ライフサイエンスコーパス: paramagnetic resonance

1 ATPase is investigated by spin-echo electron paramagnetic resonance.

2 ction, Amplex Red fluorescence, and electron paramagnetic resonance.

3 ed complementary techniques such as electron paramagnetic resonance, absorption spectroscopy, and pho

4 Electron paramagnetic resonance analysis showed that MCPyV sT coo

5 The electron paramagnetic resonance analysis suggests that with the e

6 orescence, confocal microscopy, and electron paramagnetic resonance analysis.

7 Electron paramagnetic resonance and (1)H electron nuclear double

8 acterization of the intermediate by electron paramagnetic resonance and (13)C, (57)Fe electron nuclea

9 e/spin exchange rates determined by electron paramagnetic resonance and by molecular structural level

10 Electron paramagnetic resonance and computational studies reveal

11 Continuous-wave electron paramagnetic resonance and electron-nuclear double-reson

12 man cytochrome P450 3A4 (CYP3A4) by electron paramagnetic resonance and fluorescence spectroscopy.

13 perimental data, in particular from electron paramagnetic resonance and Fourier transform infrared (F

14 been characterized by 9 and 130 GHz electron paramagnetic resonance and high-field electron nuclear d

15 at pH 1, which is characterized by electron paramagnetic resonance and in situ X-ray absorption spec

16 Continuous wave-electron paramagnetic resonance and in vivo molybdate uptake stud

17 derived from a combined analysis of electron paramagnetic resonance and inductively coupled plasma sp

18 Electron paramagnetic resonance and infrared spectroscopic analys

19 Electron paramagnetic resonance and Mott-Schottky plots reveal th

20 analyzed by X-ray crystallography, electron paramagnetic resonance and optical spectroscopy, and den

21 By using time-resolved electron paramagnetic resonance and optical spectroscopy, we have

22 and nitric oxide bioavailability by electron paramagnetic resonance and phosphorylation of vasodilato

23 CbiH(60) was characterized by electron paramagnetic resonance and shown to contain a [4Fe-4S] c

24 Electron paramagnetic resonance and solution magnetic moment dete

25 obtained from variable-temperature electron paramagnetic resonance and ultraviolet-visible spectrosc

26 application of Raman spectroscopy, electron paramagnetic resonance and UV-vis absorption spectroscop

27 easured by fluorescence anisotropy, electron paramagnetic resonance, and differential scanning calori

28 Molecular dynamics, electron paramagnetic resonance, and immunospin trapping analysis

29 L3 and MmpL11 utilizing absorption, electron paramagnetic resonance, and magnetic circular dichroism

30 assessed by electronic absorption, electron paramagnetic resonance, and Mn K-edge X-ray absorption m

31 high-resolution mass spectrometry, electron paramagnetic resonance, and nuclear magnetic resonance s

32 A combination of NMR spectroscopy, electron paramagnetic resonance, and small-angle X-ray scattering

33 n characterized by resonance Raman, electron paramagnetic resonance, and X-ray absorption spectroscop

34 UV-vis, nuclear magnetic resonance, electron paramagnetic resonance), computational, and electrochemi

35 Here we use circular dichroism and electron paramagnetic resonance (continuous wave and pulsed) to e

36 ed by comparing the continuous-wave electron paramagnetic resonance (cw-EPR) behaviors of radical Au2

37 reproduction of its continuous wave electron paramagnetic resonance (CW-EPR), hyperfine sublevel corr

38 ntibody fragment by continuous-wave electron paramagnetic resonance (cw-EPR), which we report here fo

39 Electron paramagnetic resonance data show unambiguously that the

40 These results, combined with recent electron paramagnetic resonance data, allowed us to deduce a deta

41 m nitrite in erythrocytes including electron paramagnetic resonance detection of nitrosyl hemoglobin,

42 Using spin probes and electron paramagnetic resonance detection, we confirmed that carn

43 erformance of nanometer-range pulse electron paramagnetic resonance distance measurements (pulsed ele

44 n oligomer, as determined by sparse electron paramagnetic resonance distance measurements.

45 e spectroscopically (UV/visible and electron paramagnetic resonance) distinct heme environments were

46 xperiments that use electrochemical electron paramagnetic resonance (EC-EPR) and electrochemical magn

47 te ion-pair states, as suggested by electron paramagnetic resonance/electron-nuclear double resonance

48 e probed the protomer arrangement by solvent paramagnetic resonance enhancement, analysis of chemical

49 od agreement with residual dipolar coupling, paramagnetic resonance enhancement, small-angle X-ray sc

50 Pulse techniques in electron paramagnetic resonance (EPR) allow for a reduction in me

51 Both DFT and electron paramagnetic resonance (EPR) analyses further indicate t

52 Electron paramagnetic resonance (EPR) analysis detected signals o

53 mers were investigated by transient Electron Paramagnetic Resonance (EPR) and Electron Nuclear DOuble

54 Electron paramagnetic resonance (EPR) and electron-nuclear double

55 rHydA1) affects the H-cluster using electron paramagnetic resonance (EPR) and Fourier transform infra

56 In contrast, electron paramagnetic resonance (EPR) and nuclear magnetic resona

57 ted in more detail by time-resolved electron paramagnetic resonance (EPR) and quantum chemical calcul

58 Using a combination of electron paramagnetic resonance (EPR) and X-ray absorption spectr

59 a, to our knowledge, new spin-probe electron paramagnetic resonance (EPR) approach for assessing the

60 We studied the N-terminus using two electron paramagnetic resonance (EPR) approaches: the rotational

61 on by standard continuous wave (CW) electron paramagnetic resonance (EPR) challenging.

62 d by continuous wave (CW) and pulse electron paramagnetic resonance (EPR) characterization.

63 We show that electron paramagnetic resonance (EPR) combined with atomic absorp

64 two PEDRI acquisitions performed at electron paramagnetic resonance (EPR) frequencies of protonated a

65 Electron paramagnetic resonance (EPR) has been used to measure th

66 Electron paramagnetic resonance (EPR) hyperspectral imaging is a

67 of MCR-ALS, for the first time, on electron paramagnetic resonance (EPR) imaging data sets that will

68 ur previous studies have shown that electron paramagnetic resonance (EPR) in continuous wave (CW) mod

69 Pulse electron paramagnetic resonance (EPR) is being applied to ever mo

70 ong inhomogeneous broadening of the electron paramagnetic resonance (EPR) line shapes and nonexponent

71 Electron paramagnetic resonance (EPR) measurements are found to b

72 Pulsed electron paramagnetic resonance (EPR) measurements enabled the in

73 rized including electrochemical and electron paramagnetic resonance (EPR) measurements.

74 mulations, coarse-grained analysis, electron paramagnetic resonance (EPR) membrane docking geometry,

75 ng thiol-specific spin labeling and electron paramagnetic resonance (EPR) of a (5)Ile-->Ala and (12)I

76 Using electron paramagnetic resonance (EPR) of a bifunctional spin labe

77 Electron paramagnetic resonance (EPR) of biomolecules spin-labele

78 High-frequency (263 GHz) pulse electron paramagnetic resonance (EPR) of the NH2Y*s reported the

79 Moreover, our extensive electron paramagnetic resonance (EPR) results demonstrate that th

80 il spill have shown the presence of electron paramagnetic resonance (EPR) spectra characteristic of o

81 Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-ray-irradi

82 Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-ray-irradi

83 Biochemical and electron paramagnetic resonance (EPR) spectroscopic analyses demo

84 Here, we used hyperfine electron paramagnetic resonance (EPR) spectroscopic methods, comb

85 the substrate, in combination with electron paramagnetic resonance (EPR) spectroscopic studies estab

86 In-situ temperature dependent electron paramagnetic resonance (EPR) spectroscopic studies show

87 Electron paramagnetic resonance (EPR) spectroscopic studies with

88 family by magnetometry, optical and electron paramagnetic resonance (EPR) spectroscopies and modellin

89 ants were studied by UV-visible and electron paramagnetic resonance (EPR) spectroscopies coupled to p

90 ption (XAS), and emission (XES) and electron paramagnetic resonance (EPR) spectroscopies in the solid

91 and continuous wave (CW) and pulsed electron paramagnetic resonance (EPR) spectroscopies revealed tha

92 oupled to UV/visible absorption and electron paramagnetic resonance (EPR) spectroscopies support a me

93 uclear Magnetic Resonance (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopies to distingui

94 l as continuous-wave (CW) and pulse electron paramagnetic resonance (EPR) spectroscopies.

95 ctron-electron resonance (DEER) and electron paramagnetic resonance (EPR) spectroscopies.

96 sbauer and dual-frequency/dual-mode electron paramagnetic resonance (EPR) spectroscopies.

97 (Ph4P)2[VO(C3S4O)2] (4), by pulsed electron paramagnetic resonance (EPR) spectroscopy and compared t

98 A combination of electron paramagnetic resonance (EPR) spectroscopy and computatio

99 Electron paramagnetic resonance (EPR) spectroscopy and Fourier tr

100 site-directed spin labeling (SDSL) electron paramagnetic resonance (EPR) spectroscopy and functional

101 e been employed in combination with electron paramagnetic resonance (EPR) spectroscopy at defined ele

102 impact of processing examined using electron paramagnetic resonance (EPR) spectroscopy at X-band (9.3

103 Here, using electron paramagnetic resonance (EPR) spectroscopy combined with

104 n of magnetic anisotropy using both electron paramagnetic resonance (EPR) spectroscopy for its experi

105 n nitrides, were investigated using electron paramagnetic resonance (EPR) spectroscopy in combination

106 Electron paramagnetic resonance (EPR) spectroscopy is a powerful

107 el was fitted to 180 data points of electron paramagnetic resonance (EPR) spectroscopy measurements o

108 , we report that absorption-display electron paramagnetic resonance (EPR) spectroscopy of nonirradiat

109 Electron paramagnetic resonance (EPR) spectroscopy reveals that t

110 prepared and interrogated by pulsed electron paramagnetic resonance (EPR) spectroscopy to assess quan

111 In the first use of high-field electron paramagnetic resonance (EPR) spectroscopy to characteriz

112 his series of molecules with pulsed electron paramagnetic resonance (EPR) spectroscopy to determine t

113 Electron paramagnetic resonance (EPR) spectroscopy was employed t

114 N-oxide (DMPO), in conjunction with electron paramagnetic resonance (EPR) spectroscopy was employed.

115 Using cyclic voltammetry (CV), electron paramagnetic resonance (EPR) spectroscopy, and flash-ind

116 as been investigated extensively by electron paramagnetic resonance (EPR) spectroscopy, but the prese

117 mplex, as demonstrated by (1)H NMR, electron paramagnetic resonance (EPR) spectroscopy, equilibrium d

118 (1)H and (31)P NMR spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matrix-assist

119 hilic carbon clusters (PEG-HCCs) by electron paramagnetic resonance (EPR) spectroscopy, oxygen electr

120 Using electron paramagnetic resonance (EPR) spectroscopy, the process o

121 te-directed spin labeling method of electron paramagnetic resonance (EPR) spectroscopy, we have deter

122 nx protein complex were examined by electron paramagnetic resonance (EPR) spectroscopy.

123 escence (PL) microscopy imaging and electron paramagnetic resonance (EPR) spectroscopy.

124 ) and time-resolved W-band (94 GHz) electron paramagnetic resonance (EPR) spectroscopy.

125 (DMPO) as a spin trap coupled with electron paramagnetic resonance (EPR) spectroscopy.

126 of ATII-infused mice as assessed by electron paramagnetic resonance (EPR) spectroscopy.

127 ds of beers were investigated using electron paramagnetic resonance (EPR) spectroscopy.

128 tating disk voltammetry (RDV)), and electron paramagnetic resonance (EPR) spectroscopy.

129 able temperature using steady-state electron paramagnetic resonance (EPR) spectroscopy.

130 Mnx protein complex was examined by electron paramagnetic resonance (EPR) spectroscopy.

131 ) analysis and multifrequency pulse electron paramagnetic resonance (EPR) spectroscopy.

132 ometry, continuous wave, and pulsed electron paramagnetic resonance (EPR) spectroscopy.

133 The electron paramagnetic resonance (EPR) spectrum of the complex [V(

134 The X-band electron paramagnetic resonance (EPR) spectrum reveals the presen

135 The compound exhibits an electron paramagnetic resonance (EPR) spectrum with an unusually

136 n aqueous solution using an in situ electron paramagnetic resonance (EPR) spin trapping technique and

137 Electron paramagnetic resonance (EPR) studies using nucleotide an

138 centers, which is also supported by electron paramagnetic resonance (EPR) studies.

139 g step usually required for protein electron paramagnetic resonance (EPR) studies.

140 ional trityl paramagnetic probe and electron paramagnetic resonance (EPR) technique for in vivo concu

141 sing Trp fluorescence quenching and electron paramagnetic resonance (EPR) techniques.

142 aphy mass spectrometry (GC-MS); and electron paramagnetic resonance (EPR) to assess oxidative stress.

143 peroxide (H(2)O(2)) was studied by electron paramagnetic resonance (EPR) to determine the properties

144 transferring spin polarization from electron paramagnetic resonance (EPR) to NMR.

145 We have used electron paramagnetic resonance (EPR) to probe the homo- and hete

146 stigated by time-resolved and pulse electron paramagnetic resonance (EPR) with laser excitation.

147 oated vesicles were investigated by electron paramagnetic resonance (EPR) with site-directed and non-

148 Electron paramagnetic resonance (EPR), absorption, and magnetic c

149 visible-near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic re

150 We have used chemical synthesis, electron paramagnetic resonance (EPR), and circular dichroism to

151 s nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR), and magnetic resonance ima

152 d by infrared, ultraviolet-visible, electron paramagnetic resonance (EPR), and X-ray absorption spect

153 of protein structure in solution by electron paramagnetic resonance (EPR), fluorescence spectroscopy

154 magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption,

155 Here, we used a combination of electron paramagnetic resonance (EPR), stopped flow freeze quench

156 OHPA or formate and fumarate, using electron paramagnetic resonance (EPR), visible spectroscopy, and

157 rn ideally suited for dual function electron paramagnetic resonance (EPR)-based applications.

158 at these probes in combination with electron paramagnetic resonance (EPR)-based spectroscopy and imag

159 at physiological temperature using electron paramagnetic resonance (EPR).

160 e spin density on the oxyl group by Electron Paramagnetic Resonance (EPR).

161 as investigated with spectroscopic (electron paramagnetic resonance [EPR] and UV-vis) and theoretical

162 in the literature, the technique of electron paramagnetic resonance (ESR) was implemented herein to c

163 Time-resolved electron paramagnetic resonance experiments confirm that triplet

164 Electron paramagnetic resonance experiments revealed a [4Fe-4S] c

165 of these mutants led us to a set of electron paramagnetic resonance experiments that provide evidence

166 ciation of Fe and As was studied by electron paramagnetic resonance (Fe) and X-ray absorption spectro

167 ted from peroxide, was confirmed by electron paramagnetic resonance for the first time.

168 350 and 452 nm and a relatively low electron paramagnetic resonance gz value of 2.169 in comparison w

169 its metallocofactors by UV-visible, electron paramagnetic resonance, hyperfine sublevel correlation (

170 is study, continuous-wave and pulse electron paramagnetic resonance in a native outer-membrane prepar

171 lved the T and R states not only by electron paramagnetic resonance in the absence of SERCA but also

172 oscopy, nuclear magnetic resonance, electron paramagnetic resonance, infrared and Raman spectroscopy,

173 tive measurements of (17)O and (1)H electron paramagnetic resonance line-broadening studies to wild-t

174 Electron paramagnetic resonance measurements confirmed the D1-D5

175 Lastly, electron paramagnetic resonance measurements evidence the formati

176 Electron paramagnetic resonance measurements on singly labeled co

177 ion of the triplet ground state via electron paramagnetic resonance measurements.

178 rized by continuous-wave and pulsed electron paramagnetic resonance methods.

179 By using EM and electron paramagnetic resonance of endophilin A1, we find that tu

180 ing tunneling microscopy to measure electron paramagnetic resonance of individual iron (Fe) atoms pla

181 High-frequency and -field electron paramagnetic resonance on polycrystalline samples of 1 a

182 nts such as chemical cross-linking, electron paramagnetic resonance, or Forster resonance energy tran

183 Electron paramagnetic resonance oxygen imaging (EPR O2 imaging) p

184 Time-domain Cu(2+) electron paramagnetic resonance, quantum mechanical calculations,

185 using site-directed spin labelling electron paramagnetic resonance (SDSL EPR) spectroscopy.

186 Electron paramagnetic resonance shows that their binding globally

187 as identified a low-intensity g=2.7 electron paramagnetic resonance signal in such catalytic systems

188 We have also characterized the electron paramagnetic resonance signal of the molybdenum center i

189 Furthermore, an electron paramagnetic resonance signal was observed when the N-be

190 we are able to clearly identify the electron paramagnetic resonance signals for four of the iron/sulf

191 Echo-detected electron paramagnetic resonance spectra from native membranes are

192 quency-domain Fourier-transform THz electron paramagnetic resonance spectra obtained on Mn2Os.7MeOH a

193 by pressure-induced changes in the electron paramagnetic resonance spectra of a nitroxide side chain

194 Here we report the first pulsed electron paramagnetic resonance spectra of actinide compounds.

195 nfrared, electronic absorption, and electron paramagnetic resonance spectra of MeC3Me ((3)3) are comp

196 Electrochemical analysis and electron paramagnetic resonance spectra suggest that in aerobic c

197 indicate little or no difference in electron paramagnetic resonance spectra, while X-ray absorption s

198 ox potentials (242 and 251 mV), and electron paramagnetic resonance spectra, with only the latter cle

199 served UV-vis, resonance Raman, and electron paramagnetic resonance spectra.

200 Electron paramagnetic resonance spectral parameters were compared

201 d by in situ vis-NIR absorption and electron paramagnetic resonance spectroelectrochemistry.

202 Electron paramagnetic resonance spectroscopic spin-trapping exper

203 in-depth time-resolved optical and electron-paramagnetic resonance spectroscopic study of two crypto

204 Time-resolved optical and electron paramagnetic resonance spectroscopies show that photogen

205 erized by UV-visible, Mossbauer and electron paramagnetic resonance spectroscopies.

206 n, magnetic circular dichroism, and electron paramagnetic resonance spectroscopies.

207 asurement in the nanometer range by electron paramagnetic resonance spectroscopy (EPR) in combination

208 azyl (DPPH) assay and by the use of electron paramagnetic resonance spectroscopy (EPR).

209 uding single crystal measurements), electron paramagnetic resonance spectroscopy (including measureme

210 Furthermore, our electron paramagnetic resonance spectroscopy and circular dichroi

211 m(III) ions through multi-frequency electron paramagnetic resonance spectroscopy and other techniques

212 Here we have combined electron paramagnetic resonance spectroscopy and potential-of-mea

213 Rapid freeze-quench electron paramagnetic resonance spectroscopy and rapid chemical-q

214 pre-steady state kinetic analyses, electron paramagnetic resonance spectroscopy and single crystal X

215 By combining continuous wave-electron paramagnetic resonance spectroscopy and substrate uptake

216 of Singlet Oxygen Sensor Green, by electron paramagnetic resonance spectroscopy and the induction of

217 zed using high-frequency and -field electron paramagnetic resonance spectroscopy and UV-visible absor

218 (PSII) were investigated in vivo by electron paramagnetic resonance spectroscopy and variable fluores

219 reduced FeS cluster is observed by electron paramagnetic resonance spectroscopy as a mixture of two

220 nd characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as by quantu

221 Using high-power pulse electron paramagnetic resonance spectroscopy at Q-band frequencie

222 sequent distance measurements using electron paramagnetic resonance spectroscopy combined with molecu

223 Mn(II) competition titrations, and electron paramagnetic resonance spectroscopy establish that the C

224 Electron paramagnetic resonance spectroscopy has been long known

225 molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a pivotal r

226 Here, using electron paramagnetic resonance spectroscopy in combination with

227 Characterization of this species by electron paramagnetic resonance spectroscopy in concert with stra

228 However, electron paramagnetic resonance spectroscopy indicates that a lip

229 irected spin labeling combined with electron paramagnetic resonance spectroscopy is a powerful approa

230 Site-directed spin-labeling electron paramagnetic resonance spectroscopy is a useful tool to

231 zed by spin probing continuous wave electron paramagnetic resonance spectroscopy is reminiscent of a

232 Electron paramagnetic resonance spectroscopy of 2(*+) reveals the

233 Electron paramagnetic resonance spectroscopy of BciD indicated th

234 studied oils was also confirmed by electron paramagnetic resonance spectroscopy of superoxide anion

235 xplain our findings on the basis of electron paramagnetic resonance spectroscopy of the Cr(III) site

236 Electronic and variable-temperature electron paramagnetic resonance spectroscopy of the mixed-valence

237 Electron paramagnetic resonance spectroscopy of the recombinant e

238 High-field, high-frequency electron paramagnetic resonance spectroscopy performed on a singl

239 on, near-UV circular dichroism, and electron paramagnetic resonance spectroscopy provide evidence tha

240 UV/Vis and electron paramagnetic resonance spectroscopy resolves the discrep

241 Furthermore, flow cytometry and electron paramagnetic resonance spectroscopy results suggested th

242 Tests with electron paramagnetic resonance spectroscopy showed that Ag NPs w

243 cavities, and variable-temperature electron paramagnetic resonance spectroscopy shows that a dilute

244 tion spectroscopy and freeze-quench electron paramagnetic resonance spectroscopy support the presence

245 Here, we use electron paramagnetic resonance spectroscopy to characterize conf

246 Here we used electron paramagnetic resonance spectroscopy to delineate protein

247 We used electron paramagnetic resonance spectroscopy to detect and charac

248 rein, voltammetry was combined with electron paramagnetic resonance spectroscopy to identify and defi

249 electron-electron resonance (DEER) electron paramagnetic resonance spectroscopy to identify the mole

250 we use site-directed spin-labeling electron paramagnetic resonance spectroscopy to investigate confo

251 he use of time-resolved optical and electron paramagnetic resonance spectroscopy to probe singlet fis

252 ) in its resting conformation using electron paramagnetic resonance spectroscopy together with bioche

253 is-copper six-porphyrin nanoring by electron paramagnetic resonance spectroscopy via measurement of t

254 X-band continuous-wave electron paramagnetic resonance spectroscopy was used to monitor

255 e mechanism of maltose stimulation, electron paramagnetic resonance spectroscopy was used to study th

256 Using electron paramagnetic resonance spectroscopy we have characterize

257 Using electron paramagnetic resonance spectroscopy with spin-labeled AT

258 ray absorption spectroscopy, X-band electron paramagnetic resonance spectroscopy, and (57)Fe Mossbaue

259 ectrometry, cyclic voltammetry, and electron paramagnetic resonance spectroscopy, coupled with comput

260 Here we use electron paramagnetic resonance spectroscopy, electrophysiology a

261 We present results from electron paramagnetic resonance spectroscopy, nuclear magnetic re

262 raphy, four (4+, 6+, 7+, and 8+) by electron paramagnetic resonance spectroscopy, one (7+) by superco

263 tein and O2 with reduced protein by electron paramagnetic resonance spectroscopy, providing a firm su

264 n bond in photosystem II and, using electron paramagnetic resonance spectroscopy, the thermal relaxat

265 hroism and site-directed spin label electron paramagnetic resonance spectroscopy, to show how a stagg

266 , inelastic neutron scattering, and electron paramagnetic resonance spectroscopy, we have investigate

267 ng site-directed spin labelling and electron paramagnetic resonance spectroscopy, we measured the con

268 combination of X-ray absorption and electron paramagnetic resonance spectroscopy, we show that, prior

269 we use time-resolved, full-spectrum electron paramagnetic resonance spectroscopy, with temperature-st

270 y delocalized spin, as evidenced by electron paramagnetic resonance spectroscopy.

271 ated, and EPFRs on PM quantified by electron paramagnetic resonance spectroscopy.

272 mal chemical vapor deposition, from electron paramagnetic resonance spectroscopy.

273 nfirmed by site-directed spin-label electron paramagnetic resonance spectroscopy.

274 ediates using X-ray diffraction and electron paramagnetic resonance spectroscopy.

275 fferential scanning calorimetry and electron paramagnetic resonance spectroscopy.

276 ith copper transfer as monitored by electron paramagnetic resonance spectroscopy.

277 omposition, which was verified with electron paramagnetic resonance spectroscopy.

278 n of the radical intermediate using electron paramagnetic resonance spectroscopy.

279 troscopies, cyclic voltammetry, and electron paramagnetic resonance spectroscopy.

280 g structure determination with EPR (electron paramagnetic resonance) spectroscopy and simulation, sho

281 Electron paramagnetic resonance spin trapping experiments demonst

282 )-derived radical was identified by electron paramagnetic resonance spin trapping, immunospin trappin

283 were discriminated by the means of electron paramagnetic resonance spin-trapping spectroscopy.

284 Radical clock experiments, electron paramagnetic resonance studies and density functional th

285 Electron paramagnetic resonance studies of this self-assembled ma

286 lar dichroism, resonance Raman, and electron paramagnetic resonance studies on CuA Az (WT) and its M1

287 Continuous-wave electron paramagnetic resonance studies revealed changes in mobil

288 UV-vis and electron paramagnetic resonance studies show that homologues of s

289 Electron paramagnetic resonance studies verify a clocklike transi

290 In this report, measurements by advanced paramagnetic resonance techniques [electron-spin-echo (E

291 Characterization by electron paramagnetic resonance techniques of several variants of

292 uration procedure allowing advanced electron paramagnetic resonance techniques to probe the electroni

293 High magnetic field high frequency electron paramagnetic resonance techniques were used to measure i

294 Using electron paramagnetic resonance techniques, we characterized the

295 porphyrin oligomers is explored by electron paramagnetic resonance techniques.

296 a,meso,beta fused structures, using electron paramagnetic resonance techniques.

297 ransmission electron microscopy and electron paramagnetic resonance to show that the presence of anio

298 directed spin labeling coupled with electron paramagnetic resonance to test the first 88 amino acids

299 terizations (electronic absorption, electron paramagnetic resonance, X-ray absorption spectroscopies)

300 tivity profiles, and spectroscopic (electron paramagnetic resonance, XAS, and Fourier transform infra