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1 similar light powers but with well-separated action spectra.
2 engths of excitation, and their photocurrent action spectra.
3 ters at 0.37 K to measure high-resolution IR action spectra.
4 e-response curves were used to generate four action spectra, all of which had maxima at 300 nm.
5 oal of this investigation was to measure the action spectra and absolute sensitivities of the UV-cone
6 evive the well-established tool of measuring action spectra and adapt the technique to map wavelength
7 roximately 1.7, respectively, but invariable action spectra and effective antenna sizes of the photos
8      Similarities between these mtDNA damage action spectra and previously determined nDNA damage wer
9                                 Based on the action spectra and the known excited states of psoralen,
10                                              Action spectra are important biological weighting functi
11                                        Dimer action spectra between 300 and 360 nm were independent o
12 ing the early receptor current amplitude and action spectra between WT and the Opn4-expressing Drosop
13                             The derived cone action spectra can be described as retinal1 pigments wit
14                                              Action spectra, catalyst mass-activity, light-management
15                                          The action spectra conformed to the spectrum of green cone o
16 r action spectra were compared with erythema action spectra determined from the same volunteers and u
17                      Because the ultraviolet action spectra for DNA damage, skin cancer, and vitamin
18                                         Here action spectra for DNA inactivation and isolated chlorop
19                       We have determined the action spectra for DNA photodamage in different human ep
20                                  Comparative action spectra for DNA-DNA cross-linking and DNA-protein
21 nce between the sunscreens indicates similar action spectra for erythema and DNA photodamage and that
22 d the S cones since the previously published action spectra for melatonin suppression [1,2] pointed t
23 e constructed irradiance-response curves and action spectra for melatonin suppression and circadian r
24  The latter included a careful assessment of action spectra for photorelaxation, taking into account
25        The remarkable similarity between the action spectra for the blue light responses of guard cel
26 n this model, these results suggest that the action spectra for the induction of melanoma and NMSTs i
27 rnative splicing events, expanding the known action spectra for these 2 key players in energy signali
28                           The efficiency and action spectra for this latter photoactive process are p
29                                              Action spectra for transport had indicated that light ab
30 ift is in accord with the published in vitro action spectra for vitamin D(3) synthesis.
31                                              Action spectra implicated an opsin-based photopigment sy
32 atic photon-to-current conversion efficiency action spectra in the visible and NIR region, with a fur
33 teaux are lower than the cone threshold, and action spectra indicate rod mediation.
34                                Photochemical action spectra indicate that doping involves reaction of
35                                         Both action spectra match the absorption spectrum of zeaxanth
36  both tyrosine and tryptophan exhibit unique action spectra, meaning that the identity of the donatin
37                                              Action spectra obtained during the plateaux were consist
38 tra are consistent with the zero-phonon hole action spectra obtained in absorption mode, the profiles
39                            Photodissociation action spectra of cation-Irg complexes show that absorpt
40                                              Action spectra of GR SA in the WS fraction from HL withi
41    Photoreactivity was assessed by measuring action spectra of photo-induced oxygen uptake and photog
42 the room temperature gas phase infrared (IR) action spectra of protonated amino acids and their isome
43      The kinetics, fluence dependencies, and action spectra of the photoreceptor currents differ grea
44 the skin that quantitatively account for the action spectra of the physiological responses of photoag
45                                     Infrared action spectra of these ions at cluster sizes near the t
46                                 Shifting the action spectra of these proton pumps beyond 700 nm would
47 argely wavelength-dependent, as shown by the action spectra of UVR-induced erythema and nuclear DNA (
48                              Experimental IR action spectra recorded in the fundamental CH stretch re
49                       In contrast, published action spectra suggest that the photopigment underlying
50   Data from fluence rate-response curves and action spectra suggested that there were at least two li
51                    Shortcircuit photocurrent action spectra were acquired to evaluate the influence o
52    Melatonin suppression and phase resetting action spectra were best fit by a single-opsin template
53                          The epidermal dimer action spectra were compared with erythema action spectr
54 tion in mammals should have fluorescence and action spectra within the near-infrared window.