ライフサイエンスコーパス: resonance Raman spectroscopy

1 Tyr75Ala, and His83Ala were characterized by resonance Raman spectroscopy.

2 hieved using isotope-edited surface enhanced resonance Raman spectroscopy.

3 field (VSCF) calculations and time-resolved resonance Raman spectroscopy.

4 ound carotenoid neoxanthin, identified using resonance Raman spectroscopy.

5 LC-coupled mass spectrometry and noninvasive resonance Raman spectroscopy.

6 observed spectroscopically and probed using resonance Raman spectroscopy.

7 re independently monitored via time-resolved resonance Raman spectroscopy.

8 oxidized form has also been investigated by resonance Raman spectroscopy.

9 y, the A. thaliana enzyme has been probed by resonance Raman spectroscopy.

10 using a new coherent two-dimensional form of resonance Raman spectroscopy.

11 soform of NOS (iNOS(oxy)) were examined with resonance Raman spectroscopy.

12 ex with the Ycf39 protein is evaluated using resonance Raman spectroscopy.

13 t of Ascaris suum hemoglobin (Hb) studied by resonance Raman spectroscopy.

14 low spin character at 90 K, as determined by resonance Raman spectroscopy.

15 d mixed valence species has been examined by resonance Raman spectroscopy.

16 ed mitochondria have been investigated using resonance Raman spectroscopy.

17 is studied using picosecond time-resolved UV resonance Raman spectroscopy.

18 eme-ligated CO, similar to those observed by resonance Raman spectroscopy.

19 Coordination changes are corroborated by resonance Raman spectroscopy.

20 d benzene) by UV-visible (UV-Vis), FTIR, and resonance Raman spectroscopy.

21 in both the ferric and ferrous states using resonance Raman spectroscopy.

22 ng species was additionally characterized by resonance Raman spectroscopy.

23 ic growth phase have been investigated by UV resonance Raman spectroscopy.

24 n grown aerobically, that we have studied by resonance Raman spectroscopy.

25 structures have been previously assigned by resonance Raman spectroscopy.

26 acid mutants by EPR, optical absorbance, and resonance Raman spectroscopy.

27 was 5-coordinate, high-spin as indicated by resonance Raman spectroscopy.

28 e probed using visible (Soret band enhanced) resonance Raman spectroscopy.

29 haracterized using steady-state kinetics and resonance Raman spectroscopy.

30 reduced, has been followed by time-resolved resonance Raman spectroscopy.

31 l changes, as evidenced by visible, EPR, and resonance Raman spectroscopy.

32 d on mitochondrial function and injury using resonance Raman spectroscopy.

33 (2) H NMR, EPR, applied field Mossbauer, and resonance Raman spectroscopy.

34 )](BF4)3 (2a), are characterized by FTIR and resonance Raman spectroscopy.

35 ed by UV-visible absorption spectroscopy and resonance Raman spectroscopy.

36 e parent Mn(V)(O)(TBP8Cz) complex as seen by resonance Raman spectroscopy.

37 ectroelectrochemistry, DFT calculations, and resonance Raman spectroscopy.

38 stimate organic analytes present in water by resonance Raman spectroscopy.

39 f a deprotonated chromophore as confirmed by resonance Raman spectroscopy.

40 tal redox states of proteins not amenable to resonance Raman spectroscopy.

41 for protein separation was tested by in situ resonance Raman spectroscopy.

42 aging and total skin carotenoids measured by resonance Raman spectroscopy.

43 copy as well as by electronic absorption and resonance Raman spectroscopy.

44 n DFT calculations and UV-vis, NMR, EPR, and resonance Raman spectroscopy.

45 optical spectroscopy, and Fourier-transform resonance Raman spectroscopy.

46 ree energy landscape was determined using UV resonance Raman spectroscopy.

47 of LTI at pH 6.8 was followed by UV/vis and resonance Raman spectroscopies.

48 atically studied with optical absorption and resonance Raman spectroscopies.

49 has been studied by (1)H NMR, (13)C NMR, and resonance Raman spectroscopies.

50 AT) has been studied using optical, EPR, and resonance Raman spectroscopies.

51 agnetic circular dichroism (VTMCD), EPR, and resonance Raman spectroscopies.

52 was examined by optical absorption, EPR, and resonance Raman spectroscopies.

53 and (diacetoxyiodo)benzene using UV-vis and resonance Raman spectroscopies.

54 )](+) (2(S)), as characterized by UV-vis and resonance Raman spectroscopies.

55 ange of 3.9-9.5, using EXAFS, Mossbauer, and resonance Raman spectroscopies.

56 V-vis absorption/CD/MCD, EPR, Mossbauer, and resonance Raman spectroscopies.

57 ectron paramagnetic resonance, Mossbauer and resonance Raman spectroscopies.

58 rption, electron paramagnetic resonance, and resonance Raman spectroscopies.

59 sm of this inhibition using fluorescence and resonance Raman spectroscopies.

60 cterized by low-temperature UV-vis, EPR, and resonance Raman spectroscopies.

61 rized by two-dimensional correlation deep UV resonance Raman spectroscopy (2D-DUVRR) in terms of the

62 Characterization of I435 by resonance Raman spectroscopy allowed its identification

63 Optical, Mossbauer, resonance Raman spectroscopies and native mass spectrome

64 315G] was characterized by optical, EPR, and resonance Raman spectroscopy and by studies of the INH a

65 troscopy (FCS) in combination with polarized resonance Raman spectroscopy and density functional theo

66 for hydroxylase and lyase chemistries using resonance Raman spectroscopy and drawing a comparison wi

67 zine unit to an aromatic group is studied by resonance Raman spectroscopy and electronic absorption s

68 Here, we employed resonance Raman spectroscopy and extended it to the enti

69 ing efficiency, and structurally probed with resonance Raman spectroscopy and FTIR difference spectro

70 Resonance Raman spectroscopy and MD simulations support

71 By using resonance Raman spectroscopy and NO as a probe of the he

72 Using resonance Raman spectroscopy and rapid-freeze quench tec

73 Here, with resonance Raman spectroscopy and serial femtosecond X-ra

74 Resonance Raman spectroscopy and step-scan Fourier trans

75 n protoporphyrin IX has been investigated by resonance Raman spectroscopy and stopped-flow visible sp

76 calized to a localized state is addressed by resonance Raman spectroscopy and supported by theoretica

77 determined to be approximately 630 cm(-1) by resonance Raman spectroscopy and verified by isotopic la

78 Ultraviolet resonance Raman spectroscopy and visible resonance Raman

79 ography, electronic absorption spectroscopy, resonance Raman spectroscopy, and bonding calculations r

80 re absorption and fluorescence spectroscopy, resonance Raman spectroscopy, and circular dichroism.

81 solved absorption and emission spectroscopy, resonance Raman spectroscopy, and electrochemical techni

82 spectroscopy and fluorescence spectroscopy, resonance Raman spectroscopy, and electrochemistry.

83 , UV-visible absorption, circular dichroism, resonance Raman spectroscopy, and enzyme kinetics were u

84 zation high resolution mass spectrometry and resonance Raman spectroscopy, and formulated as [(mcp)Fe

85 binding measurements, X-ray crystallography, resonance Raman spectroscopy, and hydrogen-deuterium exc

86 We used CD, UV resonance Raman spectroscopy, and molecular dynamics sim

87 UV resonance Raman spectroscopy appears to be an excellent

88 Visible and UV resonance Raman spectroscopies are used to characterize

89 tion, magnetic circular dichroism (MCD), and resonance Raman spectroscopies are used to investigate t

90 riable-temperature electronic absorption and resonance Raman spectroscopies are used to probe the exc

91 ption, Soret-enhanced Raman, and UV (229 nm) resonance Raman spectroscopies are used to probe the lig

92 Site-directed mutagenesis experiments and resonance Raman spectroscopy are consistent with the pre

93 brational frequency nu(Fe-NO) as measured by resonance Raman spectroscopy are reported for the distal

94 Absorption and resonance Raman spectroscopy are used here to establish

95 Visible and UV resonance Raman spectroscopy are used to probe the proxi

96 let resonance Raman spectroscopy and visible resonance Raman spectroscopy are used to probe, respecti

97 This work continually proves resonance Raman spectroscopy as a powerful probe for the

98 tructure at the iron-containing hemes and UV resonance Raman spectroscopy as a probe of elements of t

99 tional properties were studied using visible resonance Raman spectroscopy as a probe of local tertiar

100 Unproductive reactions are characterized by resonance Raman spectroscopy as dinitrosyl complexes, wh

101 2 has been characterized using UV/Vis, NMR, resonance Raman spectroscopy, as well as by mass spectro

102 cence (emission and excitation), normal, and resonance Raman spectroscopies associated with principal

103 we use UV-vis, CD, XAS, EPR, VT/VH-MCD, and resonance Raman spectroscopies, augmented with mass spec

104 Resonance Raman spectroscopy can probe both ET kinetics

105 ored by front-face fluorescence, ultraviolet resonance Raman spectroscopy, circular dichroism, and ox

106 er, crystallographic studies, UV and visible resonance Raman spectroscopy, CO combination kinetic mea

107 the two steps of the reaction, we have used resonance Raman spectroscopy combined with a homemade co

108 Resonance Raman spectroscopy confirms this increase in n

109 Surface enhanced resonance Raman spectroscopy coupled to dynamic electroc

110 Ir-cations, and TEM-EDX, XPS, (17)O NMR, and resonance-Raman spectroscopy data are most consistent wi

111 Resonance Raman spectroscopy demonstrates that substitut

112 rophobic for HbS > HbC > HbA, 2) ultraviolet resonance Raman spectroscopy detects alterations in Tyr

113 EPR and resonance Raman spectroscopy did not detect the proposed

114 rization was done using UV-vis spectroscopy, resonance Raman spectroscopy, electron paramagnetic reso

115 s spectroscopy, magnetic circular dichroism, resonance Raman spectroscopy, electron paramagnetic reso

116 Resonance Raman spectroscopy, electronic absorption spec

117 -on copper-sulfenate species is supported by resonance Raman spectroscopy, electrospray mass spectrom

118 Resonance Raman spectroscopy has been applied for the fi

119 Deep-UV resonance Raman spectroscopy has been shown to offer gre

120 Resonance Raman spectroscopy has been used to define act

121 Resonance Raman spectroscopy has been used to observe ch

122 Resonance Raman spectroscopy has been used to study the

123 X-ray absorption, EPR, and resonance Raman spectroscopy highlight the chemically di

124 We show that the values determined by resonance Raman spectroscopy in acetonitrile solutions a

125 nated sulfur products is provided by EPR and resonance Raman spectroscopy in addition to density func

126 ooA mutational variants have been studied by resonance Raman spectroscopy, in vivo activity measureme

127 absorption, magnetic circular dichroism, and resonance Raman spectroscopies indicate that reduction o

128 UV-visible and resonance Raman spectroscopy indicate that the distal wa

129 these mutants bind heme, but absorption and resonance Raman spectroscopy indicate that the water coo

130 Resonance Raman spectroscopy indicates that the inhibito

131 ligand binding by electronic absorption and resonance Raman spectroscopy indicates that the other ra

132 Resonance Raman spectroscopy indicates the formation of

133 Skin carotenoid status assessed by resonance Raman spectroscopy is a noninvasive, objective

134 Resonance Raman spectroscopy is a powerful analytical to

135 Resonance Raman spectroscopy is an excellent technique f

136 Resonance Raman spectroscopy is applied to the cyanide a

137 Resonance Raman spectroscopy is employed to characterize

138 Combining magnetic circular dichroism and resonance Raman spectroscopy is especially powerful.

139 Deep UV resonance Raman spectroscopy is introduced as an analyti

140 Fiber enhanced UV resonance Raman spectroscopy is introduced for chemical

141 Rotating disk electrochemistry coupled to resonance Raman spectroscopy is reported for iron porphy

142 f the visible spectrum suitable for detailed resonance Raman spectroscopy is studied in detail.

143 First, resonance Raman spectroscopy is used to assess mitochond

144 In this study resonance Raman spectroscopy is used to assign the blue

145 Resonance Raman spectroscopy is used to determine the ex

146 In this study ultraviolet (UV) resonance Raman spectroscopy is used to directly observe

147 Resonance Raman spectroscopy is used to enhance the spec

148 In this study UV resonance Raman spectroscopy is used to monitor the form

149 Time-resolved resonance Raman spectroscopy is used to obtain chromopho

150 Nanosecond time-resolved visible resonance Raman spectroscopy is used to probe conformati

151 ach, combining dynamic electrochemistry with resonance Raman spectroscopy, may be routinely used to i

152 Resonance Raman spectroscopy of copper oxochlorins show

153 Steady-state fluorescence and UV resonance Raman spectroscopy of F6W and F17W reveal mole

154 ry motion previously detected by ultraviolet resonance Raman spectroscopy of fully photolyzed HbCO.

155 On the basis of static and time-resolved resonance Raman spectroscopy of HbA and of a mutant, HbK

156 ics of the hydrated electron are probed with resonance Raman spectroscopy of isotopic mixtures of H(2

157 However, elemental analyses and resonance Raman spectroscopy of isotopically labeled enz

158 Resonance Raman spectroscopy of NCB5OR presents typical

159 ns using electron paramagnetic resonance and resonance Raman spectroscopy of rapid freeze quench samp

160 Resonance Raman spectroscopy of the carbonyl stretching

161 Comparison with low-temperature resonance Raman spectroscopy of the corresponding trappe

162 Resonance Raman spectroscopy of the wild-type and H89A m

163 UV-vis and resonance Raman spectroscopy of the wild-type protein an

164 Resonance Raman spectroscopy of the WT protein indicates

165 Resonance Raman spectroscopy offers a mechanism for the

166 llent anticorrelation of nuFeN and nuNO, via resonance Raman spectroscopy on (N-methylimidazole)Fe(II

167 (S = 1/2) species, electronic absorption and resonance Raman spectroscopy presented here demonstrate

168 absorption coupled with rapid-freeze-quench resonance Raman spectroscopy provide a detailed map of t

169 The same in situ IR setup, combined with resonance Raman spectroscopy, provided detailed insights

170 on by anionic ligands to ferric heme iron by resonance Raman spectroscopy provides a basis for compar

171 Resonance Raman spectroscopy provides direct evidence fo

172 rried out using electrochemistry, UV-vis and resonance Raman spectroscopy, pulse radiolysis, stopped

173 ding electrochemistry, UV-vis absorption and resonance Raman spectroscopy, quartz crystal microbalanc

174 Electronic absorption and resonance Raman spectroscopy reveal that Ni(II)PPIX rema

175 Electronic absorption, EPR, and resonance Raman spectroscopies revealed that CooA, the C

176 In situ resonance Raman spectroscopy reveals the accumulation of

177 nation with quantum chemical simulations and resonance Raman spectroscopy reveals the complex relatio

178 Resonance Raman spectroscopy (rR) shows that the H-bondi

179 We have used kinetic analyses and resonance Raman spectroscopy (RR) to investigate the int

180 Resonance Raman spectroscopy (RRS) has been suggested as

181 Resonance Raman spectroscopy (RRS) is an innovative meth

182 of spontaneous Raman spectroscopy, including resonance Raman spectroscopy (RRS), coherent anti-Stokes

183 e a micro-Raman setup allowing for efficient resonance Raman spectroscopy (RRS), i.e., mapping of Ram

184 red mother and infant skin carotenoids using resonance Raman spectroscopy (RRS), serum carotenoids by

185 I) were investigated using optical, EPR, and resonance Raman spectroscopy, SDS-PAGE, and X-ray crysta

186 ommonly used substrates in surface-enhanced (resonance) Raman spectroscopy (SE(R)RS).

187 To satisfy this demand, surface-enhanced resonance Raman spectroscopy (SERRS) in the deep-UV (DUV

188 Surface enhanced resonance Raman spectroscopy (SERRS) is a powerful molec

189 of DNA sequences through a surface enhanced resonance Raman spectroscopy (SERRS)-based competitive d

190 MPOD with skin carotenoid levels measured by resonance Raman spectroscopy, serum carotenoids measured

191 X-ray absorption and resonance Raman spectroscopies show that CmlA, the beta-

192 Ligand-binding analyses and resonance Raman spectroscopy show that its heme a(3)-Cu(

193 Resonance Raman spectroscopy showed a single Lorentzian

194 Optical and resonance Raman spectroscopy showed that ebselen altered

195 Resonance Raman spectroscopy shows that ferric hHO-1-hem

196 Resonance Raman spectroscopy shows that this absorption

197 Resonance Raman spectroscopy shows two Cu-S vibrations a

198 -UV circular dichroism spectroscopy, deep-UV resonance Raman spectroscopy, size exclusion chromatogra

199 traviolet visible absorption and ultraviolet resonance Raman spectroscopy supports this assignment.

200 gnal of heterogeneous catalysts by use of UV resonance Raman spectroscopy, surface-enhanced Raman spe

201 In situ resonance Raman spectroscopy technique, SERRS-RDE, is us

202 ton of this group is acidic, and variable-pH resonance Raman spectroscopy tentatively assigns it a pK

203 sing circular dichroism and deep ultraviolet resonance Raman spectroscopy, the reactive species was f

204 as ascertained by electronic absorption and resonance Raman spectroscopy, the two Cu-O-Cu active sit

205 Abs), magnetic circular dichroism (MCD), and resonance Raman spectroscopies to characterize the elect

206 ariable-temperature, variable-field MCD, and resonance Raman spectroscopies to determine ground-state

207 rehensive use of time-resolved and transient resonance Raman spectroscopies to examine photoinduced E

208 We have used resonance Raman spectroscopy to characterize heme struct

209 re, we have used ligand binding kinetics and resonance Raman spectroscopy to characterize the effect

210 l role of R481 in the bo(3) oxidase, we used resonance Raman spectroscopy to compare the nonfunctiona

211 escence, circular dichroism, and ultraviolet resonance Raman spectroscopy to confirm the spontaneous

212 ships of this new heme protein, we have used resonance Raman spectroscopy to determine the structure

213 have used a rapid continuous flow mixer and resonance Raman spectroscopy to generate and identify th

214 ponding enzyme, ferrochelatase, are shown by resonance Raman spectroscopy to induce distortion in the

215 In this paper, we have used resonance Raman spectroscopy to monitor the effect of lo

216 d temperature resolved Raman and ultraviolet-resonance Raman spectroscopy to reveal novel features of

217 We have used UV resonance Raman spectroscopy to study the acid denaturat

218 We have used UV resonance Raman spectroscopy to study the acid-induced d

219 We used CD and UV resonance Raman spectroscopy to study the impact of alco

220 ion, we here report the first application of resonance Raman spectroscopy to study the inactivation o

221 ic absorption, S and Cu K-edge XAS, EPR, and resonance Raman spectroscopies together with QM/MM compu

222 uct complex, compound T, using time-resolved resonance Raman spectroscopy (TR(3)).

223 a-hematin were derived with a combination of resonance Raman spectroscopy, two-dimensional correlatio

224 enic temperatures and characterized by using resonance Raman spectroscopy under single-turnover condi

225 ted by UV-visible absorption, Mossbauer, and resonance Raman spectroscopies, using dithionite as the

226 We utilize 198 and 204 nm excited UV resonance Raman spectroscopy (UVRR) and circular dichroi

227 We used UV resonance Raman spectroscopy (UVRR) excited within the p

228 Ultraviolet resonance Raman spectroscopy (UVRR) in combination with

229 We utilized UV resonance Raman spectroscopy (UVRS) with 204 and 229 nm

230 Resonance Raman spectroscopy was used to characterize th

231 UV resonance Raman spectroscopy was used to detect and esti

232 EPR and resonance Raman spectroscopy was used to show that the h

233 Using resonance Raman spectroscopy, we compared the effect of

234 Using off-resonance Raman spectroscopy, we have examined each comp

235 Using UV-vis and resonance Raman spectroscopy, we identify a [Cu(2)O](2+)

236 temperature magnetic circular dichroism, and resonance Raman spectroscopies were used to show that th

237 Electronic absorption and resonance Raman spectroscopy were used to show that nitr

238 is metal-ligand pi bond is probed by MCD and resonance Raman spectroscopies which show that the CT st

239 ld is determined by picosecond time-resolved resonance Raman spectroscopy, which allows direct charac

240 e presence of an oxo ligand was supported by resonance Raman spectroscopy, which revealed O-isotope-s

241 folding into NDs was provided by ultraviolet resonance Raman spectroscopy, which revealed the intense

242 By combining UV-visible, MS, NMR, and resonance Raman spectroscopies with reconstitution exper

243 ys stretching mode of gsNOS was monitored by resonance Raman spectroscopy with 363.8 nm excitation.

244 is study combines the spectral resolution of resonance Raman spectroscopy with site-directed mutagene

245 Resonance Raman spectroscopy with three distinct laser w

246 ted with UV-visible absorption spectroscopy, resonance Raman spectroscopy, X-ray crystallography, cla

247 , magnetic susceptibility, electrochemistry, resonance Raman spectroscopy, X-ray crystallography, X-r