References and Related Papers


[1] Rust, M. J., Bates, M., Zhuang, X. 2006. Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM). Nat. Meth. 10:793-795.

[2] Hell, S. W., Wichmann, J. 1994. Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy. Optics Letters 19: 780-782.

[3] Schrader, M., Bahlmann, K., Giese, G., Hell, S. 1998. 4Pi-Confocal Imaging in Fixed Biological Specimens. Biophys J. 75: 1659-1668.

[4] Hess, S., Girirajan, T., Mason, M. 2006. Ultra-High Resolution Imaging by Fluorescence Photoactivation Localization Microscopy. Biophys J. 91:4258-4272.

[5] Huang, B., Wang, W., Bates, M., Zhuang, X. 2008. Three-Dimensional Super-Resolution Imaging by Stochastic Optical Reconstruction Microscopy. Science 319:810-813.

[6] Harke, B., Ullal, C., Keller, J., Hell, S. 2008. Three-Dimensional Nanoscopy of Colloidal Crystals. Nano Letters 8:1309-1313.

[7] Juette, M., et. al. 2008. Three-dimensional sug-100nm resolution fluorescence microscopy of thick samples. Nat. Meth. 5:527-529.

[8] Shetengel, G. et. al. 2009. Interferometric fluorescent super-resolution microscopy resolves 3D cellular ultrastructure. PNAS 106:3125-3130.

[9] Kao, H. P., Verkman, A. S. 1994. Tracking of Single Fluorescent Particles in Three Dimensions: Use of Cylindrical Optics to Encode Particle Position. Biophys J. 67:1291-1300.

[10] Mlodzianowski, M., Juette, M., Beane, G., Bewersdorf, J. 2009. Experimental characterization of 3D localization techniques for particle-tracking and super-resolution microscopy. Optics Express 17:8264-8277.

[11] Hess, S., Webb, W. 2002. Focal Volume Optics and Experimental Artifacts in Confocal Fluorescence Correlation Spectroscopy. Biophys J. 83:2300-2317.

[12] Gould, T. J., Hess, S. T. 2009. Methods in Cell Biology. Elsevier, Inc. Vol89, Ch12.