ライフサイエンスコーパス: electron paramagnetic resonance

1 ous Na,K-ATPase is investigated by spin-echo electron paramagnetic resonance.

2 me c reduction, Amplex Red fluorescence, and electron paramagnetic resonance.

3 We used complementary techniques such as electron paramagnetic resonance, absorption spectroscopy

4 Electron paramagnetic resonance analysis showed that MCP

5 The electron paramagnetic resonance analysis suggests that w

6 neous fluorescence, confocal microscopy, and electron paramagnetic resonance analysis.

7 Electron paramagnetic resonance and (1)H electron nuclea

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

9 the charge/spin exchange rates determined by electron paramagnetic resonance and by molecular structu

10 Electron paramagnetic resonance and computational studie

11 Continuous-wave electron paramagnetic resonance and electron-nuclear dou

12 ape of human cytochrome P450 3A4 (CYP3A4) by electron paramagnetic resonance and fluorescence spectro

13 d with experimental data, in particular from electron paramagnetic resonance and Fourier transform in

14 eta2 has been characterized by 9 and 130 GHz electron paramagnetic resonance and high-field electron

15 V vs NHE at pH 1, which is characterized by electron paramagnetic resonance and in situ X-ray absorp

16 Continuous wave-electron paramagnetic resonance and in vivo molybdate up

17 olution, derived from a combined analysis of electron paramagnetic resonance and inductively coupled

18 Electron paramagnetic resonance and infrared spectroscop

19 Electron paramagnetic resonance and Mott-Schottky plots

20 By using time-resolved electron paramagnetic resonance and optical spectroscopy

21 which was analyzed by X-ray crystallography, electron paramagnetic resonance and optical spectroscopy

22 elemetry and nitric oxide bioavailability by electron paramagnetic resonance and phosphorylation of v

23 CbiH(60) was characterized by electron paramagnetic resonance and shown to contain a [

24 Electron paramagnetic resonance and solution magnetic mo

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

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

27 es were measured by fluorescence anisotropy, electron paramagnetic resonance, and differential scanni

28 Molecular dynamics, electron paramagnetic resonance, and immunospin trapping

29 both MmpL3 and MmpL11 utilizing absorption, electron paramagnetic resonance, and magnetic circular d

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

31 ized with high-resolution mass spectrometry, electron paramagnetic resonance, and nuclear magnetic re

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

33 ) has been characterized by resonance Raman, electron paramagnetic resonance, and X-ray absorption sp

34 oscopic (UV-vis, nuclear magnetic resonance, electron paramagnetic resonance), computational, and ele

35 Here we use circular dichroism and electron paramagnetic resonance (continuous wave and pul

36 s addressed by comparing the continuous-wave electron paramagnetic resonance (cw-EPR) behaviors of ra

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

38 labeled antibody fragment by continuous-wave electron paramagnetic resonance (cw-EPR), which we repor

39 Electron paramagnetic resonance data show unambiguously

40 These results, combined with recent electron paramagnetic resonance data, allowed us to dedu

41 ction from nitrite in erythrocytes including electron paramagnetic resonance detection of nitrosyl he

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

43 ent the performance of nanometer-range pulse electron paramagnetic resonance distance measurements (p

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

45 that three spectroscopically (UV/visible and electron paramagnetic resonance) distinct heme environme

46 es, and experiments that use electrochemical electron paramagnetic resonance (EC-EPR) and electrochem

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

48 Pulse techniques in electron paramagnetic resonance (EPR) allow for a reduct

49 Both DFT and electron paramagnetic resonance (EPR) analyses further i

50 Electron paramagnetic resonance (EPR) analysis detected

51 rin oligomers were investigated by transient Electron Paramagnetic Resonance (EPR) and Electron Nucle

52 Electron paramagnetic resonance (EPR) and electron-nucle

53 genase (CrHydA1) affects the H-cluster using electron paramagnetic resonance (EPR) and Fourier transf

54 In contrast, electron paramagnetic resonance (EPR) and nuclear magnet

55 investigated in more detail by time-resolved electron paramagnetic resonance (EPR) and quantum chemic

56 Using a combination of electron paramagnetic resonance (EPR) and X-ray absorpti

57 describe a, to our knowledge, new spin-probe electron paramagnetic resonance (EPR) approach for asses

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

59 e detection by standard continuous wave (CW) electron paramagnetic resonance (EPR) challenging.

60 rroborated by continuous wave (CW) and pulse electron paramagnetic resonance (EPR) characterization.

61 We show that electron paramagnetic resonance (EPR) combined with atom

62 ted from two PEDRI acquisitions performed at electron paramagnetic resonance (EPR) frequencies of pro

63 Electron paramagnetic resonance (EPR) has been used to m

64 Electron paramagnetic resonance (EPR) hyperspectral imag

65 plication of MCR-ALS, for the first time, on electron paramagnetic resonance (EPR) imaging data sets

66 Our previous studies have shown that electron paramagnetic resonance (EPR) in continuous wave

67 Pulse electron paramagnetic resonance (EPR) is being applied t

68 st by strong inhomogeneous broadening of the electron paramagnetic resonance (EPR) line shapes and no

69 Electron paramagnetic resonance (EPR) measurements are f

70 Pulsed electron paramagnetic resonance (EPR) measurements enabl

71 characterized including electrochemical and electron paramagnetic resonance (EPR) measurements.

72 s (MD) simulations, coarse-grained analysis, electron paramagnetic resonance (EPR) membrane docking g

73 mains using thiol-specific spin labeling and electron paramagnetic resonance (EPR) of a (5)Ile-->Ala

74 Using electron paramagnetic resonance (EPR) of a bifunctional

75 Electron paramagnetic resonance (EPR) of biomolecules sp

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

77 Moreover, our extensive electron paramagnetic resonance (EPR) results demonstrat

78 the BP oil spill have shown the presence of electron paramagnetic resonance (EPR) spectra characteri

79 Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-r

80 Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-r

81 Biochemical and electron paramagnetic resonance (EPR) spectroscopic anal

82 Here, we used hyperfine electron paramagnetic resonance (EPR) spectroscopic meth

83 Electron paramagnetic resonance (EPR) spectroscopic stud

84 alyst and the substrate, in combination with electron paramagnetic resonance (EPR) spectroscopic stud

85 In-situ temperature dependent electron paramagnetic resonance (EPR) spectroscopic stud

86 is 5f(1) family by magnetometry, optical and electron paramagnetic resonance (EPR) spectroscopies and

87 these mutants were studied by UV-visible and electron paramagnetic resonance (EPR) spectroscopies cou

88 ray absorption (XAS), and emission (XES) and electron paramagnetic resonance (EPR) spectroscopies in

89 urements and continuous wave (CW) and pulsed electron paramagnetic resonance (EPR) spectroscopies rev

90 inetics coupled to UV/visible absorption and electron paramagnetic resonance (EPR) spectroscopies sup

91 We used Nuclear Magnetic Resonance (NMR) and Electron Paramagnetic Resonance (EPR) spectroscopies to

92 hy as well as continuous-wave (CW) and pulse electron paramagnetic resonance (EPR) spectroscopies.

93 ouble electron-electron resonance (DEER) and electron paramagnetic resonance (EPR) spectroscopies.

94 using Mossbauer and dual-frequency/dual-mode electron paramagnetic resonance (EPR) spectroscopies.

95 Here, by using electron paramagnetic resonance (EPR) spectroscopy and (

96 A combination of electron paramagnetic resonance (EPR) spectroscopy and c

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

98 re, using site-directed spin labeling (SDSL) electron paramagnetic resonance (EPR) spectroscopy and f

99 Electron paramagnetic resonance (EPR) spectroscopy and F

100 tions have been employed in combination with electron paramagnetic resonance (EPR) spectroscopy at de

101 and the impact of processing examined using electron paramagnetic resonance (EPR) spectroscopy at X-

102 Here, using electron paramagnetic resonance (EPR) spectroscopy combi

103 estigation of magnetic anisotropy using both electron paramagnetic resonance (EPR) spectroscopy for i

104 of carbon nitrides, were investigated using electron paramagnetic resonance (EPR) spectroscopy in co

105 Electron paramagnetic resonance (EPR) spectroscopy is a

106 The model was fitted to 180 data points of electron paramagnetic resonance (EPR) spectroscopy measu

107 Instead, we report that absorption-display electron paramagnetic resonance (EPR) spectroscopy of no

108 Electron paramagnetic resonance (EPR) spectroscopy revea

109 s), were prepared and interrogated by pulsed electron paramagnetic resonance (EPR) spectroscopy to as

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

111 rrogate this series of molecules with pulsed electron paramagnetic resonance (EPR) spectroscopy to de

112 yrroline-N-oxide (DMPO), in conjunction with electron paramagnetic resonance (EPR) spectroscopy was e

113 Electron paramagnetic resonance (EPR) spectroscopy was e

114 Using cyclic voltammetry (CV), electron paramagnetic resonance (EPR) spectroscopy, and

115 e, pMMO has been investigated extensively by electron paramagnetic resonance (EPR) spectroscopy, but

116 ernary complex, as demonstrated by (1)H NMR, electron paramagnetic resonance (EPR) spectroscopy, equi

117 (1)H and (31)P NMR spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, matr

118 d) hydrophilic carbon clusters (PEG-HCCs) by electron paramagnetic resonance (EPR) spectroscopy, oxyg

119 Using electron paramagnetic resonance (EPR) spectroscopy, the

120 ng the site-directed spin labeling method of electron paramagnetic resonance (EPR) spectroscopy, we h

121 taining Mnx protein complex were examined by electron paramagnetic resonance (EPR) spectroscopy.

122 hotoluminescence (PL) microscopy imaging and electron paramagnetic resonance (EPR) spectroscopy.

123 d (34 GHz) and time-resolved W-band (94 GHz) electron paramagnetic resonance (EPR) spectroscopy.

124 e-N-oxide (DMPO) as a spin trap coupled with electron paramagnetic resonance (EPR) spectroscopy.

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

126 rious kinds of beers were investigated using electron paramagnetic resonance (EPR) spectroscopy.

127 V) and rotating disk voltammetry (RDV)), and electron paramagnetic resonance (EPR) spectroscopy.

128 )(17)O- and (2)H(2)O-labeling and high-field electron paramagnetic resonance (EPR) spectroscopy.

129 n at variable temperature using steady-state electron paramagnetic resonance (EPR) spectroscopy.

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

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

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

133 The electron paramagnetic resonance (EPR) spectrum of the co

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

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

136 xamined in aqueous solution using an in situ electron paramagnetic resonance (EPR) spin trapping tech

137 Electron paramagnetic resonance (EPR) studies using nucl

138 be the Fe-S relay, continuous wave and pulse electron paramagnetic resonance (EPR) studies were condu

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

140 l labeling step usually required for protein electron paramagnetic resonance (EPR) studies.

141 ultifunctional trityl paramagnetic probe and electron paramagnetic resonance (EPR) technique for in v

142 studied using Trp fluorescence quenching and electron paramagnetic resonance (EPR) techniques.

143 hromatography mass spectrometry (GC-MS); and electron paramagnetic resonance (EPR) to assess oxidativ

144 hydrogen peroxide (H(2)O(2)) was studied by electron paramagnetic resonance (EPR) to determine the p

145 itude by transferring spin polarization from electron paramagnetic resonance (EPR) to NMR.

146 We have used electron paramagnetic resonance (EPR) to probe the homo-

147 r is investigated by time-resolved and pulse electron paramagnetic resonance (EPR) with laser excitat

148 d and uncoated vesicles were investigated by electron paramagnetic resonance (EPR) with site-directed

149 Electron paramagnetic resonance (EPR), absorption, and m

150 raviolet-visible-near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear ma

151 We have used chemical synthesis, electron paramagnetic resonance (EPR), and circular dich

152 s, such as nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR), and magnetic reso

153 racterized by infrared, ultraviolet-visible, electron paramagnetic resonance (EPR), and X-ray absorpt

154 he study of protein structure in solution by electron paramagnetic resonance (EPR), fluorescence spec

155 9)Sn-NMR, magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis abs

156 Here, we used a combination of electron paramagnetic resonance (EPR), stopped flow free

157 e and Cl-OHPA or formate and fumarate, using electron paramagnetic resonance (EPR), visible spectrosc

158 hfs pattern ideally suited for dual function electron paramagnetic resonance (EPR)-based applications

159 strate that these probes in combination with electron paramagnetic resonance (EPR)-based spectroscopy

160 leic acid at physiological temperature using electron paramagnetic resonance (EPR).

161 essing the spin density on the oxyl group by Electron Paramagnetic Resonance (EPR).

162 ofuran, was investigated with spectroscopic (electron paramagnetic resonance [EPR] and UV-vis) and th

163 entioned in the literature, the technique of electron paramagnetic resonance (ESR) was implemented he

164 Time-resolved electron paramagnetic resonance experiments confirm that

165 Electron paramagnetic resonance experiments revealed a [

166 of some of these mutants led us to a set of electron paramagnetic resonance experiments that provide

167 phase speciation of Fe and As was studied by electron paramagnetic resonance (Fe) and X-ray absorptio

168 l, generated from peroxide, was confirmed by electron paramagnetic resonance for the first time.

169 tions at 350 and 452 nm and a relatively low electron paramagnetic resonance gz value of 2.169 in com

170 ation of its metallocofactors by UV-visible, electron paramagnetic resonance, hyperfine sublevel corr

171 In this study, continuous-wave and pulse electron paramagnetic resonance in a native outer-membra

172 We resolved the T and R states not only by electron paramagnetic resonance in the absence of SERCA

173 tron microscopy, nuclear magnetic resonance, electron paramagnetic resonance, infrared and Raman spec

174 quantitative measurements of (17)O and (1)H electron paramagnetic resonance line-broadening studies

175 Electron paramagnetic resonance measurements confirmed t

176 Lastly, electron paramagnetic resonance measurements evidence th

177 Electron paramagnetic resonance measurements on singly l

178 verification of the triplet ground state via electron paramagnetic resonance measurements.

179 characterized by continuous-wave and pulsed electron paramagnetic resonance methods.

180 By using EM and electron paramagnetic resonance of endophilin A1, we fin

181 ith scanning tunneling microscopy to measure electron paramagnetic resonance of individual iron (Fe)

182 High-frequency and -field electron paramagnetic resonance on polycrystalline sampl

183 experiments such as chemical cross-linking, electron paramagnetic resonance, or Forster resonance en

184 Electron paramagnetic resonance oxygen imaging (EPR O2 i

185 Time-domain Cu(2+) electron paramagnetic resonance, quantum mechanical calc

186 of EcMscL using site-directed spin labelling electron paramagnetic resonance (SDSL EPR) spectroscopy.

187 Electron paramagnetic resonance shows that their binding

188 Talsi has identified a low-intensity g=2.7 electron paramagnetic resonance signal in such catalytic

189 We have also characterized the electron paramagnetic resonance signal of the molybdenum

190 Furthermore, an electron paramagnetic resonance signal was observed when

191 duction, we are able to clearly identify the electron paramagnetic resonance signals for four of the

192 Echo-detected electron paramagnetic resonance spectra from native memb

193 g and frequency-domain Fourier-transform THz electron paramagnetic resonance spectra obtained on Mn2O

194 revealed by pressure-induced changes in the electron paramagnetic resonance spectra of a nitroxide s

195 Here we report the first pulsed electron paramagnetic resonance spectra of actinide comp

196 The infrared, electronic absorption, and electron paramagnetic resonance spectra of MeC3Me ((3)3)

197 Electrochemical analysis and electron paramagnetic resonance spectra suggest that in

198 , and A) indicate little or no difference in electron paramagnetic resonance spectra, while X-ray abs

199 nM), redox potentials (242 and 251 mV), and electron paramagnetic resonance spectra, with only the l

200 their observed UV-vis, resonance Raman, and electron paramagnetic resonance spectra.

201 Electron paramagnetic resonance spectral parameters were

202 racterized by in situ vis-NIR absorption and electron paramagnetic resonance spectroelectrochemistry.

203 Electron paramagnetic resonance spectroscopic spin-trapp

204 resent an in-depth time-resolved optical and electron-paramagnetic resonance spectroscopic study of t

205 Time-resolved optical and electron paramagnetic resonance spectroscopies show that

206 d characterized by UV-visible, Mossbauer and electron paramagnetic resonance spectroscopies.

207 absorption, magnetic circular dichroism, and electron paramagnetic resonance spectroscopies.

208 stance measurement in the nanometer range by electron paramagnetic resonance spectroscopy (EPR) in co

209 icrylhydrazyl (DPPH) assay and by the use of electron paramagnetic resonance spectroscopy (EPR).

210 ing (including single crystal measurements), electron paramagnetic resonance spectroscopy (including

211 Furthermore, our electron paramagnetic resonance spectroscopy and circula

212 dysprosium(III) ions through multi-frequency electron paramagnetic resonance spectroscopy and other t

213 Here we have combined electron paramagnetic resonance spectroscopy and potenti

214 Rapid freeze-quench electron paramagnetic resonance spectroscopy and rapid c

215 ther with pre-steady state kinetic analyses, electron paramagnetic resonance spectroscopy and single

216 By combining continuous wave-electron paramagnetic resonance spectroscopy and substra

217 orescence of Singlet Oxygen Sensor Green, by electron paramagnetic resonance spectroscopy and the ind

218 haracterized using high-frequency and -field electron paramagnetic resonance spectroscopy and UV-visi

219 ystem II (PSII) were investigated in vivo by electron paramagnetic resonance spectroscopy and variabl

220 This reduced FeS cluster is observed by electron paramagnetic resonance spectroscopy as a mixtur

221 d argon and characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as

222 Using high-power pulse electron paramagnetic resonance spectroscopy at Q-band f

223 Subsequent distance measurements using electron paramagnetic resonance spectroscopy combined wi

224 tography, Mn(II) competition titrations, and electron paramagnetic resonance spectroscopy establish t

225 Electron paramagnetic resonance spectroscopy has been lo

226 genesis, molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a

227 Here, using electron paramagnetic resonance spectroscopy in combinat

228 Characterization of this species by electron paramagnetic resonance spectroscopy in concert

229 However, electron paramagnetic resonance spectroscopy indicates t

230 Site-directed spin labeling combined with electron paramagnetic resonance spectroscopy is a powerf

231 Site-directed spin-labeling electron paramagnetic resonance spectroscopy is a useful

232 haracterized by spin probing continuous wave electron paramagnetic resonance spectroscopy is reminisc

233 Electron paramagnetic resonance spectroscopy of 2(*+) re

234 Electron paramagnetic resonance spectroscopy of BciD ind

235 pacity of studied oils was also confirmed by electron paramagnetic resonance spectroscopy of superoxi

236 further explain our findings on the basis of electron paramagnetic resonance spectroscopy of the Cr(I

237 Electronic and variable-temperature electron paramagnetic resonance spectroscopy of the mixe

238 Electron paramagnetic resonance spectroscopy of the reco

239 High-field, high-frequency electron paramagnetic resonance spectroscopy performed o

240 absorption, near-UV circular dichroism, and electron paramagnetic resonance spectroscopy provide evi

241 UV/Vis and electron paramagnetic resonance spectroscopy resolves th

242 Furthermore, flow cytometry and electron paramagnetic resonance spectroscopy results sug

243 Tests with electron paramagnetic resonance spectroscopy showed that

244 l tubular cavities, and variable-temperature electron paramagnetic resonance spectroscopy shows that

245 al absorption spectroscopy and freeze-quench electron paramagnetic resonance spectroscopy support the

246 Here, we use electron paramagnetic resonance spectroscopy to characte

247 Here we used electron paramagnetic resonance spectroscopy to delineat

248 We used electron paramagnetic resonance spectroscopy to detect a

249 nd double electron-electron resonance (DEER) electron paramagnetic resonance spectroscopy to identify

250 Herein, voltammetry was combined with electron paramagnetic resonance spectroscopy to identify

251 is study, we use site-directed spin-labeling electron paramagnetic resonance spectroscopy to investig

252 port on the use of time-resolved optical and electron paramagnetic resonance spectroscopy to probe si

253 nel (hHv1) in its resting conformation using electron paramagnetic resonance spectroscopy together wi

254 na in a bis-copper six-porphyrin nanoring by electron paramagnetic resonance spectroscopy via measure

255 tigate the mechanism of maltose stimulation, electron paramagnetic resonance spectroscopy was used to

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

257 Using electron paramagnetic resonance spectroscopy we have cha

258 Using electron paramagnetic resonance spectroscopy with spin-l

259 zed by X-ray absorption spectroscopy, X-band electron paramagnetic resonance spectroscopy, and (57)Fe

260 y mass spectrometry, cyclic voltammetry, and electron paramagnetic resonance spectroscopy, coupled wi

261 Here we use electron paramagnetic resonance spectroscopy, electrophy

262 We present results from electron paramagnetic resonance spectroscopy, nuclear ma

263 rystallography, four (4+, 6+, 7+, and 8+) by electron paramagnetic resonance spectroscopy, one (7+) b

264 dized protein and O2 with reduced protein by electron paramagnetic resonance spectroscopy, providing

265 l hydrogen bond in photosystem II and, using electron paramagnetic resonance spectroscopy, the therma

266 cular dichroism and site-directed spin label electron paramagnetic resonance spectroscopy, to show ho

267 surements, inelastic neutron scattering, and electron paramagnetic resonance spectroscopy, we have in

268 Using site-directed spin labelling and electron paramagnetic resonance spectroscopy, we measure

269 Using a combination of X-ray absorption and electron paramagnetic resonance spectroscopy, we show th

270 Here, we use time-resolved, full-spectrum electron paramagnetic resonance spectroscopy, with tempe

271 partially delocalized spin, as evidenced by electron paramagnetic resonance spectroscopy.

272 fractionated, and EPFRs on PM quantified by electron paramagnetic resonance spectroscopy.

273 apid thermal chemical vapor deposition, from electron paramagnetic resonance spectroscopy.

274 ich we confirmed by site-directed spin-label electron paramagnetic resonance spectroscopy.

275 of intermediates using X-ray diffraction and electron paramagnetic resonance spectroscopy.

276 bed by differential scanning calorimetry and electron paramagnetic resonance spectroscopy.

277 incides with copper transfer as monitored by electron paramagnetic resonance spectroscopy.

278 olution composition, which was verified with electron paramagnetic resonance spectroscopy.

279 centration of the radical intermediate using electron paramagnetic resonance spectroscopy.

280 ient spectroscopies, cyclic voltammetry, and electron paramagnetic resonance spectroscopy.

281 combining structure determination with EPR (electron paramagnetic resonance) spectroscopy and simula

282 Electron paramagnetic resonance spin trapping experiment

283 a Cys(222)-derived radical was identified by electron paramagnetic resonance spin trapping, immunospi

284 ts, which were discriminated by the means of electron paramagnetic resonance spin-trapping spectrosco

285 Radical clock experiments, electron paramagnetic resonance studies and density func

286 Electron paramagnetic resonance studies of this self-ass

287 tic circular dichroism, resonance Raman, and electron paramagnetic resonance studies on CuA Az (WT) a

288 Continuous-wave electron paramagnetic resonance studies revealed changes

289 UV-vis and electron paramagnetic resonance studies show that homolo

290 Electron paramagnetic resonance studies verify a clockli

291 Characterization by electron paramagnetic resonance techniques of several va

292 vitro maturation procedure allowing advanced electron paramagnetic resonance techniques to probe the

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

294 Using electron paramagnetic resonance techniques, we character

295 near zinc porphyrin oligomers is explored by electron paramagnetic resonance techniques.

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

297 We used transmission electron microscopy and electron paramagnetic resonance to show that the presenc

298 and site-directed spin labeling coupled with electron paramagnetic resonance to test the first 88 ami

299 ic characterizations (electronic absorption, electron paramagnetic resonance, X-ray absorption spectr

300 ty, pH-activity profiles, and spectroscopic (electron paramagnetic resonance, XAS, and Fourier transf