[1] 李帅, 匡翠方, 丁志华, 等.受激发射损耗显微术(STED)的机理及进展研究[J].激光生物学报, 2013, 2:103-113. doi: 10.3969/j.issn.1007-7146.2013.02.002

LI SH, KUANG C F, DING ZH H, et al.. A review on concept and development of stimulated emission depletion microscopy(STED)[J]. Acta Laser Biology Sinica, 2013, 2:103-113.(in Chinese) doi: 10.3969/j.issn.1007-7146.2013.02.002
[2] HUANG B, BATES M, ZHUANG X. Super-resolution fluorescence microscopy[J]. Annual Review of Biochemistry, 2009, 78:993-1016. doi: 10.1146/annurev.biochem.77.061906.092014
[3] HELL S W, WICHMANN J. Breaking the diffraction resolution limit by stimulated emission:stimulated-emission-depletion fluorescence microscopy[J]. Optics Letters, 1994, 19(11):780-782. doi: 10.1364/OL.19.000780
[4] KLAR T A, JAKOBS S, DYBA M, et al.. Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission[J]. Proceedings of the National Academy of Sciences, 2000, 97(15):8206-8210. doi: 10.1073/pnas.97.15.8206
[5] KUANG C, LI S, LIU W, et al.. Breaking the diffraction barrier using fluorescence emission difference microscopy[J]. Scientific Reports, 2013, 3:1441. doi: 10.1038/srep01441
[6] 李帅. 超分辨荧光显微方法与系统研究[D]. 杭州: 浙江大学, 2014. http://cdmd.cnki.com.cn/Article/CDMD-10335-1014269194.htm

LI SH. Research on super-resolution fluorescence microscopy method and system[D]. Huangzhou: Zhejiang University, 2014. (in Chinese) http://cdmd.cnki.com.cn/Article/CDMD-10335-1014269194.htm
[7] MEYER L, WILDANGER D, MEDDA R, et al.. Dual-color STED microscopy at 30-nm focal-plane resolution[J]. Small, 2008, 4(8):1095-1100. doi: 10.1002/smll.v4:8
[8] LI S, KUANG C, HAO X, et al.. Enhancing the performance of fluorescence emission difference microscopy using beam modulation[J]. Journal of Optics, 2013, 15(12):125708. doi: 10.1088/2040-8978/15/12/125708
[9] YOU S, KUANG C, RONG Z, et al.. Eliminating deformations in fluorescence emission difference microscopy[J]. Optics Express, 2014, 22(21):26375-26385. doi: 10.1364/OE.22.026375
[10] RONG Z, LI S, KUANG C, et al.. Real-time super-resolution imaging by high-speed fluorescence emission difference microscopy[J]. Journal of Modern Optics, 2014, 61(16):1364-1371. doi: 10.1080/09500340.2014.933272
[11] HAO X, KUANG C F, WANG T T, et al.. Effects of polarization on the de-excitation dark focal spot in STED microscopy[J]. Journal of Optics, 010, 12(11):115707. http://cn.bing.com/academic/profile?id=076fc5db3c528172e3bafe865a738aff&encoded=0&v=paper_preview&mkt=zh-cn
[12] WILSON T. Resolution and optical sectioning in the confocal microscope[J]. Journal of Microscopy, 2011, 244(2):113-121. doi: 10.1111/jmi.2011.244.issue-2
[13] BINGEN P, REUSS M, ENGELHARDT J, et al.. Parallelized STED fluorescence nanoscopy[J]. Optics Express, 2011, 19(24):23716-23726. doi: 10.1364/OE.19.023716
[14] RANKIN B R, KELLNER R R, HELL S W. Stimulated-emission-depletion microscopy with a multicolor stimulated-Raman-scattering light source[J]. Optics Letters, 2008, 33(21):2491-2493. doi: 10.1364/OL.33.002491
[15] STAUDT T M. Strategies to reduce photobleaching, dark state transitions and phototoxicity in subdiffraction optical microscopy[D]. Ruperto-Carola University of Heidelberg, Germany, 2009. https://www.researchgate.net/publication/33429512_Strategies_to_reduce_photobleaching_dark_state_transitions_and_phototoxicity_in_subdiffraction_optical_microscopy
[16] HAO X, ALLGEYER E S, BOOTH M J, et al.. Point-spread function optimization in isoSTED nanoscopy[J]. Optics Letters, 2015, 40(15):3627-3630. doi: 10.1364/OL.40.003627
[17] HIGDON P D, T R K P, WILSON T. Imaging properties of high aperture multiphoton fluorescence scanning optical microscopes[J]. Journal of Microscopy, 1999, 193(2):127-141. doi: 10.1046/j.1365-2818.1999.00448.x
[18] RUST M J, BATES M, ZHUANG X. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy(STORM)[J]. Nature Methods, 2006, 3(10):793. doi: 10.1038/nmeth929
[19] BRODEHL A, HEDDE P N, DIEDING M, et al.. Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants[J]. Journal of Biological Chemistry, 2012, 287(19):16047-16057. doi: 10.1074/jbc.M111.313841
[20] CARRINGTON W A, LYNCH R M, MOORE E D, et al.. Superresolution three-dimensional images of fluorescence in cells with minimal light exposure[J]. Science, 1995, 268(5216):1483-1487. doi: 10.1126/science.7770772