Highly nonlinear photodamage in two-photon fluorescence microscopy.

[1]  Roderick K. Clayton,et al.  Light and living matter: A guide to the study of photobiology , 1970 .

[2]  M. Scully,et al.  The Quantum Theory of Light , 1974 .

[3]  C. Sheppard,et al.  Theory and practice of scanning optical microscopy , 1984 .

[4]  W. Denk,et al.  Two-photon laser scanning fluorescence microscopy. , 1990, Science.

[5]  S. Terakawa,et al.  Quantitative analysis of exocytosis directly visualized in living chromaffin cells , 1991, Neuroscience Letters.

[6]  W. Webb,et al.  Two‐photon molecular excitation provides intrinsic 3‐dimensional resolution for laser‐based microscopy and microphotochemistry , 1994, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  G. Brakenhoff,et al.  Femtosecond pulse width control in microscopy by two‐photon absorption autocorrelation , 1995 .

[8]  K. König,et al.  Cell damage by near-IR microbeams , 1995, Nature.

[9]  W. Webb,et al.  Measurement of two-photon excitation cross sections of molecular fluorophores with data from 690 to 1050 nm , 1996 .

[10]  B. Tromberg,et al.  Cell damage in near-infrared multimode optical traps as a result of multiphoton absorption. , 1996, Optics letters.

[11]  D. Linde,et al.  Breakdown Threshold and Plasma Formation in Femtosecond Laser-Solid Interaction , 1994, High Field Interactions and Short Wavelength Generation.

[12]  Richard P. Haugland,et al.  Handbook of fluorescent probes and research chemicals , 1996 .

[13]  K. König,et al.  3D resolved two-photon fluorescence microscopy of living cells using a modified confocal laser scanning microscope. , 1996, Cellular and Molecular Biology.

[14]  Jean-Claude Diels,et al.  Ultrashort Laser Pulse Phenomena , 1996 .

[15]  C. Sheppard.  Image formation in three‐photon fluorescence microscopy , 1996 .

[16]  K. Svoboda,et al.  Photon Upmanship: Why Multiphoton Imaging Is More than a Gimmick , 1997, Neuron.

[17]  P. So,et al.  Cellular response to near-infrared femtosecond laser pulses in two-photon microscopes. , 1997, Optics letters.

[18]  S W Hell,et al.  Heating by absorption in the focus of an objective lens. , 1998, Optics letters.

[19]  Hell,et al.  Continuous wave excitation two‐photon fluorescence microscopy exemplified with the 647‐nm ArKr laser line , 1998, Journal of microscopy.

[20]  Hell,et al.  Picosecond pulsed two‐photon imaging with repetition rates of 200 and 400 MHz , 1998 .

[21]  S W Hell,et al.  Two-photon near- and far-field fluorescence microscopy with continuous-wave excitation. , 1998, Optics letters.

[22]  E Neher,et al.  Fast scanning and efficient photodetection in a simple two-photon microscope , 1999, Journal of Neuroscience Methods.

[23]  Corey A. Smith.  A Persistent Activity-Dependent Facilitation in Chromaffin Cells Is Caused by Ca2+ Activation of Protein Kinase C , 1999, The Journal of Neuroscience.

[24]  K J Halbhuber,et al.  Pulse-length dependence of cellular response to intense near-infrared laser pulses in multiphoton microscopes. , 1999, Optics letters.

[25]  S W Hell,et al.  Ca2+ fluorescence imaging with pico- and femtosecond two-photon excitation: signal and photodamage. , 1999, Biophysical journal.