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

4 e homonuclear (1)H-(1)H and (19)F-(19)F, and heteronuclear (1)H-(19)F correlations of the crystalline

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

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

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

8 parameters and permit homo- ((1)H-(1)H) and heteronuclear ((1)H-(13)C) 2D NMR experiments at natural

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 r selective 1D and 2D (1)H experiments and a heteronuclear 2D (1)H-(31)P HSQC-NOESY experiment by tak

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

23 edures, enabling challenging homonuclear and heteronuclear 2D NMR experiments on CdS, Si, and Cd(3)P(

24 ucturally characterized using MicroCryoProbe heteronuclear 2D NMR techniques.

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

26 The combination of NH-based heteronuclear adiabatic relaxation dispersion (HARD) exp

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

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

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

30 symmetry breaking relies on the presence of heteronuclear constituents.

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

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

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

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

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

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

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

38 2D) (13)C-(1)H, (13)C-(19)F and (19)F-(29)Si heteronuclear correlation (HETCOR) spectra were obtained

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

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

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

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

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

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

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

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

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

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

49 Furthermore, 2D proton-detected (1)H-(17)O heteronuclear correlation NMR experiments allow for a ra

50 2D (29)Si{(1)H} and (27)Al{(1)H} heteronuclear correlation NMR spectra of hydrated cement

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

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

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

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

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

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 suitable for sign-sensitive determination of heteronuclear couplings, as demonstrated here by measuri

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

66 Relying on heteronuclear cross-polarization experiments, phospholip

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

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

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

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

71 monuclear dimers (Br(2), I(2) and Te(2)) and heteronuclear dimers (CsBr and CsI) in a single cage is

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

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

74 Heteronuclear dipolar coupling modulation schemes allowe

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

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

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

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

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

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

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

82 o alignments and accurately measure numerous heteronuclear dipolar couplings.

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

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

85 mprovements in instrumental sensitivity made heteronuclear direct detection possible for biomolecular

86 tical resonance, and report the discovery of heteronuclear dissipative Kerr soliton molecules.

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

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

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

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

91 So far only heteronuclear examples have been isolated.

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

93 zation of proteins by NMR typically utilizes heteronuclear experiments.

94 pling relationships, NOESY correlations, and heteronuclear experiments.

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

96 (31)P-(1)H heteronuclear (HETCOR) experiments ascertained the two e

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

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

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

100 Homonuclear (H,H COSY) and heteronuclear (HSQC) methods were developed, validated,

101 1, and that IL-1beta and IL-1alpha stimulate heteronuclear I-1beta splicing and translation of the ne

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

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

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

105 derably expands the number of stable aqueous heteronuclear ions.

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

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

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

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

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

111 For example, heteronuclear molecules possess permanent electric dipol

112 Heteronuclear multidemensional NMR spectroscopy experime

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

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

115 We have used heteronuclear multidimensional NMR to determine the stru

116 Here we report the heteronuclear, multidimensional NMR spectroscopy solutio

117 Heteronuclear, multidimensional nuclear magnetic resonan

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

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

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

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

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

123 Using COSY and heteronuclear multiple quantum correlation spectroscopy

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

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

126 Heteronuclear multiple-quantum coherence (HMQC) analysis

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

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

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

130 structure, as determined by multidimensional heteronuclear NMR analysis.

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

132 Heteronuclear NMR chemical shift mapping revealed that T

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

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

135 We propose a set of exclusively heteronuclear NMR experiments to investigate these featu

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

137 Heteronuclear NMR experiments were performed to assign r

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

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

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

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

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

143 15N-labeled PSA, we applied a combination of heteronuclear NMR methods, such as heteronuclear single

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

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

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

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

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

149 Previous mutagenesis and heteronuclear NMR spectroscopy studies directed toward t

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

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

152 Using heteronuclear NMR spectroscopy, we demonstrated that the

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

154 gnaling partner, TSG101-UEV, as evidenced by heteronuclear NMR spectroscopy.

155 dodecylphosphocholine micelles by homo- and heteronuclear NMR spectroscopy.

156 hydrogen isotope exchange experiments using heteronuclear NMR spectroscopy.

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

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

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

160 Heteronuclear NMR spin relaxation is a uniquely powerful

161 Heteronuclear NMR studies established that His148 was ne

162 Heteronuclear NMR studies indicated that the L43A mutati

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

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

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

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

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

168 rminal EF-hand domain using multidimensional heteronuclear NMR.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 Heteronuclear nuclear Overhauser effect experiments show

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

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

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

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

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

190 Proton-nitrogen heteronuclear Overhauser enhancement measurements reveal

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

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

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

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

195 NMR heteronuclear relaxation experiments, residual dipolar c

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

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

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

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

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

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

202 oire of mRNA through coordinated splicing of heteronuclear RNAs.

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

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

205 ucture of mono-MAs is verified by proton and heteronuclear single quantum coherence (2D (1)H-(13)C) n

206 NMR heteronuclear single quantum coherence (HSQC) analyses r

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

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

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

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

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

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

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

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

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

216 1H-(15)N heteronuclear single quantum coherence (HSQC) spectra of

217 Heteronuclear single quantum coherence (HSQC) spectrosco

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

219 SCB/1000C and demonstrate the proper use of heteronuclear single quantum coherence (HSQC) to measure

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

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

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

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

224 Heteronuclear single quantum coherence experiments on ho

225 2D heteronuclear single quantum coherence NMR analysis of s

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

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

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

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

230 Using (15)N-heteronuclear single quantum coherence NMR, the optimal

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

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

233 r dichroism (CD) spectroscopy and (1)H-(13)C heteronuclear single quantum coherence nuclear magnetic

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

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

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

237 tra to those from two-dimensional (1)H-(15)N heteronuclear single quantum coherence spectra.

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

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

240 Analysis of heteronuclear single quantum coherence titration binding

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

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

243 ow-cost, and fast alternative to traditional heteronuclear single quantum coherence-based experiments

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

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

246 NMR heteronuclear single quantum correlation (HSQC) analysis

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

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

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

250 A heteronuclear single quantum correlation (HSQC) spectrum

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

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

253 is real-time pure shift sensitivity-improved heteronuclear single quantum correlation method provides

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

255 Using 2D heteronuclear single quantum correlation NMR experiments

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

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

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

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

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

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

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

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

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

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

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

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

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

269 se relaxation optimized spectroscopy (TROSY) heteronuclear single-quantum coherence (HSQC) NMR to cha

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

271 1H-15N heteronuclear single-quantum coherence NMR spectra colle

272 ve analysis using two-dimensional (15)N-(1)H heteronuclear single-quantum coherence NMR spectra of Cc

273 Microscale thermophoresis and heteronuclear single-quantum coherence NMR spectroscopy

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

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

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

277 Using NMR heteronuclear single-quantum coherence spectra, kinetics

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

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

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

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

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

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

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

285 dynamics in complex nonlinear systems, such heteronuclear soliton molecules yield coherent frequency

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

294 Heteronuclear tetrametallic lanthanide complexes have be

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

296 HyperW NMR can also accommodate heteronuclear transfers, facilitating the rapid acquisit

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.