ライフサイエンスコーパス: NMR spectroscopy

1 les their characterization by solution-state NMR spectroscopy.

2 ncement (PRE) to characterize Cu(II)-LPMO by NMR spectroscopy.

3 rief contact in the skin was assayed by (1)H NMR spectroscopy.

4 nctional theory calculations and solid-state NMR spectroscopy.

5 th those obtained by P K-edge XANES or (31)P NMR spectroscopy.

6 uthentication by application of non-targeted NMR spectroscopy.

7 those obtained from orthogonal analysis via NMR spectroscopy.

8 g (129) Xe, (1) H, and pulsed-field gradient NMR spectroscopy.

9 amenable to neither solid-state nor solution NMR spectroscopy.

10 r, TSG101-UEV, as evidenced by heteronuclear NMR spectroscopy.

11 he atomic level with high-resolution protein NMR spectroscopy.

12 ve been extensively studied with solid-state NMR spectroscopy.

13 e characterized by X-ray crystallography and NMR spectroscopy.

14 a log P determination method based on (19)F NMR spectroscopy.

15 to the Val66Met mutation, when compared with NMR spectroscopy.

16 study peptide-protein interactions by (19) F NMR spectroscopy.

17 re of hGMPK in the apo form, determined with NMR spectroscopy.

18 mall molecules to large proteins by solution NMR spectroscopy.

19 ernate approach for structure calculation by NMR spectroscopy.

20 the SET-FTY720 or SET-ceramide complexes by NMR spectroscopy.

21 e type that differ only in style, using (1)H NMR spectroscopy.

22 f chemical transformations by hyperpolarized NMR spectroscopy.

23 and cooperativity factors were confirmed by NMR spectroscopy.

24 id bilayers using two-dimensional J-resolved NMR spectroscopy.

25 lymer products, other than ester bonds, with NMR spectroscopy.

26 e domain (ETM), determined using solid-state NMR spectroscopy.

27 which are typically the exclusive domain of NMR spectroscopy.

28 efficients at 298.15 K were calculated using NMR spectroscopy.

29 esonances is applicable to other contexts in NMR spectroscopy.

30 )](2+) ) forms two isomers as shown by (1) H NMR spectroscopy.

31 alently attached Ub and Ub(2) moieties using NMR spectroscopy.

32 interactions via nuclear magnetic resonance (NMR) spectroscopy.

33 mino acids using nuclear magnetic resonance (NMR) spectroscopy.

34 imetry (DSF) and nuclear magnetic resonance (NMR) spectroscopy.

35 11)B solid-state nuclear magnetic resonance (NMR) spectroscopy.

36 ha-helical using nuclear magnetic resonance (NMR) spectroscopy.

37 sing proton nuclear magnetic resonance ((1)H NMR) spectroscopy.

38 ometry (MS), and nuclear magnetic resonance (NMR) spectroscopy.

39 diffuse reflectance UV-vis, and solid-state NMR spectroscopies.

40 D, IR, TGA, and solid-state (1) H and (13) C NMR spectroscopy, 2) in solution by (1) H, (13) C NMR an

41 catalytic resting state as observed by (31)P NMR spectroscopy; (3) there are no long-lived nitroarene

42 -reduction intermediates observable by (15)N NMR spectroscopy; (4) the reaction is sensitive to solve

43 Using nuclear magnetic resonance (NMR) spectroscopy, a worldwide consortium of NMR researc

44 Herein, we demonstrate that solid-state NMR spectroscopy allows the unambiguous assignment of or

45 In metabolomics, nuclear magnetic resonance (NMR) spectroscopy allows to identify and quantify compou

46 Our in vitro studies using NMR spectroscopy and (54)Fe LC-ICP-MS confirm the Fe(III

47 rrent snapshot of this important subfield of NMR spectroscopy and a basis and framework for including

48 taneously enantiospecifically detected using NMR spectroscopy and a chiral solvating agent.

49 Using (19) F NMR spectroscopy and advanced molecular dynamics simulat

50 structure of BTNL2 as determined by solution NMR spectroscopy and also the picosecond-nanosecond time

51 l dynamics in hI-BABP was investigated using NMR spectroscopy and biophysical tools.

52 By using NMR spectroscopy and circular dichroism spectropolarimet

53 27)Al, and (71)Ga magic angle spinning (MAS) NMR spectroscopy and density-functional theory (DFT) cal

54 Aromaticity is assigned by NMR spectroscopy and density-functional theory calculati

55 ic junction, quantified via fluorescence and NMR spectroscopy and DFT calculations.

56 ation of the ion atmosphere around DNA using NMR spectroscopy and directly detect the release of coun

57 We measured metabolites by HR-MAS (1)H NMR spectroscopy and DNA cytosine modifications by LC/MS

58 compounds and the FOXO3-DBD was assessed via NMR spectroscopy and docking studies.

59 gated by applying (17)O and (1)H solid-state NMR spectroscopy and dynamic nuclear polarization, combi

60 ogy approach using X-ray crystallography and NMR spectroscopy and evaluate their role in PMT function

61 ymers were characterized by (1) H and (13) C NMR spectroscopy and gel-permeation chromatography.

62 sines A and B, were elucidated by 1D- and 2D-NMR spectroscopy and HR-ESI-MS/MS spectrometry, while a

63 NMR spectroscopy and hydrogen/deuterium exchange mass sp

64 ix[3]arene-based receptors was studied using NMR spectroscopy and in silico methods.

65 In this study, using NMR spectroscopy and interaction assays, we investigated

66 In this study, we used NMR spectroscopy and isothermal titration calorimetry (I

67 Finally, using NMR spectroscopy and isothermal titration calorimetry, w

68 s, including diesters and diamides, via (1)H NMR spectroscopy and isothermal titration calorimetry.

69 Use of NMR spectroscopy and isotope effects, with the support o

70 e identity of the rotaxanes was confirmed by NMR spectroscopy and mass spectrometry.

71 Here, we used NMR spectroscopy and molecular dynamics (MD) simulations

72 Here, using NMR spectroscopy and molecular dynamics simulations comp

73 ure of the carrier protein by using solution NMR spectroscopy and molecular dynamics simulations.

74 e, using a combination of chemical kinetics, NMR spectroscopy and other biophysical methods, we ident

75 s work, by combination of organic synthesis, NMR spectroscopy and quantum chemical modeling, we show

76 re consistent with ring currents measured in NMR spectroscopy and simulated in time-dependent density

77 e of 5 was unambiguously established by both NMR spectroscopy and single-crystal X-ray diffraction.

78 Using NMR spectroscopy and small angle x-ray scattering, we sh

79 Rumen fluid samples were analysed by (1)H-NMR spectroscopy and the resulting spectra were used to

80 mprehensive metabolic phenotyping platforms (NMR spectroscopy and UHPLC-MS) to probe the urinary meta

81 EM, XRD, Raman spectroscopy and static (13)C NMR spectroscopy and used as a basis to correct the C/Zr

82 e interaction is provided by (1)H-(15)N HMBC NMR spectroscopy and X-ray crystallographic structures.

83 We employed NMR spectroscopy and X-ray crystallography coupled with

84 thyl transverse relaxation optimized (TROSY) NMR spectroscopy and X-ray crystallography, we establish

85 plexes of these ligands were investigated by NMR spectroscopy and X-ray crystallography, which reveal

86 omic level by saturation transfer difference NMR spectroscopy and X-ray crystallography.

87 350 nm), and key products were identified by NMR spectroscopy and X-ray crystallography.

88 (2)H(5))(12)](-1), was characterized by (1)H NMR spectroscopy and X-ray crystallography.

89 he individual stereoisomers were revealed by NMR spectroscopy and X-ray structure analysis.

90 were analyzed by nuclear magnetic resonance (NMR) spectroscopy and compared using multivariate and un

91 Solid-state nuclear magnetic resonance (NMR) spectroscopy and computational modeling implied tha

92 investigated by Nuclear Magnetic Resonance (NMR) spectroscopy and Fourier Transform Ion Cyclotron Re

93 hniques, such as nuclear magnetic resonance (NMR) spectroscopy and inductively coupled plasma mass sp

94 ny) by (1)H Nuclear Magnetic Resonance ((1)H NMR) spectroscopy and its in vitro antioxidant propertie

95 lysed using (1)H nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS).

96 Nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry of active fracti

97 as studied using Nuclear Magnetic Resonance (NMR) spectroscopy and multivariate analysis (MVA).

98 rus-mimetic lipid bilayers using solid-state NMR spectroscopy, and augmented these experimental data

99 labeling studies, variable-temperature (1)H NMR spectroscopy, and density functional theory calculat

100 ng paramagnetic relaxation enhancement (PRE) NMR spectroscopy, and determined distinct structures of

101 al methods, including x-ray crystallography, NMR spectroscopy, and small angle x-ray scattering, to c

102 the Zn frameworks is quantified using (13)C NMR spectroscopy, and spatially resolved EDX spectroscop

103 Circular dichroism spectra, 2D-NMR spectroscopy, and the computational simulations sugg

104 zed by X-ray crystallography, electronic and NMR spectroscopy, and theoretical calculations.

105 pectroscopy, solid-state deuterium NMR ((2)H NMR) spectroscopy, and molecular dynamics (MD) simulatio

106 lution solid-state (1)H, (71)Ga, and (115)In NMR spectroscopy; and discrete Fourier transform (DFT) a

107 X-ray diffraction; UV/vis, MCD, IR, EPR, and NMR spectroscopy; and quantum chemistry.

108 lution-phase proteins (X-ray diffraction and NMR spectroscopy) are not well-suited for studying prote

109 is determined by hyperpolarized (13)C SABRE-NMR spectroscopy as 0.056 +/- 0.003 dm(3) mol(-1) s(-1)

110 ication and development of (17)O solid-state NMR spectroscopy as a probe of molecular structure and d

111 3) by using two-dimensional (2D) solid-state NMR spectroscopy at high field.

112 ies derived from nuclear magnetic resonance (NMR) spectroscopy-based metabolic phenotyping studies, w

113 ependent behavior, cannot be investigated by NMR spectroscopy because of the supramolecular, soft nat

114 een hGrx1, Atox1 and WLN5-6 were detected by NMR spectroscopy both in the presence and absence of Cu

115 y and industrially important materials using NMR spectroscopy but suggests that further investigation

116 t operando (7)Li nuclear magnetic resonance (NMR) spectroscopy can be applied to full LIBs.

117 (1)H NMR spectroscopy combined with chemometrics was applied

118 roscopy, mass spectrometry, and multinuclear NMR spectroscopy confirm that the organic byproducts con

119 Nuclear magnetic resonance (NMR) spectroscopy contributes to this thrust through its

120 (19)F NMR spectroscopy could thus be adapted to allow contact

121 In this study, (1)H NMR spectroscopy coupled with multivariate statistical a

122 ation of data and multiple views afforded by NMR spectroscopy, cryo-electron microscopy, cryo-electro

123 Here, using diffusion ordered NMR spectroscopy, cryo-EM, and CD analyses, along with s

124 tion and confirmed by high-temperature (31)P NMR spectroscopy, crystallizes in space group Pm3n and h

125 ptides in solution were determined using the NMR spectroscopy data.

126 ound complexes of LCo, as determined by (1)H NMR spectroscopy, demonstrate high selectivity toward Ca

127 However, proton NMR spectroscopy demonstrated that these derivatives ret

128 Using NMR spectroscopy, detailed enzyme kinetics of WT and mut

129 ive protonnuclear magnetic resonance (q-(1)H NMR) spectroscopy detection.

130 ved and saturation transfer difference (STD) NMR spectroscopy, differential scanning fluorimetry (DSF

131 ynamic nuclear polarization surface enhanced NMR spectroscopy (DNP SENS) has previously been demonstr

132 ynamic nuclear polarization surface enhanced NMR spectroscopy (DNP-SENS), to obtain the (195)Pt solid

133 In the last few years, solid-state NMR spectroscopy enabled the determination of the struct

134 ered valine was observed directly by protein NMR spectroscopy, establishing the intermediacy of the h

135 Moreover, one- and two-dimensional NMR spectroscopy experiments have allowed us to determin

136 ecA and YchJ, also copurified with iron, and NMR spectroscopy experiments indicated that YecA binds i

137 change, electron paramagnetic resonance, and NMR spectroscopy experiments reveal that a disorder-to-o

138 scY is proposed to refer to the class of all NMR spectroscopy experiments that rely on viscous solven

139 In this contribution, we combine advanced NMR spectroscopy experiments with scanning electron micr

140 stic studies have been conducted using (31)P NMR spectroscopy for reaction progress monitoring, isoto

141 ablishes the power of DNP-enhanced (19)F MAS NMR spectroscopy for structural characterization of HIV-

142 t the utility of high-resolution solid-state NMR spectroscopy for studying ligand binding and the sur

143 These results underline the suitability of NMR spectroscopy for the identification and quantificati

144 use a combination of X-ray crystallography, NMR spectroscopy, functional analyses, and kinetic model

145 In-situ NMR spectroscopy has become a powerful technique for the

146 Solution-state NMR spectroscopy has emerged as a leading structural tec

147 The use of NMR spectroscopy has emerged as a premier tool to charac

148 To date, however, NMR spectroscopy has not been used to analyze these impo

149 aracterization and quantification by (29) Si NMR spectroscopy has received significant attention, it

150 Using liposome fusion assays, FRET and NMR spectroscopy, here we provide a comprehensive view o

151 High-resolution magic-angle-spinning (1)H NMR spectroscopy (HR-MAS NMR) is a well-established tech

152 the crystalline state, and FT-IR absorption/NMR spectroscopies in solution the extended vs folded pr

153 mode using two-dimensional solid-state (19)F NMR spectroscopy in conjunction with density functional

154 , the structural features were determined by NMR spectroscopy in micelles and solved by using restrai

155 s can exceed those of high-resolution MS and NMR spectroscopy in terms of selectivity, resolution, an

156 hese cations were studied by low-temperature NMR spectroscopy in the superacids, which shed light on

157 bserved by both (13) C-MR imaging and (13) C-NMR spectroscopy in vivo.

158 FTIR, operando UV/Vis and (1) H-(13) C HSQC NMR spectroscopy indicate that activity arises from isol

159 Accordingly, NMR spectroscopy indicated that the SH3 domains may comp

160 s and heteronuclear single-quantum coherence NMR spectroscopy indicated the C-lobe of Ca(2+)-free CaM

161 A combination of IR and NMR spectroscopy indicates a linear correlation between

162 Saturation-transfer difference (STD) NMR spectroscopy is a fast and versatile method which ca

163 NMR spectroscopy is a powerful tool for obtaining site-s

164 Anisotropy-based NMR spectroscopy is a powerful tool for the structural a

165 Quantitative (31)P NMR spectroscopy is a promising technique for the analys

166 Among metabolomics techniques, NMR spectroscopy is a sophisticated, powerful, and gener

167 The results showed that (1)H NMR spectroscopy is an appropriate technique for the sui

168 NMR spectroscopy is an extraordinarily rich source of qu

169 ) concentrations in the range of 1-100 mM by NMR spectroscopy is demonstrated.

170 d on glass substrates and solid-state (31) P NMR spectroscopy is shown to be highly sensitive to the

171 primary source of structure determination by NMR spectroscopy is time consuming and expensive.

172 For this Nuclear Magnetic Resonance (NMR) spectroscopy is an attractive technique as it can q

173 Nuclear magnetic resonance (NMR) spectroscopy is emerging as a powerful method to st

174 Nuclear magnetic resonance (NMR) spectroscopy is ideally suited to the investigation

175 Solid-state nuclear magnetic resonance (NMR) spectroscopy is sensitive to the interfacial chemis

176 screening, (1)H nuclear magnetic resonance (NMR) spectroscopy is used extensively in the profiling o

177 ever, the narrow frequency bandwidth of (1)H NMR spectroscopy leads to a severe overlap of the spectr

178 BCAAs were quantified via NMR spectroscopy, log-transformed, and standardized.

179 1,3,5-triazine-2,4-diamine-6-ethyl moiety by NMR spectroscopy, MALDI-TOF mass spectroscopy, UV-Vis sp

180 uctures of novel products were elucidated by NMR spectroscopy, mass spectrometry and methylation anal

181 Compound 3 was characterized by multinuclear NMR spectroscopy, mass spectrometry, single crystal X-ra

182 lation times obtained from (13)C solid-state NMR spectroscopy measurements establish the occurrence o

183 Using NMR spectroscopy, molecular dynamics simulations, and is

184 tance (LP-IR), and GlycA were measured using NMR spectroscopy (n = 8385), while acylcarnitines and am

185 nickel iminyl was determined by multinuclear NMR spectroscopy observed during catalysis.

186 was conducted using high-sensitivity (29)Si NMR spectroscopy of isotopically enriched solutions comb

187 Pgamma to GAFab in conjunction with solution NMR spectroscopy of isotopically labeled Pgamma identifi

188 ys of such sensors for parallel DNP-enhanced NMR spectroscopy of nanoliter and subnanoliter samples.

189 Using ultrahigh-field (21.14 T) NMR spectroscopy of quadrupolar nuclei ((115)In, (133)Cs

190 sion EM, biochemical assays, and solid-state NMR spectroscopy of representative isolates and "leaky m

191 s-polarization magic angle spinning (CP-MAS) NMR spectroscopy of the framework and of its (13)C-isoto

192 structure, we investigated the effect, using NMR spectroscopy, of substituting key charged Arg, Lys,

193 ased modeling approaches in conjunction with NMR spectroscopy offer great potential for understanding

194 Using (31)P NMR spectroscopy offers a simple and rapid tool to quant

195 hniques, the technique of quantitative (31)P NMR spectroscopy offers unique advantages in measuring h

196 s, Magnetic Resonance Imaging (MRI) and (1)H NMR spectroscopy on intact berries and extracts, respect

197 e demonstrate the application of solid-state NMR spectroscopy on native, heterogeneous thylakoid memb

198 We combined NMR spectroscopy, preparative reversed-phase (RP) chroma

199 CO infrared, and (195)Pt and (13)C NMR spectroscopies provide strong evidence of Pt(1)(0),

200 In conclusion, NMR spectroscopy provides information about the metabolo

201 il technology in nuclear magnetic resonance (NMR) spectroscopy provides potential for the analysis of

202 ations were assessed using (15)N multiCP-MAS NMR spectroscopy, providing the first quantitation of yi

203 ing complexes by nuclear magnetic resonance (NMR) spectroscopy remains challenging.

204 ls with solution nuclear magnetic resonance (NMR) spectroscopy requires the extraction of these metab

205 NMR spectroscopy results show that the rigid protein mat

206 Time-dependent UV-vis absorption and NMR spectroscopy reveal that the rate and yield of fulve

207 NMR spectroscopy revealed changes in tumor lactate as a

208 Combined proteomics and NMR spectroscopy revealed that roseltide rT7 is a cystin

209 m coherence nuclear magnetic resonance (HSQC NMR) spectroscopy revealed robust helical folding propen

210 is-catechol and Ga(III)-(NE)(2) complexes by NMR spectroscopy reveals only localized structural pertu

211 y diffraction, solid-state (7) Li and (11) B NMR spectroscopy, scanning transmission electron microsc

212 NMR spectroscopy showed a significant increase (P < 0.05

213 to E66S CCL5-Evasin-4 complex formation with NMR spectroscopy showed that residues of the N terminus

214 In a rare correlation, NMR spectroscopy shows a coincident molecular signature

215 (17)O NMR spectroscopy shows that although O sites in both fra

216 NMR spectroscopy shows that CypA catalyzes isomerization

217 In this work, (71) Ga NMR spectroscopy shows the presence of [Ga(arene)(n) ](+

218 The nature of 3 was probed by multinuclear NMR spectroscopy, single-crystal X-ray diffraction, and

219 niques for IDPs: Nuclear Magnetic Resonance (NMR) spectroscopy, Small-angle X-ray Scattering (SAXS),

220 f Orb2A using a nonconventional liquid-state NMR spectroscopy strategy based on (13)C detection to af

221 Our multinuclear (31)P and (11)B NMR spectroscopy studies lend support for a two-step mec

222 metry, infrared spectroelectrochemistry, and NMR spectroscopy studies provide a detailed mechanistic

223 DFT data, as well as cyclic voltammetry and NMR spectroscopy, suggests that a proton-coupled electro

224 ray diffraction, 1D and 2D solid-state (19)F NMR spectroscopy supported by ab initio calculations are

225 ion of these oxonium ions by low-temperature NMR spectroscopy supported by density functional theory

226 Temperature-dependent (7) Li NMR spectroscopy supports the fast lithium motion.

227 e spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, tailored radio frequency (RF) irradia

228 Here, we tested the ability of 1D and 2D NMR spectroscopy techniques for the targeted and untarge

229 We demonstrate using NMR spectroscopy that a ligand from this family binds at

230 ar dichroism and nuclear magnetic resonance (NMR) spectroscopy that Spp2 is intrinsically disordered

231 While in NMR spectroscopy the effects of ring currents on the che

232 Using solid-state (15)N NMR spectroscopy, the cis/trans isomerization in a two-d

233 Using NMR spectroscopy, the conformational studies of two fluo

234 (29)Si NMR spectroscopy, the method of continuous variations, a

235 X-ray crystallography and paramagnetic (1)H NMR spectroscopy, the results of which support the struc

236 ocoa was characterized for the first time by NMR spectroscopy, then compared with the profiles of fer

237 scence and two-dimensional diffusion ordered NMR spectroscopy; these experiments suggest that the int

238 sis of the alkylidyne carbon atom and (95)Mo NMR spectroscopy; this analytical tool had been rarely u

239 n this work, we have employed solution state NMR spectroscopy to characterise the structural ensemble

240 In this work, we used NMR spectroscopy to characterize the conformational prop

241 Here, we used solution-state NMR spectroscopy to characterize the structure and dynam

242 e employed solution and magic angle spinning NMR spectroscopy to characterize the structure and dynam

243 We used NMR spectroscopy to characterize the structures of the t

244 s with site-specific resolution, we utilized NMR spectroscopy to characterize the VSD derived from Sh

245 Here, we use cryo-EM and solution NMR spectroscopy to demonstrate that a pH-dependent conf

246 e used electrophysiology, microdialysis, and NMR spectroscopy to evaluate the effect of a NMDAR PAM (

247 and mechanical properties, using solid-state NMR spectroscopy to examine a variety of nuclei ((1)H, (

248 in dynamics of nuclei in the CTT backbone by NMR spectroscopy to explore the mechanism of this change

249 sslinking and immunoprecipitation (CLIP) and NMR spectroscopy to identify and characterise physiologi

250 , we employ nondestructive (31)P solid-state NMR spectroscopy to investigate the chemical structure o

251 Here we use solid-state NMR spectroscopy to investigate the conformation of BM2(

252 signal overlap make it challenging to apply NMR spectroscopy to large biological systems.

253 Here, we utilize NMR spectroscopy to map the I942-EPAC1 interactions at a

254 ive-labeling strategy coupled with real-time NMR spectroscopy to monitor nucleotide exchange, GTP hyd

255 Here we apply NMR spectroscopy to patient-derived samples of alpha(1)-

256 an splitting for structural determination in NMR spectroscopy to polaron Zeeman splitting organic spi

257 The ability of high-resolution NMR spectroscopy to readout the response of molecular in

258 Here we use solid-state NMR spectroscopy to track the conformational dynamics of

259 XANES) and (31)P nuclear magnetic resonance (NMR) spectroscopies to determine P species in PM collect

260 sing solid-state nuclear magnetic resonance (NMR) spectroscopy to deconvolute the local structural en

261 action (XRD) and nuclear magnetic resonance (NMR) spectroscopy to demonstrate that the apparent first

262 amined employing nuclear magnetic resonance (NMR) spectroscopy to determine the reaction kinetic prof

263 We used solution nuclear magnetic resonance (NMR) spectroscopy to discover the link between intrinsic

264 me spectroscopy (PALS), FTIR and solid-state NMR spectroscopy) to demonstrate how a hierarchical desi

265 a class of methods, based on (13)C-detected NMR spectroscopy, to more generally quantify motions and

266 lication of room temperature proton-detected NMR spectroscopy under fast magic angle spinning (MAS) a

267 ntifying the metabolites of interest by (1)H NMR spectroscopy using beef.

268 d by proton nuclear magnetic resonance ((1)H NMR) spectroscopy using a 600 MHz NMR spectrometer.

269 tigated by single-crystal X-ray diffraction, NMR spectroscopy, UV-vis absorption, cyclic voltammetry,

270 nsform infrared spectroscopy and solid-state NMR spectroscopy validate the N-H(2) group as the prefer

271 Structure elucidation by NMR spectroscopy was a significant challenge due to a de

272 (45)Sc NMR spectroscopy was applied as a significant probe to e

273 quencing and fecal/urinary metabolites by 1H-NMR spectroscopy was complemented with targeted quantifi

274 mounts of quartz in amorphous silica gels by NMR spectroscopy was developed and tested on commerciall

275 ctrometry (UHPLC-HRMS) supported by 1 and 2D NMR spectroscopy was used for unambiguous metabolic prof

276 TD-NMR spectroscopy was used to measure the transverse rela

277 In situ irradiation NMR spectroscopy was used to quantify photostationary st

278 Using CD and NMR spectroscopies, we show here that G-overhangs of S.

279 Using mass spectrometry and NMR spectroscopy, we analyzed folate metabolites of L. r

280 By using NMR spectroscopy, we could show that the 50 C-terminal r

281 Here, by using in-cell NMR spectroscopy, we describe the dynamic membrane assoc

282 Using NMR spectroscopy, we found evidence for increased intrin

283 Using NMR spectroscopy, we have elucidated the solution-phase

284 sical characterization of the knot region by NMR spectroscopy, we identify the SAM-binding region and

285 Using molecular simulation and NMR spectroscopy, we observe large structural changes up

286 Using (11) B solid-state NMR spectroscopy, we show that the majority of boron spe

287 om commercially pure o-xylene (>=99%); using NMR spectroscopy, we show that the metallocycle exhibits

288 Using nuclear magnetic resonance (NMR) spectroscopy, we determine the structure of an Env

289 nd high-pressure nuclear magnetic resonance (NMR) spectroscopy, we observe that the pair of beta-stra

290 and proton nuclear magnetic resonance ((1)H NMR) spectroscopy were used in the characterization of t

291 Here we present an approach based on (1)H NMR spectroscopy which can accurately estimate the conce

292 r these molecules are essentially limited to NMR spectroscopy, which should be performed under physio

293 f microcryoprobe nuclear magnetic resonance (NMR) spectroscopy, which permits the use of low amounts

294 Using natural abundance (29)Si MAS NMR spectroscopy with CPMG acquisition and standard addi

295 re, the proposed approach that couples HRMAS NMR spectroscopy with ECa maps of vineyard soils represe

296 re, we suggest an approach combining in-cell NMR spectroscopy with perturbation experiments and model

297 study, we utilized a method based on HR-MAS NMR spectroscopy with slice localization (SLS) to achiev

298 d, 5b, and 5d) were clearly observed by (1)H NMR spectroscopy with the aid of (R)-BINOL as a chiral s

299 In standard 2D NMR spectroscopy without hyperpolarization, the acquisit

300 late salts are characterized by multinuclear NMR spectroscopy, X-ray analysis, as well as their calcu