ライフサイエンスコーパス: EPR

1 EPR analysis subsequently revealed that the {FeNO}(7) mo

2 EPR and Electron Nuclear Double Resonance spectroscopies

3 EPR and resonance Raman spectroscopy did not detect the

4 EPR experiments indicated that the two electrons from NA

5 EPR simulations of a representative spectrum indicate tw

6 EPR spectra at each state of the refolding workflow of s

7 EPR spectra obtained under different conditions are expl

8 EPR spectroscopic evidence for two rotamers of the analo

9 EPR spectroscopic evidence suggested that NHC-boryl radi

10 EPR spectroscopic investigation of CntA variants indicat

11 EPR spectroscopy and mutagenesis data support that RumMC

12 EPR spectroscopy data suggests particles cleared more sl

13 EPR spectroscopy of variant CntA proteins suggested a hi

14 EPR spectroscopy reveals an axial signal consistent with

15 EPR spectroscopy showed that the synthetic pigment conta

16 EPR spectroscopy, SQUID magnetometry, and DFT calculatio

17 EPR studies demonstrate that [Ni(IMes)(2)] undergoes ver

18 EPR studies of these two types of Abeta42 fibrils show t

19 EPR study identified a potassiated paramagnetic species

20 EPR, ENDOR, and DFT studies reveal a valence-localized [

21 EPR, ENDOR, ESEEM, and HYSCORE data indicate the presenc

22 EPR-1 associates with H3K27-methylated chromatin, and lo

23 EPR-1 is not fungal-specific; orthologs of EPR-1 are pre

24 al analysis, this indicates that the g = 4.1 EPR signal corresponds to an S = (5)/(2) form of the WOC

25 1-X exhibited an S = 1/2 EPR signal distinct from that of the parent complex 1.

26 ted into the existing Expert Panel Report-3 (EPR-3) asthma management step diagram format.

27 ase in the intensity of a new "g(eff) = 4.5" EPR signal.

28 asis of analyses using transient absorption, EPR, and optical titrations with NADH or inorganic reduc

29 Recent advanced EPR and Mn K-edge X-ray spectroscopy studies converge up

30 Furthermore, 3 is an EPR active species showing an S = 1/2 signal with clearl

31 orhombic C(2v) symmetry, which neighbours an EPR active O coordinated Er centre with monoclinic C(1h)

32 ene is produced prior to the formation of an EPR detected Mn(III)Mn(IV) bimetallic species, and 0.5 e

33 Here, we present an EPR analysis strategy and the corresponding computationa

34 Using an EPR-based detection method, we find that some protein-pr

35 he corresponding disulfide conjugate with an EPR spectrum characteristic of the trapped thiol.

36 eukaryotic lineages, suggesting an ancestral EPR-1 was a component of a primitive Polycomb repression

37 lta = 0.45, |DeltaE(Q)| = 3.6 mm s(-1)), and EPR (S = 5/2, g = [6.38, 5.53, 1.99])), obtained by one-

38 n the basis of the UV-vis-NIR absorption and EPR spectroscopy results.

39 -MS, a hydroethidine fluorescence assay, and EPR spin trapping.

40 e presence of both Fe-S and Fe-CO bonds, and EPR data of this S = 1/2 species indicate a ligand-based

41 , room-temperature X-ray crystallography and EPR spectroscopy on four SLO variants (wild-type (WT) en

42 IVIS and EPR spectroscopy data indicate a predominant amount of p

43 Here, we obtained Mossbauer and EPR spectra of Escherichia coli cells prepared under dif

44 derived from W303 cells using Mossbauer and EPR spectroscopies and liquid chromatography interfaced

45 Cysteine scanning mutagenesis and EPR spectroscopy identified Cys-261 on CblD as the sulfu

46 maging, Raman, FTIR, TGA, KPFM, XPS, NMR and EPR clearly show that the properties of C(3)N(5) are dis

47 simulations and previously obtained NMR and EPR data to derive and validate a conformational ensembl

48 supported by X-ray crystallography, NMR and EPR spectroscopies, and computational studies.

49 cked by solid-state ((1)H and (13)C) NMR and EPR spectroscopies.

50 UV-vis-near-IR, Mossbauer, NMR, and EPR spectroscopies with magnetometry, crystallography, a

51 ratures via ESI-MS and UV-vis, (2)H NMR, and EPR spectroscopies.

52 V-visible absorption/CD, resonance Raman and EPR spectroscopy, and analytical studies.

53 X-ray structural and EPR/UV-Vis spectral studies revealed that the anion-anio

54 Rapid kinetic studies and EPR measurements of rapid freeze-quenched samples of the

55 UV and EPR spectroscopy both suggested that the substrate binds

56 thoroughly characterized by vibrational and EPR techniques, including pulse EPR studies.

57 etic, reagent, and spectroscopic (UV-vis and EPR) studies suggest a mechanism involving metal-substra

58 Fe K-edge XANES and EPR spectroscopy indicated initial formation of a low-sp

59 d trityl radical (FTR) shows very attractive EPR spectroscopic properties for a manifold of applicati

60 Consequently, analogous near-axial EPR spectra with g(||) < g( ) <= 2 were measured for the

61 esolution of high-frequency (130 GHz) D-band EPR, the principal components of the g tensors were dete

62 -nitroxide systems using a commercial Q-band EPR instrument.

63 X-band EPR experiments revealed bis(phosphine)cobalt(II) bis(ca

64 Continuous wave and pulsed (HYSCORE) X-band EPR show it has a highly compact g(z) area and small A(z

65 ctors with rapid freeze-quenching and X-band EPR spectroscopy, permitting characterization of reactio

66 Compound 2 was characterized by EPR spectroscopy, elemental analysis, X-ray crystallogra

67 reduction with K metal and characterized by EPR spectroscopy.

68 itrene radical species were characterized by EPR, XANES, and UV-vis spectroscopy, high-resolution mas

69 airs (3, 2; 5, 6) have been characterized by EPR, zero-field (57)Fe Mossbauer, magnetometry, single c

70 ls showed antioxidant activity determined by EPR, and inhibition of COX-1/COX-2.

71 xtracting detailed structural information by EPR spectroscopy.

72 e spin-coupled hidden Cu(II) was observed by EPR spectroscopy.

73 substrate-based radical species observed by EPR using a slurry of small-sized single crystals.

74 roducts were characterized and quantified by EPR spectroscopy and gas chromatography (GC).

75 ed outside the mRNA channel, were studied by EPR spectroscopy methods.

76 tert-butyl ester substituents was studied by EPR spectroscopy.

77 s via a radical intermediate as supported by EPR studies.

78 The identity of [1](*+) is supported by EPR, UV-vis, multinuclear NMR ((1)H, (11)B), and X-ray p

79 The structural model, validated by EPR distance measurements, illuminates the role of the h

80 To employ in-cell EPR using nitroxide-based spin labels, the structure of

81 Therefore, the characteristic EPR signals determined for 1-3 and 5 can be used as a sp

82 ENDOR spectra collected across the A(red)-CO EPR envelope reveals a second CO bound in the d(z)(2) or

83 Collectively, EPR:CR co-activation results in significant cardiovascul

84 Combined EPR and DFT methods indicate that 2 contains a S=3/2 Fe(

85 Combining EPR and electrochemical data, we quantify the free energ

86 B7 but also validates the approach combining EPR/ENDOR spectroscopy with DFT-calculated magnetic reso

87 Computational, EPR, and X-ray analysis support the view that the oxidiz

88 Cryoreduction-EPR is broadly applicable for the study of electron tran

89 agostic interactions through single-crystal EPR spectroscopy.

90 med by single crystal X-ray crystallography, EPR spectroscopy, and DFT calculations.

91 A combination of pulsed EPR, CW EPR, and X-ray absorption spectroscopies has been employ

92 The nature of the unusual CW EPR spectrum has been re-evaluated in light of new data

93 ition, a multifrequency continuous-wave (CW)-EPR and (15)N-HYSCORE spectroscopy study on the uniforml

94 Spectral features found in our CW-EPR measurements were consistent with the overall rigid

95 nd double electron-electron resonance (DEER) EPR spectroscopy to measure a large number of intra- and

96 crowave cavity to measure the face-dependent EPR spectra of the crystal, demonstrating that it has an

97 C variants have been established by detailed EPR/DFT analyses.

98 emble multiparameter fluorescence detection, EPR spectroscopy, mutagenesis, and FRET-positioning and

99 e solutions of 1 disclose entirely different EPR spectra at 10 K when prepared under N(2) versus Ar a

100 Dipolar EPR spectroscopy has proven to be a valuable tool to det

101 ocyanide (XylNC) adducts of 1, which display EPR features akin to those observed in the putative N(2)

102 tyrosyl radicals, giving rise to a distinct EPR spectrum consistent with a stable dihydroxyphenylala

103 etely different as evidenced by its distinct EPR spectrum with g(||) < 2 < g( ).

104 kinetics, thermodynamics, electrochemistry, EPR spectroscopy, and DFT calculations support the propo

105 endering weak zero-field splitting to enable EPR addressability: [Ni(phen)(3)](BF(4))(2) (1) and [Ni(

106 ociception-related behaviors and exacerbated EPRs in the same mice.

107 ponding computational tool for batch-fitting EPR spectra and cluster analysis of the chi(2) landscape

108 Computational tools for fitting EPR spectra have enabled dynamics parameters to be deter

109 trate CSCA using a model system designed for EPR analysis: a self-assembled nanoribbon with radical e

110 of exploiting the double-histidine motif for EPR applications even at sub-mum protein concentrations

111 For two nitroxides, we present results from EPR spectroscopy, X-ray crystal structures of B-form spi

112 Methodological and technological advances in EPR spectroscopy have enabled novel insight into the str

113 erestingly, various spectroscopies including EPR and XAFS determine a high-spin state (S = 3/2) for t

114 We use light-induced EPR and ENDOR spectroscopy combined with DFT calculation

115 ch using X-ray diffraction; UV/vis, MCD, IR, EPR, and NMR spectroscopy; and quantum chemistry.

116 e [LCu(2)(mu-O)(mu-NO)](2+) complex with IR, EPR, and X-ray crystallography suggests a localized mixe

117 withstands prolonged storage at 77 K and its EPR signal is only partially lost upon annealing at 100

118 Site directed spin labeling EPR and DEER (double electron-electron resonance) studie

119 tes FAK, we used site-directed spin-labeling EPR spectroscopy-based studies coupled with bioluminesce

120 amic nuclear polarization, and spin-labeling EPR under in-cell conditions.

121 IR, UV/vis, multinuclear NMR, and dual-mode EPR spectroscopy.

122 ntermediate, and a combination of Mossbauer, EPR, and X-ray absorption spectroscopies identifies it a

123 Multifrequency EPR spectroscopy identified two distinct Fe(III) sites (

124 d characterization by XAS and multifrequency EPR spectroscopy of a Mn(IV)(4)O(4) cuboidal complex as

125 thus permitting its characterization by NMR, EPR, X-ray, and HRMS.

126 tructures elucidated using multinuclear NMR, EPR, electronic absorption spectroscopies, SQUID magneto

127 used isopycnic gradient sedimentation, NMR, EPR, high-resolution microscopy, and proteomics to analy

128 Transient nutation EPR experiments and DFT calculations confirm that the co

129 An array of EPR labels for nucleic acids are available, but they oft

130 e dramatically broadened the capabilities of EPR dynamics analysis, however, their implementation can

131 The combination of EPR with X-ray crystallographic studies has revealed the

132 with H3K27-methylated chromatin, and loss of EPR-1 de-represses H3K27-methylated genes without loss o

133 EPR-1 is not fungal-specific; orthologs of EPR-1 are present in a diverse array of eukaryotic linea

134 CA tool will increase the reproducibility of EPR fitting for the characterization of dynamics in biom

135 Through a series of EPR and biochemical characterizations, we found that Moa

136 Simulation of EPR spectra from bulk oil demonstrated that mainly alkox

137 In addition to an extensive toolkit of EPR methods, multiple spin labels have been developed an

138 a the Fenton reaction, a novel tool based on EPR spin trapping methodology was developed to quantify

139 Parallel EPR tests were performed to assess the importance of met

140 orrelation between in-phase and out-of-phase EPR intensities of radicals and vanadyl porphyrins in ba

141 -plant homeodomain (PHD)-containing protein, EPR-1 (effector of polycomb repression 1; NCU07505).

142 Pulse EPR experiments, X-band ENDOR and HYSCORE, reveal deloca

143 Although pulse EPR studies indicate the presence of two Fe-(mu-H)-Fe mo

144 tom by way of continuous-wave (CW) and pulse EPR (HYSCORE) spectroscopic measurements.

145 racterized by continuous-wave (CW) and pulse EPR techniques.

146 (+1) and [(P(6)ArC)Fe(2)(mu-H)](-1) by pulse EPR revealed that redox chemistry induces significant ch

147 -HCCH); the latter is characterized by pulse EPR spectroscopy and DFT calculations.

148 the mu-hydride ligand was evaluated by pulse EPR studies.

149 1) for 1 and 2, respectively, enabling pulse EPR measurements.

150 Variable temperature Q-band (34 GHz) pulse EPR spectroscopy, in conjunction with density functional

151 Herein, pulse EPR spectroscopy ((1,2)H HYSCORE, ENDOR) and X-ray cryst

152 rational and EPR techniques, including pulse EPR studies.

153 he best of our knowledge, there are no pulse EPR studies on Ni(2+) molecules.

154 nitrogen atoms in the adt ligand using pulse EPR to target the magnetic couplings introduced via a (1

155 By performing pulse-EPR measurements on the shortest hairpin, selective addr

156 These results demonstrate that pulse-EPR can manipulate coherent spin states in DNA hairpins,

157 nd rich binding mode scenarios, 1D/2D pulsed EPR experiments have been used and tailored to different

158 (17)O and (1)H pulsed EPR spectra show that the as-isolated Mo(V) enzyme form

159 A combination of pulsed EPR, CW EPR, and X-ray absorption spectroscopies has bee

160 pically and structurally by resonance Raman, EPR, and X-ray absorption spectroscopies as well as dens

161 gestion rate (IR) and egg reproduction rate (EPR)) of the numerically dominant neritic copepod Acarti

162 Although the exercise pressor reflex (EPR) and the chemoreflex (CR) are recognized for their s

163 ctive effect of the exercise pressor reflex (EPR) and the chemoreflex (CR) on the cardiovascular resp

164 The exercise pressor reflex (EPR) is defined by a rise in mean arterial pressure (MAP

165 orking model of the exercise pressor reflex (EPR).

166 nals and modulate exercise pressor reflexes (EPRs).

167 It is found that the relative EPR intensity of radicals and vanadyl porphyrins is sens

168 fluorescence emission, NMR and time-resolved EPR spectroscopies, cyclic voltammetry, mass spectrometr

169 ia theoretical computation and time-resolved EPR spectroscopy, we confirmed that the ISC of the bodip

170 oupled with electron paramagnetic resonance (EPR) analyses and DFT calculations, allowed the identifi

171 tato) using electron paramagnetic resonance (EPR) and (57)Fe Mossbauer spectroscopy coupled with wave

172 the use of electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) spect

173 uench (RFQ) electron paramagnetic resonance (EPR) and magnetic circular dichroism (MCD) yields two in

174 Electron paramagnetic resonance (EPR) at the X-band, combining in-phase and out-of-phase

175 Electron paramagnetic resonance (EPR) distance measurements are making increasingly impor

176 biomedical electron paramagnetic resonance (EPR) due to their unmatched stability in biological medi

177 temperature electron paramagnetic resonance (EPR) experiments show that the nitroxides couple to one

178 Electron paramagnetic resonance (EPR) has become an important tool to probe conformationa

179 A focus on electron paramagnetic resonance (EPR) imaging shows the validation of treating hypoxic tu

180 chanism via electron paramagnetic resonance (EPR) is not generally possible.

181 temperature electron paramagnetic resonance (EPR) measurements and relaxation studies suggest a stron

182 coupled to electron paramagnetic resonance (EPR) measurements to study electron transfer from the ex

183 ed using an electron paramagnetic resonance (EPR) method, which is based on a semiempirical correlati

184 rectly with electron paramagnetic resonance (EPR) parameters such as the tyrosyl g-tensor, allowing u

185 ation of an electron paramagnetic resonance (EPR) signal by a tuneable optical field.

186 The S(3)' electron paramagnetic resonance (EPR) signal is significantly broader than the untreated

187 a multiline electron paramagnetic resonance (EPR) signal with effective total spin of S = 1/2 in the

188 with X-band electron paramagnetic resonance (EPR) spectral analysis, this indicates that the g = 4.1

189 genesis and electron paramagnetic resonance (EPR) spectroscopic approaches.

190 optical and electron paramagnetic resonance (EPR) spectroscopic signatures of the PmoD Cu(A) bear sim

191 d and pulse electron paramagnetic resonance (EPR) spectroscopies are used to probe their spin dynamic

192 mple, using electron paramagnetic resonance (EPR) spectroscopy and a trityl-radical-based probe (MTST

193 gated using electron paramagnetic resonance (EPR) spectroscopy and compared with hydroperoxides and h

194 Electron paramagnetic resonance (EPR) spectroscopy indicates the presence of ROS on titan

195 e show that electron paramagnetic resonance (EPR) spectroscopy of oligonucleotides spin-labelled with

196 abeling and electron paramagnetic resonance (EPR) spectroscopy of protein bound to standard, commerci

197 Electron-paramagnetic resonance (EPR) spectroscopy of stretched rat tail tendon, atomisti

198 Electron paramagnetic resonance (EPR) spectroscopy proved that these did indeed add to th

199 esults from Electron Paramagnetic Resonance (EPR) spectroscopy to explain the nature and stability of

200 with pulsed electron paramagnetic resonance (EPR) spectroscopy under electric fields to assess their

201 rent study, electron paramagnetic resonance (EPR) spectroscopy was employed to measure environmentall

202 (GPC), and electron paramagnetic resonance (EPR) spectroscopy were used to estimate structural chara

203 metry (CV), electron paramagnetic resonance (EPR) spectroscopy, and theoretical studies.

204 ectroscopy, electron paramagnetic resonance (EPR) spectroscopy, and X-ray crystallography.

205 Electron paramagnetic resonance (EPR) spectroscopy, coupled with site-directed spin label

206 structures, electron paramagnetic resonance (EPR) spectroscopy, quantum mechanics/molecular mechanics

207 eptibility, electron paramagnetic resonance (EPR) spectroscopy, X-ray absorption near-edge spectrosco

208 alysed by electronic paramagnetic resonance (EPR) spectroscopy.

209 observed by electron paramagnetic resonance (EPR) spectroscopy.

210 ex vivo via electron paramagnetic resonance (EPR) spectroscopy.

211 gatus using electron paramagnetic resonance (EPR) spectroscopy: E(m) Q(B)/Q(B) (*-) ~ 90 mV, and E(m)

212 probe whose electron paramagnetic resonance (EPR) spectrum is highly sensitive to molecular tumbling

213 Electron paramagnetic resonance (EPR) studies of the rhenium(II) complex Re(eta(5)-Cp)(BD

214 Detailed electron paramagnetic resonance (EPR) studies, isotopic labeling, and other control exper

215 egrated NMR/electron paramagnetic resonance (EPR) study into the detailed aspects of an AA10 LPMO-sub

216 ties of the electron paramagnetic resonance (EPR) technique make it suitable for use in such media.

217 using pulse electron paramagnetic resonance (EPR) techniques at low temperature.

218 n, by using electron paramagnetic resonance (EPR) to measure conformational dynamics.

219 via UV-vis, electron paramagnetic resonance (EPR), (57)Fe Mossbauer, Fe X-ray absorption (XAS), and (

220 absorption, electron paramagnetic resonance (EPR), and X-ray absorption spectroscopies (XAS), which t

221 Here, using electron paramagnetic resonance (EPR), Mossbauer, and UV-visible spectroscopies, we explo

222 ring (DLS), electron paramagnetic resonance (EPR), UV-vis, fluorescence, and density functional theor

223 stigated by electron paramagnetic resonance (EPR).

224 verified by electron paramagnetic resonance (EPR)/electron nuclear double-resonance spectra.

225 by ESR (or electron paramagnetic resonance, EPR) is suitable to evaluate, either qualitatively or qu

226 on the enhanced permeability and retention (EPR) effect observed in tumour vasculature to deliver an

227 d on the enhance permeability and retention (EPR) effect remain insufficient to satisfy the clinical

228 such as enhanced permeability and retention (EPR) effect, active targeting, and tumor microenvironmen

229 ased on enhanced permeability and retention (EPR) effects show only an ~5% targeting rate.

230 ant reaction pathway is characterized by RFQ EPR and kinetic modeling to directly produce Cu(II)-HjLP

231 duced dipolar modulation enhancement (RIDME) EPR experiments.

232 50' N; 104 degrees 17.5 W East Pacific Rise (EPR) vent field are a source for (sub)micron-sized graph

233 Frozen-solution EPR data demonstrate the formation of an interesting bio

234 lectron paramagnetic resonance spectroscopy (EPR) is a uniquely powerful technique for characterizing

235 surprisingly, X-ray absorption spectroscopy, EPR, and electron nuclear double resonance revealed that

236 In addition, they show strong EPR signals, have long phase memory times at room temper

237 We term this technique EPR thiol-trapping.

238 und state by theory and variable temperature EPR.

239 The EPR and hypercapnia-induced CR interaction results in a

240 The EPR and hypoxia-induced CR interaction is hyper-additive

241 The EPR measurements and mass spectrometry analyses further

242 The EPR spectroscopic properties of the trityl radicals 1 an

243 ing trials through buffer exchanges, and the EPR spectra are collected on the order of seconds under

244 mechanism, which is very different from the EPR effect.

245 dynamics, the interaction resulting from the EPR:CO(2) -CR co-activation is simply additive for all c

246 peripheral haemodynamics, resulting from the EPR:CR interaction in hypoxia, likely having the most cr

247 re, while the interaction resulting from the EPR:O(2) -CR co-activation is hyper-additive for blood p

248 role of the TRPV1 receptor in mediating the EPR.

249 rent feedback from lower limbs to modify the EPR, while breathing either ambient air, normocapnic hyp

250 Moreover, the EPR data provide evidence for the location of the intera

251 During co-activation of the EPR and the hypercapnia-induced CR (CO(2) -CR), the haem

252 During co-activation of the EPR and the hypoxia-induced CR (O(2) -CR), mean arterial

253 A cumulative assessment of the EPR data, when combined with insights provided by near-i

254 ew, we summarize the current findings of the EPR effect and assess its limitations in the context of

255 umor-targeting rate from less than 5% of the EPR effect to more than 50%.

256 se models can define exact mechanisms of the EPR in health and disease.

257 model will allow for extensive study of the EPR in unlimited transgenic and mutant mouse lines, and

258 The decerebrate mouse model of the EPR is similar to the previously described decerebrate r

259 acid and detected by the oscillation of the EPR nitrogen splitting of a dialkyl nitroxide function m

260 The line shape of the EPR spectra and the quantity of radicals can be modulate

261 e have developed a novel murine model of the EPR to allow for mechanistic studies in various mouse mo

262 hile structural interpretations based on the EPR spectroscopic features of the S(3) state provide val

263 o five adjacent guanines in a G-tract on the EPR time scale.

264 Since the EPR:CR co-activation with hypoxia potentiates the presso

265 Studying the EPR in transgenic mouse models can define exact mechanis

266 creates a similar phenomenon compared to the EPR effect arising from tumour tissues, its drug deliver

267 While the EPR effect offers a possible route for drug passage, we

268 ide content analyses in conjunction with the EPR and Mossbauer spectroscopy measurements and the site

269 ts was measured, over storage time, with the EPR spin trapping method under forced ageing conditions.

270 their rubber-like property to enhance their EPR as well as the receptor-mediated endocytosis by hepa

271 of these radicals were identified from their EPR spectra.

272 Nitroxides which exhibit a change in their EPR hyperfine coupling constants upon enzymatic activity

273 Thus, EPR:CR co-activation results in significant interactions

274 This novel approach to EPR spectral analysis provides insight into the position

275 Transient EPR spectroscopy shows that the photoexcited QDs strongl

276 it distances, and are probed using transient EPR spectroscopy.

277 first time spectral characterization of two EPR-active Fe(mu-C)(mu-H)Fe model complexes linked by a

278 reveals low- to sub-mum Cu(II) K(D) s under EPR distance measurement conditions at cryogenic tempera

279 We further use EPR spectroscopy to identify a mixed-valent M-M bonded P

280 mplexes under photochemical activation using EPR.

281 etailed analysis of the Cu2+-DPA motif using EPR and molecular dynamics (MD) simulations.

282 ive triradical species has been probed using EPR spectroscopy, magnetic susceptibility measurements,

283 We were able to characterize 1-X using EPR spectroscopy and DFT calculations.

284 Here, we utilize EPR spectroscopy to target the conformational changes th

285 Temperature-varied EPR spectroscopy with spectral simulation reveals large

286 intermediates, as well as interrogation via EPR spectroscopy, UV-vis spectroscopy, radical probes, a

287 omo- or hetero-oligomeric Bcl-2 proteins via EPR.

288 icle distribution was quantified ex vivo via EPR spectroscopy.

289 UV-vis, EPR, and Mossbauer spectroscopy of purified wild-type Ap

290 us spectroscopic techniques, such as UV/Vis, EPR, CSI-MS, resonance Raman, XANES, and EXAFS, showing

291 Combined UV-vis/EPR spectroelectrochemistry indicates that a two-electro

292 in the solid state, i.e. Raman, UV-visible, EPR, NMR and X-ray absorption spectroscopy, X-ray crysta

293 sed purification methods as well as in vivo, EPR spectroscopy, and MALDI measurements, we show that s

294 We used continuous wave EPR experiments to characterize Cu2+ binding to DPA as w

295 Continuous-wave EPR spectroscopy reveals the exchange interactions betwe

296 anions activate (cleave) dihydrogen, whilst EPR spectroscopic characterization, supported by computa

297 The NADH photo-activation coupled with EPR is broadly applicable to trap reactive intermediates

298 ved oxygen centered, secondary radicals with EPR g values of 2.0041 for mainstream and 2.0044 for sid

299 Herein, we use UV-vis, CD, XAS, EPR, VT/VH-MCD, and resonance Raman spectroscopies, augm

300 R paramagnetic shifts, but are evident in Yb EPR and Eu emission spectra.