| 參考文獻 |
1. S. W. Hell, J. Wichmann, ”Breaking the diffraction resolution limit by stimulated emission stimulated-emission-depletion fluorescence microscopy,” Opt. Lett. 19(11), 780-782 (1994).
2. T. A. Klar, S. W. Hell, ”Subdiffraction resolution in far-field fluorescence microscopy,” Opt. Lett. 24(14), 954-956 (1999).
3. X. Liu, W. Rudolph, and J. L. Thomas, ”Photobleaching resistance of stimulated parametric emission in microscopy,” Opt. Lett. 34(3), 304-306 (2009).
4. T. Scheul, C. D’Amico, I. Wang, and J. C. Vial, ”Two-photon excitation and stimulated emission depletion by a single wavelength,” Opt. Express 19(19), 18036-18048 (2011).
5. S.W. Hell, M. Kroug, ”Ground-state-depletion fluorscence microscopy: a concept for breaking the diffraction resolution limit,” Appl. Phys. B 60, 495-497 (1995).
6. S. W. Hell, ”Increasing the Resolution of Far-Field Fluorescence Light Microscopy by Point-Spread-Function Engineering,” in Topics in Fluorescence Spectroscopy 5, J. Lakowicz. Plenum Press, ed. (New York, 1997), pp.361-426.
7. J. Fölling, M. Bossi, H. Bock, R. Medda, C. A. Wurm, B. Hein, S. Jakobs, C. Eggeling, and S. W. Hell, ”Fluorescence nanoscopy by ground-state depletion and single-molecule return,” Nat. Methods 5(11), 943-945 (2008).
8. K. Y. Han, S. K. Kim, C. Eggeling, and S. W. Hell, ”Metastable Dark States Enable Ground State Depletion Microscopy of Nitrogen Vacancy Centers in Diamond with Diffraction-Unlimited Resolution,” Nano Lett. 10, 3199-3203 (2010).
9. M. J. Rust, M. Bates, and X. W. Zhuang, ”Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM),” Nat. Methods 3(10), 793-795 (2006).
10. B. O. Huang, W. Q. Wang, M. Bates, and X. W. Zhuang, ”Three-Dimensional Super-Resolution Imaging by Stochastic Optical Reconstruction Microscopy,” Science 319, 810-813 (2008).
11. M. W. Gramlich, J. Bae, R. C. Hayward, and J. L. Ross, ”Fluorescence imaging of nanoscale domains in polymer blends using stochastic optical reconstruction microscopy (STORM),” Opt. Express 22(7), 8438-8450 (2014).
12. M. G. L. GUSTAFSSON, ”Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy,” J. Microsc. 198(2), 82-87 (2000).
13. M. G. L. GUSTAFSSON, ”Nonlinear structured-illuminati microscopy: Wide-field fluorescence imaging with theoretically unlimited resolution,” PNAS. 102(37), 13081-13086 (2005).
14. M. Saxena, G. Eluru, and S. S. Gorthi, ”Structured illumination microscopy,” Adv. Opt. Photonics 7, 241-275 (2015).
15. M. A. A. Neil, R. Juškaitis, and T. Wilson, ”Method of obtaining optical sectioning by using structured light in a conventional microscope,” Opt. Lett. 22(24), 1905-1907 (1997).
16. M. A. A. Neil, A. Squire, R. Juškaitis, P. I. H. Bastiaens, and T. Wilson, ”Wide-field optically sectioning fluorescence microscopy with laser illumination,” J. Microsc. 197(1), 1-4 (2000).
17. S. Lin, B. Isaac, S. Uzawa, D. A. Agard, J. W. Sedat, and M. G. L. Gustafsson, ”I5S: Wide-Field Light Microscopy with 100-nm-Scale Resolution in Three Dimensions,” Biophys. J. 94, 4971-4983 (2008).
18. J. T. Frohn, H. F. Knapp, and A. Stemmer, ”True optical resolution beyond the Rayleigh limit achieved by standing wave illumination,” PNAS. 97(13), 7232-7236 (2000).
19. P. Křížek, I. Raška, and G. M. Hagen, ”Flexible structured illumination microscope with a programmable illumination array,” Opt. Express 20(22), 24585-24599 (2012).
20. C. F. Jiang, B. W. Li, and S. Zhang, ”Pixel-by-pixel absolute phase retrieval using three phase-shifted fringe patterns without markers,” Opt. Laser. Eng. 91, 232–241 (2017).
21. N. Bozinovic, C. Ventalon, T. Ford, and J. Mertz, ”Fluorescence endomicroscopy with structured illumination,” Opt. Express 16(11), 8016-8025 (2008).
22. D. W. Piston, M. S. Kirby, H. P. Cheng, W. J. Lederer, and W. W. Webb, ”Two-photon-excitation fluorescence imaging of three-dimensional calcium-ion activity,” Appl. Opt. 33(4), 662-669 (1994).
23. M. Gu, ”Resolution in three-photon fluorescence scanning microscopy,” Opt. Lett. 21(13), 988-990 (1996).
24. C. H. Yeh, S. Y. Chen, ”Resolution enhancement of two-photon microscopy via intensity-modulated laser scanning structured illumination,” Appl. Opt. 54(9), 2309-2317 (2015).
25. O. Mandula, M. Kielhorn, K. Wicker, G. Krampert, I. Kleppe, and R. Heintzmann, ”Line scan - structured illumination microscopy super-resolution imaging in thick fluorescent samples,” Opt. Express 20(22), 24167-24174 (2012).
26. B. E. Urban, J. Yi, S. Y. Chen, B. Q. Dong, Y. L. Zhu, S. H. DeVries, V. Backman, and H. F. Zhang, ”Super-resolution two-photon microscopy via scanning patterned illumination,” Phy. Rev. E 91(042703), 1-6 (2015).
27. P. J. Campagnola, L. M. Loew, ”Second-harmonic imaging microscopy for visualizing biomolecular arrays in cells, tissues and organisms,” Nat. Biotechnol. 21(11), 1356-1360 (2003).
28. P. J. Campagnola, M. D. Wei, A. Lewis, and L. M. Loew, ”High-Resolution Nonlinear Optical Imaging of Live Cells by Second Harmonic Generation,” Biophys. J. 77, 3341-3349 (1999).
29. P. Mahou, N. Olivier, G. Labroille, L. Duloquin, J. M. Sintes, N. Peyriéras, R. Legouis, D. Débarre, and E. Beaurepaire, ”Combined third-harmonic generation and four-wave mixing microscopy of tissues and embryos,” Biomed. Opt. Express 2(10), 2837-1849 (2011).
30. ”Nonlinear susceptibility,” in Principles of nonlinear optics, Y. C. Huang, eds. (2016), pp.97-124.
31. M. Sheik-Bahea, A. A. Said, T. H. Wei, D. J. Hagan and E. W. Van Stryland, ”Sensitive measurement of optical nonlinearities using a single beam,” IEEE J. Quantum Electron 26(4), 760-769(1990)
32. ”Frequency analysis of optical image systems,” in Fourier Optics, J. W. Goodman, 3rd eds. (2004), pp.127-172.
33. A. Lal, C. Y. Shan, and P. Xi, ”Structured Illumination Microscopy Image Reconstruction Algorithm,” IEEE J. Sel. Top. Quant. 22(4), 1-14 (2016). |
[Endnote RIS 格式]
[相關文章]
[文章引用]
[完整記錄]
[館藏目錄]
至系統瀏覽論文 (2025-1-16以後開放)
plurk
funp
live
udn
HD
myshare
netvibes
friend
youpush
delicious
baidu
Google bookmarks
del.icio.us
hemidemi
facebook
twitter
google
reddit