[1] Huang B, Babcock H, Zhuang X. Breaking the diffraction barrier: super-resolution imaging of cells[J]. Cell, 2010, 143(7): 1047-1058.
[2] Abbe E. Beitrge zur Theorie des Mikroskops und der mikroskopischen Wahrnehmung[J]. Archiv für mikroskopische Anatomie, 1873, 9(1): 413-418.
[3] Shi Shunxiang, Wang Xue′ en, Liu Jingsong. Physical Optics and Applied Optics[M]. Xi′ an: Xidian University Press, 2008, 139-142.
[4] Huang B, Bates M, Zhuang X. Super resolution fluorescence microscopy[J]. Annual review of biochemistry, 2009, 78: 993.
[5] Schermelleh L, Heintzmann R, Leonhardt H. A guide to super-resolution fluorescence microscopy[J]. The Journal of Cell Biology, 2010, 190(2): 165-175.
[6] Lü Zhijian, Lu Jingze, Wu Yaqiong, et al.. Introduction to theories of several super-resolution fluorescence microscopy methods and recent advance in the field[J]. Progress in Biochemistry and Biophysics, 2009, 36(12): 1626-1634.
[8] Betzig E, Patterson G H, Sougrat R, et al.. Imaging intracellular fluorescent proteins at nanometer resolution[J]. Science, 2006, 313(5793): 1642-1645.
[9] Rust M J, Bates M, Zhuang X. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM) [J]. Nature methods, 2006, 3(10): 793-796.
[10] Hell S W, Wichmann J. Breaking the diffraction resolution limit by stimulated emission: stimulated-emissiondepletion fluorescence microscopy[J]. Opt Lett, 1994, 19(11): 780-782.
[11] Gustafsson M G. Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy[J]. Journal of microscopy, 2000, 198(2): 82-87.
[12] Gustafsson M G, Agard D A, Sedat J W. Doubling the lateral resolution of wide-field fluorescence microscopy using structured illumination[C]. BiOS 2000 The International Symposium on Biomedical Optics, 2000. 141-150.
[13] Su Xianyu, Zhang Qican, Chen Wenjing. Three-dimensional imaging based on structured illumination[J]. Chinese J Lasers, 2014, 41(2): 0209001.
[14] Liu Di, Yao Zhenning, Li Haifeng, et al.. Structured light acquisition system based on waveband separation[J]. Acta Optica Sinica, 2012, 32(6): 0612003.
[15] Peng Yifan, Tao Yiyang, Yu Chao, et al.. Three-dimenaional display interaction device based on infrared structured light[J]. Acta Optica Sinica, 2013, 33(4): 0412005.
[16] Su Xianyu, Li Jitao. Information Optics[M]. Chengdu: Sichuan University Press, 1999. 20-26.
[17] Zhang B, Zerubia J, Olivo-Marin J-C. Gaussian approximations of fluorescence microscope point-spread function models[J]. Applied Optics, 2007, 46(10): 1819-1829.
[18] Chang B J, Chou L J, Chang Y C, et al.. Isotropic image in structured illumination microscopy patterned with a spatial light modulator[J]. Optics Express, 2009, 17(17): 14710-14721.
[19] Stokseth P A. Properties of a defocused optical system[J]. J Opt Soc Am, 1969, 59(10): 1314-1321.
[20] Sedat J W. Fluorescence microscopy in three dimensions[M]// Methods in Cell Biology, fluorescence microscopy of living cells in culture, part B: quantitative fluorescence microscopy-imaging and spectroscopy: fluorescence microscopy of living cells in culture, 1989, 30: 353.
[21] Gustafsson M G, Shao L, Carlton P M, et al.. Three-dimensional resolution doubling in wide-field fluorescence microscopy by structured illumination[J]. Biophysical Journal, 2008, 94(12): 4957-4970.
[22] Neil M, Juskaitis R, Wilson T. Method of obtaining optical sectioning by using structured light in a conventional microscope[J]. Opt Lett, 1997, 22(24): 1905-1907.
[23] Karadagli c′ D, Wilson T. Image formation in structured illumination wide-field fluorescence microscopy[J]. Micron, 2008, 39(7): 808-818.
[24] Heintzmann R, Jovin T M, Cremer C. Saturated patterned excitation microscopy—a concept for optical resolution improvement[J]. J Opt Soc Am A, 2002, 19(8): 1599-1609.
[25] Heintzmann R. Saturated patterned excitation microscopy with two-dimensional excitation patterns[J]. Micron, 2003, 34(6): 283-291.
[26] Hao Xiang, Kuang Cuifang, Li Yanghui, et al.. Reversible saturable optical transitions based fluorescence nanoscopy[J]. Laser & Optoelectronics Progress, 2012, 49(3): 030005.
[27] Gustafsson M G. 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, 2005, 102(37): 13081-13086.
[28] Heintzmann R, Cremer C G. Laterally modulated excitation microscopy: improvement of resolution by using a diffraction grating[C]. BiOS Europe′98, 1999. 185-196.
[29] Thomas B, Momany M, Kner P. Optical sectioning structured illumination microscopy with enhanced sensitivity[J]. Journal of Optics, 2013, 15(9): 094004.
[30] Neil M, Jukaitis R, Wilson T. Real time 3D fluorescence microscopy by two beam interference illumination[J]. Opt Commun, 1998, 153(1): 1-4.
[31] Beversluis M R, Bryant G W, Stranick S J. Effects of inhomogeneous fields in superresolving structured-illumination microscopy[J]. J Opt Soc Am A, 2008, 25(6): 1371-1377.
[32] Hirvonen L M, Wicker K, Mandula O, et al.. Structured illumination microscopy of a living cell[J]. European Biophysics Journal, 2009, 38(6): 807-812.
[33] Shao L, Kner P, Rego E H, et al.. Super-resolution 3D microscopy of live whole cells using structured illumination[J]. Nature Methods, 2011, 8(12): 1044-1046.
[34] Kner P, Chhun B B, Griffis E R, et al.. Super-resolution video microscopy of live cells by structured illumination[J]. Nature Methods, 2009, 6(5): 339-342.
[35] Dan D, Lei M, Yao B, et al.. DMD-based LED-illumination Super-resolution and optical sectioning microscopy[J]. Scientific Reports, 2013, 3(1116): 1-7.
[36] Xu D, Jiang T, Li A, et al.. Fast optical sectioning obtained by structured illumination microscopy using a digital mirror device[J]. Journal of Biomedical Optics, 2013, 18(6): 060503.
[37] Fukano T, Miyawaki A. Whole-field fluorescence microscope with digital micromirror device: imaging of biological samples[J]. Appl Opt, 2003, 42(19): 4119-4124.
[38] Cai Dongmei, Yang Huizhen, Ling Ning, et al.. Diffraction effect of liquid crystal spatial light modulator using for beam deflection[J]. Chinese J Lasers, 2008, 35(4): 491-495.
[39] Du Yanli, Ma Fengying, Gong Qiaoxia, et al.. Optical microscopic imaging technology based on spatial light modulator [J]. Laser & Optoelectronics Progress, 2014, 51(2): 020002.
[40] 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, 2012, 109(3): E135-E143.
[41] Fitzgibbon J, Bell K, King E, et al.. Super-resolution imaging of plasmodesmata using three-dimensional structured illumination microscopy[J]. Plant Physiology, 2010, 153(4): 1453-1463.
[42] Schermelleh L, Carlton P M, Haase S, et al.. Subdiffraction multicolor imaging of the nuclear periphery with 3D structured illumination microscopy[J]. Science, 2008, 320(5881): 1332-1336.
[43] Rahman M, Abd-El-Barr M, Mack V, et al.. Optical imaging of cervical pre-cancers with structured illumination: an integrated approach[J]. Gynecologic Oncology, 2005, 99(3): S112-S115.
[44] Best G, Amberger R, Baddeley D, et al.. Structured illumination microscopy of autofluorescent aggregations in human tissue[J]. Micron, 2011, 42(4): 330-335.
[45] Sonnen K F, Schermelleh L, Leonhardt H, et al.. 3D-structured illumination microscopy provides novel insight into architecture of human centrosomes[J]. Biology Open, 2012, 1(10): 965-976.
[46] Carlton P M. Three-dimensional structured illumination microscopy and its application to chromosome structure[J]. Chromosome Research, 2008, 16(3): 351-365.
[47] York A G, Parekh S H, Dalle Nogare D, et al.. Resolution doubling in live, multicellular organisms via multifocal structured illumination microscopy[J]. Nature Methods, 2012, 9(7): 749-754.
[48] Lefman J, Scott K, Stranick S. Live, video-rate super-resolution microscopy using structured illumination and rapid GPU-based parallel processing[J]. Microscopy and Microanalysis, 2011, 17(2): 191-196.
[49] Isobe K, Takeda T, Mochizuki K, et al.. Enhancement of lateral resolution and optical sectioning capability of twophoton fluorescence microscopy by combining temporal-focusing with structured illumination[J]. Biomedical Optics Express, 2013, 4(11): 2396-2410.
[50] Rossberger S, Best G, Baddeley D, et al.. Combination of structured illumination and single molecule localization microscopy in one setup[J]. Journal of Optics, 2013, 15(9): 094003.
[51] Fedosseev R, Belyaev Y, Frohn J, et al.. Structured light illumination for extended resolution in fluorescence microscopy[J]. Optics and Lasers in Engineering, 2005, 43(3): 403-414.
