ライフサイエンスコーパス: heteronuclear

1 Using two-dimensional heteronuclear (1)H-(15)N correlation spectra recorded wi

2 e monitored in situ by recording a series of heteronuclear (1)H-(15)N correlation spectra.

3 5% dichloroacetic acid (DCA) and successive heteronuclear (1)H-(15)N HSQC spectra were collected to

4 H-(1)H nuclear Overhauser effects (NOEs) and heteronuclear (1)H-(15)N NOEs if the paramagnetic contri

5 Heteronuclear (1)H-(15)N nuclear Overhauser effect spect

6 pin-coupled hyperpolarized (13)C signal in a heteronuclear (1)H/(13)C spin-echo experiment.

7 lycan binding, we performed multidimensional heteronuclear ((1)H, (13)C, (15)N) NMR (nuclear magnetic

8 t LPS was analyzed by homonuclear ((1)H) and heteronuclear ((1)H,(13)C, and (1)H,(31)P) correlated on

9 Heteronuclear (13)C-(17)O and (15)N-(17)O J couplings we

10 ift values as well as both one- and two-bond heteronuclear (13)C-(77)Se coupling constants, and the c

11 two-dimensional ((1)H-(1)H) homonuclear and heteronuclear ((13)C-(1)H) single quantum correlations (

12 that combines measurements of R1, R1rho, and heteronuclear 13C{1H} NOEs for protonated base (C2, C5,

13 By use of heteronuclear (15)N NMR relaxation measurements in a ser

14 relaxation data ((15)N-T(1), (15)N-T(2), and heteronuclear (15)N-{(1)H}-nOe) recorded on all three ap

15 Heteronuclear 19F-1H cross-polarization can be used effe

16 Fluorine observed homonuclear 19F-19F and heteronuclear 19F-1H NOE experiments providing selective

17 The aromatic region of two-dimensional heteronuclear 1H, 13C NMR spectra of natural organic mat

18 so evident in the F2 hydrogen dimension from heteronuclear 1H-13C HSQC spectroscopy, which did not de

19 hydrophobic core of a protein, demonstrating heteronuclear 1H-15N NMR data on the Lys-66 side chain a

20 LC, and combined analysis of homonuclear and heteronuclear (2,3)J couplings, along with ROE data.

21 have been proposed to reduce the duration of heteronuclear 2D experiments.

22 ucturally characterized using MicroCryoProbe heteronuclear 2D NMR techniques.

23 ive nuclei of the ChB-donor chalcogen atoms, heteronuclear (77)Se and (125)Te NMR were used to direct

24 nt of the integrated intensity obtained in a heteronuclear and a homonuclear spin-echo experiment, S(

25 ling scheme, termed sel-SHARPER, removes all heteronuclear and homonuclear couplings of the selected

26 asis for the formation of both the homo- and heteronuclear bimetallics, for the observed two-electron

27 ted, such as in the acquisition dimension of heteronuclear broadband decoupled HSQC (heteronuclear si

28 symmetry breaking relies on the presence of heteronuclear constituents.

29 ermined by experiments that probe long-range heteronuclear contacts for fibrils templated from a 1:1

30 Two-dimensional (1)H-(13)C heteronuclear correlation (2D HETCOR) NMR indicated aryl

31 A (1)H-(13)C two-dimensional heteronuclear correlation (HETCOR) experiment with frequ

32 Two-dimensional (1)H/(31)P dipolar heteronuclear correlation (HETCOR) magic-angle spinning

33 solid-state two-dimensional (2D) (13)C{(1)H} heteronuclear correlation (HETCOR) NMR analyses support

34 resolved in the two-dimensional (2-D) 1H-17O heteronuclear correlation (HETCOR) NMR spectra allowing

35 al-echo double resonance (CP-REDOR) NMR, and heteronuclear correlation (HETCOR) NMR spectroscopy to d

36 2D) (13)C-(1)H, (13)C-(19)F and (19)F-(29)Si heteronuclear correlation (HETCOR) spectra were obtained

37 h-resolution two-dimensional (2D) (1)H-(15)N heteronuclear correlation (HETCOR) spectroscopy has been

38 1)H-based SSNMR study [1D (1)H and 2D (1)H-X heteronuclear correlation (HETCOR, X = (13)C, (29)Si) ex

39 ple set, the quality of a protein's [15N-1H]-heteronuclear correlation (HSQC) spectrum recorded under

40 D (29)Si{(1)H}, (13)C{(1)H}, and (31)P{(1)H} heteronuclear correlation and 1D (29)Si{(13)C} rotationa

41 A (1)H-(31)P heteronuclear correlation experiment provided unambiguou

42 ydroxide ion was found, through a (1)H-(31)P heteronuclear correlation experiment, to be confined to

43 lica has been established by two-dimensional heteronuclear correlation experiments involving 1H, 11B,

44 On the basis of (1)H/(13)C/(15)N heteronuclear correlation experiments selective for lysi

45 on was obtained with 2D F1-1H-coupled 1H-15N heteronuclear correlation experiments.

46 CH(n) selection, two-dimensional (1)H-(13)C heteronuclear correlation NMR (2D HETCOR), 2D HETCOR com

47 h (15)N-ethanolamine and detected using a 2D heteronuclear correlation NMR experiment.

48 2D (29)Si{(1)H} and (27)Al{(1)H} heteronuclear correlation NMR spectra of hydrated cement

49 uantum, exchange, and RFDR), and (1)H-(29)Si heteronuclear correlation NMR.

50 Multidimensional homo- and heteronuclear correlation spectra of CA assemblies of un

51 tion of two- and three-dimensional homo- and heteronuclear correlation spectra.

52 present new sensitivity enhanced schemes for heteronuclear correlation spectroscopy (HETCOR) in solid

53 omolecular NMR sensitivity in the context of heteronuclear correlation spectroscopy.

54 high magnetic field, and carefully chosen 2D heteronuclear correlation techniques.

55 ss-polarization, (13)C{(1)H} two-dimensional heteronuclear correlation, and (1)H relaxation technique

56 MBC) optimized to detect four- and five-bond heteronuclear correlations and the use of computer-assis

57 the spectral coordinates observed in the 2D heteronuclear correlations, previously postulated interm

58 s determined from a combination of homo- and heteronuclear coupling constants in conjunction with mol

59 mplished by consideration of homonuclear and heteronuclear coupling constants in tandem with ROESY da

60 ional NMR approaches based on both homo- and heteronuclear couplings ((1)H-(1)H COSY; (1)H-(13)C HSQC

61 , we introduce the application of scaling of heteronuclear couplings by optimal tracking (SHOT) to ac

62 single selected signal, SHARPER removes all heteronuclear couplings of a selected nucleus without th

63 pectra in natural abundance samples based on heteronuclear couplings to these same, (13)C-bonded nucl

64 to 4-, 5-, and even 6-bond long-range (n)JCH heteronuclear couplings.

65 times than are generally associated with 2D heteronuclear cross-correlation experiments.

66 ediate-sized molecules, however, show strong heteronuclear cross-relaxation effects: spontaneous proc

67 r the accurate measurement of intermolecular heteronuclear cross-relaxation rates by simultaneous acq

68 n a broader context, accurate measurement of heteronuclear cross-relaxation rates may enable the stud

69 The use of low-power heteronuclear decoupling is essential in the (1)H-(29)Si

70 e applied here combines both homonuclear and heteronuclear details and therefore provides complete in

71 yielded site-specific (1)H-(13)C/(1)H-(15)N heteronuclear dipolar coupling constants for CAP-Gly and

72 sociated (15)N chemical shift and (1)H-(15)N heteronuclear dipolar coupling frequencies as orientatio

73 SLF techniques to accurately measure strong heteronuclear dipolar couplings between directly bonded

74 On the other hand, weak heteronuclear dipolar couplings can be measured using la

75 used for the measurement of a broad range of heteronuclear dipolar couplings, allowing for a complete

76 t suitable for the measurement of long-range heteronuclear dipolar couplings, and that they provide i

77 conformational order parameters are based on heteronuclear dipolar couplings, and they are correlated

78 xation of the hyperpolarized LLS, induced by heteronuclear dipolar couplings, generates strongly enha

79 (15)N chemical shifts as well as (1)H-(15)N heteronuclear dipolar couplings.

80 o alignments and accurately measure numerous heteronuclear dipolar couplings.

81 resent an approach for (1)H-(13)C/(1)H-(15)N heteronuclear dipolar recoupling under fast MAS conditio

82 age the static chemical shift anisotropy and heteronuclear dipole-dipole coupling powder patterns to

83 We employ our recently developed heteronuclear double resonance method to determine the t

84 ysed dehydrocoupling reactions as a route to heteronuclear element-element bonds.

85 A two-step heteronuclear enhancement approach was combined with che

86 In addition to these spontaneous heteronuclear enhancement experiments, single-shot acqui

87 hievement of two-dimensional (2D) (1)H-(13)C heteronuclear experiments with a precision of a few per

88 pling relationships, NOESY correlations, and heteronuclear experiments.

89 zation of proteins by NMR typically utilizes heteronuclear experiments.

90 the reactants are aligned and activated by a heteronuclear four-metal-ion center that contains a meta

91 lude a homonuclear all-Ru hexamer as well as heteronuclear hexamer and nonamer with alternating Ru/Ru

92 d to selected peaks from the two-dimensional heteronuclear HSQC spectrum of a sample of natural organ

93 ced homonuclear TOCSY-based DemixC method to heteronuclear HSQC-TOCSY NMR spectroscopy.

94 1, and that IL-1beta and IL-1alpha stimulate heteronuclear I-1beta splicing and translation of the ne

95 Platelets contain unspliced heteronuclear IL-1beta RNA, which is rapidly spliced and

96 e 15N transverse coherence (termed HISQC for heteronuclear in-phase single quantum coherence spectros

97 on between local homonuclear and long-ranged heteronuclear ionisation mechanisms.

98 derably expands the number of stable aqueous heteronuclear ions.

99 NMR spectroscopy, multiple-pulse echoes, and heteronuclear J spectroscopy.

100 transfer of population double resonance) and heteronuclear J-spin-echoes.

101 Detailed biochemical and heteronuclear magnetic resonance spectroscopy (NMR) stud

102 on protein A (hRPA70) was investigated using heteronuclear magnetic resonance spectroscopy.

103 ipolar dephasing followed by proton-assisted heteronuclear magnetization transfer yields long-range (

104 ransmetalation agents for the preparation of heteronuclear molecular gold carbido complexes such as [

105 owing to multiphoton absorption, which in a heteronuclear molecular system occurs predominantly loca

106 For example, heteronuclear molecules possess permanent electric dipol

107 Heteronuclear multidemensional NMR spectroscopy experime

108 P7B N-domain in the presence of ATP by using heteronuclear multidimensional NMR spectroscopy.

109 ocapsid domains (referred to as DeltaGag) by heteronuclear multidimensional NMR spectroscopy.

110 We have used heteronuclear multidimensional NMR to determine the stru

111 Here we report the heteronuclear, multidimensional NMR spectroscopy solutio

112 Heteronuclear, multidimensional nuclear magnetic resonan

113 eronuclear Multiple Quantum Coherence and 2D Heteronuclear Multiple Bond Coherence spectroscopic anal

114 eteronuclear sequential quantum correlation, heteronuclear multiple bond correlation) analysis identi

115 ties for NH3 cross-peaks than either HSQC or heteronuclear multiple quantum coherence (HMQC) correlat

116 e site loop is suppressed and the (1)H-(13)C heteronuclear multiple quantum coherence (HMQC) spectrum

117 Application of (1)H, (13)C, 2D Heteronuclear Multiple Quantum Coherence and 2D Heteronu

118 Using COSY and heteronuclear multiple quantum correlation spectroscopy

119 r single quantum correlation) and fast-HMQC (heteronuclear multiple quantum correlation) pulse sequen

120 Cimicifuga) species as a test case, heteronuclear multiple-bond correlation (HMBC) barcodes

121 Heteronuclear multiple-quantum coherence (HMQC) analysis

122 pectroscopy, total correlation spectroscopy, heteronuclear multiple-quantum coherence, and NOE, were

123 Levels of heteronuclear NaV1.8 RNA were unaffected by SNE or shRNA

124 effects (fluoro, nitrobenzoate), handles for heteronuclear NMR ((19)F:fluoro; pentafluorophenyl or pe

125 rometry (MS), tandem MS, and homonuclear and heteronuclear NMR analyses.

126 structure, as determined by multidimensional heteronuclear NMR analysis.

127 Here, using both heteronuclear NMR and single crystal X-ray diffraction,

128 Heteronuclear NMR chemical shift mapping revealed that T

129 We used a combination of heteronuclear NMR experiments and molecular dynamics sim

130 In this paper, we present a series of heteronuclear NMR experiments for the direct observation

131 or enzymatic oxidation in rat liver cytosol; heteronuclear NMR experiments revealed that oxidation oc

132 ing one- and two-dimensional (1)H, (13)C and heteronuclear NMR experiments under continuous flow.

133 Heteronuclear NMR experiments were performed to assign r

134 achieved by two-dimensional homonuclear and heteronuclear NMR experiments, is reported for the first

135 near-UV CD, fluorescence, urea titration and heteronuclear NMR experiments, we show that three amino

136 reliable way of enhancing the sensitivity of heteronuclear NMR in dilute mixtures of metabolites.

137 tural (13)C abundance, metabolomics based on heteronuclear NMR is limited by sensitivity.

138 he T and A bases, as previously deduced from heteronuclear NMR measurements by Zhao et al.

139 Heteronuclear NMR methods were used to determine the sol

140 15N-labeled PSA, we applied a combination of heteronuclear NMR methods, such as heteronuclear single

141 eptide bound to BIV TAR RNA determined using heteronuclear NMR methods.

142 nt helix at low temperature as identified by heteronuclear NMR relaxation measurements, secondary che

143 ns and the first equivalent of metal through heteronuclear NMR relaxation measurements.

144 ntent, leading to remarkably clean homo- and heteronuclear NMR spectra of the serum metabolome that c

145 Here, we used heteronuclear NMR spectroscopy and molecular modeling to

146 flexibility in the native state as probed by heteronuclear NMR spectroscopy and multiple conformer si

147 red the autocatalytic conversion of BACE1 by heteronuclear NMR spectroscopy and used chemical shift p

148 Previous mutagenesis and heteronuclear NMR spectroscopy studies directed toward t

149 Here, we employ heteronuclear NMR spectroscopy to characterize a monomer

150 of the two sequences using multidimensional heteronuclear NMR spectroscopy, and the structure was fo

151 Using heteronuclear NMR spectroscopy, we demonstrated that the

152 dodecylphosphocholine micelles by homo- and heteronuclear NMR spectroscopy.

153 hydrogen isotope exchange experiments using heteronuclear NMR spectroscopy.

154 get RNA, has been solved by multidimensional heteronuclear NMR spectroscopy.

155 nd the catalytic domain of FKBP38 derived by heteronuclear NMR spectroscopy.

156 A high quality heteronuclear NMR spectrum of HCV NS5B(Delta21) has been

157 h as may be obtained from a two-dimensional, heteronuclear NMR spectrum), the inverse mode of SPARIA

158 Heteronuclear NMR spin relaxation is a uniquely powerful

159 Heteronuclear NMR studies established that His148 was ne

160 Heteronuclear NMR studies indicated that the L43A mutati

161 A multidimensional heteronuclear NMR study has demonstrated that a guanine-

162 er acidic conditions, using a combination of heteronuclear NMR, analytical ultracentrifugation, and c

163 Using UV melting, gel electrophoresis and heteronuclear NMR, we investigated effects of various si

164 d the pH titration of individual residues by heteronuclear NMR.

165 rminal EF-hand domain using multidimensional heteronuclear NMR.

166 protein unfolded in 6 M urea in detail using heteronuclear NMR.

167 P with and without bound ligands by means of heteronuclear NMR.

168 An analysis of heteronuclear-NMR-based screening data is used to derive

169 e serine were analyzed using R(1), R(2), and heteronuclear NOE experiments, variable temperature TROS

170 R(1) and R(2), relaxation and heteronuclear NOE measurements showed that the protein i

171 btained by conventional NOE spectroscopy and heteronuclear NOE spectroscopy NMR experiments.

172 The low (15) N-{(1) H} heteronuclear NOE values (</=0.4), the close to zero val

173 The (1)H/(15)N heteronuclear NOE values for residues 1-25 are significa

174 In contrast, (15)N{(1)H} heteronuclear NOE values for the N-terminal subdomain ar

175 tion rates ( (15)N R 1, R 2) and (1)H- (15)N heteronuclear NOE values indicated that HscB is rigid al

176 lyses, d(NN)(i, i + 1) NOEs, and (15)N{(1)H} heteronuclear NOE values show that the C-terminal subdom

177 These regions also have small but positive heteronuclear NOEs, interresidue d(NN) NOEs, and small b

178 ) and T(2) relaxation times and {(1)H}-(15)N heteronuclear NOEs, reveal residue flexibility at the ac

179 dom-coil values, and by measuring (1)H-(15)N heteronuclear NOEs, which are all consistent with an unf

180 e frameshift site RNA using multidimensional heteronuclear nuclear magnetic resonance (NMR) methods.

181 Here, we use UV/vis and heteronuclear nuclear magnetic resonance (NMR) spectrosc

182 tween PIDD-DD and RAIDD-DD in solution using heteronuclear nuclear magnetic resonance (NMR) spectrosc

183 High-resolution heteronuclear nuclear magnetic resonance (NMR) spectrosc

184 -human tRNA(Lys)(3) initiation complex using heteronuclear nuclear magnetic resonance methods.

185 e (R1), transverse relaxation rate (R2), and heteronuclear nuclear Overhauser effect (NOE)] measured

186 Heteronuclear nuclear Overhauser effect experiments show

187 We measure (13)C T(1), T(1rho) and heteronuclear nuclear Overhauser effects (NOEs) for suga

188 Steady-state {(1)H}-(15)N heteronuclear nuclear Overhauser effects indicate that t

189 ied beta-strand was confirmed by T1, T2, and heteronuclear nuclear Overhauser enhancement (NOE) measu

190 Using high-resolution NMR experiments of heteronuclear nuclear Overhauser enhancement (NOE), spin

191 , is introduced that allows the detection of heteronuclear one-bond correlations in less than 30 s on

192 and transverse relaxation rates and [1H]-15N heteronuclear Overhauser effects of the backbone amides

193 Proton-nitrogen heteronuclear Overhauser enhancement measurements reveal

194 iffusion-ordered NMR spectroscopy as well as heteronuclear Overhauser enhancement NMR spectroscopy.

195 substances was verified by either (19)F-(1)H heteronuclear Overhauser spectroscopy (HOESY) or X-ray c

196 The heteronuclear oxo-cluster [VPO4](*+) is generated via el

197 timulated splicing and translation of stored heteronuclear pro-IL-1beta RNA.

198 terminal 22 residues of the alpha subunit by heteronuclear protein NMR spectroscopy.

199 NMR heteronuclear relaxation experiments, residual dipolar c

200 uence of anisotropic rotational diffusion on heteronuclear relaxation.

201 Hadamard-encoded heteronuclear-resolved NMR diffusion and relaxation meas

202 ntrast, acute stress increased levels of PPG heteronuclear RNA (hnRNA) in a glucocorticoid-dependent

203 ing that SAA increased expression of sPLA(2) heteronuclear RNA and that inhibiting transcription elim

204 bserved increased claudin-7 mRNA and nascent heteronuclear RNA levels during differentiation.

205 n histochemistry using an intron-specific VP heteronuclear RNA probe.

206 PSF3), an essential component for converting heteronuclear RNA to mRNA, binds with high affinity to t

207 transcriptional activation of egr-1 mRNA and heteronuclear RNA.

208 thought to arise by alternative splicing of heteronuclear RNA.

209 oire of mRNA through coordinated splicing of heteronuclear RNAs.

210 gh-resolution-MS and NMR ((1)H, (13)C, COSY, heteronuclear sequential quantum correlation, heteronucl

211 construction, and J-compensated quantitative heteronuclear single quantum (HSQC) (1)H-(13)C NMR spect

212 INEPT), correlation spectroscopy (COSY), and heteronuclear single quantum coherence (HSQC) are also d

213 ches have been proposed utilizing (1)H-(15)N heteronuclear single quantum coherence (HSQC) as well as

214 apes of NH3 signals in a conventional 1H-15N heteronuclear single quantum coherence (HSQC) correlatio

215 oton-nitrogen correlations measured with the heteronuclear single quantum coherence (HSQC) experiment

216 (1)H-(13)C heteronuclear single quantum coherence (HSQC) HR-MAS NMR

217 s-[Pt(15NH3)2Cl2]1, are studied using 1H-15N heteronuclear single quantum coherence (HSQC) NMR and in

218 First, an NUS heteronuclear single quantum coherence (HSQC) NMR pulse

219 ects (KIEs) by (1)H-detected 2D [(13)C,(1)H]-heteronuclear single quantum coherence (HSQC) NMR spectr

220 erial completely and gave high-resolution 2D heteronuclear single quantum coherence (HSQC) NMR spectr

221 Results of NMR studies including 1H{15N} heteronuclear single quantum coherence (HSQC) show that

222 1H-(15)N heteronuclear single quantum coherence (HSQC) spectra of

223 (1)H-(15)N heteronuclear single quantum coherence (HSQC) spectra, l

224 Heteronuclear single quantum coherence (HSQC) spectrosco

225 A 1H-15N heteronuclear single quantum coherence (HSQC) titration

226 ive K296R kinase domain, and performed (15)N-heteronuclear single quantum coherence (HSQC) titrations

227 ar- and far-UV CD, and 1D and 2D ((1)H-(15)N heteronuclear single quantum coherence (HSQC)) NMR.

228 at straw, respectively, and characterized by heteronuclear single quantum coherence (HSQC), nuclear m

229 (1)H-(15)N heteronuclear single quantum coherence analysis of the p

230 Analysis of (1)H-(15)N heteronuclear single quantum coherence and nuclear Overh

231 Heteronuclear single quantum coherence experiments on ho

232 2D heteronuclear single quantum coherence NMR analysis of s

233 Mass spectrometry and 2D heteronuclear single quantum coherence NMR revealed that

234 In two-dimensional [(1)H,(13)C]heteronuclear single quantum coherence NMR spectra, seve

235 Here, we have utilized two-dimensional heteronuclear single quantum coherence NMR spectroscopy

236 In addition, heteronuclear single quantum coherence NMR was used to m

237 n agonist-bound conformation, as measured by heteronuclear single quantum coherence NMR, and lead to

238 n using one-dimensional (1)H gradient carbon heteronuclear single quantum coherence NMR.

239 ensional (1)H and two-dimensional (1)H/(13)C heteronuclear single quantum coherence nuclear magnetic

240 Two-dimensional (1)H,(15)N heteronuclear single quantum coherence spectra reveal ch

241 al shift perturbation analysis by (1)H-(15)N heteronuclear single quantum coherence spectra reveals d

242 nd hydrogen-deuterium exchange (using 1H-15N heteronuclear single quantum coherence spectra) reveal t

243 inities as assessed by changes in (1)H,(15)N heteronuclear single quantum coherence spectra.

244 Analysis of NMR (1)H-(15)N-heteronuclear single quantum coherence spectral peak int

245 l (2D) NMR spectra, namely, (13)C-(1)H HSQC (heteronuclear single quantum coherence spectroscopy), (1

246 Analysis of heteronuclear single quantum coherence titration binding

247 nation of heteronuclear NMR methods, such as heteronuclear single quantum coherence, HNCA, and HNCO,

248 lations (correlation spectroscopy, COSY, and heteronuclear single quantum coherence, HSQC) nuclear ma

249 substituents and can be readily assigned by heteronuclear single quantum coherence-nuclear magnetic

250 intermediate was undetectable in a series of heteronuclear single quantum coherences, revealing the d

251 NMR heteronuclear single quantum correlation (HSQC) analysis

252 correlation spectroscopy (COSY), (1)H-(31)P heteronuclear single quantum correlation (HSQC) and (1)H

253 or organophosphorus compounds via (31)P-(1)H heteronuclear single quantum correlation (HSQC) and prov

254 r Overhauser effect spectroscopy (NOESY) and heteronuclear single quantum correlation (HSQC) NMR spec

255 To address this issue, we recorded 1H-15N heteronuclear single quantum correlation (HSQC) spectra

256 A heteronuclear single quantum correlation (HSQC) spectrum

257 adening of certain cross-peaks in the 15N-1H heteronuclear single quantum correlation (HSQC) spectrum

258 nuclear Overhauser enhancement spectroscopy heteronuclear single quantum correlation (NOESY-HSQC) NM

259 Furthermore our (1)H-(15)N heteronuclear single quantum correlation NMR data illust

260 Using 2D heteronuclear single quantum correlation NMR experiments

261 hat the protein fold was not disturbed using heteronuclear single quantum correlation NMR spectra.

262 ding monitored both by changes in (1)H-(15)N heteronuclear single quantum correlation spectra and by

263 and from natural abundance (13)C NMR, where heteronuclear single quantum correlation spectra reveal

264 in Escherichia coli and has a well dispersed heteronuclear single quantum correlation spectrum and a

265 Comparison of the (1)H-(15)N heteronuclear single quantum correlation spectrum of CPR

266 ks for residues G13 to H19 in the (1)H-(15)N heteronuclear single quantum correlation spectrum sugges

267 oduced dispersed cross-peaks in a (1)H-(15)N heteronuclear single quantum correlation spectrum that e

268 Two-dimensional 1H-13C HSQC (heteronuclear single quantum correlation) and fast-HMQC

269 il) can be reached with the (1)H-(13)C HSQC (Heteronuclear Single Quantum Correlation) experiment, th

270 n of heteronuclear broadband decoupled HSQC (heteronuclear single quantum correlation) spectra.

271 a time, together with structural analysis by heteronuclear single quantum correlation-NMR spectroscop

272 cluster were fully elucidated by (13)C-(1)H heteronuclear single-quantum coherence (HSQC) in conjunc

273 Two-dimensional (15)N-heteronuclear single-quantum coherence (HSQC) NMR studie

274 r dichroism (CD) spectroscopy and (1)H-(15)N heteronuclear single-quantum coherence (HSQC) nuclear ma

275 1H-15N heteronuclear single-quantum coherence NMR spectra colle

276 ding, the kinetics of trypsin digestion, and heteronuclear single-quantum coherence nuclear magnetic

277 evidenced by multiple two-dimensional (15)N heteronuclear single-quantum coherence peaks for certain

278 F structure using nuclear magnetic resonance heteronuclear single-quantum coherence spectra of these

279 The (1)H/(15)N heteronuclear single-quantum correlated (HSQC) spectra f

280 Using two-dimensional (1)H-(15)N heteronuclear single-quantum correlation (HSQC) experime

281 er dereplication, a differential analysis of heteronuclear single-quantum correlation (HSQC) spectra

282 A series of (1)H-(15)N heteronuclear single-quantum correlation NMR spectra wer

283 ion spectroscopy (TOCSY) experiments, and 2D heteronuclear single-quantum correlation spectroscopy (H

284 n order of magnitude, compared to typical 2D heteronuclear single-quantum correlation-resolved diffus

285 Heteronuclear solid-state magic-angle spinning (MAS) NMR

286 and a controlled catalytic production of the heteronuclear species HD.

287 Following a heteronuclear spin-pair selection using a DANTE pulse tr

288 The relevant homo- and heteronuclear spin-spin couplings are reported.

289 st-free agents via SABRE with hyperpolarized heteronuclear spins, and thus is promising for biomedica

290 his approach into two- and three-dimensional heteronuclear SSNMR experiments to examine the MSP1D1 re

291 We present a novel application of the heteronuclear statistical total correlation spectroscopy

292 samples and between 1H and 31P-{1H} spectra (heteronuclear STOCSY) to recover latent metabolic inform

293 Heteronuclear syn-facial and anti-facial bimetallics are

294 nt sensitivities to specific homonuclear and heteronuclear terms in the interaction potential.

295 Heteronuclear tetrametallic lanthanide complexes have be

296 ombined with LC-MS, three-dimensional 19F-1H heteronuclear TOCSY filtered experiments based on this a

297 The heteronuclear triple resonance NMR study reported here o

298 5)N chemical shift degeneracy we developed a heteronuclear zero-quantum (and double-quantum) coherenc

299 We expect our heteronuclear zero-quantum coherence N(z)-exchange exper

300 t time scale are frequently studied using 2D heteronuclear ZZ or N(z)-exchange spectroscopy.