumination[J]. Nature Methods, 6, 339-342(2009).

[36] LI D, SHAO L, CHEN B CH, et al. Extended-resolution structured illumination imaging of endocytic and cytoskeletal dynamics[J]. Science, 349, aab3500(2015).

[37] NIXON-ABELL J, OBARA C J, WEIGEL A V, et al. Increased spatiotemporal resolution reveals highly dynamic dense tubular matrices in the peripheral ER[J]. Science, 354, aaf3928(2016).

[38] GUO Y T, LI D, ZHANG S W, et al. Visualizing intracellular organelle and cytoskeletal interactions at nanoscale resolution on millisecond timescales[J]. Cell, 175, 1430-1442.e17(2018).

[39] YORK A G, PAREKH S H, NOGARE D D, et al. Resolution doubling in live, multicellular organisms via multifocal structured illumination microscopy[J]. Nature Methods, 9, 749-754(2012).

[40] YORK A G, CHANDRIS P, NOGARE D D, et al. Instant super-resolution imaging in live cells and embryos via analog image processing[J]. Nature Methods, 10, 1122-1126(2013).

[41] MO Y Q, FENG F, MAO H, et al. Structured illumination microscopy artefacts caused by illumination scattering[J]. Philosophical Transactions of the Royal Society A:Mathematical, Physical and Engineering Sciences, 379, 20200153(2021).

[42] INGARAMO M, YORK A G, WAWRZUSIN P, et al. Two-photon excitation improves multifocal structured illumination microscopy in thick scattering tissue[J]. Proceedings of the National Academy of Sciences of the United States of America, 111, 5254-5259(2014).

[43] WINTER P W, YORK A G, NOGARE D D, et al. Two-photon instant structured illumination microscopy improves the depth penetration of super-resolution imaging in thick scattering samples[J]. Optica, 1, 181-191(2014).

[44] GREGOR I, SPIECKER M, PETROVSKY R, et al. Rapid nonlinear image scanning microscopy[J]. Nature Methods, 14, 1087-1089(2017).

[45] HEINTZMANN R, JOVIN T M, CREMER C. Saturated patterned excitation microscopy-a concept for optical resolution improvement[J]. Journal of the Optical Society of America A, 19, 1599-1609(2002).

[46] GUSTAFSSON M G L. Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution[J]. Proceedings of the National Academy of Sciences of the United States of America, 102, 13081-13086(2005).

[47] ZHANG H, ZHAO M, PENG L L. Nonlinear structured illumination microscopy by surface plasmon enhanced stimulated emission depletion[J]. Optics Express, 19, 24783-24794(2011).

[48] [48] DAKE F, NAKAYAMA S, TAKI Y. Optical resolution enhancement background reduction by stimulated emission depletion structured illumination microscopy with structured excitation[C]. Novel Techniques in Microscopy 2015, OSA, 2015: NM2C. 4.

[49] XUE Y, SO P T C. Three-dimensional super-resolution high-throughput imaging by structured illumination STED microscopy[J]. Optics Express, 26, 20920-20928(2018).

[50] REGO E H, SHAO L, MACKLIN J J, et al. Nonlinear structured-illumination microscopy with a photoswitchable protein reveals cellular structures at 50-nm resolution[J]. Proceedings of the National Academy of Sciences of the United States of America, 109, E135-E143(2012).