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1 d imaging of the fluorescence lifetime using multiphoton excitation.
2 rmediates in photoredox catalysis, including multiphoton excitation and electrophotocatalytic process
3  recent achievements in the understanding of multiphoton excitation and the resulting photoluminescen
4 ection, NIR-II excitation capabilities under multiphoton excitation, and high dye brightness; all hig
5 sm, red-edge excitation, chemical stability, multiphoton excitation, and protein conjugation, were pr
6 e heterogeneity, and poor compatibility with multiphoton excitation because of local heating.
7          These challenges are exacerbated in multiphoton excitation by the lower excitation efficienc
8                                      Through multiphoton excitation experiments in aqueous solutions,
9 linear optical processes for imaging include multiphoton excitation fluorescence (MPEF), second harmo
10 omerization interactions in living cells via multiphoton excitation fluorescence correlation spectros
11               By simultaneous observation of multiphoton excitation fluorescence emission and second
12                                              Multiphoton excitation fluorescence imaging generates an
13                                              Multiphoton excitation fluorescence microscopy (MPM) can
14                                              Multiphoton excitation fluorescence microscopy is a powe
15      We present comparisons of confocal with multiphoton excitation imaging of identical optical sect
16 et further improvements in the capability of multiphoton excitation imaging to produce good quality i
17                                      Because multiphoton excitation imaging with 1,047-nm wavelength
18 ght pulses excites fluorescent molecules via multiphoton excitation in an ellipsoidal focal volume an
19                            In this approach, multiphoton excitation is used to focally excite noncyto
20                Using styryl dye staining and multiphoton excitation microscopy, we visualized vesicul
21                                              Multiphoton excitation (MPE) lithography offers an effec
22                                              Multiphoton excitation (MPE) of fluorescent probes has b
23 ntaneous intensities great enough to promote multiphoton excitation of a photosensitizer and subseque
24 nd states of NAD(P)H and FAD are achieved by multiphoton excitation of a pulsed femto-second infra-re
25                          We demonstrate that multiphoton excitation of DNA in live cells with visible
26 ined in all three spatial dimensions, making multiphoton excitation of DNA with visible light an idea
27  capillary electrophoresis, and detection by multiphoton excitation of fluorescence.
28                                      Because multiphoton excitation of fluorophores is intrinsically
29          We demonstrated this approach using multiphoton excitation of the Blastochloris viridis phot
30 escent probe molecules by density-dependent, multiphoton excitation processes.
31 e created by a direct-write process in which multiphoton excitation promotes photochemical cross-link
32                                              Multiphoton excitation provides a new means for producin
33  the imaging penetration depth obtained with multiphoton excitation relative to confocal imaging.
34 py, a method integrating one-shot multicolor multiphoton excitation through wavelength mixing and ser
35 scence in this focal volume is measured with multiphoton excitation, using the attenuated laser beam
36          Excitation of this pair by a single multiphoton excitation wavelength (MPE, 850 nm) yields w
37 cond laser pulses on the plasma membrane for multiphoton excitation, we directly induced Ca(2+) influ