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1 present in the oxidized form (determined by electron paramagnetic resonance spectroscopy).
2 partially delocalized spin, as evidenced by electron paramagnetic resonance spectroscopy.
3 ient spectroscopies, cyclic voltammetry, and electron paramagnetic resonance spectroscopy.
4 xide rotational motions were monitored using electron paramagnetic resonance spectroscopy.
5 the [4Fe-4S] cluster that can be studied by electron paramagnetic resonance spectroscopy.
6 r magnetic resonance (NMR) spectroscopy, and electron paramagnetic resonance spectroscopy.
7 d D = -2.0(5) as determined by parallel-mode electron paramagnetic resonance spectroscopy.
8 I to a proamyloidogenic form was examined by electron paramagnetic resonance spectroscopy.
9 pecies are quantitatively characterized with electron paramagnetic resonance spectroscopy.
10 iron-sulfur cluster as shown by optical and electron paramagnetic resonance spectroscopy.
11 uorescent and biochemical assays, as well as electron paramagnetic resonance spectroscopy.
12 heme environment in catalase, as detected by electron paramagnetic resonance spectroscopy.
13 using reductive chemiluminescent assays and electron paramagnetic resonance spectroscopy.
14 volts, using site-directed spin labeling and electron paramagnetic resonance spectroscopy.
15 nt of iron nitrosyl hemoglobin detectable by electron paramagnetic resonance spectroscopy.
16 absorption, magnetic circular dichroism, and electron paramagnetic resonance spectroscopy.
17 fractionated, and EPFRs on PM quantified by electron paramagnetic resonance spectroscopy.
18 (SOD)-inhibitable cytochrome c reduction or electron paramagnetic resonance spectroscopy.
19 ity was determined using saturation transfer electron paramagnetic resonance spectroscopy.
20 mpound I was confirmed using low-temperature electron paramagnetic resonance spectroscopy.
21 tography, and Mn(II) binding was assessed by electron paramagnetic resonance spectroscopy.
22 d by site-directed spin-labeling methods and electron paramagnetic resonance spectroscopy.
23 examined by UV-visible, resonance Raman, and electron paramagnetic resonance spectroscopy.
24 xamined by conventional and power saturation electron paramagnetic resonance spectroscopy.
25 f yeast cytochrome c oxidase (Cox IVp) using electron paramagnetic resonance spectroscopy.
26 were studied by UV-visible spectroscopy and electron paramagnetic resonance spectroscopy.
27 loenzyme as determined by metal analyses and electron paramagnetic resonance spectroscopy.
28 ified in the corrinoid/iron-sulfur enzyme by electron paramagnetic resonance spectroscopy.
29 absorption, magnetic circular dichroism, and electron paramagnetic resonance spectroscopy.
30 ic emission spectroscopy metal analysis, and electron paramagnetic resonance spectroscopy.
31 apid thermal chemical vapor deposition, from electron paramagnetic resonance spectroscopy.
32 ich we confirmed by site-directed spin-label electron paramagnetic resonance spectroscopy.
33 of intermediates using X-ray diffraction and electron paramagnetic resonance spectroscopy.
34 bed by differential scanning calorimetry and electron paramagnetic resonance spectroscopy.
35 incides with copper transfer as monitored by electron paramagnetic resonance spectroscopy.
36 olution composition, which was verified with electron paramagnetic resonance spectroscopy.
37 centration of the radical intermediate using electron paramagnetic resonance spectroscopy.
38 ith the polar-end of a paramagnetic lipid by electron paramagnetic resonance spectroscopy.
39 rified using both chemical cross-linking and electron paramagnetic resonance spectroscopy.
40 iquinone radical, which was characterized by electron paramagnetic resonance spectroscopy.
41 ard-facing intermediate was identified using electron paramagnetic resonance spectroscopy.
42 imD, a binding mode confirmed in solution by electron paramagnetic resonance spectroscopy.
43 d characterized by UV-visible, Mossbauer and electron paramagnetic resonance spectroscopies.
44 absorption, magnetic circular dichroism, and electron paramagnetic resonance spectroscopies.
45 tic circular dichroism, resonance Raman, and electron paramagnetic resonance spectroscopies about the
49 Using a combination of X-ray absorption and electron paramagnetic resonance spectroscopies and varia
52 enhanced superoxide levels as determined by electron paramagnetic resonance spectroscopy and dihydro
57 variant D131H+E134H of HuHF were studied by electron paramagnetic resonance spectroscopy and gel per
59 flow (SF) absorption and rapid freeze quench electron paramagnetic resonance spectroscopy and has fai
60 After i.v. infusion of nitroxides, in vivo electron paramagnetic resonance spectroscopy and imaging
61 dysprosium(III) ions through multi-frequency electron paramagnetic resonance spectroscopy and other t
66 ther with pre-steady state kinetic analyses, electron paramagnetic resonance spectroscopy and single
68 ryotic mechanosensitive channel (MscL) using electron paramagnetic resonance spectroscopy and site-di
70 orescence of Singlet Oxygen Sensor Green, by electron paramagnetic resonance spectroscopy and the ind
71 roperties of FA and FB were characterized by electron paramagnetic resonance spectroscopy and time-re
73 haracterized using high-frequency and -field electron paramagnetic resonance spectroscopy and UV-visi
74 ystem II (PSII) were investigated in vivo by electron paramagnetic resonance spectroscopy and variabl
76 manganese cofactors were identified by using electron paramagnetic resonance spectroscopy and were qu
77 combining structure determination with EPR (electron paramagnetic resonance) spectroscopy and simula
78 , is widely used for NO detection (mainly by electron paramagnetic resonance spectroscopy) and for mo
79 ped-flow UV-visible, and rapid-freeze-quench electron paramagnetic resonance spectroscopies, and anae
80 I by UV-visible spectra, circular dichroism, electron paramagnetic resonance spectroscopies, and by x
81 le, resonance Raman, and rapid freeze-quench electron paramagnetic resonance spectroscopies, and spec
82 zed by X-ray absorption spectroscopy, X-band electron paramagnetic resonance spectroscopy, and (57)Fe
83 , a chemical assay, magnetic susceptibility, electron paramagnetic resonance spectroscopy, and absorp
84 of ischemic murine hippocampal neurons using electron paramagnetic resonance spectroscopy, and also t
85 in membranes, using functorial measurements, electron paramagnetic resonance spectroscopy, and comput
86 ceptibility measurement, cyclic voltammetry, electron paramagnetic resonance spectroscopy, and densit
87 erated in the presence of NO was shown using electron paramagnetic resonance spectroscopy, and format
88 Nitric oxide production was documented by electron paramagnetic resonance spectroscopy, and found
89 No metmyoglobin formation was detected by electron paramagnetic resonance spectroscopy, and micros
90 ere, we combine site-directed spin labeling, electron paramagnetic resonance spectroscopy, and molecu
91 ic oxide-generated radicals were assessed by electron paramagnetic resonance spectroscopy, and protei
93 d argon and characterized by IR, UV-vis, and electron paramagnetic resonance spectroscopy as well as
96 stals were analyzed by UV-vis absorption and electron paramagnetic resonance spectroscopies before an
97 ] cluster were detected in hydrogenase II by electron paramagnetic resonance spectroscopy, but amino
98 le electron-electron resonance (DEER) pulsed electron paramagnetic resonance spectroscopy by measurin
99 ric oxide, and peroxynitrite was measured by electron paramagnetic resonance spectroscopy, chemilumin
100 and magnitude of NO generation from nitrite, electron paramagnetic resonance spectroscopy, chemilumin
101 sformation of organic nitrate, studies using electron paramagnetic resonance spectroscopy, chemilumin
102 antitative importance in biological systems, electron paramagnetic resonance spectroscopy, chemilumin
107 y mass spectrometry, cyclic voltammetry, and electron paramagnetic resonance spectroscopy, coupled wi
108 he yield of tyrosyl formation measured using electron paramagnetic resonance spectroscopy decreased s
109 UV-visible, magnetic circular dichroism, and electron paramagnetic resonance spectroscopies demonstra
110 min E-deficient and Ttp-/- mice, measured by electron paramagnetic resonance spectroscopy, demonstrat
111 Electron paramagnetic resonance spectroscopy demonstrate
113 Here we use electron paramagnetic resonance spectroscopy, electrophy
114 ng semiquinone free radicals, as detected by electron paramagnetic resonance spectroscopy (EPR alias
116 stance measurement in the nanometer range by electron paramagnetic resonance spectroscopy (EPR) in co
117 ed for sample packing in rapid freeze-quench electron paramagnetic resonance spectroscopy (EPR) kinet
118 ated under dilute solution conditions, using electron paramagnetic resonance spectroscopy (EPR) to de
121 igated using atomic absorption spectroscopy, electron paramagnetic resonance spectroscopy (EPR), and
122 and have studied the role of Trp(208) using electron paramagnetic resonance spectroscopy (EPR), muta
123 lectivity studies, catalytic lifetime tests, electron paramagnetic resonance spectroscopy (EPR), nega
124 xamined by conventional and power saturation electron paramagnetic resonance spectroscopy (EPR).
125 icrylhydrazyl (DPPH) assay and by the use of electron paramagnetic resonance spectroscopy (EPR).
126 f the trapped intermediate) by Mossbauer and electron paramagnetic resonance spectroscopies establish
127 tography, Mn(II) competition titrations, and electron paramagnetic resonance spectroscopy establish t
128 or this phenomenon, site-directed spin label electron paramagnetic resonance spectroscopy experiments
130 genesis, molecular dynamics simulations, and electron paramagnetic resonance spectroscopy identify a
134 a nitroxide free radical and investigated by electron paramagnetic resonance spectroscopy in the abse
135 ing (including single crystal measurements), electron paramagnetic resonance spectroscopy (including
139 Site-directed spin labeling combined with electron paramagnetic resonance spectroscopy is a powerf
141 haracterized by spin probing continuous wave electron paramagnetic resonance spectroscopy is reminisc
143 mmunological analysis and nitroxide-scanning electron paramagnetic resonance spectroscopy, it is show
148 sing low-temperature and ambient-temperature electron paramagnetic resonance spectroscopy of H(2)O(2)
151 pacity of studied oils was also confirmed by electron paramagnetic resonance spectroscopy of superoxi
152 further explain our findings on the basis of electron paramagnetic resonance spectroscopy of the Cr(I
159 esult was confirmed by depth measurements by electron paramagnetic resonance spectroscopy on several
160 here use double site-directed spin-labeling electron paramagnetic resonance spectroscopy on the bact
161 rystallography, four (4+, 6+, 7+, and 8+) by electron paramagnetic resonance spectroscopy, one (7+) b
164 absorption, near-UV circular dichroism, and electron paramagnetic resonance spectroscopy provide evi
165 dized protein and O2 with reduced protein by electron paramagnetic resonance spectroscopy, providing
172 nce analysis, similar to that performed with electron paramagnetic resonance spectroscopy, revealed t
176 C1)) and the principal g-factors measured by electron paramagnetic resonance spectroscopy (rho(C1) on
178 nalysis, absorption, circular dichroism, and electron paramagnetic resonance spectroscopies show that
189 l tubular cavities, and variable-temperature electron paramagnetic resonance spectroscopy shows that
191 al absorption spectroscopy and freeze-quench electron paramagnetic resonance spectroscopy support the
193 ytical methods in concert with Mossbauer and electron paramagnetic resonance spectroscopies, the prot
194 l hydrogen bond in photosystem II and, using electron paramagnetic resonance spectroscopy, the therma
196 from Cmpd I was shown by rapid freeze-quench electron paramagnetic resonance spectroscopy to be a tyr
197 We used site-directed spin-labeling and electron paramagnetic resonance spectroscopy to characte
203 this issue establishes a method using pulse electron paramagnetic resonance spectroscopy to determin
205 viously used site-directed spin labeling and electron paramagnetic resonance spectroscopy to establis
206 -steady-state kinetics, motility assays, and electron paramagnetic resonance spectroscopy to examine
207 , we carried out site-directed spin-labeling electron paramagnetic resonance spectroscopy to examine
209 Here, we use site-directed spin labeling and electron paramagnetic resonance spectroscopy to identify
211 nd double electron-electron resonance (DEER) electron paramagnetic resonance spectroscopy to identify
212 is study, we use site-directed spin-labeling electron paramagnetic resonance spectroscopy to investig
213 nd hyperfine sublevel correlation (HYSCORE)) electron paramagnetic resonance spectroscopy to investig
214 ic methanethiosulfonate spin-label, and used electron paramagnetic resonance spectroscopy to measure
215 We have used site-directed spin-labeling and electron paramagnetic resonance spectroscopy to monitor
216 eling of recombinant tau in conjunction with electron paramagnetic resonance spectroscopy to obtain s
217 port on the use of time-resolved optical and electron paramagnetic resonance spectroscopy to probe si
218 ave used visible absorbance spectroscopy and electron paramagnetic resonance spectroscopy to probe th
219 ibited form of the bovine enzyme is shown by electron paramagnetic resonance spectroscopy to result i
220 In the present work, we use UV/visible and electron paramagnetic resonance spectroscopy to show tha
222 udy, we used site-directed spin labeling and electron paramagnetic resonance spectroscopy to study th
224 ed the site-directed spin labeling method of electron paramagnetic resonance spectroscopy to the pro-
225 cular dichroism and site-directed spin label electron paramagnetic resonance spectroscopy, to show ho
226 powder x-ray diffraction and laser Raman and electron paramagnetic resonance spectroscopies-to show t
227 nel (hHv1) in its resting conformation using electron paramagnetic resonance spectroscopy together wi
229 na in a bis-copper six-porphyrin nanoring by electron paramagnetic resonance spectroscopy via measure
230 ce for one such intermediate was provided by electron paramagnetic resonance spectroscopy via photoly
231 ies associated with the oxidation of copper, electron paramagnetic resonance spectroscopy was employe
234 tigate the mechanism of maltose stimulation, electron paramagnetic resonance spectroscopy was used to
237 of oxygen-derived free radicals (measured by electron paramagnetic resonance spectroscopy) was attenu
241 surements, inelastic neutron scattering, and electron paramagnetic resonance spectroscopy, we have in
246 Using a combination of X-ray absorption and electron paramagnetic resonance spectroscopy, we show th
249 , fluorescence resonance energy transfer and electron paramagnetic resonance spectroscopy were used t
250 ng at amino acids 101, 105-109, 111, 112 and electron paramagnetic resonance spectroscopy were used t
251 vasodilatation [FMD]) and oxidative stress (electron paramagnetic resonance spectroscopy) were measu
252 Lipid radical formation was detected by electron paramagnetic resonance spectroscopy with in viv
254 Here, we use time-resolved, full-spectrum electron paramagnetic resonance spectroscopy, with tempe
256 ray crystal structures, variable-temperature electron paramagnetic resonance spectroscopy, zero-field
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