ライフサイエンスコーパス: Raman spectra

1 nd human subjects by statistical analysis of Raman spectra.

2 and necrotic cell death based on single cell Raman spectra.

3 TOF experiments can be utilized to interpret Raman spectra.

4 t and retrieve the corresponding vibrational Raman spectra.

5 nsistent with and extends previous resonance Raman spectra.

6 performance is evaluated by comparison with Raman spectra.

7 (WMRS) may suppress the background from the Raman spectra.

8 nd a detailed analysis of the rich resonance Raman spectra.

9 a computer algorithm to analyze the measured Raman spectra.

10 ter functions may be used to regenerate full Raman spectra.

11 s of the analyte of interest and the mixture Raman spectra.

12 acid-microwaved CNTs, as indicated by their Raman spectra.

13 al contribution of the above proteins to the Raman spectra.

14 rbidity correction procedure to the observed Raman spectra.

15 rnate acquisition of diffuse reflectance and Raman spectra.

16 of nu(Fe-CO)/nu(C-O) modes in the resonance Raman spectra.

17 e microorganisms when compared to the native Raman spectra.

18 lent agreement with conventionally collected Raman spectra.

19 luorescence that does not interfere with the Raman spectra.

20 y via numerical simulations and experimental Raman spectra.

21 hierarchical cluster analysis (HCA) of their Raman spectra.

22 exhibit strikingly similar changes in their Raman spectra.

23 yphil cells) were characterized by their own Raman spectra.

24 by their transient absorption and stimulated Raman spectra.

25 d to characterize them on the basis of their Raman spectra.

26 copic analysis to improve analyte signals in Raman spectra.

27 ectra as well as label-free plasmon-enhanced Raman spectra.

28 per TEM and the presence of a 2D mode in the Raman spectra.

29 s, and provide a basis for interpretation of Raman spectra.

30 g the ratio of the amplitudes of the ROA and Raman spectra.

31 us solutions through chemometric analysis of Raman spectra.

32 environment, as indicated in the solid-state Raman spectra.

33 ation hierarchy via multivariate analysis of Raman spectra.

34 onsistent with characteristic changes in the Raman spectra.

35 A total of 94 HW Raman spectra (22 normal sites, 72 tumor sites) were acq

36 a (800-1800 cm(-1)) and high-wavenumber (HW) Raman spectra (2800-3600 cm(-1)) from the subsurface of

37 A total of 476 in vivo FP/HW Raman spectra (356 normal and 120 precancer) are acquire

38 ultifocal detection scheme that enables full Raman spectra (~500-2000 cm(-1)) from a 2-D focal array

39 Chemometric analyses of far-field Raman spectra accurately classified their internal struc

40 In situ Raman spectra acquired in 0.1 M KOH at OER potentials sh

41 In particular, we show that Raman spectra acquired with an inexpensive noncooled det

42 Subsequently, using field data (Raman spectra) acquired from a glucose clamping study on

43 A quantitative model based on Raman spectra allowed an estimation of the exchange rate

44 The Raman spectra analyzed for water and for the components

45 n microscopy (TEM), X-ray diffraction (XRD), Raman spectra and Brunauer-Emmett-Teller (BET) method.

46 ves including simulation of NMR, infrared or Raman spectra and calculation of other properties such a

47 v) the degree of similarity between solution Raman spectra and DCDR spectra.

48 According to the matrix isolated Raman spectra and DFT calculations, we proposed aggregat

49 f simultaneously acquiring both single point Raman spectra and digital holographic images of single c

50 .15 K), as shown from the dramatic change in Raman spectra and fluctuations in AL/AS values.

51 ultaneously measuring phase-contrast images, Raman spectra and fluorescence images of the optically c

52 However, the resonance Raman spectra and global fit analysis of the UV-visible

53 Based upon the Raman spectra and HRTEM images of the composite, it is c

54 Micro-Raman spectra and imaging were acquired across the denti

55 llent agreement between our newly remeasured Raman spectra and our model system further supports the

56 ial was characterized by means of FTIR, XRD, Raman spectra and TEM analyses.

57 probed by the low-frequency range of IR and Raman spectra and the applications of vibrational spectr

58 the OH stretching bands in the infrared and Raman spectra and their isotropic-anisotropic Raman nonc

59 Raman spectra and X-ray diffraction characterization sug

60 phase transition shows a hysteretic loop in Raman spectra, and can be reversed by increasing or decr

61 fficiency in the near-infrared (NIR) region, Raman spectra, and light attenuation spectra in the UV,

62 Analysis of X-ray diffraction, Raman spectra, and Mossbauer spectra confirm the presenc

63 arable to one derived from the corresponding Raman spectra, and the considerably higher intensity of

64 In this study, 130 Raman spectra are acquired from ex vivo samples of human

65 e parallel and perpendicular polarized light Raman spectra are also reported.

66 d dipole moment, as well as the infrared and Raman spectra are in excellent agreement with experiment

67 The CDW modes from Raman spectra are observed in x = 0.04 and 0.1 crystals,

68 Electronic absorption and resonance Raman spectra are presented.

69 ies of the enhanced modes from the resonance Raman spectra are used together with the time-dependent

70 ), rates of absorption-desorption as well as Raman spectra as a function of depth (a total of 124 inf

71 e Raman spectroscopy (RRS), i.e., mapping of Raman spectra as a function of tunable laser excitation

72 coefficients (FC) derived by modeling tissue Raman spectra as a linear combination of the Raman spect

73 differentiation capability using spontaneous Raman spectra as well as label-free plasmon-enhanced Ram

74 We observe changes in the Raman spectra associated with the interactions between t

75 s in the CH region of HWVN (high-wavenumber) Raman spectra between melanoma and benign melanocytic le

76 nal residues has been previously observed in Raman spectra, but atomic-resolution evidence for this i

77 rate that relative peak intensity changes in Raman spectra can be caused by morphological changes in

78 ormation in the CH-stretching region of HWVN Raman spectra can discriminate melanoma from benign mela

79 Raman spectra changes observed during the lysis from "wi

80 scattering and exhibited distinctive dynamic Raman spectra changes.

81 ata collection in conjunction with resonance Raman spectra collected before and after diffraction dat

82 We found that Raman spectra collected from these products are characte

83 Raman spectra confirm the increased intensity of carbon

84 gahertz- to terahertz-frequency infrared and Raman spectra contain a wealth of information concerning

85 The acquired Raman spectra display excellent reproducibility of spect

86 The Raman spectra do not change with temperature for molecul

87 Structural changes observed in the Raman spectra during permeabilization indicated acyl cha

88 t electrode surface stability as verified by Raman spectra, electrochemical impedance spectroscopy (E

89 nant analysis (PLS-DA) models of single cell Raman spectra enable identifying four dissimilar hematop

90 of principal component analysis (PCA) to the Raman spectra enabled accurate identification of the dif

91 Raman spectra exhibit a major line at 1080 cm(-1) and l

92 tructures were studied by X-ray diffraction, Raman spectra, field-emission scanning electron microsco

93 Multivariate analysis results of single-cell Raman spectra followed the same trend, exhibiting a sepa

94 Electronic absorption and resonance-enhanced Raman spectra for ketimido (azavinylidene) complexes of

95 By comparing Raman spectra for low-energy structures found in DFT sea

96 h onto a CCD detector, giving 16 independent Raman spectra formed as 16 bands with different heights

97 emission scanning electron microscopy (SEM), Raman spectra, Fourier Transform infrared spectroscopy (

98 We provided an important database for Raman spectra from a broad range of AGEs and ALEs, each

99 Notably, Raman spectra from a human sample with nemaline-myopathy

100 Raman spectra from as-prepared type I collagen (Col-I) a

101 are described, as well as the first reported Raman spectra from live, priority pathogens, including B

102 Raman spectra from Ni cermet anodes at open circuit volt

103 We have collected 31 Raman spectra from nine patients undergoing partial mast

104 been used to compile a reference library of Raman spectra from several species of microfungi typical

105 rapid buildup of the acrylate product in the Raman spectra from the dideutero analogue.

106 Principal component analyses of Raman spectra further demonstrated that the crystallinit

107 eir FT-IR spectra had the sp (2) bond, their Raman spectra had matching D, G, G', D +G, and D '' band

108 ts FT-IR spectra lacked the sp (2) bond, its Raman spectra had no detectable G' band at 2700 cm (-1),

109 Fluorescence measurements and Raman spectra have also shown that chloroform significan

110 With this design characteristic Raman spectra have been collected and explored for diffe

111 Room-temperature Raman spectra have broad CdSe peaks at 175 and 200 cm(-1

112 f bacteria allows for obtaining high quality Raman spectra in dilute suspensions with an integration

113 report, we demonstrate the effectiveness of Raman spectra, in conjunction with multivariate analysis

114 Infrared and Raman spectra indicate a weakening of the intramolecular

115 se in coordination number, whereas resonance Raman spectra indicate a weaker Cu-S bond.

116 The Raman spectra indicate that the materials quality of the

117 Raman spectra indicated formation of an amorphous Ge fil

118 Raman spectra indicated the composition of the resultant

119 arance of graphite intensity measured in the Raman spectra is accompanied by a steep approximately 0.

120 A normalization procedure for the Raman spectra is proposed based on the equilibria taking

121 On the basis of the resonance Raman spectra, it is clear that the actual heme conforma

122 lyzed, we provide instructions for acquiring Raman spectra, maps and images for fresh plant tissue, f

123 calculations also reproduce the experimental Raman spectra measured for the ambient and high-pressure

124 we apply biomolecular component analysis for Raman spectra measured in the same nucleoli of HeLa cell

125 In addition, the Raman spectra not only indicated the morphological chang

126 upon application of TCRS, the widely varying Raman spectra observed from a set of tissue phantoms hav

127 ated and validated based on surface-enhanced Raman spectra obtained from adjacent cantilevers that we

128 Many of the Raman spectra obtained from areas painted with ultramari

129 The Raman spectra obtained from cresyl fast violet (CFV) dep

130 sing AuNPs@mesoSiO2 compared with the normal Raman spectra obtained from the aqueous solution and the

131 The Raman spectra obtained from these solutions were in agre

132 This work presents Raman spectra obtained from thin films of protein materi

133 Raman spectra obtained on eC/Ag surfaces were indistingu

134 Comparison of the UV-vis and resonance Raman spectra of 2 with adduct I in WT, D383E, D383N, an

135 abase containing more than 10000 single-cell Raman spectra of 34 bacterial strains out of 13 differen

136 Raman spectra as a linear combination of the Raman spectra of 9 chemical and morphologic components o

137 through the changes in photoluminescence and Raman spectra of a bare bilayer MoS2 (Molybdenum disulfi

138 The isotropic and anisotropic Raman spectra of acetone and deuterated acetone isolated

139 beta-CD: rGO sheets to record the resonance Raman spectra of adsorbed and included organic chromopho

140 eory calculations were used to determine the Raman spectra of all botryococcenes to compare computed

141 Finally, Raman spectra of an AZD2811-pamoate salt compared well w

142 that the contribution of cellular DNA to the Raman spectra of bacterial cells is negligible compared

143 Remarkably, the Raman spectra of Bi2Se3 from this work (two independent

144 Changes in Raman spectra of boronate-substituted polyaniline after

145 is method requires the transformation of the Raman spectra of both API and finished drug products int

146 first demonstration of in vivo collection of Raman spectra of breast tissue.

147 sence of gold nanorods afforded good quality Raman spectra of carbendazim at micromolar concentration

148 ional modes were identified in the resonance Raman spectra of CcO from bovine (bCcO) and Rhodobacter

149 Raman spectra of cells and nuclei from cultures in the p

150 The Raman spectra of cells exposed to Cefazolin at the end o

151 his data corresponds well with the simulated Raman spectra of chiral peropyrenes.

152 Differences in the average Raman spectra of cocoa beans from different sites but wi

153 Finally, resonance Raman spectra of CODH reveal the presence of FAD, Fe/S c

154 We also provide a mapping between the Raman spectra of defective graphene and its mechanical p

155 s is constructed to collect the superimposed Raman spectra of different multifocal patterns.

156 The Raman spectra of E. coli cells sampled at different time

157 mical experiments by Raman spectroscopy, the Raman spectra of each phase were successfully identified

158 Resonance Raman spectra of ferrous-nitrosyl RCCP confirm the prese

159 o of the intensities of the D and G bands in Raman spectra of graphene films.

160 Herein we reanalyse the Raman spectra of graphenes and show that traditional met

161 Statistically averaged Raman spectra of H(2) in hydrogen clathrate are calculat

162 Raman spectra of hairs from TTD patients and normal dono

163 We report temperature-dependent Raman spectra of HfO2, TiO2 and Ge2Sb2Te5 (GST) films, a

164 Assignments of the Raman spectra of Hg(OTeF5)2 and Hg(OTeF5)2.1.5NgF2 are b

165 The resonance Raman spectra of Hmx1 reveal a heme binding pocket simil

166 ads to distinct changes in the coherence and Raman spectra of HRP that are consistent with the stabil

167 spectral flow cytometer capable of acquiring Raman spectra of individual SERS-tags at flow rates of h

168 In the present study, ROA and Raman spectra of insulin under a range of various condit

169 Vibrational frequencies observed in IR and Raman spectra of ionic liquids based on different anions

170 Some basic care needed while recording IR or Raman spectra of ionic liquids is explained.

171 a singular value decomposition analysis for Raman spectra of liquid indene.

172 obleaching effects observed in the resonance Raman spectra of live cells.

173 The Raman spectra of live, hematopoietic cells provide relia

174 effect spectroscopy to study the depolarized Raman spectra of lysozyme and its complex with the inhib

175 ng multivariate analysis techniques to micro-Raman spectra of mineralized nodules formed in vitro, we

176 Raman spectra of Mo/SiO2 show a feature at 975 cm(-1), a

177 Comparison to solution resonance Raman spectra of MTHF suggests that the carbonyl of its

178 In contrast to the wild-type enzyme, Raman spectra of NADD bound to F149A InhA resemble those

179 Raman spectra of NaTFSI/DMSO electrolytes and ab initio

180 ce Fourier transform infrared (ATR-FTIR) and Raman spectra of non-extracted seed material have been r

181 The Raman spectra of normal modes primarily involving the ch

182 The differences between Raman spectra of NSCs and glial cells indicated that the

183 in formaldehyde does not strongly affect the Raman spectra of nucleolar biomolecular components, but

184 We present a systematic study of the Raman spectra of optical phonons in graphene monolayers

185 have been compared to experimental resonance Raman spectra of oxidized A. thaliana sulfite oxidase ca

186 ectronic absorption and stimulated resonance Raman spectra of P(r) and P(fr) are presented; vibronic

187 Raman spectra of phosphorylated amino acids and peptides

188 approximately 980 and 1080cm(-1) in solution Raman spectra of phosphoserine and phosphothreonine are

189 The Raman spectra of regions with a large moire period revea

190 applied to compile a large-scale database of Raman spectra of single Bacillus endospores and to calcu

191 We measured Raman spectra of single E. coli cells at different cultu

192 We acquired Raman spectra of skin of patients undergoing treatment w

193 In situ Raman spectra of solution-phase electrogenerated species

194 dispersion of the G-band was present in the Raman spectra of sub-nm SWNTs with diameters <0.7 nm.

195 Raman spectra of the 1T '-MoTe2 nanostructures exhibit a

196 Raman spectra of the as-prepared and illuminated samples

197 Low-temperature resonance Raman spectra of the beta1(1-194)-NO and beta2(1-217)-NO

198 greement between calculated and experimental Raman spectra of the biliverdin cofactor is in line with

199 Resonance Raman spectra of the charge-transfer complex reveals mul

200 01 M) concentrations of dissolved As(2)O(3), Raman spectra of the electrodeposited films were consist

201 For ABS, the Raman spectra of the filament and the printed part were

202 The Raman spectra of the graphene layers grown on hBN and sa

203 Time-resolved Raman spectra of the initial species with (16)O(18)O oxy

204 After capturing, single cell Raman spectra of the isolated species were acquired.

205 In the analysis of the Raman spectra of the meat mixtures, the integral intensi

206 ls to determine the alumina content from the Raman spectra of the molten NaF-AlF3-CaF2-Al2O3 electrol

207 The Raman spectra of the natural abundance and (18)O-enriche

208 Raman spectra of the oxy complex of Y171F indicate that

209 nate recombination and the visible resonance Raman spectra of the photoproduct of alpha alpha-fumaryl

210 Close similarities in the low-wavenumber Raman spectra of the title compound and starch-iodine po

211 hical cluster analysis were able to separate Raman spectra of the two most abundant leukocytes, the n

212 Raman spectra of the yolk extracts were recorded in the

213 Comparison of the resonance Raman spectra of this adduct and a phenylhydrazine-label

214 Here, we report the resonance Raman spectra of this naturally occurring Fe(2)S(2)(His)

215 Variations in the enhanced Raman spectra of three peptide ligands (i.e., cyclic-RGD

216 Ultraviolet resonance Raman spectra of Trp-170 and Trp-7 reveal evolution of a

217 discriminant analysis (LDA) models based on Raman spectra of undifferentiated NSCs and NSC-derived g

218 trate dianion at the enzyme active site, and Raman spectra of urate oxidase-bound 8-nitroxanthine sug

219 lar dichroism, and isotropic and anisotropic Raman spectra of XAO, where, for each residue, the backb

220 o retrieve background-free and noise-reduced Raman spectra over the whole frequency range including b

221 With an acquisition rate of 333 Raman spectra per second, chemical information was obtai

222 Advances in the interpretation of Raman spectra permit identifying the fate decisions of i

223 short distances into cloth targets, and the Raman spectra produced by the GSR were measured and comp

224 We demonstrate that single-cell Raman spectra provide a highly reproducible biomolecular

225 Moreover, the distinct peak structures of Raman spectra provide detailed insight into the overall

226 The Raman spectra provide real-time information about polyme

227 These changes in the Raman spectra provide us with a powerful tool for probin

228 he 2D correlation analysis of time dependent Raman spectra readily identified small sequential change

229 study presented here relies on reproducible Raman spectra recorded on molten mixtures whose composit

230 m(-1)) vibrations in infrared absorption and Raman spectra, respectively, identifies this intermediat

231 Atomic force microscopy and Raman spectra reveal that the flake thickness actually i

232 ate spectral data analysis of space-resolved Raman spectra revealed the intrinsic spectra and relativ

233 he absence of the disorder-induced D band in Raman spectra revealed the single-crystalline feature of

234 studies of reporter plasmids using confocal Raman spectra, S1 nuclease and restriction enzymes demon

235 ome", which is the collection of Single-cell Raman Spectra (SCRS) from a number of cells randomly sel

236 demonstrates the application of single-cell Raman spectra (SCRS) to differentiate Rhizobium legumino

237 tion band at 2070-2300 cm(-1) in single-cell Raman spectra (SCRS) when Escherichia coli used deuterat

238 Raman spectra separately showed that the electrodeposite

239 Optical images and Raman spectra separately showed the composition of the a

240 Raman spectra show a significant and gradual red shift f

241 The Raman spectra show for cells with wild-type K-Ras altera

242 Raman spectra show that nonameric rings formed by subuni

243 Symmetry arguments together with first-order Raman spectra show that the single layer graphene (1LG),

244 Raman spectra showed that both molecules produce a simil

245 Analyses of the Raman spectra showed that Mo and W substituted for V and

246 PCA analysis of Raman spectra shows a clear discrimination between nativ

247 roach that allows recording surface-enhanced Raman spectra simultaneously with electrical measurement

248 spectra was achieved by SERS enhancement of Raman spectra specific for the Raman reporter dyes Infra

249 Here, we present resonance Raman spectra, statistical analysis on multiple data set

250 ectron paramagnetic resonance, and resonance Raman spectra strongly support the formation of a neutra

251 The Raman spectra taken both in aqueous dispersion and in th

252 Raman spectra taken within the interior of the particle

253 To help in the interpretation of the Raman spectra, the absorption properties in the UV-visib

254 ition of the amide I vibrational band in the Raman spectra, the secondary structure of the peptide wa

255 n to B produces C, determined from resonance Raman spectra to be a Cu(II)-semiquinone complex.

256 loy factor analysis of temperature-dependent Raman spectra to characterize the thermostability of the

257 spectroscopy, scanning electron microscopy, Raman spectra, transmission electron microscopy, positro

258 cal absorption, ligand binding and resonance Raman spectra typical of mu-oxo-bridged di-iron containi

259 r verified with resistivity measurements and Raman spectra under high pressure.

260 optical trap while simultaneously collecting Raman spectra upon application of sugar to the medium.

261 omophore ground-state features, we collected Raman spectra using 752-nm excitation.

262 from key leaders in the field for obtaining Raman spectra using a microspectrometer.

263 r and with infrared absorption and resonance Raman spectra using a Styryl 9 M dye as a model system.

264 Raman spectra using light polarized along the orientatio

265 re implemented to calculate IR and isotropic Raman spectra, using the SPC/E simulation model, and the

266 maps were obtained by collecting individual Raman spectra via a Raman microspectrometer in a raster

267 n of WNV and RVFV antigen detection in mixed Raman spectra was achieved by SERS enhancement of Raman

268 The data mining process of collected Raman spectra was performed with principal component ana

269 Principal component analysis (PCA) of the Raman spectra was used to build a classification model f

270 peak at 1594 cm(-1) in the second derivative Raman spectra was used to generate linear calibration mo

271 and optimizing the signal-to-noise ratio of Raman spectra, we observed a large-scale transition from

272 Raman spectra were acquired at spatial resolutions of 2-

273 dual C18-functionalized silica particle, and Raman spectra were acquired from a small confocal sampli

274 Raman spectra were acquired in mapping mode from multipl

275 Raman spectra were acquired, using a 532 nm excitation w

276 FT-Raman spectra were again obtained at the same 12 points

277 Raman spectra were collected from "splinted" full thickn

278 Raman spectra were collected from a 1.25 M aqueous pyrid

279 Raman spectra were collected from indirect flight muscle

280 Resonance Raman spectra were consistent with the loss of a hydroge

281 dine were concentrated at the tips and their Raman spectra were detected in real time.

282 Raman spectra were first collected by the Raman spectros

283 Resonance Raman spectra were measured for the wild type Heme-Nitri

284 The Raman spectra were modeled on the basis of the breast ti

285 Raman spectra were obtained ex vivo from 146 tissue site

286 FT-Raman spectra were obtained from samples of whole lactos

287 To measure this pKa directly, Raman spectra were recorded on single ribozyme crystals

288 lly trapped in a focused laser beam, and its Raman spectra were recorded sequentially in time after e

289 The Raman spectra were retrieved from CARS spectra and found

290 Raman spectra were subjected to principal component anal

291 hemical-morphological constituents, acquired Raman spectra were translated to characterize chemical m

292 odel was developed based on multidimensional Raman spectra, which classified the mutants according to

293 This was further evidenced by the Raman spectra, which displayed up-field shift of the pho

294 Many materials have characteristic Raman spectra, which means that Raman spectroscopy has p

295 out the protein composition derived from the Raman spectra with data of the lipids analyzed by the MA

296 Systematic changes in the X-ray Raman spectra with increasing pressure and temperature a

297 in HiPCO-SWNTs leads to large changes in the Raman spectra with the appearance of new peaks at 319, 3

298 pores through direct comparison of the spore Raman spectra with the reference spectral signatures in

299 ther PLS-DA modeling on in vivo FP/HW tissue Raman spectra yielded a diagnostic accuracy of 88.8% (se

300 e subject-out, cross-validation method on HW Raman spectra yielded a diagnostic sensitivity of 90.3%