Extended resolution fluorescence microscopy.
暂无分享,去创建一个
[1] D A Agard,et al. Tilted view reconstruction in optical microscopy. Three-dimensional reconstruction of Drosophila melanogaster embryo nuclei. , 1989, Biophysical journal.
[2] Pekka Hänninen,et al. Nonlinear fluorescence through intermolecular energy transfer and resolution increase in fluorescence microscopy , 1999 .
[3] R Freimann,et al. Development of a standing‐wave fluorescence microscope with high nodal plane flatness , 1997, Journal of microscopy.
[4] S. Hell,et al. Properties of a 4Pi confocal fluorescence microscope , 1992 .
[5] Bernd Rinke,et al. A versatile 2π‐tilting device for fluorescence microscopes , 1994 .
[6] Emil Wolf,et al. Principles of Optics: Contents , 1999 .
[7] K Bahlmann,et al. Three-photon excitation in fluorescence microscopy. , 1996, Journal of biomedical optics.
[8] T. Wilson,et al. Real time 3D fluorescence microscopy by two beam interference illumination , 1998 .
[9] P. Shaw,et al. Three‐dimensional optical microscopy using tilted views , 1990, Journal of microscopy.
[10] Steffen Lindek,et al. Single‐lens theta microscopy — a new implementation of confocal theta microscopy , 1997 .
[11] Monty Glass,et al. The experimental effect of detector size on confocal lateral resolution , 1991 .
[12] Daniel L. Farkas,et al. Enhancement of axial resolution in fluorescence microscopy by standing-wave excitation , 1993, Nature.
[13] E Gratton,et al. Fluorescence lifetime imaging by asynchronous pump-probe microscopy. , 1995, Biophysical journal.
[14] Rainer Heintzmann,et al. Laterally modulated excitation microscopy: improvement of resolution by using a diffraction grating , 1999, European Conference on Biomedical Optics.
[15] T. Wilson,et al. Method of obtaining optical sectioning by using structured light in a conventional microscope. , 1997, Optics letters.
[16] Brent Bailey,et al. Image processing in 3D standing-wave fluorescence microscopy , 1996, Electronic Imaging.
[17] S. Hell,et al. Subdiffraction resolution in far-field fluorescence microscopy. , 1999, Optics letters.
[18] Tony Wilson,et al. Imaging properties of high aperture multiphoton fluorescence scanning optical microscopes , 1999 .
[19] S W Hell,et al. Confocal microscopy with an increased detection aperture: type-B 4Pi confocal microscopy. , 1994, Optics letters.
[20] B Bailey,et al. Standing-wave excitation for fluorescence microscopy. , 1994, Trends in cell biology.
[21] Neil,et al. A light efficient optically sectioning microscope , 1998 .
[22] Agard,et al. I5M: 3D widefield light microscopy with better than 100 nm axial resolution , 1999, Journal of microscopy.
[23] M. Kozubek,et al. Confocal microscopy by aperture correlation. , 1996, Optics letters.
[24] D. L. Taylor,et al. The actin-based nanomachine at the leading edge of migrating cells. , 1999, Biophysical journal.
[25] Colin J. R. Sheppard,et al. Comparison of three‐dimensional imaging properties between two‐photon and single‐photon fluorescence microscopy , 1995 .
[26] S. Hell,et al. Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy. , 1994, Optics letters.
[27] David A. Agard,et al. 3D widefield microscopy with two objective lenses: experimental verification of improved axial resolution , 1996, Electronic Imaging.
[28] W. Denk,et al. Two-photon laser scanning fluorescence microscopy. , 1990, Science.
[29] M. Kozubek,et al. Efficient real-time confocal microscopy with white light sources , 1996, Nature.
[30] P. Verveer,et al. A comparison of image restoration approaches applied to three‐dimensional confocal and wide‐field fluorescence microscopy , 1999, Journal of microscopy.
[31] Martin Schrader,et al. Three-dimensional super-resolution with a 4Pi-confocal microscope using image restoration , 1998 .
[32] S. Hell,et al. 4Pi-confocal imaging in fixed biological specimens. , 1998, Biophysical journal.
[33] J. Swoger,et al. Single-lens theta microscopy: Resolution, efficiency and working distance , 1999 .
[34] Daniel L. Farkas,et al. Three-dimensional imaging of biological specimens with standing wave fluorescence microscopy , 1994, Electronic Imaging.
[35] Daniel L. Farkas,et al. Excitation field synthesis as a means for obtaining enhanced axial resolution in fluorescence microscopes , 1993 .
[36] David A. Agard,et al. Sevenfold improvement of axial resolution in 3D wide-field microscopy using two objective lenses , 1995, Electronic Imaging.
[37] S W Hell,et al. 4Pi-confocal microscopy provides three-dimensional images of the microtubule network with 100- to 150-nm resolution. , 1998, Journal of structural biology.
[38] S. Hell,et al. Far-field fluorescence microscopy with repetitive excitation , 1999 .
[39] Pekka Hänninen,et al. Two-photon excitation 4Pi confocal microscope: enhanced axial resolution microscope for biological research , 1995 .
[40] Enrico Gratton,et al. Spatial resolution in scanning pump-probe fluorescence microscopy , 1997 .
[41] Steffen Lindek,et al. Fundamental reduction of the observation volume in far-field light microscopy by detection orthogonal to the illumination axis: confocal theta microscopy , 1994 .
[42] W. Webb,et al. Quantitative comparison of background rejection, signal-to-noise ratio, and resolution in confocal and full-field laser scanning microscopes. , 1995, Applied optics.
[43] J. Pawley,et al. Handbook of Biological Confocal Microscopy , 1990, Springer US.
[44] T. Wilson,et al. Optical sectioning in confocal fluorescent microscopes , 1989 .
[45] S W Hell,et al. 4Pi confocal microscopy with alternate interference. , 1998, Optics letters.
[46] Stefan W. Hell,et al. Measurement of the 4Pi‐confocal point spread function proves 75 nm axial resolution , 1994 .
[47] E. Abbe. Beiträge zur Theorie des Mikroskops und der mikroskopischen Wahrnehmung , 1873 .
[48] T. Wilson,et al. The Role of the Pinhole in Confocal Imaging Systems , 1990 .
[49] Christoph Cremer,et al. HIGH PRECISION LOCALIZATION OF FLUORESCENT TARGETS IN THE NANOMETER RANGE BY SPATIALLY MODULATED EXCITATION FLUORESCENCE MICROSCOPY , 1998 .
[50] S W Hell,et al. Far‐field fluorescence microscopy with three‐dimensional resolution in the 100‐nm range , 1997, Journal of microscopy.
[51] D. Agard,et al. Fluorescence microscopy in three dimensions. , 1989, Methods in cell biology.
[52] F S Fay,et al. Superresolution three-dimensional images of fluorescence in cells with minimal light exposure. , 1995, Science.