ライフサイエンスコーパス: spin labeling

1 nsory cortex activity (quantitative arterial spin labeling).

2 ually activated region (measured by arterial spin labeling).

3 e thiosulfonate spin label for site-directed spin labeling.

4 erfusion decrement using continuous arterial spin labeling.

5 cosahedral protein cages using site-directed spin labeling.

6 nanosecond backbone motions by site-directed spin labeling.

7 es into calmodulin by means of site-directed spin labeling.

8 cerebral perfusion was examined by arterial 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 images and to perfusion images from arterial spin labeling.

13 hia coli, were investigated by site-directed spin labeling.

14 the Ton box was examined with site-directed spin labeling.

15 s on T4 lysozyme introduced by site-directed spin labeling.

16 seudo-continuous magnetic resonance-arterial spin labeling 20 +/- 6 hours before and after TMS treatm

17 In site-directed spin labeling, a covalently attached nitroxide probe con

18 In site-directed spin labeling, a nitroxide-containing side chain is intr

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 the substituted domains using thiol-specific spin labeling and electron paramagnetic resonance (EPR)

30 ious compositions, and initial site-directed spin labeling and electron paramagnetic resonance (EPR)

31 Here we used site-directed spin labeling and electron paramagnetic resonance (EPR)

32 a prokaryotic homologue, using site-directed spin labeling and electron paramagnetic resonance (EPR)

33 Here we use site-directed spin labeling and electron paramagnetic resonance (EPR)

34 previously been identified by site-directed spin labeling and electron paramagnetic resonance (EPR)

35 ding cleft of myosin, based on site-directed spin labeling and electron paramagnetic resonance (EPR)

36 come this problem by utilizing site-directed spin labeling and electron paramagnetic resonance (EPR)

37 In this study, site-directed spin labeling and electron paramagnetic resonance (SDSL-

38 This model is supported by site-directed spin labeling and electron paramagnetic resonance spectr

39 Here, we used spin labeling and electron paramagnetic resonance spectr

40 Here, we use site-directed spin labeling and electron paramagnetic resonance spectr

41 We have previously used site-directed spin labeling and electron paramagnetic resonance spectr

42 Site-directed spin labeling and electron paramagnetic resonance spectr

43 (KvAP) at 0 millivolts, using site-directed spin labeling and electron paramagnetic resonance spectr

44 In this study, we used site-directed spin labeling and electron paramagnetic resonance spectr

45 e distance data gathered using site-directed spin labeling and electron paramagnetic resonance spectr

46 We used site-directed spin labeling and electron paramagnetic resonance to ana

47 sly established the utility of site-directed spin labeling and electron paramagnetic resonance to det

48 Site-directed spin labeling and electron paramagnetic resonance were u

49 onal changes were investigated by systematic spin labeling and EPR analysis.

50 We have used site-directed spin labeling and EPR spectroscopy to detect structural

51 e-mediated misfolding, we used site-directed spin labeling and EPR spectroscopy to generate a three-d

52 Here we have used site-directed spin labeling and EPR spectroscopy to probe the molecula

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 dy support the possibility of using arterial spin labeling and pattern analysis of dynamic susceptibi

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 Site-directed spin labeling and pulsed electron-electron double resona

63 Using 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 Site-directed spin-labeling and EPR spectroscopy were carried out for

74 Previous spin-labeling and fluorescence resonance energy transfer

75 Site-directed spin-labeling and Forster resonance energy transfer expe

76 Spin-labeling and multifrequency EPR spectroscopy were u

77 Here we employ spin-labeling and pressure-resolved double electron-elec

78 ns in GPCR catalytic function; 2) the use of spin-labeling and variable-pressure electron paramagneti

79 en; mean age, 72.9 years) underwent arterial spin-labeling and volumetric T1-weighted structural MR i

80 re prepared by overexpression of apoprotein, spin labeling, and reconstitution with hemin.

81 netic resonance imaging methods for Arterial Spin Labeling (ASL) and Blood Oxygenation Level Dependen

82 Purpose To compare arterial spin labeling (ASL) data between low- and high-grade bra

83 Arterial spin labeling (ASL) is a magnetic resonance (MR) imaging

84 Arterial spin labeling (ASL) is a neuroimaging technique used to

85 collateral vessels identified using arterial spin labeling (ASL) magnetic resonance imaging, a techni

86 the emergence and potential role of arterial spin labeling (ASL) MRI, which measures cerebral blood f

87 Here, we investigated arterial spin labeling (ASL) perfusion CMR as a novel approach to

88 ate pattern recognition analysis of arterial spin labeling (ASL) perfusion maps can be used for class

89 Arterial spin labeling (ASL) provides an endogenous and completel

90 diffusion tensor imaging (DTI) and arterial spin labeling (ASL) to discriminate patients with early

91 graphy, carotid plaque imaging, and arterial spin labeling (ASL) to identify imaging parameters that

92 el-encoded multi-postlabeling delay arterial spin labeling (ASL) was used to separately quantify the

93 ical magnetic resonance scans using arterial spin labeling (ASL) were performed to study the haemodyn

94 Arterial spin labeling (ASL), as a non-invasive and non-contrast

95 plementary neuroimaging techniques: arterial spin labeling (ASL), blood oxygen level-dependent (BOLD)

96 nges, as assessed using whole-brain arterial spin labeling (ASL), during tDCS applied to the left DLP

97 nsor imaging (DTI) acquisitions and arterial spin labeling (ASL).

98 ents obtained with different pulsed arterial spin-labeling (ASL) magnetic resonance (MR) imaging meth

99 anges after enzyme activation, site-directed spin labeling at amino acids 101, 105-109, 111, 112 and

100 of brain activity using continuous arterial spin labeling based functional magnetic resonance imagin

101 ful tool in the development of site-directed spin labeling by resolving rotamers of the nitroxide spi

102 ructure determination, but EPR site-directed spin-labeling can provide a detailed medium-resolution v

103 the novel application of continuous arterial spin-labeling (CASL) magnetic resonance imaging (MRI) fo

104 l blood flow (CBF) using continuous arterial spin-labeling (CASL) MRI.

105 Site-directed spin labeling combined with electron paramagnetic resona

106 omer, called globulomer, using site-directed spin labeling complemented by other techniques.

107 pin resonance spectroscopy and site-specific spin-labeling confirm that the Tsr HAMP maintains a four

108 We used circular dichroism and site-directed spin labeling coupled with electron paramagnetic resonan

109 relating crystallographic and site-directed spin labeling data, and hence comparing crystal and solu

110 NMR studies in combination with paramagnetic spin labeling demonstrate that this interaction is media

111 , MDR769, are characterized by site-directed spin labeling double electron-electron resonance spectro

112 Here, we combine spin-labeling double electron-electron resonance (DEER)

113 S I) complex was studied using site-specific spin labeling electron paramagnetic resonance (EPR) spec

114 l activity assays coupled with site-directed spin labeling electron paramagnetic resonance (EPR) spec

115 Site-directed spin labeling electron paramagnetic resonance methods ha

116 Using site-directed spin labeling electron paramagnetic resonance spectrosco

117 Site-directed spin labeling electron paramagnetic resonance spectrosco

118 Here we report site-directed spin labeling electron paramagnetic resonance studies ex

119 these studies, we carried out site-directed spin-labeling electron paramagnetic resonance spectrosco

120 We here use double site-directed spin-labeling electron paramagnetic resonance spectrosco

121 In this study, we used site-directed spin-labeling electron paramagnetic resonance spectrosco

122 In this study, we use site-directed spin-labeling electron paramagnetic resonance spectrosco

123 Site-directed spin-labeling electron paramagnetic resonance spectrosco

124 Here, we combine site-directed spin labeling, electron paramagnetic resonance spectrosc

125 A hybrid approach combining spin labeling EPR and cryoelectron microscopy imaging at

126 Site directed spin labeling EPR and DEER (double electron-electron res

127 Site-directed spin labeling EPR spectroscopy was used to study the ope

128 Using spin labeling EPR spectroscopy, we studied a 38-residue

129 ructural biology studies using site-directed spin labeling EPR techniques.

130 ing fluorescence quenching and site-directed spin labeling EPR.

131 High-pressure site-directed spin-labeling EPR (SDSL-EPR) was developed recently to m

132 h STAM1 activates FAK, we used site-directed spin-labeling EPR spectroscopy-based studies coupled wit

133 e imaging, dynamic nuclear polarization, and spin-labeling EPR under in-cell conditions.

134 Using spin-labeling EPR, trans-SNARE complex formation was mon

135 tigated by solid-state NMR and site-directed spin labeling/EPR with a synthetic peptide, hCB(1)(T377-

136 These findings, in combination with spin-labeling/EPR spectroscopic measurements in reconsti

137 amate (Glu) and glutamine (Gln) and arterial spin labeling evaluation for rCBF.

138 -binding domain of apo-MntR, a site-directed spin labeling experiment was performed on a mutant of Mn

139 which was further validated by site-directed spin labeling experiments.

140 Spin-labeling experiments show that the complex of the f

141 NMR and spin-labeling experiments showed that GH5_pMut bound to

142 of W14A determined by NMR and site-directed spin labeling features a flexible kink that points out o

143 dient-recalled echo to assess CMBs, arterial spin labeling for CBF, and T1- and T2-weighted imaging f

144 tial of double-histidine (dHis)-based Cu(II) spin labeling for the identification of various conforma

145 n healthy individuals (n=23) during arterial spin labeling functional magnetic resonance imaging (fMR

146 Pseudocontinuous arterial spin labeling functional magnetic resonance imaging and

147 ces the sensory experience, we used arterial spin labeling functional magnetic resonance imaging to a

148 Using arterial spin labeling functional magnetic resonance imaging, we

149 tivity, which was assessed by using arterial spin-labeling functional magnetic resonance imaging 4 h

150 and disease parameters, we used an arterial-spin-labeling functional MRI stress paradigm in 36 MS pa

151 Site-directed spin labeling has been employed in this work to address

152 resonance in conjunction with site-directed spin labeling has been used to probe natural conformatio

153 Site-directed spin labeling has previously been employed to detect con

154 Site-directed spin labeling has qualitatively shown that a key event d

155 ce (DEER), in conjunction with site-directed spin-labeling, has emerged in the past decade as a power

156 Pseudo-continuous arterial spin labeling imaging was used to measure resting region

157 clear magnetic resonance, combining arterial spin-labeling imaging of perfusion, and (31)P-spectrosco

158 eutral pH was investigated via site-directed spin labeling in combination with conventional electron

159 Site-directed spin labeling in combination with double electron-electr

160 Site-directed spin labeling in combination with EPR is a powerful meth

161 A goal in the development of site-directed spin labeling in proteins is to correlate the motion of

162 are similar to the WT protein, site-directed spin labeling in solution reveals additional conformatio

163 pin resonance spectroscopy and site-directed spin labeling in what to our knowledge is a new approach

164 stituted synaptotagmin 1 using site-directed spin labeling in which we characterize the linker region

165 We have therefore used site-specific spin-labeling in conjunction with EPR distance measureme

166 In the current studies, site-directed spin labeling, in combination with electron paramagnetic

167 copy (EPR) in combination with site-directed spin labeling is a very powerful tool to monitor the str

168 lowing overexpression of the target protein, spin labeling is performed with E. coli or isolated oute

169 copy (PDS) in combination with site-directed spin labeling is unique in providing nanometer-range dis

170 Site-directed spin labeling is used to determine the orientation and d

171 Here, site-directed spin labeling is used to examine a conformational equili

172 Continuous arterial spin-labeling is a noninvasive MRI method capable of mea

173 uble resonance (PELDOR), using site-directed spin labeling, is most commonly employed to accurately d

174 total blood flow to the retina with Arterial Spin Labeling Magnetic Resonance Imaging (ASL-MRI) has b

175 r for two imaging modalities-pulsed arterial spin labeling magnetic resonance imaging (PASL-MRI) and

176 We acquired pulsed arterial spin labeling magnetic resonance imaging data in 44 gene

177 Arterial spin labeling magnetic resonance imaging was used to col

178 c flow velocity was quantified by performing spin labeling measurements as a function of postlabeling

179 RE is confirmed in solution by site-directed spin labeling measurements.

180 We applied the site-directed spin labeling method of electron paramagnetic resonance

181 Using the site-directed spin labeling method of electron paramagnetic resonance

182 rane insertion by applying the site-directed spin labeling method of EPR to 13 different amino acid l

183 n by using NMR residual dipolar coupling and spin labeling methods and is based on available crystal

184 multisection continuous and pulsed arterial spin-labeling methods at 3.0 T showed a 33% improvement

185 We used cysteine-scanning and spin-labeling methods to prepare singly spin labeled rec

186 ion-recovery electron paramagnetic resonance spin-labeling methods, in which bimolecular collisions o

187 Guided by these parameters, an arterial spin labeling MR imaging approach was adapted to measure

188 Arterial spin-labeling MR imaging showed regional hypoperfusion w

189 etinas were imaged using continuous arterial spin labeling MRI at 90 x 90 x 1500 microm.

190 but no agonists, we acquired pulsed arterial spin labeling MRI at the end of each treatment period.

191 absolute myocardial blood flow (MBF) using a spin-labeling MRI (SL-MRI) method after transplantation

192 We then used arterial spin-labeling MRI to noninvasively measure CBF and asses

193 Spin labeling nucleic acids at specific sites requires t

194 ce tools that rely on site-specific electron spin labeling of Deltatau187.

195 We used site-directed spin labeling of N-WASP peptides in conjunction with met

196 s and distance restraints from site-specific spin labeling of Pdx has been applied.

197 Here, we used site-directed spin labeling of recombinant tau in conjunction with ele

198 Using site-directed spin labeling of Ser(155)Cys with a nitroxide side chain

199 ed experimental data involving site-directed spin labeling of the intact RLC bound to the two-headed

200 f monocysteine variants and by site-specific spin labeling of the Q-helix followed by EPR-based inter

201 Site-specific spin labeling of the recombinant protein allowed the mea

202 Site-directed spin labeling of the SCAMP-E peptide indicates that the

203 We have used site-specific spin-labeling of single cysteine mutations within a wate

204 We used pulsed continuous arterial spin labeling (pCASL), a perfusion magnetic resonance im

205 subsequent protein expression, OM isolation, spin labeling, PELDOR experiment, and data analysis typi

206 Here, we combined arterial spin labeling perfusion and blood oxygen level-dependent

207 Arterial spin labeling perfusion and blood-oxygen level-dependent

208 ndividuals with schizophrenia using arterial spin labeling perfusion MRI.

209 hunting ranging from (37-60%) using arterial spin labeling perfusion.

210 ood-oxygenation-level-dependent and arterial-spin-labeling perfusion contrasts to investigate the rel

211 (CBF) was measured with continuous arterial spin-labeling perfusion magnetic resonance (MR) imaging

212 noninvasive neuroimaging technique, arterial spin-labeling perfusion MRI, to measure cerebral blood f

213 and derivatives thereof using site-directed spin labeling, pressure-resolved double electron-electro

214 three-dimensional pulsed-continuous arterial spin labeling provided measurements of regional cerebral

215 We exploited arterial spin-labeling quantitative perfusion imaging and a newly

216 Moreover, NMR and spin-labeling results from the study of the nucleosome i

217 Recent site-directed spin labeling (SDSL) and double electron-electron resona

218 context of the ribozyme using site-directed spin labeling (SDSL) and electron paramagnetic resonance

219 We have used site-directed spin labeling (SDSL) and electron paramagnetic resonance

220 Here, site-directed spin labeling (SDSL) and electron paramagnetic resonance

221 ombine ESEEM spectroscopy with site-directed spin labeling (SDSL) and X-ray crystallography in order

222 using circular dichroism (CD), Site-Directed Spin Labeling (SDSL) coupled to EPR spectroscopy, and en

223 Here, using site-directed spin labeling (SDSL) electron paramagnetic resonance (EP

224 Site-directed spin labeling (SDSL) electron paramagnetic resonance (EP

225 Site-directed spin labeling (SDSL) electron paramagnetic resonance (EP

226 Site-directed spin labeling (SDSL) ESR is a valuable tool to probe pro

227 For this study, we used a site-directed spin labeling (SDSL) experimental approach to investigat

228 Site-directed spin labeling (SDSL) has potential for mapping protein f

229 osecond backbone dynamics with site-directed spin labeling (SDSL) in soluble proteins has been well e

230 Spectroscopic studies using site-directed spin labeling (SDSL) indicate that the N-terminus of Btu

231 Here, site-directed spin labeling (SDSL) is used to show that a range of sol

232 The traditional site-directed spin labeling (SDSL) method, which utilizes cysteine res

233 en carried out using site directed nitroxide spin labeling (SDSL) of cysteine residues.

234 Site-directed spin labeling (SDSL) studies revealed that C265 lies clo

235 In the present study, site-directed spin labeling (SDSL) together with double electron-elect

236 The method of site-directed spin labeling (SDSL) utilizes a stable nitroxide radical

237 Here, site-directed spin labeling (SDSL) was used to determine the position

238 Site-directed spin labeling (SDSL) was used to examine and compare tra

239 etic resonance (EPR) method of site-directed spin labeling (SDSL) with double electron-electron reson

240 In site-directed spin labeling (SDSL), a nitroxide moiety containing a st

241 he hemolytic anemia phenotype, site-directed spin labeling (SDSL), in combination with continuous wav

242 PR) spectroscopy, coupled with site-directed spin labeling (SDSL), is a useful method for studying co

243 In site-directed spin labeling (SDSL), local structural and dynamic infor

244 Site-directed spin labeling (SDSL), the site-specific incorporation of

245 two mutant cycle analysis with site-directed spin labeling (SDSL).

246 With an arterial spin labeling sequence, three networks were first identi

247 e-chain interactions, and that site-directed spin labeling should be a powerful means of monitoring c

248 photoconversions monitored by site-directed spin labeling show that opposite structural changes in h

249 or resonances more than 20 residues from the spin-labeling site.

250 ctive insights into these processes, but new spin-labeling strategies are needed.

251 binding interface in MHV with site-directed spin labeling studies consistent with a model in which t

252 Remarkably, site-directed spin labeling studies reveal that these fibrils possess

253 ng environments encountered in site-directed spin labeling studies.

254 the use of this technique for site-directed spin-labeling studies of biologically relevant samples,

255 The results of these site-directed spin-labeling studies reveal that phosphorylation at a d

256 Spin-labeling studies show that residue A62 of MMOB is l

257 Here we describe site-directed spin-labeling studies that identify interactions of LF w

258 A spin-labeling study of interactions of a fusion peptide

259 The method relies on sparse spin-labeling, supplemented by deuteration of protein an

260 d with echo-planar imaging using an arterial spin labeling technique and a custom-made eye coil at 7

261 s in DNA are studied using the site-directed spin labeling technique.

262 A continuous arterial spin-labeling technique with an amplitude-modulated cont

263 easured using the pseudo-continuous arterial-spin-labeling technique with background suppression and

264 Site directed spin-labeling technology has enabled the insertion of ni

265 In site-directed spin labeling, the relative solvent accessibility of spi

266 e-matched healthy controls, we used arterial spin labeling to assess the effects of kidney transplant

267 simulations were combined with site-directed spin labeling to define its structure and dynamics.

268 Here, we use site-specific spin labeling to demonstrate that relaxation enhancement

269 We generated seven mutants suitable for spin labeling to enable application of pulsed EPR techni

270 Here, we used site-directed spin labeling to map the conformation of a pRNA three-wa

271 e imaging based on pseudocontinuous arterial spin labeling to measure CBF at normocapnia (ie, breathi

272 a placebo-controlled study, we used arterial spin labeling to measure IN-OT-induced changes in restin

273 e validity of this model using site-directed spin labeling to obtain long-range distance information

274 n resonance spectroscopy using site-directed spin labeling to understand the structure and interfacia

275 This work points the way for spin-labeling to investigate oligonucleotide-protein com

276 tudy utilizes site-directed fluorescence and spin-labeling to map out the membrane docking surface of

277 ce spectroscopy, together with site-directed spin labeling, to investigate the structural features of

278 We used site-directed spin-labeling together with electron spin-resonance line

279 Site-directed spin labeling utilizes site-specific attachment of a sta

280 performed using velocity-selective arterial spin labeling (VSASL) and 3D image acquisition with whol

281 thod based on the technique of site-directed spin labeling was developed to experimentally map shapes

282 Continuous arterial spin labeling was interleaved with TMS to directly asses

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 Site-directed spin labeling was used to obtain bilayer depth restraint

288 Here, site-directed spin labeling was used to probe the solution structures

289 gnetic resonance imaging technique (arterial spin labeling) was used to quantify spatial pulmonary bl

290 Using site-directed spin labeling, we demonstrated that the pressure- and te

291 Using site-directed spin labeling, we found that the local structure around

292 Using arterial spin labeling, we measured resting-state cerebral blood

293 ectroscopy in combination with site-directed spin labeling, we show that familial PD-associated varia

294 mages and perfusion images by using arterial spin labeling were obtained for comparison.

295 The cysteine mutations used for spin-labeling were distributed throughout the cytosolic

296 MRI arterial spin labeling, white matter hyperintensities (WMHs) and

297 oped an approach that combines site-directed spin labeling with continuous wave and pulsed EPR to inv

298 Here, we used site-directed spin labeling with power saturation electron paramagneti

299 el system, we introduce a method of parallel spin-labeling with paramagnetic and diamagnetic labels a

300 omogeneity and investigated by site-directed spin-labeling with pulse-dipolar electron-spin resonance