ライフサイエンスコーパス: action spectrum

1 (kmod) computed using a previously published action spectrum.

2 nger wavelengths compared with the erythemal action spectrum.

3 gate its spectral sensitivity and produce an action spectrum.

4 for lens filtering and used to construct an action spectrum.

5 y, which is reflected by a blue shift of the action spectrum.

6 , PSmOrange2 has blue-shifted photoswitching action spectrum, 9-fold higher photoconversion contrast,

7 The CPGE action spectrum above the bandgap reveals spin-polarized

8 The action spectrum, absolute sensitivity, and recovery of t

9 We present action spectrum and genetic data indicating that the lig

10 rformance in terms of inactivation efficacy, action spectrum, and energy efficiency was determined.

11 bit bacterial growth, yet their mechanism of action, spectrum, and clinical relevance remain unknown.

12 t between kobs and kmod, suggesting that the action spectrum can be used to estimate the decrease in

13 n the summer and winter, suggesting that the action spectrum can be used to predict changes in the in

14 The cis-UCA action spectrum can be used to predict the ability of su

15 pha(q)/Galpha(11) G protein pathway, with an action spectrum closely matching that of melanopsin-expr

16 The action spectrum conformed to the sensitivity of rhodopsi

17 to short-wavelength light, demonstrating an action spectrum consistent with cryptochrome rather than

18 The action spectrum constructed from these data fit an opsin

19 The resulting action spectrum demonstrated maximal cis-UCA production

20 The action spectrum deviated significantly from the absorpti

21 levels, as weighting the UVR doses with this action spectrum did not result in a common regression li

22 The action spectrum exhibits a major peak at approximately 2

23 and a shoulder at 430 nm, closely matched an action spectrum for blue light-stimulated coleoptile pho

24 This spectrum matched closely an action spectrum for blue light-stimulated stomatal openi

25 ctral properties are not consistent with the action spectrum for circadian entrainment.

26 e different spectral dependence and (ii) the action spectrum for dermal damage in the UVA is broad, e

27 ch of the UVR sources and cell types, and an action spectrum for each cell type was determined by mat

28 The aim of this study was to establish an action spectrum for light-induced melatonin suppression

29 ls in the skin of this model and derived the action spectrum for melanin-photosensitized oxidant prod

30 The derived action spectrum for NFAT activation indicates that NFAT

31 mice lacking rods and cones, we measured the action spectrum for phase-shifting the circadian rhythm

32 The action spectrum for photodamage exhibits minima at 830 a

33 The action spectrum for photooxidation in full fat bovine mi

34 These spectral features correspond to the action spectrum for phototropism in higher plants.

35 of the recombinant protein is similar to the action spectrum for phototropism, consistent with the co

36 ies of the chromopeptides are similar to the action spectrum for phototropism, implying that the LOV

37 This paper reports that the in vitro action spectrum for singlet oxygen generation after exci

38 The ultraviolet action spectrum for stomatal opening was measured using

39 An action spectrum for the blue light-induced enhancement o

40 In addition, the two-photon fluorescence action spectrum for the fluorescent photoproduct was det

41 mal collagen cross-links and to determine an action spectrum for the induced changes.

42 trans-urocanic acid mimics the in vivo UV-A action spectrum for the photosagging of mouse skin.

43 An action spectrum for the PLR in rd/rd cl mice demonstrate

44 es which generate LIBM in high yield, and an action spectrum for the PM-->LIBM photoconversion all in

45 The action spectrum for the ultraviolet A effect on the in v

46 An action spectrum for the WS-LMW fraction from human lens

47 f 7-dehydrocholesterol to previtamin D(3) An action spectrum for this process that is followed by oth

48 to monochromatic UV radiation at 254 nm and action spectrum for wavelengths ranging from 214 to 289

49 An action spectrum from 320 to 400 nm was determined for bo

50 We tested this action spectrum in vivo by full- or partial-body suberyt

51 The generic form of an action spectrum [in our experiments, photoluminescence e

52 Their action spectrum (lambda(max) approximately 480 nm) impli

53 zation increases with stimulus size, and its action spectrum matches that of cones.

54 s by transient-absorption and photocatalysis action spectrum measurement.

55 bda(max) at 350 nm, which was similar to the action spectrum obtained for the photobleaching of the l

56 ollect the 935-1600 cm(-1) (6.2-10.7 mum) IR action spectrum of a collection of amino acids and a dip

57 o develop a detailed spectral sensitivity or action spectrum of adenovirus 2.

58 n opsin shift above 440 nm is induced in the action spectrum of charge motions caused by visible flas

59 A wider action spectrum of intrinsic photosensitivity was obtain

60 The only model for which the action spectrum of melanoma causation is known is a gene

61 m that is coincident with the maximum of the action spectrum of most UV-induced photobiologic respons

62 for quite some time, but a detailed in vivo action spectrum of mutation formation has not yet been r

63 Furthermore, the inactivation action spectrum of PBCV-1 was similar to that of adenovi

64 The presence of features in the action spectrum of the +3 charge state of both quenched

65 The action spectrum of the major R(2) charge motion is consi

66 The action spectrum of the wild-type response was consistent

67 t of this finding and the recently published action spectrum of this class of Crys, we conclude that

68 The action spectrum of this response, showing a major peak a

69 study solves this problem by determining the action spectrum of UVR-induced mtDNA damage in human ski

70 of omadacycline, including its mechanism of action; spectrum of activity; protein binding; activity

71 ambdamax = 532 nm) with a non-rhodopsin-like action spectrum peaking at 610 nm for stationary photocu

72 mates based on the human photocarcinogenesis action spectrum predict that narrowband UVB lamps will b

73 We observe a red shift of the action spectrum relative to the absorption spectrum of t

74 lar UVR based on the ex vivo previtamin D(3) action spectrum require revision.

75 An action spectrum showed that ascorbate oxidation occurred

76 The resulting action spectrum showed unique short-wavelength sensitivi

77 Irradiance-response curves yield an action spectrum similar to absorption spectra for prokar

78 velengths but does not alter the form of the action spectrum, suggesting that cryptochrome does not f

79 ion of wavelength and calculated a composite action spectrum that allowed extrapolation from the 254-

80 ity to respond to light while shifting their action spectrum to 355 nm.

81 ns and wildlife to solar UV, and use the DNA action spectrum to model how differences in water transp

82 The action spectrum was also used to predict the endogenous

83 The action spectrum was determined by following the increase

84 This action spectrum was identical to that for melanoma induc

85 It was established that the previtamin D(3) action spectrum was not valid when related to the serum

86 The excitation wavelength dependence (action spectrum) was measured and found to be comparable

87 The lack of fit (r(2) < 0.1) of our action spectrum with the published rod and cone absorpti