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1 ually activated region (measured by arterial spin labeling).
2 nsory cortex activity (quantitative arterial spin labeling).
3 images and to perfusion images from arterial spin labeling.
4 e thiosulfonate spin label for site-directed spin labeling.
5 erfusion decrement using continuous arterial spin labeling.
6 cosahedral protein cages using site-directed spin labeling.
7 nanosecond backbone motions by site-directed spin labeling.
8 es into calmodulin by means of site-directed spin labeling.
9 n overexpression of holo-protein followed by spin labeling.
10 ssion imaging both with and without arterial spin labeling.
11 and C2B) were determined using site-directed spin labeling.
12 hia coli, were investigated by site-directed spin labeling.
13  the Ton box was examined with site-directed spin labeling.
14 s on T4 lysozyme introduced by site-directed spin labeling.
15 seudo-continuous magnetic resonance-arterial spin labeling 20 +/- 6 hours before and after TMS treatm
16                             In site-directed spin labeling, a covalently attached nitroxide probe con
17                             In site-directed spin labeling, a nitroxide-containing side chain is intr
18 h the undocking of this region proposed from spin-labeling analyses.
19                   Here, we use site-directed spin labeling and a novel total internal reflection fluo
20 ealthy volunteers were scanned with arterial spin labeling and a separate 15 with BOLD.
21                                     Arterial spin labeling and asymmetric spin echo sequences measure
22                                Site-directed spin labeling and both continuous wave (CW) and pulsed E
23        We have quantified both site-directed spin labeling and dehydroalanine formation.
24                  Here we report a systematic spin labeling and double electron electron resonance (DE
25                 In this study, site-directed spin labeling and double electron-electron resonance spe
26  structures in a mechanistic context, we use spin labeling and double electron-electron resonance spe
27  the cytoplasmic surface using site-directed spin labeling and double electron-electron resonance spe
28 hyl-based labels, approach for site-directed spin labeling and efficient immobilization procedure tha
29                   Here we used site-directed spin labeling and electron paramagnetic resonance (EPR)
30 a prokaryotic homologue, using site-directed spin labeling and electron paramagnetic resonance (EPR)
31                    Here we use site-directed spin labeling and electron paramagnetic resonance (EPR)
32  previously been identified by site-directed spin labeling and electron paramagnetic resonance (EPR)
33 ding cleft of myosin, based on site-directed spin labeling and electron paramagnetic resonance (EPR)
34 the substituted domains using thiol-specific spin labeling and electron paramagnetic resonance (EPR)
35 ious compositions, and initial site-directed spin labeling and electron paramagnetic resonance (EPR)
36                 In this study, site-directed spin labeling and electron paramagnetic resonance (SDSL-
37 stance restraints derived from site-directed spin labeling and electron paramagnetic resonance (SDSL-
38                                Here, we used spin labeling and electron paramagnetic resonance spectr
39                   Here, we use site-directed spin labeling and electron paramagnetic resonance spectr
40        We have previously used site-directed spin labeling and electron paramagnetic resonance spectr
41                                Site-directed spin labeling and electron paramagnetic resonance spectr
42  (KvAP) at 0 millivolts, using site-directed spin labeling and electron paramagnetic resonance spectr
43         In this study, we used site-directed spin labeling and electron paramagnetic resonance spectr
44                        We used site-directed spin labeling and electron paramagnetic resonance to ana
45 sly established the utility of site-directed spin labeling and electron paramagnetic resonance to det
46                                Site-directed spin labeling and electron paramagnetic resonance were u
47 onal changes were investigated by systematic spin labeling and EPR analysis.
48                          Using site-directed spin labeling and EPR distance measurement we show that
49                   We have used site-directed spin labeling and EPR spectroscopy to detect structural
50 e-mediated misfolding, we used site-directed spin labeling and EPR spectroscopy to generate a three-d
51              Here we have used site-directed spin labeling and EPR spectroscopy to probe the molecula
52                                Site-directed spin labeling and EPR spectroscopy were used to map two
53 changes in loop C, measured by site-directed spin labeling and EPR spectroscopy, reveal immobilizatio
54                          Using site-directed spin labeling and EPR spectroscopy, we show that the ove
55  yeast, was investigated using site-directed spin labeling and EPR spectroscopy.
56            Here we developed a site-directed spin labeling and EPR-based approach for determining the
57 e assessed using voxel-based pulsed arterial spin labeling and morphometric analyses and tested for a
58 in has been characterized using paramagnetic spin labeling and NMR.
59 consistent with the results of site-directed spin labeling and places the peptide backbone in the bil
60                                Site-specific spin labeling and pulsed dipolar ESR spectroscopy (PDS)
61                   We have used site-directed spin labeling and pulsed electron paramagnetic resonance
62                          Using site-directed spin labeling and pulsed electron-electron double resona
63                                Site-directed spin labeling and pulsed electron-electron double resona
64 SH2 and iSH2 of p85alpha using site-directed spin labeling and pulsed EPR.
65  The present study employs EPR site-directed spin labeling and relaxation methods to generate a mediu
66                                     Arterial spin labeling and seed-based resting state functional co
67                          Here, site-directed spin labeling and simulated annealing were used to locat
68 ng two biophysical techniques: site-directed spin labeling and surface plasmon resonance.
69          Participants underwent two arterial spin labeling and two blood oxygen level-dependent scans
70 terized using a combination of site-directed spin labeling and vesicle sedimentation.
71                                Site-directed spin-labeling and electron paramagnetic resonance are po
72                        We used site-directed spin-labeling and electron paramagnetic resonance spectr
73                   We have used site-directed spin-labeling and electron paramagnetic resonance spectr
74                                Site-directed spin-labeling and EPR spectroscopy were carried out for
75                                Site-directed spin-labeling and Forster resonance energy transfer expe
76                                              Spin-labeling and multifrequency EPR spectroscopy were u
77 en; mean age, 72.9 years) underwent arterial spin-labeling and volumetric T1-weighted structural MR i
78 re prepared by overexpression of apoprotein, spin labeling, and reconstitution with hemin.
79 netic resonance imaging methods for Arterial Spin Labeling (ASL) and Blood Oxygenation Level Dependen
80                  Purpose To compare arterial spin labeling (ASL) data between low- and high-grade bra
81                                     Arterial spin labeling (ASL) is a magnetic resonance (MR) imaging
82 collateral vessels identified using arterial spin labeling (ASL) magnetic resonance imaging, a techni
83 the emergence and potential role of arterial spin labeling (ASL) MRI, which measures cerebral blood f
84               Here, we investigated arterial spin labeling (ASL) perfusion CMR as a novel approach to
85 ate pattern recognition analysis of arterial spin labeling (ASL) perfusion maps can be used for class
86                                     Arterial spin labeling (ASL) provides an endogenous and completel
87  diffusion tensor imaging (DTI) and arterial spin labeling (ASL) to discriminate patients with early
88 ical magnetic resonance scans using arterial spin labeling (ASL) were performed to study the haemodyn
89 plementary neuroimaging techniques: arterial spin labeling (ASL), blood oxygen level-dependent (BOLD)
90 nges, as assessed using whole-brain arterial spin labeling (ASL), during tDCS applied to the left DLP
91 nsor imaging (DTI) acquisitions and arterial spin labeling (ASL).
92 ents obtained with different pulsed arterial spin-labeling (ASL) magnetic resonance (MR) imaging meth
93 anges after enzyme activation, site-directed spin labeling at amino acids 101, 105-109, 111, 112 and
94  of brain activity using continuous arterial spin labeling based functional magnetic resonance imagin
95 ful tool in the development of site-directed spin labeling by resolving rotamers of the nitroxide spi
96 e that restraints derived from site-directed spin labeling can contribute significantly to defining t
97 ructure determination, but EPR site-directed spin-labeling can provide a detailed medium-resolution v
98 the novel application of continuous arterial spin-labeling (CASL) magnetic resonance imaging (MRI) fo
99 l blood flow (CBF) using continuous arterial spin-labeling (CASL) MRI.
100                                Site-directed spin labeling combined with electron paramagnetic resona
101 omer, called globulomer, using site-directed spin labeling complemented by other techniques.
102 pin resonance spectroscopy and site-specific spin-labeling confirm that the Tsr HAMP maintains a four
103 We used circular dichroism and site-directed spin labeling coupled with electron paramagnetic resonan
104  relating crystallographic and site-directed spin labeling data, and hence comparing crystal and solu
105 NMR studies in combination with paramagnetic spin labeling demonstrate that this interaction is media
106 , MDR769, are characterized by site-directed spin labeling double electron-electron resonance spectro
107                             Here, we combine spin-labeling double electron-electron resonance (DEER)
108 S I) complex was studied using site-specific spin labeling electron paramagnetic resonance (EPR) spec
109 l activity assays coupled with site-directed spin labeling electron paramagnetic resonance (EPR) spec
110                                Site-directed spin labeling electron paramagnetic resonance methods ha
111                          Using site-directed spin labeling electron paramagnetic resonance spectrosco
112                                Site-directed spin labeling electron paramagnetic resonance spectrosco
113                 Here we report site-directed spin labeling electron paramagnetic resonance studies ex
114 terface were investigated with site-specific spin labeling electron paramagnetic resonance.
115          In this study, we use site-directed spin-labeling electron paramagnetic resonance spectrosco
116  these studies, we carried out site-directed spin-labeling electron paramagnetic resonance spectrosco
117             We here use double site-directed spin-labeling electron paramagnetic resonance spectrosco
118                                Site-directed spin-labeling electron paramagnetic resonance spectrosco
119               Here, we combine site-directed spin labeling, electron paramagnetic resonance spectrosc
120                                Site-directed spin labeling EPR (SDSL-EPR) was used to determine the s
121                  A hybrid approach combining spin labeling EPR and cryoelectron microscopy imaging at
122 tide by using a combination of site directed spin labeling EPR and homology modeling and molecular dy
123                                Site-directed spin labeling EPR spectroscopy was used to study the ope
124                                        Using spin labeling EPR spectroscopy, we studied a 38-residue
125 ructural biology studies using site-directed spin labeling EPR techniques.
126 ing fluorescence quenching and site-directed spin labeling EPR.
127 omplex were investigated using site-directed spin labeling EPR.
128                  High-pressure site-directed spin-labeling EPR (SDSL-EPR) was developed recently to m
129                                        Using spin-labeling EPR, trans-SNARE complex formation was mon
130 tigated by solid-state NMR and site-directed spin labeling/EPR with a synthetic peptide, hCB(1)(T377-
131          These findings, in combination with spin-labeling/EPR spectroscopic measurements in reconsti
132 amate (Glu) and glutamine (Gln) and arterial spin labeling evaluation for rCBF.
133 -binding domain of apo-MntR, a site-directed spin labeling experiment was performed on a mutant of Mn
134 re then directly compared with site-directed spin labeling experimental results obtained by preparing
135 y a series of tetraalkylammonium ions and 2) spin labeling experiments.
136 which was further validated by site-directed spin labeling experiments.
137                                              Spin-labeling experiments show that the complex of the f
138                                      NMR and spin-labeling experiments showed that GH5_pMut bound to
139  of W14A determined by NMR and site-directed spin labeling features a flexible kink that points out o
140 dient-recalled echo to assess CMBs, arterial spin labeling for CBF, and T1- and T2-weighted imaging f
141 n healthy individuals (n=23) during arterial spin labeling functional magnetic resonance imaging (fMR
142                    Pseudocontinuous arterial spin labeling functional magnetic resonance imaging and
143 ces the sensory experience, we used arterial spin labeling functional magnetic resonance imaging to a
144                               Using arterial spin labeling functional magnetic resonance imaging, we
145 tivity, which was assessed by using arterial spin-labeling functional magnetic resonance imaging 4 h
146  and disease parameters, we used an arterial-spin-labeling functional MRI stress paradigm in 36 MS pa
147                                Site-directed spin labeling has been employed in this work to address
148  resonance in conjunction with site-directed spin labeling has been used to probe natural conformatio
149                                Site-directed spin labeling has previously been employed to detect con
150                                Site-directed spin labeling has qualitatively shown that a key event d
151 ce (DEER), in conjunction with site-directed spin-labeling, has emerged in the past decade as a power
152                   Pseudo-continuous arterial spin labeling imaging was used to measure resting region
153 clear magnetic resonance, combining arterial spin-labeling imaging of perfusion, and (31)P-spectrosco
154                    Here we use site-directed spin labeling in combination with circular dichroism and
155 eutral pH was investigated via site-directed spin labeling in combination with conventional electron
156                                Site-directed spin labeling in combination with double electron-electr
157                                Site-directed spin labeling in combination with EPR is a powerful meth
158   A goal in the development of site-directed spin labeling in proteins is to correlate the motion of
159 are similar to the WT protein, site-directed spin labeling in solution reveals additional conformatio
160 pin resonance spectroscopy and site-directed spin labeling in what to our knowledge is a new approach
161         We have therefore used site-specific spin-labeling in conjunction with EPR distance measureme
162        In the current studies, site-directed spin labeling, in combination with electron paramagnetic
163       Crosslinking to TonB and site-directed spin labeling indicated that the Ton box of BtuB undergo
164 copy (EPR) in combination with site-directed spin labeling is a very powerful tool to monitor the str
165 copy (PDS) in combination with site-directed spin labeling is unique in providing nanometer-range dis
166                                Site-directed spin labeling is used to determine the orientation and d
167                          Here, site-directed spin labeling is used to examine a conformational equili
168                          Continuous arterial spin-labeling is a noninvasive MRI method capable of mea
169 uble resonance (PELDOR), using site-directed spin labeling, is most commonly employed to accurately d
170 total blood flow to the retina with Arterial Spin Labeling Magnetic Resonance Imaging (ASL-MRI) has b
171 r for two imaging modalities-pulsed arterial spin labeling magnetic resonance imaging (PASL-MRI) and
172                                     Arterial spin labeling magnetic resonance imaging was used to col
173 c flow velocity was quantified by performing spin labeling measurements as a function of postlabeling
174 RE is confirmed in solution by site-directed spin labeling measurements.
175                 We applied the site-directed spin labeling method of electron paramagnetic resonance
176                      Using the site-directed spin labeling method of electron paramagnetic resonance
177 rane insertion by applying the site-directed spin labeling method of EPR to 13 different amino acid l
178 n by using NMR residual dipolar coupling and spin labeling methods and is based on available crystal
179  multisection continuous and pulsed arterial spin-labeling methods at 3.0 T showed a 33% improvement
180                We used cysteine-scanning and spin-labeling methods to prepare singly spin labeled rec
181 ion-recovery electron paramagnetic resonance spin-labeling methods, in which bimolecular collisions o
182      Guided by these parameters, an arterial spin labeling MR imaging approach was adapted to measure
183                                     Arterial spin-labeling MR imaging showed regional hypoperfusion w
184 etinas were imaged using continuous arterial spin labeling MRI at 90 x 90 x 1500 microm.
185 but no agonists, we acquired pulsed arterial spin labeling MRI at the end of each treatment period.
186 absolute myocardial blood flow (MBF) using a spin-labeling MRI (SL-MRI) method after transplantation
187                        We then used arterial spin-labeling MRI to noninvasively measure CBF and asses
188                                              Spin labeling nucleic acids at specific sites requires t
189                                Site-directed spin labeling of Cys-299 reveals a flexible hinge-like d
190 ce tools that rely on site-specific electron spin labeling of Deltatau187.
191                        We used site-directed spin labeling of N-WASP peptides in conjunction with met
192 s and distance restraints from site-specific spin labeling of Pdx has been applied.
193                  Here, we used site-directed spin labeling of recombinant tau in conjunction with ele
194                          Using site-directed spin labeling of Ser(155)Cys with a nitroxide side chain
195 ed experimental data involving site-directed spin labeling of the intact RLC bound to the two-headed
196 f monocysteine variants and by site-specific spin labeling of the Q-helix followed by EPR-based inter
197                                Site-specific spin labeling of the recombinant protein allowed the mea
198                                Site-directed spin labeling of the SCAMP-E peptide indicates that the
199                                Site-directed spin labeling of this peptide shows that the position an
200                                Site-directed spin-labeling of proteins whereby the spin-label methyl
201                   We have used site-specific spin-labeling of single cysteine mutations within a wate
202           We used pulsed continuous arterial spin labeling (pCASL), a perfusion magnetic resonance im
203                   Here, we combined arterial spin labeling perfusion and blood oxygen level-dependent
204                                     Arterial spin labeling perfusion and blood-oxygen level-dependent
205 ndividuals with schizophrenia using arterial spin labeling perfusion MRI.
206 ood-oxygenation-level-dependent and arterial-spin-labeling perfusion contrasts to investigate the rel
207  (CBF) was measured with continuous arterial spin-labeling perfusion magnetic resonance (MR) imaging
208 noninvasive neuroimaging technique, arterial spin-labeling perfusion MRI, to measure cerebral blood f
209  and derivatives thereof using site-directed spin labeling, pressure-resolved double electron-electro
210 three-dimensional pulsed-continuous arterial spin labeling provided measurements of regional cerebral
211                        We exploited arterial spin-labeling quantitative perfusion imaging and a newly
212                            Moreover, NMR and spin-labeling results from the study of the nucleosome i
213                         Recent site-directed spin labeling (SDSL) and double electron-electron resona
214  context of the ribozyme using site-directed spin labeling (SDSL) and electron paramagnetic resonance
215                   We have used site-directed spin labeling (SDSL) and electron paramagnetic resonance
216                          Here, site-directed spin labeling (SDSL) and electron paramagnetic resonance
217 ombine ESEEM spectroscopy with site-directed spin labeling (SDSL) and X-ray crystallography in order
218 using circular dichroism (CD), Site-Directed Spin Labeling (SDSL) coupled to EPR spectroscopy, and en
219                                Site-directed spin labeling (SDSL) electron paramagnetic resonance (EP
220                                Site-directed spin labeling (SDSL) electron paramagnetic resonance (EP
221                    Here, using site-directed spin labeling (SDSL) electron paramagnetic resonance (EP
222      For this study, we used a site-directed spin labeling (SDSL) experimental approach to investigat
223                                Site-directed spin labeling (SDSL) has potential for mapping protein f
224 osecond backbone dynamics with site-directed spin labeling (SDSL) in soluble proteins has been well e
225    Spectroscopic studies using site-directed spin labeling (SDSL) indicate that the N-terminus of Btu
226                          Here, site-directed spin labeling (SDSL) is used to show that a range of sol
227                The traditional site-directed spin labeling (SDSL) method, which utilizes cysteine res
228 en carried out using site directed nitroxide spin labeling (SDSL) of cysteine residues.
229                                Site-directed spin labeling (SDSL) studies revealed that C265 lies clo
230          In the present study, site-directed spin labeling (SDSL) together with double electron-elect
231                  The method of site-directed spin labeling (SDSL) utilizes a stable nitroxide radical
232                          Here, site-directed spin labeling (SDSL) was used to determine the position
233                                Site-directed spin labeling (SDSL) was used to examine and compare tra
234                                Site-directed spin labeling (SDSL) was used to explore the structural
235 etic resonance (EPR) method of site-directed spin labeling (SDSL) with double electron-electron reson
236                             In site-directed spin labeling (SDSL), a nitroxide moiety containing a st
237 he hemolytic anemia phenotype, site-directed spin labeling (SDSL), in combination with continuous wav
238                             In site-directed spin labeling (SDSL), local structural and dynamic infor
239                                Site-directed spin labeling (SDSL), the site-specific incorporation of
240 two mutant cycle analysis with site-directed spin labeling (SDSL).
241                             With an arterial spin labeling sequence, three networks were first identi
242 e-chain interactions, and that site-directed spin labeling should be a powerful means of monitoring c
243  photoconversions monitored by site-directed spin labeling show that opposite structural changes in h
244 or resonances more than 20 residues from the spin-labeling site.
245 ctive insights into these processes, but new spin-labeling strategies are needed.
246 ng the phenomena which they measure, but our spin labeling strategy has reported common kinetic theme
247  binding interface in MHV with site-directed spin labeling studies consistent with a model in which t
248                    Remarkably, site-directed spin labeling studies reveal that these fibrils possess
249 ng environments encountered in site-directed spin labeling studies.
250  the use of this technique for site-directed spin-labeling studies of biologically relevant samples,
251           The results of these site-directed spin-labeling studies reveal that phosphorylation at a d
252                                              Spin-labeling studies show that residue A62 of MMOB is l
253                                Site-directed spin-labeling studies showed that the N-terminus of the
254               Here we describe site-directed spin-labeling studies that identify interactions of LF w
255                                            A spin-labeling study of interactions of a fusion peptide
256                  The method relies on sparse spin-labeling, supplemented by deuteration of protein an
257 d with echo-planar imaging using an arterial spin labeling technique and a custom-made eye coil at 7
258 s in DNA are studied using the site-directed spin labeling technique.
259 tem to explore and enhance the site-directed spin labeling technique.
260                        A continuous arterial spin-labeling technique with an amplitude-modulated cont
261 easured using the pseudo-continuous arterial-spin-labeling technique with background suppression and
262                                Site directed spin-labeling technology has enabled the insertion of ni
263                             In site-directed spin labeling, the relative solvent accessibility of spi
264 simulations were combined with site-directed spin labeling to define its structure and dynamics.
265                   Here, we use site-specific spin labeling to demonstrate that relaxation enhancement
266      We generated seven mutants suitable for spin labeling to enable application of pulsed EPR techni
267 iol-specific cross-linking and site-directed spin labeling to identify specific protein-protein assoc
268                  Here, we used site-directed spin labeling to map the conformation of a pRNA three-wa
269 e imaging based on pseudocontinuous arterial spin labeling to measure CBF at normocapnia (ie, breathi
270 a placebo-controlled study, we used arterial spin labeling to measure IN-OT-induced changes in restin
271 e validity of this model using site-directed spin labeling to obtain long-range distance information
272 n resonance spectroscopy using site-directed spin labeling to understand the structure and interfacia
273                 This work points the way for spin-labeling to investigate oligonucleotide-protein com
274 tudy utilizes site-directed fluorescence and spin-labeling to map out the membrane docking surface of
275 ce spectroscopy, together with site-directed spin labeling, to investigate the structural features of
276                        We used site-directed spin-labeling together with electron spin-resonance line
277                                Site-directed spin labeling utilizes site-specific attachment of a sta
278  performed using velocity-selective arterial spin labeling (VSASL) and 3D image acquisition with whol
279                                Site-directed spin labeling was carried out on the C2 domain of cytoso
280 thod based on the technique of site-directed spin labeling was developed to experimentally map shapes
281                          Continuous arterial spin labeling was interleaved with TMS to directly asses
282                                Site-directed spin labeling was used to determine the membrane orienta
283                          Here, site-directed spin labeling was used to examine the complex formed bet
284                          Here, site-directed spin labeling was used to examine the structural basis f
285                          Here, site-directed spin labeling was used to generate models for the soluti
286 emic clamp sessions in which pulsed arterial spin labeling was used to measure regional cerebral bloo
287 lectron paramagnetic resonance site-directed spin labeling was used to monitor loss of tertiary struc
288                                Site-directed spin labeling was used to obtain bilayer depth restraint
289                          Here, site-directed spin labeling was used to probe the solution structures
290 gnetic resonance imaging technique (arterial spin labeling) was used to quantify spatial pulmonary bl
291                          Using site-directed spin labeling, we demonstrated that the pressure- and te
292                          Using site-directed spin labeling, we found that the local structure around
293                               Using arterial spin labeling, we measured resting-state cerebral blood
294 ectroscopy in combination with site-directed spin labeling, we show that familial PD-associated varia
295 mages and perfusion images by using arterial spin labeling were obtained for comparison.
296              The cysteine mutations used for spin-labeling were distributed throughout the cytosolic
297                                 MRI arterial spin labeling, white matter hyperintensities (WMHs) and
298 oped an approach that combines site-directed spin labeling with continuous wave and pulsed EPR to inv
299                  Here, we used site-directed spin labeling with power saturation electron paramagneti
300 el system, we introduce a method of parallel spin-labeling with paramagnetic and diamagnetic labels a

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