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

1 plasma-based metabolites assessed by proton nuclear magnetic resonance.

2 oscopy, size particle, X-ray diffraction and nuclear magnetic resonance.

3 , we measured lipoprotein subfractions using nuclear magnetic resonance.

4 s experiments with infrared spectroscopy and nuclear magnetic resonance.

5 y stable isotope-labeled GPCR for studies by nuclear magnetic resonance.

6 zed by means of dynamic light scattering and nuclear magnetic resonance.

7 hrotron X-ray nano-tomography and unilateral nuclear magnetic resonance.

8 capped HIV-1 leader RNAs by deuterium-edited nuclear magnetic resonance.

9 terized using Diffusion ordered spectroscopy-Nuclear Magnetic Resonance ((1)H DOSY-NMR) and Fourier-t

10 solvent holding capacity as shown by proton nuclear magnetic resonance ((1)H NMR) experiments in pre

11 fagnana (Province of Lucca, Tuscany) by (1)H Nuclear Magnetic Resonance ((1)H NMR) spectroscopy and i

12 ct of the soft tissue was analyzed by proton nuclear magnetic resonance ((1)H NMR) spectroscopy using

13 Fourier Transform Infrared (FTIR) and proton nuclear magnetic resonance ((1)H NMR) spectroscopy were

14 ing the human faecal metabolome using proton nuclear magnetic resonance ((1)H NMR) spectroscopy.

15 the resonance frequency of water in the (1)H nuclear magnetic resonance ((1)H NMR) spectrum, enabling

16 ion product, benzaldehyde, was detected with Nuclear Magnetic Resonance ((1)H NMR), in line with MNP-

17 y is to analyze in depth, by means of proton nuclear magnetic resonance, (1)H NMR, the changes caused

18 Nuclear magnetic resonance(11), X-ray photoelectron spec

19 e aim of this study was to investigate if 1H-nuclear magnetic resonance (1H-NMR) analysis of serum sa

20 Here we use R(1rho) relaxation-dispersion nuclear magnetic resonance(2) and molecular simulations(

21 on mass spectrometry, UV-vis, (1)H and (19)F nuclear magnetic resonance, (57)Fe Mossbauer, and electr

22 rochemical Scanning Tunneling Microscopy and Nuclear Magnetic Resonance among many other techniques w

23 Nuclear magnetic resonance analyses of Der p 2 in comple

24 says to distinguish overlapping epitopes and nuclear magnetic resonance analyses to identify specific

25 cript of DUX4 through circular dichroism and nuclear magnetic resonance analysis.

26 rometry, one-dimensional and two-dimensional nuclear magnetic resonance and absorption spectroscopies

27 ic nuclear polarization-enhanced solid-state nuclear magnetic resonance and cryo-electron microscopy,

28 teraction has been elucidated by solid-state nuclear magnetic resonance and density functional theory

29 (iPr4) radicals in solution as shown by (1)H nuclear magnetic resonance and electron paramagnetic res

30 XAD-8 and XAD-4 resins and analyzed by C-13 nuclear magnetic resonance and liquid chromatography tim

31 lear magnetic resonance followed by in vitro nuclear magnetic resonance and mass spectrometry analysi

32 A La assay to detect reactive molecules by nuclear magnetic resonance and mass spectrometry peptide

33 We exploited this model through WaterLOGSY nuclear magnetic resonance and microscale thermophoresis

34 2D proton nuclear magnetic resonance and SAXS data provided constr

35 nonselective hits that were optimized using nuclear magnetic resonance and X-ray-derived structural

36 onal methods, such as X-ray crystallography, nuclear magnetic resonance, and cryo-electron microscopy

37 Specialty Coffee Association protocol, nuclear magnetic resonance, and denaturing gradient gel

38 fied with the guidance of mass spectrometry, nuclear magnetic resonance, and molecular ion networking

39 olic profiling with multiple platforms (both nuclear magnetic resonance- and mass spectrometry-based

40 Mass spectrometry and nuclear magnetic resonance are the most commonly reporte

41 Nuclear magnetic resonance-based lipoprotein profiling w

42 esiduals of the postprandial response of 149 nuclear magnetic resonance-based metabolite measures.

43 K9 methyltransferase, with nucleosomes using nuclear magnetic resonance, biochemical and genetic assa

44 GlycA, a nuclear magnetic resonance composite marker of systemic

45 Applying a suite of nuclear magnetic resonance, crystallography, and stopped

46 Using nuclear magnetic resonance data and molecular dynamics s

47 We used this existing villin headpiece nuclear magnetic resonance data and performed mutational

48 Here, we present in-situ high-pressure nuclear magnetic resonance data on molecular hydrogen in

49 We analyzed nuclear magnetic resonance-derived lipoprotein and metab

50 Comparison of nuclear magnetic resonance-derived structures revealed s

51 tically by comparative pulsed field gradient nuclear magnetic resonance diffusion measurements, which

52 Comparison to Diffusion Ordered Spectroscopy Nuclear Magnetic Resonance (DOSY NMR) results allows the

53 These constructs were interrogated using nuclear magnetic resonance, electrophysiology, and cell

54 e probed by variable temperature solid-state nuclear magnetic resonance experiments and periodic dens

55 c analysis using 1-dimension and 2-dimension nuclear magnetic resonance experiments in addition to ga

56 opioid endomorphin-1 (EM-1) via an array of nuclear magnetic resonance experiments in both aqueous c

57 Atomistic molecular dynamics simulations and nuclear magnetic resonance experiments suggest that tran

58 This work explores what Fast Field-Cycling Nuclear Magnetic Resonance (FFC-NMR) relaxometry brings

59 ed with (13)C LCFA during dynamic-mode (13)C nuclear magnetic resonance followed by in vitro nuclear

60 pH probing of biofilm colonies, solid-state nuclear magnetic resonance for macromolecular interactio

61 (1)H NMR (hydrogen-1 nuclear magnetic resonance), FT-IR (Fourier transform-in

62 (13)C heteronuclear single quantum coherence nuclear magnetic resonance (HSQC NMR) spectroscopy revea

63 es on a combination of mass spectrometry and nuclear magnetic resonance imaging to provide insights i

64 ide range of fields, from radio astronomy to nuclear magnetic resonance imaging.

65 Single-crystal x-ray diffraction as well as nuclear magnetic resonance, infrared, and Mossbauer spec

66 isotope (89)Y is proving to be suitable for nuclear magnetic resonance investigations, where initial

67 Low-field proton nuclear magnetic resonance (LF-(1)H NMR) devices based o

68 Using molecular docking, nuclear magnetic resonance, lipid-binding assays, and su

69 (31)P magic-angle spinning nuclear magnetic resonance (MAS NMR) and Fourier-transfo

70 effective hydrogen atom donor, confirmed by nuclear magnetic resonance, mass spectrometry, and deute

71 roups of botanical samples, including proton nuclear magnetic resonance, mass, and ultraviolet spectr

72 Nuclear magnetic resonance measurements additionally sho

73 h-resolution X-ray structures, combined with nuclear magnetic resonance measurements and structural a

74 sigma interactions via temperature-dependent nuclear magnetic resonance measurements.

75 y diffraction structural analysis as well as nuclear magnetic resonance measurements.

76 nical, demographic, and one-dimensional (1)H nuclear magnetic resonance metabolic variables.

77 We have compiled a vast resource of proton nuclear magnetic resonance metabolomics and phenotypic d

78 A proton nuclear magnetic resonance metabolomics platform provide

79 was performed using a high-throughput proton nuclear magnetic resonance metabolomics platform, which

80 , microfabrication and novel chemistry, NMR (Nuclear Magnetic Resonance) methods, embodied in miniatu

81 le also recapitulating earlier findings from nuclear magnetic resonance, modeling and crystallography

82 Extensive nuclear magnetic resonance, molecular dynamics, and ense

83 Furthermore, in operando nuclear magnetic resonance monitoring of the catalytic r

84 Here, we use structural and dynamic nuclear magnetic resonance (NMR) analysis to demonstrate

85 n of the sensitivity-relevant electronics of nuclear magnetic resonance (NMR) and electron spin reson

86 Nuclear magnetic resonance (NMR) and gas chromatography

87 Nuclear magnetic resonance (NMR) and H1 tail-swapping cr

88 Furthermore, we use nuclear magnetic resonance (NMR) and molecular dynamics

89 ixture in its raw form using high resolution Nuclear Magnetic Resonance (NMR) and previously develope

90 ed its excellent suitability to mimic ZEA by nuclear magnetic resonance (NMR) and surface plasmon res

91 uranyl(VI) complex were characterized using nuclear magnetic resonance (NMR) and UV-vis spectroscopi

92 Nuclear magnetic resonance (NMR) and X-ray photoelectron

93 Quantum mechanical/nuclear magnetic resonance (NMR) approaches are widely u

94 ances in X-ray crystallography, cryo-EM, and nuclear magnetic resonance (NMR) are closing this gap by

95 In this study, we report nuclear magnetic resonance (NMR) based metabolomic analy

96 lysaccharide, based on chemical analysis and nuclear magnetic resonance (NMR) data.

97 l [15N-1H] separated local field solid-state nuclear magnetic resonance (NMR) experiments of membrane

98 We address this problem through nuclear magnetic resonance (NMR) experiments on BiCu[For

99 Time-series nuclear magnetic resonance (NMR) has advanced our knowle

100 iology techniques are X-ray crystallography, nuclear magnetic resonance (NMR) imaging, and cryogenic

101 on generation of acoustic-Brownian noise in nuclear magnetic resonance (NMR) induced as a result of

102 In vivo nuclear magnetic resonance (NMR) is a powerful analytica

103 Nuclear magnetic resonance (NMR) is a powerful method fo

104 Zero- to ultralow-field (ZULF) nuclear magnetic resonance (NMR) is an emerging tool for

105 In vivo nuclear magnetic resonance (NMR) is rapidly evolving as

106 Nuclear magnetic resonance (NMR) measurements of the mit

107 inflammatory cytokine gene expression and 1H nuclear magnetic resonance (NMR) metabolomics measuremen

108 cancer cell lines using [Formula: see text] nuclear magnetic resonance (NMR) metabolomics, Seahorse,

109 Here we report two in situ nuclear magnetic resonance (NMR) methods of studying red

110 nce of N, N-diisopropylethylamine (DIPEA) by nuclear magnetic resonance (NMR) monitoring of the react

111 This is made possible by real-time nuclear magnetic resonance (NMR) monitoring using dissol

112 ials can be studied by pulsed field gradient nuclear magnetic resonance (NMR) non-invasively and with

113 hod for measurement of elemental analysis by nuclear magnetic resonance (NMR) of unknown samples is d

114 tylsalicylic acid (aspirin) and its use as a nuclear magnetic resonance (NMR) probe.

115 pect to control samples were studied by (1)H nuclear magnetic resonance (NMR) relaxometry and thermog

116 State-of-the-art nuclear magnetic resonance (NMR) selective experiments a

117 This prediction is confirmed by (1)H nuclear magnetic resonance (NMR) signals of bound guest

118 olution and solid state magic-angle-spinning nuclear magnetic resonance (NMR) spectra provide atomic

119 Nuclear magnetic resonance (NMR) spectra showed that dep

120 a combination of experimental (1)H and (13)C nuclear magnetic resonance (NMR) spectra, high-resolutio

121 rption near-edge structure (XANES) and (31)P nuclear magnetic resonance (NMR) spectroscopies to deter

122 In metabolomics, nuclear magnetic resonance (NMR) spectroscopy allows to

123 Metabolic profiles were analyzed by nuclear magnetic resonance (NMR) spectroscopy and compar

124 Solid-state nuclear magnetic resonance (NMR) spectroscopy and comput

125 e, HWE buried green tea, was investigated by Nuclear Magnetic Resonance (NMR) spectroscopy and Fourie

126 Metabolomic techniques, such as nuclear magnetic resonance (NMR) spectroscopy and induct

127 Nuclear magnetic resonance (NMR) spectroscopy and mass s

128 Sera were analysed using (1)H nuclear magnetic resonance (NMR) spectroscopy and mass s

129 ra virgin olive oil (EVOO) was studied using Nuclear Magnetic Resonance (NMR) spectroscopy and multiv

130 his work, we demonstrate that operando (7)Li nuclear magnetic resonance (NMR) spectroscopy can be app

131 Nuclear magnetic resonance (NMR) spectroscopy contribute

132 Solution nuclear magnetic resonance (NMR) spectroscopy has emerge

133 Nuclear magnetic resonance (NMR) spectroscopy in solutio

134 For this Nuclear Magnetic Resonance (NMR) spectroscopy is an attr

135 Nuclear magnetic resonance (NMR) spectroscopy is emergin

136 Nuclear magnetic resonance (NMR) spectroscopy is ideally

137 Solid-state nuclear magnetic resonance (NMR) spectroscopy is sensiti

138 pability for high-throughput screening, (1)H nuclear magnetic resonance (NMR) spectroscopy is used ex

139 Here we use nuclear magnetic resonance (NMR) spectroscopy of oxygen-

140 e HP observations with high-resolution (13)C-nuclear magnetic resonance (NMR) spectroscopy of tissue

141 mass sensitivity of microcoil technology in nuclear magnetic resonance (NMR) spectroscopy provides p

142 s in membrane protein signaling complexes by nuclear magnetic resonance (NMR) spectroscopy remains ch

143 iles of solid sample materials with solution nuclear magnetic resonance (NMR) spectroscopy requires t

144 Here we show by circular dichroism and nuclear magnetic resonance (NMR) spectroscopy that Spp2

145 atography-mass spectrometry (GC-MS) and (1)H nuclear magnetic resonance (NMR) spectroscopy to charact

146 monstrate the advantage of using solid-state nuclear magnetic resonance (NMR) spectroscopy to deconvo

147 ando synchrotron X-ray diffraction (XRD) and nuclear magnetic resonance (NMR) spectroscopy to demonst

148 on reaction mechanism was examined employing nuclear magnetic resonance (NMR) spectroscopy to determi

149 We used solution nuclear magnetic resonance (NMR) spectroscopy to discove

150 Proton nuclear magnetic resonance (NMR) spectroscopy was used t

151 High-resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy were used

152 Using nuclear magnetic resonance (NMR) spectroscopy, a worldwi

153 most common structural techniques for IDPs: Nuclear Magnetic Resonance (NMR) spectroscopy, Small-ang

154 ple, by combining magic-angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, tailored

155 Using nuclear magnetic resonance (NMR) spectroscopy, we determ

156 sing relaxation dispersion and high-pressure nuclear magnetic resonance (NMR) spectroscopy, we observ

157 success is the utilization of microcryoprobe nuclear magnetic resonance (NMR) spectroscopy, which per

158 r identifying molecular species derived from nuclear magnetic resonance (NMR) spectroscopy-based meta

159 crimination of derivatized amino acids using nuclear magnetic resonance (NMR) spectroscopy.

160 and analysis of its glycan interactions via nuclear magnetic resonance (NMR) spectroscopy.

161 differential scanning fluorimetry (DSF) and nuclear magnetic resonance (NMR) spectroscopy.

162 scopy (XPS), and (10)B and (11)B solid-state nuclear magnetic resonance (NMR) spectroscopy.

163 model epoxide-nucleophile experiments using nuclear magnetic resonance (NMR) spectroscopy.

164 ng site structure, which can be achieved via nuclear magnetic resonance (NMR) spectroscopy.

165 termined and found to be alpha-helical using nuclear magnetic resonance (NMR) spectroscopy.

166 chromatography, mass spectrometry (MS), and nuclear magnetic resonance (NMR) spectroscopy.

167 new in situ magic angle spinning (MAS) (7)Li nuclear magnetic resonance (NMR) strategy allowing for t

168 Here, we report the nuclear magnetic resonance (NMR) structure of a stem-loo

169 The nuclear magnetic resonance (NMR) structures of the P22,

170 st Field-Cycling (FFC) is a well-established Nuclear Magnetic Resonance (NMR) technique that exploits

171 (23)Na magnetic resonance imaging (MRI) and nuclear magnetic resonance (NMR) techniques, along with

172 erovskite CH(3)NH(3)PbBr(3) were studied via nuclear magnetic resonance (NMR) to determine the mechan

173 -angle X-ray scattering (GISAXS) while using nuclear magnetic resonance (NMR) to quantify the bound a

174 ates of a membrane protein by solution-state nuclear magnetic resonance (NMR) using uniformly (15)N-l

175 Using Nuclear Magnetic Resonance (NMR) we showed that both DDB

176 r transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR) were employed to identi

177 drogen/deuterium exchange mass spectrometry, nuclear magnetic resonance (NMR), and evolutionary seque

178 thylation reactions were confirmed by LC-MS, nuclear magnetic resonance (NMR), and rationalized using

179 approach combining high-resolution solution nuclear magnetic resonance (NMR), chemical cross-linking

180 Here, solution nuclear magnetic resonance (NMR), neutron reflectometry

181 ing (MAS) and (105)Pd static solid-state NMR nuclear magnetic resonance (NMR), synchrotron X-ray diff

182 h we name pristinin A3 (1), was solved using nuclear magnetic resonance (NMR), tandem mass spectromet

183 Through the analysis of the exometabolome by nuclear magnetic resonance (NMR), the metabolic changes

184 dependent on databases or require the use of nuclear magnetic resonance (NMR), which have their own d

185 Using nuclear magnetic resonance (NMR)- and structure-based op

186 Nuclear magnetic resonance (NMR)-based studies revealed

187 ough was monitored using low-resolution (1)H nuclear magnetic resonance (NMR).

188 ved from composite pulses widely employed in nuclear magnetic resonance (NMR).

189 s: GC/quadrupole-TOF, LC/quadrupole-TOF, and nuclear magnetic resonance (NMR).

190 s modulate the conformation of arrestin-1 by nuclear magnetic resonance (NMR).

191 ear spin singlet states are silent states in nuclear magnetic resonance (NMR).

192 as identified by gas chromatography (GC) and nuclear magnetic resonance (NMR).

193 ere the optical analogue of multidimensional nuclear magnetic resonance (NMR).

194 Nuclear-magnetic-resonance (NMR) analysis provides the s

195 Low-Field Nuclear Magnetic Resonance of proton transverse relaxati

196 Quantitative (1)H nuclear magnetic resonance (qHNMR) with an appropriate i

197 (1)H quantitative Nuclear Magnetic Resonance (qNMR) spectroscopy technique

198 gels, when measured using proton and carbon nuclear magnetic resonance relaxation methods.

199 eon was investigated with time domain proton nuclear magnetic resonance relaxometry.

200 Moreover, we discovered a diagnostic (13)C nuclear magnetic resonance signal that allows the formul

201 One consists of nuclear magnetic resonance spectra for mixtures of three

202 The proton nuclear magnetic resonance spectra for these adj-dicarba

203 The Raman, infrared, and nuclear magnetic resonance spectra show the clear presen

204 (1)H high-resolution magic angle spinning nuclear magnetic resonance spectra were acquired from ex

205 1D (1)H nuclear magnetic resonance spectra were acquired in plas

206 e recorded over time, the later using proton Nuclear Magnetic Resonance spectra.

207 sonance mass spectrometry (FT-ICR-MS), (13)C-nuclear magnetic resonance spectrometry ((13)C-NMR), and

208 eight chromophores was analyzed by 1D and 2D nuclear magnetic resonance spectroscopic studies reveali

209 ometry and ultraviolet visible, infrared and nuclear magnetic resonance spectroscopies.

210 ing their 1:1 binding properties by means of nuclear magnetic resonance spectroscopy ((1)H and (31)P

211 Proton nuclear magnetic resonance spectroscopy ((1)H NMR), hydr

212 mass spectrometry (native nESI-MS), and (1)H-nuclear magnetic resonance spectroscopy ((1)H NMR).

213 ctures elucidated by one and two-dimensional nuclear magnetic resonance spectroscopy (1D and 2D NMR)

214 nalytical techniques including proton ((1)H) nuclear magnetic resonance spectroscopy (NMR) and electr

215 Solid-state nuclear magnetic resonance spectroscopy (NMR) is potenti

216 ches to elucidation of protein structures by Nuclear Magnetic Resonance spectroscopy (NMR) rely on di

217 Solid-state (31)P nuclear magnetic resonance spectroscopy (NMR) revealed t

218 17 wines of Czech origin were analysed using nuclear magnetic resonance spectroscopy (NMR) with the a

219 Interactions were measured using Nuclear Magnetic Resonance spectroscopy (NMR), Isotherma

220 scopy (SEM), Dynamic Light Scattering (DLS), Nuclear Magnetic Resonance Spectroscopy (NMR), Thermogra

221 e-crystal X-ray crystallography, UV-vis-NIR, nuclear magnetic resonance spectroscopy (NMR), X-ray abs

222 spectrometry (ESI-HRAM-MS/MS), and 1D and 2D nuclear magnetic resonance spectroscopy (NMR).

223 anic molecules is typically determined using nuclear magnetic resonance spectroscopy (NMR).

224 ffusivities measured by pulse field gradient nuclear magnetic resonance spectroscopy (PFG-NMR, which

225 Nuclear magnetic resonance spectroscopy analysis of pote

226 scattering, cross-linking mass spectrometry, nuclear magnetic resonance spectroscopy and computationa

227 e separated and analysed using proton ((1)H)-nuclear magnetic resonance spectroscopy and direct infus

228 polymer was synthesized and characterized by nuclear magnetic resonance spectroscopy and Fourier tran

229 Here we report operando (1)H and (23)Na nuclear magnetic resonance spectroscopy and imaging expe

230 rd carbon, are observed and mapped by (23)Na nuclear magnetic resonance spectroscopy and imaging, and

231 ed and targeted metabolic profiling using 1H-nuclear magnetic resonance spectroscopy and liquid chrom

232 ear single quantum coherence (2D (1)H-(13)C) nuclear magnetic resonance spectroscopy and mass spectro

233 d de-N-acetylated by mono- and bidimensional Nuclear Magnetic Resonance spectroscopy and mass spectro

234 resolution spectroscopic techniques, such as nuclear magnetic resonance spectroscopy and mass spectro

235 f metabolomics on two mass spectrometry, one nuclear magnetic resonance spectroscopy and one fluxomic

236 omposition and speciation of Tc using (99)Tc nuclear magnetic resonance spectroscopy and X-ray absorp

237 hermal titration calorimetry and solid-state nuclear magnetic resonance spectroscopy as well as bacte

238 Solid-state (13) C nuclear magnetic resonance spectroscopy demonstrated tha

239 We used proton nuclear magnetic resonance spectroscopy for metabolic pr

240 Here, using (1)H- and (19)F-nuclear magnetic resonance spectroscopy in combination w

241 ear-edge X-ray absorption fine structure and nuclear magnetic resonance spectroscopy reveal that a va

242 Solution nuclear magnetic resonance spectroscopy revealed that HP

243 e spectroscopic analysis performed by proton-nuclear magnetic resonance spectroscopy showed that the

244 We used nuclear magnetic resonance spectroscopy to describe in a

245 We used nuclear magnetic resonance spectroscopy to determine the

246 grown E. multilocularis metacestodes by (1)H nuclear magnetic resonance spectroscopy to identify the

247 This work uses nuclear magnetic resonance spectroscopy to investigate m

248 Nuclear magnetic resonance spectroscopy was shown to be

249 Additionally, tandem mass spectrometry and nuclear magnetic resonance spectroscopy were used to elu

250 , augmentation index, lipoprotein status (by nuclear magnetic resonance spectroscopy), and nitric oxi

251 ng circular dichroism, thermal denaturation, nuclear magnetic resonance spectroscopy, analytical ultr

252 , electrospray ionization mass spectrometry, nuclear magnetic resonance spectroscopy, and density fun

253 Milk metabolomics were evaluated using (1)H nuclear magnetic resonance spectroscopy, and multivariat

254 omplex at polymer chain ends is evidenced by nuclear magnetic resonance spectroscopy, end group analy

255 analytical platforms, mass spectrometry and nuclear magnetic resonance spectroscopy, have been used

256 Nuclear magnetic resonance spectroscopy, in addition to

257 l products were structurally confirmed using nuclear magnetic resonance spectroscopy, matrix assisted

258 tegrative biophysical approach that includes nuclear magnetic resonance spectroscopy, small-angle x-r

259 s techniques, such as infrared spectroscopy, nuclear magnetic resonance spectroscopy, ultraviolet-vis

260 n with high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy, we integrated t

261 h-resolution imaging and in situ solid-state nuclear magnetic resonance spectroscopy, we reveal the u

262 In this study, using nuclear magnetic resonance spectroscopy, we show that Ki

263 Using high-resolution solution nuclear magnetic resonance spectroscopy, we show that th

264 provides limited structural information, and nuclear magnetic resonance spectroscopy, which can achie

265 The focus is on synchrotron nuclear magnetic resonance spectroscopy, X-ray diffracti

266 spectroscopy, UV-vis spectroscopy, and (1)H nuclear magnetic resonance spectroscopy.

267 of 10 assemblies were fully characterized by nuclear magnetic resonance spectroscopy.

268 id chromatography with mass spectrometry and nuclear magnetic resonance spectroscopy.

269 hydrogen/deuterium fractionation factors by nuclear magnetic resonance spectroscopy.

270 g differential scanning calorimetry and (2)H nuclear magnetic resonance spectroscopy.

271 duplexes, molecular dynamics simulations and nuclear magnetic resonance spectroscopy.

272 detailed lipoprotein subclass profiling from nuclear magnetic resonance spectroscopy.

273 ance liquid chromatography and identified by nuclear magnetic resonance spectroscopy.

274 nd in situ X-ray diffraction and solid-state nuclear magnetic resonance spectroscopy.

275 tal analysis, thermogravimetric analysis and nuclear magnetic resonance spectroscopy.

276 e structure spectroscopy, and solution (31)P nuclear magnetic resonance spectroscopy.

277 nd characterized using X-ray diffraction and nuclear magnetic resonance spectroscopy.

278 solution mass spectrometry, and infrared and nuclear magnetic resonance spectroscopy.

279 ation, time-resolved fluorescence, and (19)F nuclear magnetic resonance spectroscopy.

280 gh spectroscopic resolution using zero-field nuclear magnetic resonance spectroscopy.

281 es using ultrahigh-field zinc-67 solid-state nuclear magnetic resonance spectroscopy.

282 mining techniques such as crystallography or nuclear magnetic resonance spectroscopy.

283 d solutions, and low-temperature solid state nuclear magnetic resonance (ssNMR) enhanced by dynamic n

284 Solid-state nuclear magnetic resonance (ssNMR) spectroscopy plays a

285 Here we used solid-state nuclear magnetic resonance (ssNMR) spectroscopy to probe

286 lear polarization (DNP)-enhanced solid-state nuclear magnetic resonance (SSNMR) spectroscopy, and X-r

287 of the Kir channel KirBac1.1 via solid-state nuclear magnetic resonance (SSNMR) spectroscopy, potassi

288 k comprises the use of different solid-state Nuclear Magnetic Resonance strategies for characterizing

289 Nuclear magnetic resonance structure of the TMH in bicel

290 Nuclear magnetic resonance studies and density functiona

291 d on the basis of mass spectrometry data and nuclear magnetic resonance studies, with the newly deter

292 mid-infrared (MIR) spectroscopy, time domain nuclear magnetic resonance (TD-NMR), and machine learnin

293 r activity (a(w)) assessment and time domain nuclear magnetic resonance (TD-NMR).

294 ) weighted signals registered by Time Domain Nuclear Magnetic Resonance (TD-NMR).

295 biota on circulating metabolites measured by Nuclear Magnetic Resonance technology in 2309 individual

296 ty classes has been evaluated by time domain Nuclear Magnetic Resonance, Thermogravimetric analysis a

297 al changes upon Ab binding were confirmed by nuclear magnetic resonance using a 7A1-single-chain vari

298 Using Nuclear Magnetic Resonance, we were able to detect DMG i

299 Chronopotentiometry, mass spectrometry and nuclear magnetic resonance were used to investigate the

300 change measurements by mass spectrometry and nuclear magnetic resonance with molecular dynamics to ev