ライフサイエンスコーパス: Raman spectrum

1 .0 is consistent with shifts observed in the Raman spectrum.

2 n/beta-carotene ratio in EVOO using a single Raman spectrum.

3 chieved within the cell-silent region of the Raman spectrum.

4 rystallinity, as indicated by a shift in the Raman spectrum.

5 iously unexplained bands in the experimental Raman spectrum.

6 ived from the O-H stretching in deconvoluted Raman spectrum.

7 nal shifts and intensity fluctuations in the Raman spectrum.

8 on-chip fusion of the different parts of the Raman spectrum.

9 tidine vibrational mode in the time-resolved Raman spectrum.

10 ed from the amide I profile in the isotropic Raman spectrum.

11 nges in the ultrafast dynamics and terahertz Raman spectrum accompanying a helix-to-coil transition o

12 y measured leak rate, separation factors and Raman spectrum agree well with models based on effusion

13 w-frequency phonon structure observed in the Raman spectrum, although the Raman spectrum does experie

14 xyapatite (959 and 1038 cm(-1)) bands in the Raman spectrum and fluorescence lifetime shortened by 0.

15 cterizing the temperature dependency of both Raman spectrum and Fourier transform infrared spectrosco

16 sure exhibits two significant changes in the Raman spectrum and indicates of phase transition.

17 Lack of change in the Raman spectrum and relative amount of borate suggested t

18 ers, the Fe-His(F8) stretch in the resonance Raman spectrum and the position of band III in the absor

19 and the graphite index was characterized by Raman spectrum and X-ray diffraction.

20 images in the high-wavenumber region of the Raman spectrum as a robust and reliable method for the s

21 ar-infrared (NIR) laser source to excite the Raman spectrum at 752 nm, vibrational signatures of both

22 three-dimensional data cube consisting of a Raman spectrum at every pixel in a microscope field of v

23 ochrome c is released from mitochondria, its Raman spectrum becomes identical to that of ferrous cyto

24 pite the polarization sensitivity of the ChC Raman spectrum, cholesterol monohydrate crystals can be

25 The resulting difference Raman spectrum contained only vibrational modes due to b

26 The high wavenumber Raman spectrum contains quantitative information about t

27 The dominant feature in the low-frequency Raman spectrum correlates quite closely with the materia

28 zed by Raman spectroscopy, no changes in the Raman spectrum could be detected with changes in pH.

29 observed in the Raman spectrum, although the Raman spectrum does experience approximately 50% reducti

30 ough the absence of interlayer models in the Raman spectrum, dominant local modes in heat capacity, l

31 e enhancement of the melamine signals in the Raman spectrum due to the formation of SERS "hot spots".

32 s in the high-wavenumber (HWN) region of the Raman spectrum enabled the segmentation of subcellular o

33 ns by monitoring its time-resolved resonance-Raman spectrum following ultrafast photoexcitation.

34 emical selectivity in imaging by providing a Raman spectrum for each pixel.

35 The latter features allow us to obtain the Raman spectrum for small molecules soaking into crystals

36 The individual Raman spectrum from each focus is then retrieved from th

37 tably, the temperature dependence of water's Raman spectrum has long been considered to be among the

38 e most intense normal modes occurring in the Raman spectrum in the 1520-1560 cm-1 region.

39 n here to concomitantly affect the resonance Raman spectrum in the region with Fe-His contribution.

40 The new catalysts exhibit an in situ Raman spectrum, in the region associated with CO stretch

41 ermediate 3 is photolabile, so, in lieu of a Raman spectrum, IR was used to obtain vibrational data f

42 When the vesicle-associated cytochrome c Raman spectrum is compared with a spectrum in buffer, he

43 the intensity of different bands within its Raman spectrum is first established computationally thro

44 the E14A variant indicate that the resonance Raman spectrum is remarkably insensitive to changes in t

45 The Raman spectrum is unique in the capability to characteri

46 mod)D form, identified by its characteristic Raman spectrum, is also present in the 'as prepared' enz

47 to the specific chemical fingerprint of the Raman spectrum, it was possible to discriminate differen

48 Raman spectrum microscopy confirmed that mouse PPy/u con

49 n the high-wavenumber region of the cellular Raman spectrum, nine discrete regions of interest can be

50 In particular, the resonance Raman spectrum of 2 reveals a diatomic Co-O vibration ba

51 The Raman spectrum of 3 has a peak at 1017 cm(-1) that can b

52 The Raman spectrum of 4-dimethylaminobenzoyl-CoA undergoes m

53 without interference from protein modes; the Raman spectrum of a 12S crystal containing 2 MM-CoA liga

54 ligands per hexamer was subtracted from the Raman spectrum of a 12S crystal containing six MM-CoA li

55 Because the Raman spectrum of a filamentous phage is strongly depend

56 when a spectral component is removed from a Raman spectrum of a multi-component sample entirely.

57 The analysis of the Raman spectrum of a real dry white wine reveals qualitat

58 al assignment of amide I marker bands in the Raman spectrum of alpha-synuclein and by extrapolation t

59 The Raman spectrum of an equimolar alpha/beta mixture exhibi

60 lly, analysis relies on pattern matching the Raman spectrum of an unknown dataset with a supporting l

61 l conversion induces distinct changes in the Raman spectrum of bilayer graphene including the broaden

62 This effect allowed us to record the Raman spectrum of bound MM-CoA without interference from

63 The similarity between the Raman spectrum of bulk red phosphorus and of the metal-o

64 d vibrational mode in the 10 ns photoproduct Raman spectrum of CO-bound H93G(dibromopyridine) support

65 The unique Raman spectrum of different combinations of intracellula

66 le in this issue, and applied to measure the Raman spectrum of ds-DNA during force-extension.

67 The reversible change in the Raman spectrum of FePc can be related to the FePc molecu

68 )Am(PO(4))(2) and compared to the calculated Raman spectrum of K(3)Am(PO(4))(2) obtained from DFT cal

69 d the online acquisition of the nonresonance Raman spectrum of LC eluates.

70 The resonance Raman spectrum of MnII cytochrome b5 indicated a high-sp

71 The resonance Raman spectrum of MnIII cytochrome b5 was consistent wit

72 The Raman spectrum of monomeric alpha-synuclein in aqueous s

73 in, for the first time, the surface-enhanced Raman spectrum of neptunyl ions in dilute aqueous soluti

74 The resonance Raman spectrum of oxidized MauG exhibits a set of marker

75 The resonance Raman spectrum of oxidized wild-type P. furiosus SOR at

76 nding, and electrostatic interactions to the Raman spectrum of phosphoryl oxygens have not been analy

77 ctral decomposition technique, uncovered the Raman spectrum of prenucleation aggregates and their cri

78 The low-frequency Raman spectrum of reduced oPGHS-1 reveals two v[Fe-His]

79 Similarity between the PC1 loading and the Raman spectrum of RNA indicated a high concentration of

80 (1) The Raman spectrum of single D2O-loaded dormant spores sugge

81 In addition, the resonance Raman spectrum of the [4Fe-4S](2+) cluster in IscU is be

82 Amide I and III frequencies in the Raman spectrum of the adsorbed protein suggest that ther

83 yr and the heme-bound NO, we examined the UV Raman spectrum of the B10 Tyr by subtracting the B10 mut

84 lity to detect bacterial spores based on the Raman spectrum of the characteristic molecule calcium di

85 By subtracting the Raman spectrum of the complex with labeled substrate fro

86 on addition of glycerol, striking changes in Raman spectrum of the deoxy form are observed that indic

87 beling using the intrinsic surfaced-enhanced Raman spectrum of the DNA-RNA complex.

88 haps more revealing is the unusual resonance Raman spectrum of the endogenous E287Q-bound porphyrin,

89 e-enhanced tyrosinate modes in the resonance Raman spectrum of the H25Y.heme complex provide direct e

90 etect a line at 1135 cm(-1) in the resonance Raman spectrum of the intermediate formed from 0.6 to 3.

91 viscosity-dependent changes in the resonance Raman spectrum of the liganded photoproduct, together im

92 bound to d(CGCGCG), changes in the resonance Raman spectrum of the metal drug complex suggest conform

93 32)S-(34)S stretching modes in the resonance Raman spectrum of the O(2)-exposed [2Fe-2S](2+) cluster-

94 (PCA) were used independently to resolve the Raman spectrum of the peptide from the background cellul

95 The resonance Raman spectrum of the simple alkyne bridge in 4,4'-dinit

96 morphologic alteration and a characteristic Raman spectrum on spore and hyphae exposed to BITC.

97 30 min, chlorine dioxide did not change the Raman spectrum or the spore structure, peracetic acid sh

98 This technology allows the acquisition of a Raman spectrum over a rastered macro spot.

99 The Raman spectrum pattern was converted into image presenta

100 observed changes in the carotenoid Resonance Raman spectrum proved that zeaxanthin was involved and i

101 The Raman spectrum provides further evidence to support the

102 be tracked by following the evolution of the Raman spectrum, providing a clear signature for the expe

103 The low-frequency region of the Raman spectrum reveals lattice-level interactions and gl

104 guanine and adenine in the surface-enhanced Raman spectrum (SERS) of a dsDNA self-assembled monolaye

105 A Raman spectrum serves as a molecular 'fingerprint' of a

106 Raman spectrum showed the intense peaks in raw rice and

107 be nicely proven by the very characteristic Raman spectrum showing, because of the (approximately) i

108 bon atoms at 72.9 parts per million; and its Raman spectrum shows an intense peak at 1890 inverse cen

109 olayers, ReS2 remains direct bandgap and its Raman spectrum shows no dependence on the number of laye

110 ar 252 cm(-1) (assigned to nu(9) in the MbCN Raman spectrum) suggests that the 75% lower limit is muc

111 e show here that many of the features of the Raman spectrum that are considered to be hallmarks of a

112 nmental dependence of the tyrosine resonance Raman spectrum, the spectrum of 3-Y(f) is found to be ex

113 redicting chromosome number from each cell's Raman spectrum, thereby linking molecular fingerprints d

114 The Raman spectrum thus provides a definitive basis for eval

115 eory calculations were used to calculate the Raman spectrum to help identify the Raman bands at 690 a

116 insensitivity of the optical absorption and Raman spectrum to interlayer distance modulated by hydro

117 separated into two categories based on their Raman spectrum: type I, calcium oxalate dihydrate, and t

118 The FT-Raman spectrum upon visible light excitation of the Cr (

119 Raman spectroscopy allows recording the full Raman spectrum using a detection system with limited spe

120 A single cell Raman spectrum usually contains more than 1000 Raman ban

121 An observation of Mb(III) bands in the Raman spectrum was made for all of the cardiomyocytes th

122 A key change in the Raman spectrum was observed after perfusion of the NO-do

123 Without Ti, the NAB surface Raman spectrum was sufficiently strong to observe previo

124 brations in the high frequency region of the Raman spectrum, we conclude that the ferrous heme is fiv

125 the OH-stretching and bending regions of the Raman spectrum were analysed, along with investigation o

126 ands in the 2200-2400 cm(-1) interval of the Raman spectrum were measured and interpreted using tenso

127 applied to recognize the virus based on its Raman spectrum, which is used as a fingerprint.

128 In clear contrast with the bovine rhodopsin Raman spectrum, which is very similar to that for the 11

129 ve terms in the potential, and the resonance Raman spectrum, which provides a direct measure of the l

130 ns were resolved by correlating the obtained Raman spectrum with the characteristic Raman peaks assoc