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

1 observed spectroscopically and probed using resonance Raman spectroscopy.

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

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

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

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

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

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

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

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

10 ed mitochondria have been investigated using resonance Raman spectroscopy.

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

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

13 Coordination changes are corroborated by resonance Raman spectroscopy.

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

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

16 ng species was additionally characterized by resonance Raman spectroscopy.

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

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

19 structures have been previously assigned by resonance Raman spectroscopy.

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

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

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

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

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

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

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

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

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

29 ectroelectrochemistry, DFT calculations, and resonance Raman spectroscopy.

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

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

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

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

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

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

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

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

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

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

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

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

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

43 ound carotenoid neoxanthin, identified using resonance Raman spectroscopy.

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

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

46 atically studied with optical absorption and resonance Raman spectroscopies.

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

48 )](+) (2(S)), as characterized by UV-vis and resonance Raman spectroscopies.

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

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

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

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

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

54 ectron paramagnetic resonance, Mossbauer and resonance Raman spectroscopies.

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

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

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

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

59 Characterization of I435 by resonance Raman spectroscopy allowed its identification

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

61 315G] was characterized by optical, EPR, and resonance Raman spectroscopy and by studies of the INH a

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

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

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

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

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

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

68 Using resonance Raman spectroscopy and rapid-freeze quench tec

69 Resonance Raman spectroscopy and step-scan Fourier trans

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

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

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

73 Ultraviolet resonance Raman spectroscopy and visible resonance Raman

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

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

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

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

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

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

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

81 UV resonance Raman spectroscopy appears to be an excellent

82 Visible and UV resonance Raman spectroscopies are used to characterize

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

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

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

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

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

88 Absorption and resonance Raman spectroscopy are used here to establish

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

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

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

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

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

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

95 Resonance Raman spectroscopy can probe both ET kinetics

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

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

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

99 Resonance Raman spectroscopy confirms this increase in n

100 Surface enhanced resonance Raman spectroscopy coupled to dynamic electroc

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

102 Resonance Raman spectroscopy demonstrates that substitut

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

104 Resonance Raman spectroscopy, electronic absorption spec

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

106 Resonance Raman spectroscopy has been applied for the fi

107 Resonance Raman spectroscopy has been used to define act

108 Resonance Raman spectroscopy has been used to observe ch

109 Resonance Raman spectroscopy has been used to study the

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

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

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

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

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

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

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

117 Resonance Raman spectroscopy indicates that the inhibito

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

119 Resonance Raman spectroscopy indicates the formation of

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

121 Resonance Raman spectroscopy is a powerful analytical to

122 Resonance Raman spectroscopy is an excellent technique f

123 Resonance Raman spectroscopy is applied to the cyanide a

124 Resonance Raman spectroscopy is employed to characterize

125 Deep UV resonance Raman spectroscopy is introduced as an analyti

126 Fiber enhanced UV resonance Raman spectroscopy is introduced for chemical

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

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

129 Resonance Raman spectroscopy is used to determine the ex

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

131 Resonance Raman spectroscopy is used to enhance the spec

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

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

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

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

136 Resonance Raman spectroscopy of copper oxochlorins show

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

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

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

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

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

142 Resonance Raman spectroscopy of NCB5OR presents typical

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

144 Resonance Raman spectroscopy of the carbonyl stretching

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

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

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

148 Resonance Raman spectroscopy of the WT protein indicates

149 Resonance Raman spectroscopy offers a mechanism for the

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

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

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

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

154 Resonance Raman spectroscopy provides direct evidence fo

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

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

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

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

159 Resonance Raman spectroscopy (RRS) has been suggested as

160 Resonance Raman spectroscopy (RRS) is an innovative meth

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

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

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

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

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

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

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

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

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

170 Resonance Raman spectroscopy showed a single Lorentzian

171 Optical and resonance Raman spectroscopy showed that ebselen altered

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

173 Resonance Raman spectroscopy shows that this absorption

174 Resonance Raman spectroscopy shows two Cu-S vibrations a

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

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

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

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

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

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

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

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

183 We have used resonance Raman spectroscopy to characterize heme struct

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 Ultraviolet resonance Raman spectroscopy (UVRR) in combination with

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

202 Resonance Raman spectroscopy was used to characterize th

203 UV resonance Raman spectroscopy was used to detect and esti

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

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

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

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

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

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

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

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

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

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

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

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