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1 d imaging of the fluorescence lifetime using multiphoton excitation.
2 sm, red-edge excitation, chemical stability, multiphoton excitation, and protein conjugation, were pr
3                                      Through multiphoton excitation experiments in aqueous solutions,
4 omerization interactions in living cells via multiphoton excitation fluorescence correlation spectros
5               By simultaneous observation of multiphoton excitation fluorescence emission and second
6                                              Multiphoton excitation fluorescence imaging generates an
7                                              Multiphoton excitation fluorescence microscopy (MPM) can
8                                              Multiphoton excitation fluorescence microscopy is a powe
9      We present comparisons of confocal with multiphoton excitation imaging of identical optical sect
10 et further improvements in the capability of multiphoton excitation imaging to produce good quality i
11                                      Because multiphoton excitation imaging with 1,047-nm wavelength
12 ght pulses excites fluorescent molecules via multiphoton excitation in an ellipsoidal focal volume an
13                            In this approach, multiphoton excitation is used to focally excite noncyto
14                Using styryl dye staining and multiphoton excitation microscopy, we visualized vesicul
15                                              Multiphoton excitation (MPE) lithography offers an effec
16                                              Multiphoton excitation (MPE) of fluorescent probes has b
17 ntaneous intensities great enough to promote multiphoton excitation of a photosensitizer and subseque
18                          We demonstrate that multiphoton excitation of DNA in live cells with visible
19 ined in all three spatial dimensions, making multiphoton excitation of DNA with visible light an idea
20  capillary electrophoresis, and detection by multiphoton excitation of fluorescence.
21                                      Because multiphoton excitation of fluorophores is intrinsically
22          We demonstrated this approach using multiphoton excitation of the Blastochloris viridis phot
23 escent probe molecules by density-dependent, multiphoton excitation processes.
24 e created by a direct-write process in which multiphoton excitation promotes photochemical cross-link
25                                              Multiphoton excitation provides a new means for producin
26  the imaging penetration depth obtained with multiphoton excitation relative to confocal imaging.
27 scence in this focal volume is measured with multiphoton excitation, using the attenuated laser beam
28          Excitation of this pair by a single multiphoton excitation wavelength (MPE, 850 nm) yields w

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