ライフサイエンスコーパス: nuclear magnetic resonance

1 and plasma metabolomes were assessed by (1)H-nuclear magnetic resonance.

2 ehydes and keto-dienes, was followed by (1)H nuclear magnetic resonance.

3 ation was monitored by pulsed low-resolution nuclear magnetic resonance.

4 the thermal treatment were monitored by (1)H Nuclear Magnetic Resonance.

5 ation products formed were studied by Proton Nuclear Magnetic Resonance.

6 sotopic labels and measuring USP7 binding by nuclear magnetic resonance.

7 on chromatography, dynamic light scattering, nuclear magnetic resonance ((1) H, (31) P{(1) H}, (195)

8 estinal digestion was investigated by Proton Nuclear Magnetic Resonance ((1)H NMR) and Solid Phase Mi

9 (1)H nuclear magnetic resonance ((1)H NMR) spectra indicated

10 ducted in developing a low resolution proton nuclear magnetic resonance ((1)H NMR) spectroscopic tech

11 ance mass spectrometry (FTICR MS) and proton nuclear magnetic resonance ((1)H NMR) spectroscopy were

12 Proton Nuclear Magnetic Resonance ((1)H NMR) was employed to st

13 Proton nuclear magnetic resonance ((1)H NMR), Fourier transform

14 c basis of meridian specificity using proton nuclear magnetic resonance ((1)H NMR)-based metabolomics

15 The study was carried out by Proton Nuclear Magnetic Resonance ((1)H NMR).

16 Profiles were based on H-nuclear magnetic resonance ((1)H-NMR) metabolomics techn

17 Urine samples were assessed by proton nuclear magnetic resonance ((1)H-NMR) spectroscopy, and

18 onization-mass spectrometry (ESI-MS), proton nuclear magnetic resonance ((1)H-NMR), and fluorescence

19 Alternatively, carbon-13 nuclear magnetic resonance ((13)C NMR) is a fast and rel

20 The proton nuclear magnetic resonance analysis indicated that all o

21 A combination of mass spectrometry and nuclear magnetic resonance analysis of bioactive fractio

22 Nuclear magnetic resonance analysis of STAT3-inhibitor c

23 Nuclear magnetic resonance analysis of the QD-molecule s

24 Nuclear magnetic resonance analysis suggests that negati

25 ccharide units, which were characterized via nuclear magnetic resonance analysis, consist preponderan

26 me include the HX pulse labeling method with nuclear magnetic resonance analysis, the fragment separa

27 around the silicon atoms is given by (29)Si nuclear magnetic resonance analysis.

28 ount of these amines was determined by (19)F nuclear magnetic resonance analysis.

29 Based on Nuclear Magnetic Resonance and Circular Dichroism, these

30 Nuclear magnetic resonance and crystal structures of the

31 anic cage using a combination of solid state nuclear magnetic resonance and dielectric spectroscopies

32 shell and ytterbium is determined using both nuclear magnetic resonance and electron microscopy measu

33 Proton nuclear magnetic resonance and enantiomeric separation i

34 f an m(6)A-switch in a cellular RNA, we used nuclear magnetic resonance and Forster resonance energy

35 ve been probed for proteins in solution with nuclear magnetic resonance and infrared methods for deca

36 We exemplify the approach for both nuclear magnetic resonance and liquid chromatography-mas

37 Its structure was established by nuclear magnetic resonance and mass spectroscopy as a he

38 Using a combination of nuclear magnetic resonance and molecular dynamics simula

39 fied in the recovered product by solid-state nuclear magnetic resonance and neutron pair distribution

40 in solution by small angle X-Ray scattering, nuclear magnetic resonance and surface-plasmon resonance

41 Using one-dimensional nuclear magnetic resonance and the pointed-end actin pol

42 ray diffraction, solid fat content by pulsed nuclear magnetic resonance and thermal behaviour by diff

43 We perform nuclear Magnetic Resonance and thermodynamic stability m

44 Freeze-trapping x-ray crystallography, nuclear magnetic resonance, and computational techniques

45 RF2 mRNA, as measured by circular dichroism, nuclear magnetic resonance, and dimethylsulfate footprin

46 ilities of T-oligo using nondenaturing PAGE, nuclear magnetic resonance, and immunofluorescence.

47 demonstrate by using ab initio calculations, nuclear magnetic resonance, and impedance spectroscopy m

48 ic Neutron Scattering, Pulsed Field Gradient Nuclear Magnetic Resonance, and Molecular Dynamics compu

49 ll wall recalcitrance by phenolic profiling, nuclear magnetic resonance, and saccharification assays

50 h as a new capillary electrophoresis method, nuclear magnetic resonance, and surface plasmon resonanc

51 tion calorimetry, surface plasmon resonance, nuclear magnetic resonance, and X-ray techniques.

52 ound that was identified by purification and nuclear magnetic resonance as syringyl lactic acid hexos

53 ble-isotope tracer experiments combined with nuclear magnetic resonance-based metabolic analysis demo

54 Nuclear magnetic resonance-based metabolomics analysis i

55 compared with placebo administration using a nuclear magnetic resonance-based metabolomics platform.

56 respect to its use in mass spectrometry- and nuclear magnetic resonance-based metabolomics studies.

57 Here, using nuclear magnetic resonance-based screening and structure

58 a-toxin (PLAT) signature domain of PC1 using nuclear magnetic resonance, biochemical, cellular, and i

59 In this study, we used nuclear magnetic resonance Carr-Purcell-Meiboom-Gill rel

60 Light-scattering, mass spectrometric, and nuclear magnetic resonance characterization of fractiona

61 inking, bacterial two-hybrid experiments and nuclear magnetic resonance chemical shift analysis, we n

62 Our results derived from nuclear magnetic resonance chemical shift perturbation a

63 an original strategy based on solution-state nuclear magnetic resonance combined with an efficient is

64 an isolated heart preparation using ex vivo nuclear magnetic resonance combined with targeted quanti

65 Solid-state nuclear magnetic resonance confirmed a cellulose deficie

66 13)C Cross polarization-magic angle spinning nuclear magnetic resonance (CP-MAS NMR) spectroscopy, an

67 d chromatographic purification were used and nuclear magnetic resonance data allowed the identificati

68 High-resolution x-ray structures and nuclear magnetic resonance data enabled the efficient de

69 uorimetry and saturation transfer difference-nuclear magnetic resonance demonstrated specific binding

70 using magneto-DNA probes and a miniaturized nuclear magnetic resonance device.

71 ure are compared with the existing data from nuclear magnetic resonance, dielectric and infrared meas

72 Solid-state nuclear magnetic resonance distance measurements capture

73 Fast field cycling nuclear magnetic resonance, electrochemical analysis and

74 e studied using a combination of solid state nuclear magnetic resonance, electron microscopy, digital

75 us structure was investigated by solid-state nuclear magnetic resonance experiments and further confi

76 judged by X-ray photoelectron spectroscopy, nuclear magnetic resonance experiments and quantificatio

77 Direct polarization and cross-polarization nuclear magnetic resonance experiments enabled us to pro

78 By using site-specific Fluorine-19 nuclear magnetic resonance experiments guided by in vivo

79 Two-dimensional nuclear magnetic resonance experiments reveal that PARP3

80 chemical exchange saturation transfer (CEST) nuclear magnetic resonance experiments that a similar, C

81 e of EXPB1 binding, we conducted solid-state nuclear magnetic resonance experiments using paramagneti

82 ical shifts of CaM upon Ng13-49 binding from nuclear magnetic resonance experiments.

83 We applied (1)H nuclear magnetic resonance exploratory metabolomics to s

84 The essential principles of nuclear magnetic resonance for the analysis of biomolecu

85 We also directly demonstrate by nuclear magnetic resonance formation of a ternary FLI1-D

86 the-art high-resolution magic-angle spinning nuclear magnetic resonance (HRMAS NMR), applied to intac

87 previously by scanning electron microscopy, nuclear magnetic resonance imaging, and electron tomogra

88 gray-scale and Doppler ultrasonography, and nuclear magnetic resonance imaging.

89 ilar to that of unfolded proteins studied by nuclear magnetic resonance in conjunction with molecular

90 In-cell nuclear magnetic resonance is a branch of biomolecular N

91 Nuclear magnetic resonance is an excellent probe to foll

92 r dichroism (CD) and magic angle solid-state nuclear magnetic resonance (MAS SS-NMR) spectroscopy est

93 situ (23)Na magic-angle spinning solid-state nuclear magnetic resonance (MAS ssNMR) spectroscopy are

94 elt viscosity, together with glass Raman and Nuclear Magnetic Resonance measurements and Molecular Dy

95 Here, we show that solid-state nuclear magnetic resonance measurements of (29)Si-enrich

96 r conformation in RNA excited states through nuclear magnetic resonance measurements of C1 and C4 rot

97 Here, using high-accuracy (75)As and (51)V nuclear magnetic resonance measurements, we investigate

98 ht lipids and metabolites were quantified by nuclear magnetic resonance metabolomics in the populatio

99 A high-throughput serum nuclear magnetic resonance metabolomics platform was use

100 Nuclear magnetic resonance metabolomics was used to anal

101 ray), genome-wide gene expression arrays and nuclear magnetic resonance metabolomics were performed f

102 ic traits were quantified by high-throughput nuclear magnetic resonance metabolomics.

103 We have used solid-state nuclear magnetic resonance methods to characterize the m

104 ontent, amylopectin retrogradation) and (1)H Nuclear Magnetic Resonance molecular mobility were chara

105 Here, we describe the use of nuclear magnetic resonance (NMR) 'cytometry' to quantify

106 Enzymatic assay and nuclear magnetic resonance (NMR) analysis demonstrated t

107 expression and in vitro assays combined with nuclear magnetic resonance (NMR) analysis identified SdC

108 Biochemical and nuclear magnetic resonance (NMR) analysis showed that th

109 Here, we employed nuclear magnetic resonance (NMR) and biochemical and bio

110 rom Caenorhabditis elegans, determined using nuclear magnetic resonance (NMR) and electron microscopy

111 We used Nuclear Magnetic Resonance (NMR) and Electron Paramagnet

112 The resulting products were characterized by nuclear magnetic resonance (NMR) and Infra-red spectrosc

113 were isolated and characterized by 1D and 2D nuclear magnetic resonance (NMR) and mass spectrometry (

114 c communications in STAT3 from studies using nuclear magnetic resonance (NMR) and other methods.

115 Here we present a sensitive nuclear magnetic resonance (NMR) approach to determine t

116 Chemical shifts from Nuclear Magnetic Resonance (NMR) are hypersensitive to c

117 Nuclear magnetic resonance (NMR) can characterize the po

118 The Nuclear Magnetic Resonance (NMR) coupled to multivariate

119 ignment of complex molecular structures from nuclear magnetic resonance (NMR) data can be prone to in

120 Our nuclear magnetic resonance (NMR) data rule out a direct

121 t shift and spin relaxation time measured in nuclear magnetic resonance (NMR) experiments.

122 cal parameters, near-infra red data and (1)H nuclear magnetic resonance (NMR) fingerprints, obtained

123 l as well as biophysical approaches based on nuclear magnetic resonance (NMR) fragment screening are

124 Nuclear magnetic resonance (NMR) has been an important s

125 e sequence was adapted to a state-of-the-art nuclear magnetic resonance (NMR) instrument, and data re

126 Nuclear magnetic resonance (NMR) is a powerful tool for

127 , and solid-state magic-angle spinning (MAS) nuclear magnetic resonance (NMR) is a unique method to e

128 Conventional solid-state (13)C Nuclear Magnetic Resonance (NMR) is widely used to exami

129 A nuclear magnetic resonance (NMR) method was developed to

130 of flight (MALDI-TOF) mass spectrometry and nuclear magnetic resonance (NMR) methods were thus used

131 Using nuclear magnetic resonance (NMR) methods, in this study

132 t, electron paramagnetic resonance (EPR) and nuclear magnetic resonance (NMR) on the isolated CNBD in

133 ization of these tails and their linkages by nuclear magnetic resonance (NMR) or mass spectrometry is

134 Specifically, the prediction of nuclear magnetic resonance (NMR) parameters through dens

135 Nuclear magnetic resonance (NMR) profiles were analyzed

136 s and one (1D) and two dimensional (2D) (1)H Nuclear Magnetic Resonance (NMR) relaxometry.

137 ollow-up characterisation by ligand observed nuclear magnetic resonance (NMR) revealed direct interac

138 Nuclear magnetic resonance (NMR) revealed that CyP40 int

139 Using them as nuclear magnetic resonance (NMR) sensitive nanoprobes ad

140 he exceptionally rich information content of nuclear magnetic resonance (NMR) spectra is routinely us

141 e Data Bank (BMRB) is a public repository of Nuclear Magnetic Resonance (NMR) spectroscopic data of b

142 lts of a two-dimensional solid-state (77) Se nuclear magnetic resonance (NMR) spectroscopic study of

143 (1)H and (13)C nuclear magnetic resonance (NMR) spectroscopies confirme

144 Using nuclear magnetic resonance (NMR) spectroscopy and bioche

145 Using solution-state nuclear magnetic resonance (NMR) spectroscopy and coarse

146 sticated instrumentation render conventional nuclear magnetic resonance (NMR) spectroscopy and imagin

147 nolic extract and structurally elucidated by Nuclear Magnetic Resonance (NMR) spectroscopy and mass s

148 ndial urine samples were analyzed using (1)H nuclear magnetic resonance (NMR) spectroscopy and multiv

149 Using nuclear magnetic resonance (NMR) spectroscopy and single

150 tion have been characterised by ATR-FTIR and nuclear magnetic resonance (NMR) spectroscopy as well as

151 Nuclear magnetic resonance (NMR) spectroscopy combined w

152 Nuclear magnetic resonance (NMR) spectroscopy evaluated

153 Nuclear magnetic resonance (NMR) spectroscopy has been i

154 esolution magic angle spinning ((1)H HR-MAS) nuclear magnetic resonance (NMR) spectroscopy in combina

155 om Russia and Kenya were analysed using (1)H nuclear magnetic resonance (NMR) spectroscopy in compari

156 The application of methyl nuclear magnetic resonance (NMR) spectroscopy in protein

157 Lipoprotein profiling of human blood by (1)H nuclear magnetic resonance (NMR) spectroscopy is a rapid

158 Nuclear Magnetic Resonance (NMR) spectroscopy is emergin

159 Nuclear magnetic resonance (NMR) spectroscopy is widely

160 High-resolution (6/7)Li solid-state nuclear magnetic resonance (NMR) spectroscopy of T-Nb2O5

161 Quantitative (13)C nuclear magnetic resonance (NMR) spectroscopy shows that

162 cted by the type of counterions, as shown by nuclear magnetic resonance (NMR) spectroscopy studies an

163 euptake mechanisms, and 5) used (1)H-[(13)C]-nuclear magnetic resonance (NMR) spectroscopy to evaluat

164 spins, yet limits the spectral resolution of nuclear magnetic resonance (NMR) spectroscopy to several

165 Here, nuclear magnetic resonance (NMR) spectroscopy with the w

166 iamond are a promising tool for small-volume nuclear magnetic resonance (NMR) spectroscopy, but the l

167 Liver study was performed by nuclear magnetic resonance (NMR) spectroscopy, followed

168 (13)C solid-state magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, supported

169 Using nuclear magnetic resonance (NMR) spectroscopy, we analys

170 By nuclear magnetic resonance (NMR) spectroscopy, we charac

171 Here by performing (7)Li-/(95)Mo-nuclear magnetic resonance (NMR) spectroscopy, we direct

172 Here, by using nuclear magnetic resonance (NMR) spectroscopy, we examin

173 Here, using nuclear magnetic resonance (NMR) spectroscopy, we show t

174 onal imaging and two-dimensional solid-state nuclear magnetic resonance (NMR) spectroscopy, we show t

175 In this study, nuclear magnetic resonance (NMR) spectroscopy-based meta

176 of the YscP binding site on YscU by means of nuclear magnetic resonance (NMR) spectroscopy.

177 ied via one- and two-dimensional solid-state nuclear magnetic resonance (NMR) spectroscopy.

178 ith Trypanosoma brucei rhodesiense, using 1H nuclear magnetic resonance (NMR) spectroscopy.

179 cal calculations, in combination with (7) Li nuclear magnetic resonance (NMR) spectroscopy.

180 d interactions are frequently screened using nuclear magnetic resonance (NMR) spectroscopy.

181 ed fluorescence, microwave spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy.

182 on MS (LC-HRMS), LC-tandem MS (LC-MS/MS) and nuclear magnetic resonance (NMR) spectroscopy.

183 pproaches for integrating light sources with nuclear magnetic resonance (NMR) spectroscopy: sample ir

184 Nuclear magnetic resonance (NMR) spin relaxation is prob

185 Here, we develop a convenient (17)O nuclear magnetic resonance (NMR) strategy to distinguish

186 Nuclear magnetic resonance (NMR) studies have benefited

187 acids, and labeling with stable isotopes for nuclear magnetic resonance (NMR) studies is desired.

188 architecture, which has been corroborated by nuclear magnetic resonance (NMR) studies.

189 g analysis, linker-scanning mutagenesis, and nuclear magnetic resonance (NMR) studies.

190 Nuclear magnetic resonance (NMR) titrations, potentiomet

191 as chromatography-mass spectrometry (GC-MS), nuclear magnetic resonance (NMR), and enzyme assays.

192 teronuclear single quantum coherence (HSQC), nuclear magnetic resonance (NMR), and py-GC/MS.

193 Therefore, nuclear magnetic resonance (NMR), electron spin resonanc

194 ays and saturation transfer difference (STD) nuclear magnetic resonance (NMR), we found that P[19] co

195 nt of serum poses significant challenges for nuclear magnetic resonance (NMR)-based metabolomics stud

196 We demonstrate using nuclear magnetic resonance (NMR)-based relaxation disper

197 dodecamers, determined herein by means of 1H nuclear magnetic resonance (NMR).

198 ture content) and molecular mobility by (1)H Nuclear Magnetic Resonance (NMR).

199 y de novo structural elucidation using 1D/2D nuclear magnetic resonance (NMR).

200 as determined by one-dimensional (1D) and 2D nuclear magnetic resonance (NMR).

201 resolution magic angle spinning (HRMAS) (1)H nuclear magnetic resonance (NMR).

202 Nuclear magnetic resonance of Skint-1 DV revealed a core

203 Using nuclear magnetic resonance, operando electrochemical pre

204 evidence, such as X-ray crystallography and nuclear magnetic resonance (primary techniques) and a br

205 as on longitudinal (T1) and transversal (T2) nuclear magnetic resonance relaxation time mapping.

206 ur was investigated using time-domain proton nuclear magnetic resonance relaxometry, and related to t

207 The observed imino proton nuclear magnetic resonance resonances and Forster resona

208 ics simulations, and by means of solid-state nuclear magnetic resonance show that the amino acids are

209 nstitution into cNDs enhanced the quality of nuclear magnetic resonance spectra for both VDAC-1, a be

210 In contrast, solid-state nuclear magnetic resonance spectra showed substantial de

211 studies including mass spectrometry (MS) and nuclear magnetic resonance spectrometry (NMR) data spann

212 33 metabolite measures were quantified using nuclear magnetic resonance spectrometry.

213 Using mass spectrometry and nuclear magnetic resonance spectroscopic techniques, a s

214 ycles by (7)Li, (19)F, and (13)C solid-state nuclear magnetic resonance spectroscopies, with the orga

215 -Cu (10 and 20 mg/L) was evaluated by proton nuclear magnetic resonance spectroscopy ((1)H NMR) and g

216 Nuclear magnetic resonance spectroscopy ((1)H NMR) was u

217 ion mass spectrometry-solid-phase extraction-nuclear magnetic resonance spectroscopy (HR-bioassay/HPL

218 Using (1)H Nuclear Magnetic Resonance spectroscopy (NMR) and Gas Ch

219 Liquid-state, one-dimension (31)P nuclear magnetic resonance spectroscopy (NMR) has greatl

220 lated Tau by activated recombinant ERK2 with nuclear magnetic resonance spectroscopy (NMR) reveals ph

221 rence fatty acid methyl esters (FAMEs), (1)H nuclear magnetic resonance spectroscopy (NMR), employing

222 y using mass spectrometry (MS) and 1D and 2D nuclear magnetic resonance spectroscopy (NMR).

223 chromatography mass spectrometry (GC-MS) and nuclear magnetic resonance spectroscopy (NMR).

224 orimetry and changes in chemical shifts from nuclear magnetic resonance spectroscopy also support the

225 age- and sex-matched healthy controls, using nuclear magnetic resonance spectroscopy and a validated

226 Here we show, using nuclear magnetic resonance spectroscopy and density func

227 using (31)P solid-state magic-angle-spinning nuclear magnetic resonance spectroscopy and differential

228 t the use of low-temperature rapid injection nuclear magnetic resonance spectroscopy and kinetic stud

229 OEGCG was carefully characterized with nuclear magnetic resonance spectroscopy and mass spectro

230 y studies, Isothermal Titration Calorimetry, Nuclear Magnetic Resonance spectroscopy and molecular mo

231 he inflorescence cell wall using solid-state nuclear magnetic resonance spectroscopy and small-angle

232 Nuclear magnetic resonance spectroscopy and thioacidolys

233 te extracts were analysed using 600 MHz (1)H Nuclear Magnetic Resonance spectroscopy and Ultra-Perfor

234 We perform (1)H and (19)F nuclear magnetic resonance spectroscopy at room temperat

235 Here we employed high-resolution (1)H nuclear magnetic resonance spectroscopy coupled with adv

236 Nuclear magnetic resonance spectroscopy demonstrated tha

237 Nuclear magnetic resonance spectroscopy demonstrates the

238 tion, levels at which circular dichroism and nuclear magnetic resonance spectroscopy fingerprinting,

239 quantitative metabolomics platform based on nuclear magnetic resonance spectroscopy has found widesp

240 While X-ray crystallography and nuclear magnetic resonance spectroscopy have revealed th

241 Nuclear magnetic resonance spectroscopy is a powerful to

242 Nuclear magnetic resonance spectroscopy of products from

243 Using methyl transverse relaxation-optimized nuclear magnetic resonance spectroscopy on a 450-kilodal

244 rahigh-resolution mass spectrometry (MS) and nuclear magnetic resonance spectroscopy reveal abundant

245 Nuclear magnetic resonance spectroscopy studies and dens

246 Here we show by nuclear magnetic resonance spectroscopy that inhibitors

247 Here, we demonstrate by nuclear magnetic resonance spectroscopy that the Escheri

248 ated using solubility enhancement as well as nuclear magnetic resonance spectroscopy to demonstrate s

249 Here, we use solid-state nuclear magnetic resonance spectroscopy to gain atomic l

250 metabolic content measured in lymphocytes by nuclear magnetic resonance spectroscopy was altered in s

251 Nuclear Magnetic Resonance spectroscopy was employed to

252 Using Nuclear Magnetic Resonance spectroscopy we reveal how di

253 by hyperpolarized in vivo pyruvate studies, nuclear magnetic resonance spectroscopy, and carbon-13 f

254 AS proteins using microscale thermophoresis, nuclear magnetic resonance spectroscopy, and isothermal

255 f conventional photophysical investigations, nuclear magnetic resonance spectroscopy, and kinetic stu

256 Here, using vibrational and solid-state nuclear magnetic resonance spectroscopy, and molecular d

257 hanced Raman spectroscopy, (27)Al and (35)Cl nuclear magnetic resonance spectroscopy, and pair distri

258 influenced by Nox1 deletion as determined by nuclear magnetic resonance spectroscopy, glucose toleran

259 nto transient HG bps, we used solution-state nuclear magnetic resonance spectroscopy, including measu

260 sing a combination of X-ray crystallography, nuclear magnetic resonance spectroscopy, SAXS and molecu

261 Using nuclear magnetic resonance spectroscopy, we first show t

262 Using time-resolved nuclear magnetic resonance spectroscopy, we found that E

263 With the use of a (1)H nuclear magnetic resonance spectroscopy-based metabolic

264 GlycA is a novel proton nuclear magnetic resonance spectroscopy-measured biomark

265 ake rats as measured by ex vivo (1)H-[(13)C]-nuclear magnetic resonance spectroscopy.

266 y, and sequential (2)H and (31)P solid-state nuclear magnetic resonance spectroscopy.

267 ometry, electron paramagnetic resonance, and nuclear magnetic resonance spectroscopy.

268 ere assessed with the use of high-throughput nuclear magnetic resonance spectroscopy.

269 pectrometry and lipidome analysis using (1)H nuclear magnetic resonance spectroscopy.

270 ve basic determinants that are identified by nuclear magnetic resonance spectroscopy.

271 s spectrometry, tandem mass spectrometry and nuclear magnetic resonance spectroscopy.

272 determined using (1)H and (7)Li solid-state nuclear magnetic resonance spectroscopy.

273 gated using solid-state magic angle spinning nuclear magnetic resonance spectroscopy.

274 ced by high resolution mass spectrometry and nuclear magnetic resonance spectroscopy.

275 Circulating amino acids were assessed by nuclear magnetic resonance spectroscopy.

276 on the innovative application of (13)C NMR (nuclear magnetic resonance) spectroscopy to determine th

277 Two-dimensional (2D) solid-state nuclear magnetic resonance (SSNMR) experiments on sample

278 heimer's disease phenotype using solid-state nuclear magnetic resonance (ssNMR) measurements on Abeta

279 We report solid state nuclear magnetic resonance (ssNMR) measurements on the i

280 uantum-filtered (DQF) J-resolved solid-state nuclear magnetic resonance (SSNMR) spectroscopy.

281 Nuclear magnetic resonance structural studies reveal tha

282 The nuclear magnetic resonance structure of [C117S]YmoB and

283 Nuclear magnetic resonance structures of 9 of 12 designe

284 Here, we describe crystal and nuclear magnetic resonance structures of KaiB-KaiC,KaiA-

285 Nuclear magnetic resonance studies confirmed that the ca

286 ng upon a model of RNA dynamics derived from nuclear magnetic resonance studies, we developed a quant

287 d without post-treatments by (31)P adsorbate nuclear magnetic resonance, supported by a range of othe

288 ability of meat microstructures, time domain nuclear magnetic resonance (TD-NMR) has gained a promine

289 l scanning calorimetry (DSC) and time domain nuclear magnetic resonance (TD-NMR) were applied to anal

290 microscopy, light microscopy and time domain nuclear magnetic resonance (TD-NMR) were respectively us

291 studied by using low resolution time domain nuclear magnetic resonance (TD-NMR).

292 Ester bond formation was confirmed by nuclear magnetic resonance technique that the chemical s

293 By using solution and solid-state nuclear magnetic resonance techniques in conjunction wit

294 This review deals with the use of Nuclear Magnetic Resonance techniques to monitor the beh

295 e-molecule studies to jump kinetics and from nuclear magnetic resonance to imaging on the microscope,

296 most cases, their poor responsivities toward nuclear magnetic resonance, ultraviolet/visible, and inf

297 Here by (63)Cu-nuclear magnetic resonance, we report the discovery of C

298 r mobility by means of time domain low-field nuclear magnetic resonance were investigated.

299 cal examinations (computer tomography and/or nuclear magnetic resonance), which are essential to conf

300 y-the synergistic combination of solid-state nuclear magnetic resonance, X-ray crystallography, and c