ライフサイエンスコーパス: NMR spectroscopy

1 ize exclusion chromatography and Solid-state NMR spectroscopy.

2 ate constant of 9 M(-1) s(-1) as measured by NMR spectroscopy.

3 pression, noncovalent mass spectrometry, and NMR spectroscopy.

4 on and was confirmed with solid-state (31) P NMR spectroscopy.

5 4,6-phosphates, which were analyzed by (31)P NMR spectroscopy.

6 characterized as intrinsically disordered by NMR spectroscopy.

7 top pan molecular balances was determined by NMR spectroscopy.

8 tural studies by crystallography or solution NMR spectroscopy.

9 ies of membrane proteins with solution-state NMR spectroscopy.

10 protein structure, function, and dynamics by NMR spectroscopy.

11 onjunction with DNP and magic-angle-spinning NMR spectroscopy.

12 rs was proved by elemental analysis, IR, and NMR spectroscopy.

13 ol of other metabolites in human blood using NMR spectroscopy.

14 icity using low-field (60MHz) bench-top (1)H NMR spectroscopy.

15 n in phospholipid bilayers using solid-state NMR spectroscopy.

16 investigated by (15)N relaxation dispersion NMR spectroscopy.

17 namics of active and inactive TNFalpha using NMR spectroscopy.

18 ed enzymatic and chemical methods as well as NMR spectroscopy.

19 s membrane topology using static solid-state NMR spectroscopy.

20 ammonium ions by direct and competitive (1)H NMR spectroscopy.

21 lin has been studied using in situ (13)C MAS NMR spectroscopy.

22 measurements using stopped-flow kinetics and NMR spectroscopy.

23 polymers, as detected by solid-state (13) C NMR spectroscopy.

24 f supramolecular machines using methyl-based NMR spectroscopy.

25 namics were assessed by variable-temperature NMR spectroscopy.

26 d pyridinium salts in combination with (19)F NMR spectroscopy.

27 s were characterized structurally using (1)H NMR spectroscopy.

28 hesized and characterized structurally using NMR spectroscopy.

29 t ambient temperature in aqueous solution by NMR spectroscopy.

30 ere confirmed by HRMS and detailed 1D and 2D NMR spectroscopy.

31 d by single crystal X-ray diffraction and/or NMR spectroscopy.

32 holine nanoparticles and studied by solution NMR spectroscopy.

33 ons with the aid of combined (1)H- and (19)F-NMR spectroscopy.

34 of the anti-sigma factor, NepR, by solution NMR spectroscopy.

35 erences in surface chemistry to be mapped by NMR spectroscopy.

36 compounds using circular dichroism and (1) H NMR spectroscopy.

37 c1, for prokaryotic production to be used in NMR spectroscopy.

38 the corresponding oils were analysed by (1)H NMR spectroscopy.

39 e O-protonation was observed by multinuclear NMR spectroscopy.

40 correlation (PAC) of gamma-rays and (113)Cd NMR spectroscopy.

41 tions at 37 degrees C and monitored by (13)C NMR spectroscopy.

42 tudied the NtrC1-sigma(54) AID complex using NMR spectroscopy.

43 e phosphatase 1B using a covalent ligand and NMR spectroscopy.

44 The binding mechanism was delineated via NMR spectroscopy.

45 tone modification crosstalk by time-resolved NMR spectroscopy.

46 h-level DFT studies and variable-temperature NMR spectroscopy.

47 structural characterization was possible by NMR spectroscopy.

48 t that has been characterized by IR and (1)H NMR spectroscopy.

49 racterized using TLC, mass spectrometry, and NMR spectroscopy.

50 itions including sugars were evaluated using NMR spectroscopy.

51 to phenols has been investigated using (19)F NMR spectroscopy.

52 NTA is similar to that determined by in vivo NMR spectroscopy.

53 symmetric conformers can be distinguished by NMR spectroscopy.

54 sensing riboswitch from Mesoplasma florum by NMR spectroscopy.

55 large size prohibits structural analysis by NMR spectroscopy.

56 fferent pulsing delays by dual-channel (19)F NMR spectroscopy.

57 onstrated for double-stranded (ds) DNA using NMR spectroscopy.

58 were established using X-ray diffraction and NMR spectroscopy.

59 tate and glucose tracers in combination with NMR spectroscopy.

60 zed Zn species in combination with EXAFS and NMR spectroscopy.

61 on barriers, as demonstrated by dynamic (1)H NMR spectroscopy.

62 YscU by means of nuclear magnetic resonance (NMR) spectroscopy.

63 onal solid-state nuclear magnetic resonance (NMR) spectroscopy.

64 siense, using 1H nuclear magnetic resonance (NMR) spectroscopy.

65 tion with (7) Li nuclear magnetic resonance (NMR) spectroscopy.

66 S (LC-MS/MS) and nuclear magnetic resonance (NMR) spectroscopy.

67 echanistically using a combination of IR and NMR spectroscopies.

68 chniques, including infrared and solid-state NMR spectroscopies.

69 Based on (77)Se NMR spectroscopy, a catalytic cycle for diselenide 8b, i

70 cterization of relative stereochemistries by NMR spectroscopy, a DFT-based theoretical model was deve

71 ne stability with no degradation detected by NMR spectroscopy after more than 1800 h in 1 M KOD/D2O a

72 ZZ-exchange NMR spectroscopy allows determination of folding and unf

73 Concepts of solid-state NMR spectroscopy and applications to fluid membranes are

74 HR mass spectrometry and extensive 1D and 2D NMR spectroscopy and based on data from synthetic arunci

75 The binding site of NF023, identified by NMR spectroscopy and biochemical assays, overlaps with t

76 in chloroform has been investigated by (1)H NMR spectroscopy and computational methods.

77 es were determined by single-crystal XRD and NMR spectroscopy and confirmed that the solid-state stru

78 Through a combination of NMR spectroscopy and control studies with and without ox

79 HBs) in 5-azopyrimidines are investigated by NMR spectroscopy and DFT computations that involve nucle

80 Here, we used NMR spectroscopy and electrophysiological characterizati

81 Perry and colleagues now combine NMR spectroscopy and electrophysiological experiments to

82 Using (1)H NMR spectroscopy and fiber X-ray diffraction, we determi

83 zed the acid-induced unfolding of HdeA using NMR spectroscopy and fluorescence measurements, and obta

84 in the cyanoindenes was determined by (13)C NMR spectroscopy and indicates the occurrence of two par

85 IMHBs is determined by variable temperature NMR spectroscopy and it is demonstrated that the barrier

86 NMR spectroscopy and mass spectrometry analyses of degra

87 sphate product was characterized using (31)P NMR spectroscopy and mass spectrometry.

88 unambiguously observed and characterized by NMR spectroscopy and mass spectrometry.

89 Characterizations by NMR spectroscopy and matrix-assisted laser ionization ti

90 NMR spectroscopy and MD simulations were used to obtain

91 used a combination of relaxation dispersion NMR spectroscopy and molecular dynamics simulations to d

92 Using methyl-TROSY solution NMR spectroscopy and molecular dynamics simulations, we

93 the native state as probed by heteronuclear NMR spectroscopy and multiple conformer simulations of c

94 Solid-state (2)H NMR spectroscopy and neutron diffraction studies reveal

95 ation, we characterized the sigma(54) AID by NMR spectroscopy and other biophysical methods and show

96 ls relating to optimization of nanodiscs for NMR spectroscopy and outline a strategy for the high-res

97 Two-dimensional NMR spectroscopy and polarimetry provided a deeper under

98 through a combination of in situ solid-state NMR spectroscopy and powder X-ray diffraction experiment

99 NMR spectroscopy and quantum chemical calculations were

100 rosix-membered ring by low temperature (13)C NMR spectroscopy and quantum chemical calculations.

101 Both (1)H NMR spectroscopy and single-crystal X-ray diffraction an

102 ilica nanostructures, using widely available NMR spectroscopy and small amounts of sample.

103 ecular aggregation have been investigated by NMR spectroscopy and supported by quantum chemical calcu

104 alkyl straps is investigated in solution by NMR spectroscopy and UV-vis titration, and in the solid

105 Based on data from (1) H, (13)C, and (31)P NMR spectroscopy and X-ray crystallography, we suspect t

106 This complex was fully characterized by NMR spectroscopy and X-ray crystallography.

107 17A1, as previously proposed on the basis of NMR spectroscopy and X-ray crystallography.

108 The latter was isolated and characterized by NMR spectroscopy and X-ray crystallography.

109 These results were confirmed both by NMR spectroscopy and X-ray diffraction analysis.

110 Using nuclear magnetic resonance (NMR) spectroscopy and biochemistry, we show that RNF169

111 der conventional nuclear magnetic resonance (NMR) spectroscopy and imaging (MRI) incompatible with sm

112 ly elucidated by Nuclear Magnetic Resonance (NMR) spectroscopy and mass spectrometry (MS).

113 lyzed using (1)H nuclear magnetic resonance (NMR) spectroscopy and multivariate data analysis.

114 in solution by (1)H DOSY (diffusion-ordered NMR spectroscopy), and a Van't Hoff analysis of the equi

115 UV-vis, (1)H NMR spectroscopies, and DFT calculations resulted approp

116 1)H-NOESY, (1)H,(13)C-HSQC, (1)H,(13)C-HMBC) NMR spectroscopies, and structures of six complexes (thr

117 these dynamics, using X-ray crystallography, NMR spectroscopy, and ab initio quantum-mechanical calcu

118 ere established by X-ray structure analysis, NMR spectroscopy, and additional independent synthetic p

119 T calculations, IR spectroscopy, solid-state NMR spectroscopy, and analysis of the Cambridge Structur

120 tructures produced by X-ray crystallography, NMR spectroscopy, and cryo electron microscopy.

121 mation of amides was studied using kinetics, NMR spectroscopy, and DFT calculations.

122 -phase electron diffraction, low-temperature NMR spectroscopy, and high-level quantum chemical calcul

123 mall-angle x-ray scattering, high-resolution NMR spectroscopy, and limited proteolysis coupled with m

124 e characterized using X-ray crystallography, NMR spectroscopy, and mass spectrometry.

125 that combines small angle X-ray scattering, NMR spectroscopy, and molecular dynamics simulations, we

126 tracts and purified proteins by top-down MS, NMR spectroscopy, and site-directed mutagenesis revealed

127 eus-independent chemical shift calculations, NMR spectroscopy, and X-ray crystallography revealed the

128 d by proton nuclear magnetic resonance ((1)H-NMR) spectroscopy, and diet-discriminatory metabolites w

129 ynamic nuclear polarization surface enhanced NMR spectroscopy approach that induces a 200-fold increa

130 ommunication will highlight the potential of NMR spectroscopy as a method for identification of probl

131 yogenic probe, demonstrates the viability of NMR spectroscopy as a powerful and complementary techniq

132 tes, and he was instrumental in establishing NMR spectroscopy as a standard analytical technique in o

133 se here in vitro kinase assays combined with NMR spectroscopy as an analytical tool to generate well-

134 hich was fully characterized by multinuclear NMR spectroscopy as well as single-crystal X-ray diffrac

135 plexes were synthesized and characterized by NMR spectroscopy as well as X-ray crystallography.

136 by ATR-FTIR and nuclear magnetic resonance (NMR) spectroscopy as well as analytical ultracentrifugat

137 Results demonstrated the suitability of NMR spectroscopy, as a robust nondestructive technique,

138 ons were fully characterized by multinuclear NMR spectroscopy at low temperature, and the reaction co

139 internal dynamics, and opens new avenues for NMR spectroscopy at very high magnetic fields.

140 In this study, nuclear magnetic resonance (NMR) spectroscopy-based metabolomic analysis was used to

141 chemical shift of Li polysulfides in (7) Li NMR spectroscopy, being both theoretically predicted and

142 By combining NMR spectroscopy, biophysical measurements, statistical

143 ancy (NV) centres in diamond can be used for NMR spectroscopy, but increased sensitivity is needed to

144 for small-volume nuclear magnetic resonance (NMR) spectroscopy, but the limited sensitivity remains a

145 Here, we demonstrate that (13)C NMR spectroscopy can also be successfully adopted to cha

146 Here, we show that solid-state (17) O NMR spectroscopy can provide unique information about th

147 to detect these modifications in proteins by NMR spectroscopy, chemical shift assignments of referenc

148 Nuclear magnetic resonance (NMR) spectroscopy combined with cross-linking experiment

149 We combine NMR spectroscopy, computational modelling and biochemist

150 Structural analysis by NMR spectroscopy confirmed that the peptides maintain an

151 (1)H and (13)C nuclear magnetic resonance (NMR) spectroscopies confirmed the isolation of the dimer

152 n neutral and acidic environments from D-DNP NMR spectroscopy, corresponding to a pre-equilibrium of

153 and and Australia were analysed using proton NMR spectroscopy coupled with chemometrics.

154 Analysis of (1)H-NMR spectroscopy data indicated that urinary metabolic p

155 le Spinning Nuclear Magnetic Resonsance (MAS-NMR) spectroscopy, demonstrated increased abundance of t

156 Compounds 1-3 were analyzed by EPR and NMR spectroscopy, DFT calculations, and X-ray crystallog

157 y)2(2A-tripy)2](4+) was confirmed using (1)H NMR spectroscopy, diffusion-ordered spectroscopy, and ro

158 ynamic nuclear polarization surface-enhanced NMR spectroscopy (DNP SENS) allows the unambiguous descr

159 nuclear polarization surface-enhanced (89)Y NMR spectroscopy (DNP SENS).

160 complexes using a (1)H NMR/diffusion-ordered NMR spectroscopy (DOSY) titration technique.

161 y, temperature- and pressure-dependent (17)O NMR spectroscopy, electrochemistry, stopped-flow kinetic

162 rystal X-ray diffraction and show by (27) Al NMR spectroscopy, electrospray-ionization mass spectrome

163 Two-field NMR spectroscopy enables the measurement of chemical shi

164 The new compounds were characterized by NMR spectroscopy, ESI-MS spectrometry, and X-ray single-

165 ) P) and two-dimensional (COSY, NOESY, DOSY) NMR spectroscopy, ESI-MS, ion-mobility mass spectrometry

166 ectures were characterized by NOESY and DOSY NMR spectroscopy, ESI-MS, TWIM-MS, and transmission elec

167 Nuclear magnetic resonance (NMR) spectroscopy evaluated the aromatic compounds and t

168 he dioxo compound, as established by dynamic NMR spectroscopy, excludes the intermediacy of mer-(ONO(

169 (1)H and (2)H NMR spectroscopy experiments on reactions using allylic

170 Comprehensive (1)H NMR spectroscopy experiments unravel the network topolog

171 Solution NMR spectroscopy experiments validated the ACPS binding

172 series of comprehensive kinetic (19)F{(1)H} NMR spectroscopy experiments, this system-level outcome

173 was performed by nuclear magnetic resonance (NMR) spectroscopy, followed by multivariate statistical

174 hird minireview highlights advances in using NMR spectroscopy for analysis of protein folding and ass

175 on the use of analytical techniques, mainly NMR spectroscopy, for authentication of honey, its botan

176 es have been characterized by (1)H and (13)C NMR spectroscopy, FTIR, EA, and melting point, and in th

177 NMR spectroscopy further demonstrated that DREB2A underw

178 Over the past few decades, NMR spectroscopy has become an established tool in drug

179 A method using (1)H NMR spectroscopy has been developed to quantify simultan

180 s especially lipids and acetate derived from NMR spectroscopy has high sensitivity and specificity to

181 The nanoprobe based NMR spectroscopy has the potential to enable rapid scree

182 Until recently, NMR spectroscopy has yielded structures of small or medi

183 Nuclear magnetic resonance (NMR) spectroscopy has been instrumental during the past

184 6,8-pentachloro-BODIPY, and characterized by NMR spectroscopy, HRMS, and X-ray crystallography.

185 ene-fused BODIPYs 4a-c were characterized by NMR spectroscopy, HRMS, DFT calculations, and, in the ca

186 onas reinhardtii has been studied using (1)H NMR spectroscopy identifying the paramagnetically shifte

187 oviding compelling evidence for the value of NMR spectroscopy in characterizing faceted oxides.

188 rning more about the potential and impact of NMR spectroscopy in environmental research.

189 yclophane structures are characterized using NMR spectroscopy in solution and single-crystal X-ray di

190 xes is assessed computationally and by (31)P NMR spectroscopy in toluene-d8 solution, where both comp

191 ng ((1)H HR-MAS) nuclear magnetic resonance (NMR) spectroscopy in combination with principal componen

192 lysed using (1)H nuclear magnetic resonance (NMR) spectroscopy in comparison to authentic products.

193 cation of methyl nuclear magnetic resonance (NMR) spectroscopy in protein side-chain structural studi

194 c acid from various structural elements, and NMR spectroscopy indicated complete de-esterification of

195 Variable-temperature (1)H NMR spectroscopy indicates fast ethyl group exchange bet

196 Variable-temperature (1) H NMR spectroscopy indicates that this transition is the r

197 , were synthesized and characterized by (1)H NMR spectroscopy, IR spectroscopy, mass spectrometry, an

198 actions with cucurbit[6]uril were studied by NMR spectroscopy, IR spectroscopy, X-ray crystallography

199 In the past, (13)C NMR spectroscopy (irm-(13)C NMR) was mainly used to meas

200 NMR spectroscopy is a powerful tool for studying molecul

201 Studying PTMs by NMR spectroscopy is a promising method to analyze protei

202 NMR spectroscopy is a versatile tool for the study of st

203 Saturation transfer difference (STD) NMR spectroscopy is extensively used to obtain epitope m

204 Naked RNAs are difficult to crystallize and NMR spectroscopy is generally limited to small RNA fragm

205 an blood by (1)H nuclear magnetic resonance (NMR) spectroscopy is a rapid and promising approach to m

206 Nuclear magnetic resonance (NMR) spectroscopy is widely used in metabolomics to perf

207 Using NMR spectroscopy, isothermal titration calorimetry and m

208 d kinetic studies using UV/vis, CD, and (1)H NMR spectroscopy, it was established that they still fun

209 ed using a combination of isotopic labeling, NMR spectroscopy, kinetic modeling, structure-activity r

210 prepared and studied by variable temperature NMR spectroscopy leading to the conclusion that the rate

211 dentifying several reaction intermediates by NMR spectroscopy, mass spectrometry and X-ray crystallog

212 ot topology and handedness were confirmed by NMR spectroscopy, mass spectrometry, and X-ray crystallo

213 The ligands and cages were characterized by NMR spectroscopy, mass spectrometry, elemental analysis,

214 lement of Abeta, have been unravelled by STD-NMR spectroscopy methods in solution.

215 Here, we used NMR spectroscopy, mutagenesis, small-angle X-ray scatter

216 Using circular dichroism, NMR spectroscopy, native mass-spectrometry and X-ray cry

217 The discovery by NMR spectroscopy of a "p53 rescue motif" in SUSP4 that d

218 igh resolution-magic angle spinning (HR-MAS) NMR spectroscopy of apple pulp was performed before and

219 we carried out metabolomic analysis by (1)H NMR spectroscopy of media from astrocyte-spinal neuron c

220 al studies by high-resolution solution-state NMR spectroscopy of membrane proteins in commonly used n

221 We demonstrate NMR spectroscopy of picoliter-volume solutions using a n

222 with a high density of NV centres, enabling NMR spectroscopy of picoliter-volume solutions.

223 the chiral recognition of small molecules by NMR spectroscopy, opening new possibilities in situation

224 hway by an experimental strategy centered on NMR spectroscopy, protein engineering, and X-ray crystal

225 Mass spectrometry and NMR spectroscopy provide complementary analytical inform

226 NMR spectroscopy provides important details of the natur

227 n secondary structures (as revealed by 2D-1H NMR spectroscopy), providing a basis for their interacti

228 ficult to detect in alkaline solutions using NMR spectroscopy, requiring alternative methods for dete

229 Mass spectrometry and NMR spectroscopy reveal that hyper-Ser5 phosphorylation

230 NMR spectroscopy revealed a marked loss of signal intens

231 ydrogen induced polarization (PHIP) transfer NMR spectroscopy revealed cis-hydrogenation of the alkyn

232 NMR spectroscopy revealed that this inhibitory compound

233 ed form of the MAL TIR domain, determined by NMR spectroscopy, reveals a remarkable structural rearra

234 The use of low-temperature, rapid injection NMR spectroscopy (RI-NMR), kinetic studies, and computat

235 ght sources with nuclear magnetic resonance (NMR) spectroscopy: sample irradiation using a "sunlight

236 ral abundance by (17) O DNP surface-enhanced NMR spectroscopy (SENS).

237 M phosphate, 25 degrees C) monitored by (1)H NMR spectroscopy show benign acetic acid as the only sig

238 The results of NMR spectroscopy show the resulting enolates to be stati

239 antitative (13)C nuclear magnetic resonance (NMR) spectroscopy shows that the presence of the iron cl

240 rmation for subsequent experiments (e.g., 2D-NMR spectroscopy, solid-phase extraction, liquid chromat

241 ca. 30 nm diameter) can be used for solution NMR spectroscopy studies whereas the magnetic-alignment

242 ons, as shown by nuclear magnetic resonance (NMR) spectroscopy studies and all-atom molecular dynamic

243 In this work we propose NMR spectroscopy such as (1)H NMR, (1)H-(1)H TOCSY and D

244 hniques routinely employed in small molecule NMR spectroscopy, such as HSQC, HMQC, HMBC, COSY, NOESY,

245 DOSY is an NMR spectroscopy technique that resolves resonances acco

246 By low-temperature NMR spectroscopy the six-membered-ring interconversion c

247 In the present work, we used UV-vis and NMR spectroscopies to investigate the electron transfer

248 We used peptide synthesis and 2D NMR spectroscopy to assign all (1)H and (13)C chemical s

249 of investigation enable high resolution (1)H NMR spectroscopy to be used for evaluation of saffron ad

250 employ isothermal titration calorimetry and NMR spectroscopy to characterize MeCP2 binding to methyl

251 In this study we use NMR spectroscopy to determine the pKa for the N-terminal

252 Modern applications of 2D NMR spectroscopy to diagnostic screening, metabolomics,

253 Here, the authors use (17)O solid-state NMR spectroscopy to discriminate between oxygen species

254 density fractionation and solid-state (13) C-NMR spectroscopy to explore the extent to which declines

255 Here, we use solid-state NMR spectroscopy to investigate the structure, dynamics,

256 Here we use solid-state NMR spectroscopy to investigate the water interactions o

257 We have used NMR spectroscopy to obtain site-specific structure and d

258 organic matter with advanced two-dimensional NMR spectroscopy to open the "black box" of uncharacteri

259 a series of 270 ternary reactions using (1)H NMR spectroscopy to quantify product selectivity.

260 continuous high-sensitivity (1)H-(15)N HMBC NMR spectroscopy to resolve scarce reaction intermediate

261 ted by variable-temperature (2)H solid-state NMR spectroscopy to reveal the reorientation mechanisms

262 measurements in combination with solid-state NMR spectroscopy to show that the cohesive properties of

263 above materials and applied solid-state (2)H NMR spectroscopy to show that these three frameworks con

264 A method based on d-DNP NMR spectroscopy to study chiral recognition is describe

265 Here, we use solution NMR spectroscopy to study phase-separated droplets forme

266 nce anisotropy measurements, and solid-state NMR spectroscopy to study the influence of physiological

267 tic relaxation enhancement (PRE) measured by NMR spectroscopy to study the transient intermolecular i

268 sed (1)H-[(13)C]-nuclear magnetic resonance (NMR) spectroscopy to evaluate the effects of RH on neuro

269 al resolution of nuclear magnetic resonance (NMR) spectroscopy to several hundred Hertz, which typica

270 Mass spectrometry and NMR spectroscopy together with computational tools have

271 sis and saturation transfer difference (STD) NMR spectroscopy using an enhanced method to interpret t

272 Lastly, NMR spectroscopy using in situ LED-irradiated samples wa

273 NMR spectroscopy was performed for backbone and side-cha

274 etails of this conformational rearrangement, NMR spectroscopy was used to discover that the JM region

275 (1)H HR-MAS NMR spectroscopy was used to track the metabolic changes

276 Using (1)H NMR spectroscopy we characterised short-term variability

277 Using methyl transverse relaxation-optimized NMR spectroscopy, we demonstrate that only three of the

278 Using NMR spectroscopy, we demonstrate that the RAP80 SIM bind

279 Using molecular modelling and 1D (1)H NOESY NMR spectroscopy, we determine the angle between the two

280 Using 2D NMR spectroscopy, we established for the first time that

281 By solid-state (13)C NMR spectroscopy, we observed that about one-third of he

282 , using isothermal titration calorimetry and NMR spectroscopy, we report that acidic residues in the

283 Using nuclear magnetic resonance (NMR) spectroscopy, we analysed the lipoprotein profile o

284 By nuclear magnetic resonance (NMR) spectroscopy, we characterized the dynamics of all

285 ng (7)Li-/(95)Mo-nuclear magnetic resonance (NMR) spectroscopy, we directly observed the charge state

286 Here, by using nuclear magnetic resonance (NMR) spectroscopy, we examine the mechanism of action of

287 onal solid-state nuclear magnetic resonance (NMR) spectroscopy, we show that mineral deposition is bi

288 Here, using nuclear magnetic resonance (NMR) spectroscopy, we show that TRIP13 and p31(comet) ca

289 High-field and low-field proton NMR spectroscopy were used to analyse lipophilic extract

290 inylphosphonium ions can only be observed by NMR spectroscopy when benzhydryl cations with high Lewis

291 ization methods improve the applicability of NMR spectroscopy when rapid acquisitions or low concentr

292 n solution have been studied by multinuclear NMR spectroscopy, which supports specific interactions b

293 single- and double-quantum (1)H solid-state NMR spectroscopy with density functional theory calculat

294 Combining quantitative NMR spectroscopy with principal component analysis we ha

295 Here, nuclear magnetic resonance (NMR) spectroscopy with the wild-type-like A2A adenosine

296 tics of this process of were investigated by NMR spectroscopy, with the determined overall second-ord

297 ds and their model analogues were studied by NMR spectroscopy, X-ray analysis, and MP2 theoretical ca

298 By means of ligand-based NMR spectroscopy, X-ray crystallography, computer simula

299 3) C cross-polarization magic-angle spinning NMR spectroscopy, X-ray diffraction, and time-resolved f

300 Comprehensive NMR spectroscopy yields a detailed picture of the polyme