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

1 ttering, analytical ultracentrifugation, and electron paramagnetic resonance.

2 trophotometric method and by continuous-wave electron paramagnetic resonance.

3 ined by X-ray photoelectron spectroscopy and electron paramagnetic resonance.

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

5 ntitatively probed with 2-dimensional pulsed electron paramagnetic resonance.

6 in vitro experiments, mass spectrometry and electron paramagnetic resonance.

7 s is spin dependent and can be controlled by electron-paramagnetic resonance, affecting device resist

8 UV-visible spectroscopy and electron paramagnetic resonance analyses confirmed the f

9 Here, we use combined mutagenesis and pulse electron paramagnetic resonance analyses to establish hi

10 its bacterial homolog leucine transporter by electron paramagnetic resonance analysis and X-ray cryst

11 Electron paramagnetic resonance analysis further reveale

12 tion revealed more perfusion, and functional electron paramagnetic resonance analysis revealed more o

13 Electron paramagnetic resonance analysis showed that MCP

14 In line with these observations, electron paramagnetic resonance analysis suggested that

15 The electron paramagnetic resonance analysis suggests that w

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

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

18 Electron paramagnetic resonance and density functional t

19 Operando X-ray absorption spectroscopy, electron paramagnetic resonance and density-functional t

20 According to electron paramagnetic resonance and diffuse-reflectance

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

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

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

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

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

26 nce of Tb(4+) was unambiguously confirmed by electron paramagnetic resonance and magnetometry.

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

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

29 Electron paramagnetic resonance and solution magnetic mo

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

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

32 Electron paramagnetic resonance and X-ray absorption spe

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

34 combination of hydrogen-deuterium exchange, electron paramagnetic resonance, and NMR spectroscopy ex

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

36 res of spin-state ice in neutron scattering, electron paramagnetic resonance, and thermodynamic exper

37 Moreover, Fourier transform infrared, electron paramagnetic resonance, and UV-visible spectros

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

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

40 Biochemical and continuous wave electron paramagnetic resonance data demonstrate the ina

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

42 X-ray diffraction, continuous wave and pulse electron paramagnetic resonance, density-functional theo

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

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

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

46 achieving high resolution in double electron-electron paramagnetic resonance distance measurements.

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

48 ious solid-state NMR data and newly acquired electron paramagnetic resonance double electron-electron

49 ental evidence (e.g., X-ray crystallography, electron paramagnetic resonance, electrochemistry) demon

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

51 oxygen consumption experiments, coupled with electron paramagnetic resonance (EPR) analyses and DFT c

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

53 Electron paramagnetic resonance (EPR) analysis detected

54 11-tetraazacyclotetradecane-1-acetato) using electron paramagnetic resonance (EPR) and (57)Fe Mossbau

55 ng-sought radical species through the use of electron paramagnetic resonance (EPR) and electron nucle

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

57 Electron paramagnetic resonance (EPR) and electron-nucle

58 low absorption and rapid freeze-quench (RFQ) electron paramagnetic resonance (EPR) and magnetic circu

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

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

61 Electron paramagnetic resonance (EPR) at the X-band, com

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

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

64 Electron paramagnetic resonance (EPR) distance measureme

65 ributed to the recent progress in biomedical electron paramagnetic resonance (EPR) due to their unmat

66 Variable-temperature electron paramagnetic resonance (EPR) experiments show t

67 Electron paramagnetic resonance (EPR) has become an impo

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

69 Electron paramagnetic resonance (EPR) hyperspectral imag

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

71 A focus on electron paramagnetic resonance (EPR) imaging shows the

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

73 vel insight into the catalytic mechanism via electron paramagnetic resonance (EPR) is not generally p

74 Variable-temperature electron paramagnetic resonance (EPR) measurements and r

75 Pulsed electron paramagnetic resonance (EPR) measurements enabl

76 light (365 nm) activation of NADH coupled to electron paramagnetic resonance (EPR) measurements to st

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

78 s alcoholic beverages is determined using an electron paramagnetic resonance (EPR) method, which is b

79 Using electron paramagnetic resonance (EPR) of a bifunctional

80 Electron paramagnetic resonance (EPR) of biomolecules sp

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

82 to Y(D) are shown to correlate directly with electron paramagnetic resonance (EPR) parameters such as

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

84 MR) gives a spectrum of the modulation of an electron paramagnetic resonance (EPR) signal by a tuneab

85 The S(3)' electron paramagnetic resonance (EPR) signal is signific

86 iginates from the observation of a multiline electron paramagnetic resonance (EPR) signal with effect

87 Combined with X-band electron paramagnetic resonance (EPR) spectral analysis,

88 Biochemical and electron paramagnetic resonance (EPR) spectroscopic anal

89 A were investigated based on mutagenesis and electron paramagnetic resonance (EPR) spectroscopic appr

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

91 Although the optical and electron paramagnetic resonance (EPR) spectroscopic sign

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

93 Electron paramagnetic resonance (EPR) spectroscopic stud

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

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

96 t pairs at 85 K, and time-resolved and pulse electron paramagnetic resonance (EPR) spectroscopies are

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

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

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

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

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

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

103 ifferent biothiols in a single sample, using electron paramagnetic resonance (EPR) spectroscopy and a

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

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

106 d and stable radicals was investigated using electron paramagnetic resonance (EPR) spectroscopy and c

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

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

109 Electron paramagnetic resonance (EPR) spectroscopy indic

110 Electron paramagnetic resonance (EPR) spectroscopy is a

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

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

113 Using several techniques, we show that electron paramagnetic resonance (EPR) spectroscopy of ol

114 by utilizing site-directed spin labeling and electron paramagnetic resonance (EPR) spectroscopy of pr

115 Electron paramagnetic resonance (EPR) spectroscopy prove

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

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

118 ith extensive highlights of the results from Electron Paramagnetic Resonance (EPR) spectroscopy to ex

119 olecular spin qubits are studied with pulsed electron paramagnetic resonance (EPR) spectroscopy under

120 In the current study, electron paramagnetic resonance (EPR) spectroscopy was e

121 D), gel permeation chromatography (GPC), and electron paramagnetic resonance (EPR) spectroscopy were

122 UV/Vis absorption, cyclic voltammetry (CV), electron paramagnetic resonance (EPR) spectroscopy, and

123 tions monitored by UV-vis microspectroscopy, electron paramagnetic resonance (EPR) spectroscopy, and

124 Electron paramagnetic resonance (EPR) spectroscopy, coup

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

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

127 igh-resolution three-dimensional structures, electron paramagnetic resonance (EPR) spectroscopy, quan

128 Magnetic susceptibility, electron paramagnetic resonance (EPR) spectroscopy, X-ra

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

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

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

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

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

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

135 ng system (IVIS), and quantified ex vivo via electron paramagnetic resonance (EPR) spectroscopy.

136 radicals at room temperature as observed by electron paramagnetic resonance (EPR) spectroscopy.

137 SII from Thermosynechococcus elongatus using electron paramagnetic resonance (EPR) spectroscopy: E(m)

138 A stable triarylmethyl spin probe whose electron paramagnetic resonance (EPR) spectrum is highly

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

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

141 Electron paramagnetic resonance (EPR) studies of the rhe

142 Detailed electron paramagnetic resonance (EPR) studies, isotopic

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

144 enzymes, we have performed an integrated NMR/electron paramagnetic resonance (EPR) study into the det

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

146 ivity in turbid media, the properties of the electron paramagnetic resonance (EPR) technique make it

147 protonation products of Cp*(2)Co using pulse electron paramagnetic resonance (EPR) techniques at low

148 to rapidly undergo bioconjugation, by using electron paramagnetic resonance (EPR) to measure conform

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

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

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

152 Characterization was carried out via UV-vis, electron paramagnetic resonance (EPR), (57)Fe Mossbauer,

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

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

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

156 opic techniques including UV-vis absorption, electron paramagnetic resonance (EPR), and X-ray absorpt

157 y substrates in addition to O(2) Here, using electron paramagnetic resonance (EPR), Mossbauer, and UV

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

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

160 ystal X-ray, dynamic light scattering (DLS), electron paramagnetic resonance (EPR), UV-vis, fluoresce

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

162 pproved for winemaking) were investigated by electron paramagnetic resonance (EPR).

163 affords (13)CN-labeled enzyme as verified by electron paramagnetic resonance (EPR)/electron nuclear d

164 Electron-paramagnetic resonance (EPR) spectroscopy of st

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

166 sults suggested that the analysis by ESR (or electron paramagnetic resonance, EPR) is suitable to eva

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

168 We make predictions for electron paramagnetic resonance experiments and analyze

169 Time-resolved electron paramagnetic resonance experiments confirm that

170 Electron paramagnetic resonance experiments provide crit

171 Electron paramagnetic resonance experiments show that th

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

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

174 High-frequency and -field electron paramagnetic resonance (HFEPR) spectroscopy con

175 eriments, deuterium labeling, radical clock, electron paramagnetic resonance, high-resolution mass sp

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

177 ere, we developed new hyperpolarized MRI and electron paramagnetic resonance imaging procedures that

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

179 ystems, and the ability to label and perform electron paramagnetic resonance in cells is expected to

180 bed using a combination of X-ray scattering, electron paramagnetic resonance (in the case where the m

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

182 Electron paramagnetic resonance measurements confirmed t

183 develop a cryoreduction approach coupled to electron paramagnetic resonance measurements to study el

184 uctural determination of CntA and subsequent electron paramagnetic resonance measurements uncover the

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

186 sitions by means of transient absorption and electron paramagnetic resonance measurements.

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

188 ation and distance measurements derived from electron paramagnetic resonance of a bifunctional spin l

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

190 ned in a previous study from continuous-wave electron paramagnetic resonance of myosin labeled at spe

191 cture determination, were investigated using electron paramagnetic resonance of spin probes doped int

192 Using a combination of electron paramagnetic resonance, on spin-labeled protein

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

194 Electron paramagnetic resonance shows that their binding

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

196 Furthermore, an electron paramagnetic resonance signal was observed when

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

198 erimental and computational methods, such as electron paramagnetic resonance, solid-state ultraviolet

199 Echo-detected electron paramagnetic resonance spectra from native memb

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

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

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

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

204 Electrochemical analysis and electron paramagnetic resonance spectra suggest that in

205 In the electron paramagnetic resonance spectra, at least two fo

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

207 nt control of this spin qubit with a 240 GHz electron paramagnetic resonance spectrometer powered by

208 We present biochemical and electron paramagnetic resonance spectroscopic characteri

209 Electron paramagnetic resonance spectroscopic spin-trapp

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

211 UV-visible and electron paramagnetic resonance spectroscopies are consi

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

213 hod, iron quantification, and UV-visible and electron paramagnetic resonance spectroscopies to invest

214 ar magnetic resonance, (57)Fe Mossbauer, and electron paramagnetic resonance spectroscopies.

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

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

217 rdination modes was done by using UV/Vis and Electron Paramagnetic Resonance spectroscopies.

218 Electron paramagnetic resonance spectroscopy (EPR) is a

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

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

221 been synthesized and analyzed by UV-vis and electron paramagnetic resonance spectroscopy and by X-ra

222 Furthermore, our electron paramagnetic resonance spectroscopy and circula

223 and size of the surfactants' monolayer using electron paramagnetic resonance spectroscopy and dynamic

224 , the formation of the former is inferred by electron paramagnetic resonance spectroscopy and its abs

225 we analyzed recombinantly produced HoxEFU by electron paramagnetic resonance spectroscopy and kinetic

226 As shown by combined high-field electron paramagnetic resonance spectroscopy and magneti

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

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

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

230 Electron paramagnetic resonance spectroscopy and X-ray p

231 Electron paramagnetic resonance spectroscopy and X-ray p

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

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

234 Electron paramagnetic resonance spectroscopy confirms th

235 Electron paramagnetic resonance spectroscopy has been lo

236 Recent advances in the application of electron paramagnetic resonance spectroscopy have demons

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

238 Here, using electron paramagnetic resonance spectroscopy in combinat

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

240 e-4S center after 7 d as determined from the electron paramagnetic resonance spectroscopy measurement

241 Electron paramagnetic resonance spectroscopy of BciD ind

242 As determined by electron paramagnetic resonance spectroscopy of intermed

243 supported by site-directed spin labeling and electron paramagnetic resonance spectroscopy of melanops

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

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

246 ogendeuterium-exchange mass spectrometry and electron paramagnetic resonance spectroscopy reveal an a

247 Tests with electron paramagnetic resonance spectroscopy showed that

248 Time-resolved electron paramagnetic resonance spectroscopy shows that

249 f the R(*) and D(*+) spin states using pulse electron paramagnetic resonance spectroscopy shows that

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

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

252 Applying cryogenic infrared and electron paramagnetic resonance spectroscopy to an [FeFe

253 we apply time-resolved mass spectrometry and electron paramagnetic resonance spectroscopy to determin

254 s study, we used site-directed spin-labeling electron paramagnetic resonance spectroscopy to examine

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

256 thered using site-directed spin labeling and electron paramagnetic resonance spectroscopy to improve

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

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

259 also exploit species-selective scavengers in electron paramagnetic resonance spectroscopy to sequeste

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

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

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

263 Continuous wave and pulsed electron paramagnetic resonance spectroscopy was used to

264 Using electron paramagnetic resonance spectroscopy we have cha

265 -crystal cryogenic X-ray diffraction at 6 K, electron paramagnetic resonance spectroscopy, and correl

266 und was characterized by means of UV-vis and electron paramagnetic resonance spectroscopy, cyclic vol

267 radical association by variable-temperature electron paramagnetic resonance spectroscopy, determinin

268 We sampled blood for oxidative (electron paramagnetic resonance spectroscopy, HPLC), nit

269 bal kinetic modeling, X-ray crystallography, electron paramagnetic resonance spectroscopy, protein el

270 9.2 cm(-1), as determined by magnetometry or electron paramagnetic resonance spectroscopy, respective

271 eld TEMPO(*) and [LCuOOH](-) on the basis of electron paramagnetic resonance spectroscopy, the produc

272 ulfate self-decomposition, while detected by electron paramagnetic resonance spectroscopy, was unlike

273 trometry, protein film electrochemistry, and electron paramagnetic resonance spectroscopy, we confirm

274 plexes were assessed by variable-temperature electron paramagnetic resonance spectroscopy, X-ray abso

275 nced by confocal fluorescence microscopy and electron paramagnetic resonance spectroscopy.

276 trap hydroxymethyl radical was evaluated by electron paramagnetic resonance spectroscopy.

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

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

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

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

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

282 zed by molecular structure determination and electron paramagnetic resonance spectroscopy.

283 omyces coelicolor using paramagnetic NMR and electron paramagnetic resonance spectroscopy.

284 shown by (1)H nuclear magnetic resonance and electron paramagnetic resonance spectroscopy.

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

286 ype of mixed valence dirhodium species whose electron paramagnetic resonance spectrum revealed a delo

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

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

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

290 Electron paramagnetic resonance studies verify a clockli

291 Continuous-wave and pulse electron paramagnetic resonance techniques are used to v

292 Characterization by electron paramagnetic resonance techniques of several va

293 Using electron paramagnetic resonance techniques, we character

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

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

296 Here, we use pulse electron paramagnetic resonance to examine the conformat

297 e use of spin-labeling and variable-pressure electron paramagnetic resonance to reveal them in a memb

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

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

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