ライフサイエンスコーパス: DNP

1 DNP boosts NMR signal intensities by factors of 10(2) to

2 DNP can enhance NMR signals by factors of 10-100, thereb

3 DNP colocalized with the myeloid cell marker CD11b on im

4 DNP enables the rapid acquisition with natural isotopic

5 DNP enhancements (epsilon) of between 40 and 90 at 105 K

6 DNP improved glucose tolerance and reduced hepatic steat

7 DNP is a sensitivity enhancement technique that transfer

8 DNP treatment also reduced circulating T3 and T4 levels,

9 DNP treatment increased energy expenditure by approximat

10 DNP-enhanced 2D (13)C correlation spectra further reveal

11 DNP-enhanced 2D (29)Si{(1)H}, (13)C{(1)H}, and (31)P{(1)

12 DNP-enhanced 2D (29)Si{(29)Si} J-mediated NMR analyses o

13 DNP-enhanced NMR provides a powerful, generalizable appr

14 DNP-enhanced ssNMR data reveal a monotonic increase in c

15 DNP-treated mice weighed 26% less than controls after 2

16 DNPs functionalized with the MUC1 aptamer and doxorubici

17 DNPs were immobilized onto a gold electrode by direct ad

18 1D DNP enhanced spectra acquired in this way are shown to c

19 rate of photolysis of 2,4-dinitrophenol (24-DNP), an important environmental toxin.

20 For example, 24-DNP and other nitro-aromatic compounds should readily ph

21 om transfer reaction to the photo-excited 24-DNP.

22 ed by more than an order of magnitude for 24-DNP dissolved in 1-octanol or embedded in secondary orga

23 stark contrast to the slow photolysis of 24-DNP in an aqueous solution, the photolysis rate is incre

24 SOM much more significantly than that of 24-DNP in octanol, with effective activation energies of 53

25 perature decreased the photolysis rate of 24-DNP in SOM much more significantly than that of 24-DNP i

26 ositional isomers of dinitrophenol, only 2,4-DNP has been used extensively by many researchers for de

27 the p-NO2 group toward the reactivity of 2,4-DNP-based probes.

28 Following a DNP and spin diffusion period, the microwave irradiation

29 In order to develop a DNPs-based biosensing platform, we have selected glucose

30 tween oppositely charged regions on adjacent DNP surfaces.

31 After DNP injection, the maximal CMRO2 in both striatum and co

32 enyl-LPS or the T cell-independent type 2 Ag DNP-Ficoll revealed minimal differences between strains.

33 munization with the T cell-dependent (TD) Ag DNP-keyhole limpet hemocyanin.

34 NH3, CO, and pyridine, and (29)Si and (27)Al DNP-enhanced solid-state NMR spectroscopy.

35 obilized conjugates of bovine serum albumin (DNP-BSA) or mobile in a supported lipid bilayer (DNP-SLB

36 ination of data obtained from high-field and DNP-enhanced MAS NMR spectroscopy together with time-res

37 mited to relatively low magnetic fields, and DNP at fields higher than 9.4 T significantly drops in e

38 ng dependence on the microwave frequency and DNP polarization time.

39 annels (incipient wetness impregnation), and DNP is performed at low temperatures in a very efficient

40 antigen-independent cytokinergic manner, and DNP-specific murine SPE-7 IgE is the most highly cytokin

41 M-to-DNP ratios, DNP charge is reversed, and DNP aggregates remain stable in suspension.

42 As a result, DBPs and DNPs exhibit stronger 2PA into the one-photon-allowed B

43 finity for PSMA and the ability to bind anti-DNP antibodies.

44 aneously and its limit of detection for anti-DNP antibody and streptavidin is 1.2x10(-10) g/ml (0.55

45 ize the biosensor platform, using model anti-DNP antibodies, with the ultimate goal of designing a ve

46 ts passively sensitized with monoclonal anti-DNP IgE also resulted in mast-cell degranulation and ove

47 Although soluble anti-DNP IgE binds uniformly across features for both pattern

48 (>10% ID/g) but had minimal binding to anti-DNP antibodies.

49 ) mice were injected intradermally with anti-DNP-IgE and intravenously with the antigen DNP-HSA.

50 cepsilonRI) and stimulated using the antigen DNP-BSA.

51 i-DNP-IgE and intravenously with the antigen DNP-HSA.

52 Here, we applied DNP NMR to investigate the structure of a protein contai

53 DNP technique, identification of appropriate DNP substrates, and approaches to increase hyperpolarize

54 estion, six molecular probes using available DNP isomers were developed and investigated to evaluate

55 The basic DNP strategy is to irradiate the EPR transitions of a st

56 BSA) or mobile in a supported lipid bilayer (DNP-SLB).

57 mediate states was generated and analyzed by DNP-enhanced solid-state NMR.

58 tically doped crystals might be increased by DNP.

59 bolic switch in dCTP production triggered by DNP inhibition is accompanied by NSP up-regulation and c

60 We report CE DNP experiments at 211, 600, and 800 MHz using a new ser

61 The CE DNP enhancement for the TEMTriPol biradicals does not de

62 ) moiety to the C7 end of ciprofloxacin (Cip-DNP) reduced protection due to resistance substitutions

63 Treatment of E. coli cultures with Cip-DNP selectively enriched an uncommon variant, GyrA-A119E

64 Comparing DNP-enhanced and conventional solid-state NMR, an absolu

65 Cryogenic DNP was required to observe the weaker external binding

66 ments at room temperature and with cryogenic DNP.

67 rage repeatability of our state-of-the-art D-DNP NMR equipment for samples of metabolomic relevance (

68 ts in neutral and acidic environments from D-DNP NMR spectroscopy, corresponding to a pre-equilibrium

69 High signal gains in D-DNP enable rapid measurement of data sets characterizing

70 f components and estimation of kinetics in D-DNP experiments, which can be applied at a high level of

71 rpolarized samples increases throughput of D-DNP by the same factor, improving the applicability to m

72 aneous signal acquisition, a limitation of D-DNP for the screening of protein-ligand interactions is

73 This first report on the repeatability of D-DNP highlights the compatibility of the technique with t

74 ion therefore extends the applicability of D-DNP to in vitro studies with a wider range of metabolite

75 A method based on d-DNP NMR spectroscopy to study chiral recognition is desc

76 dissolution dynamic nuclear polarization (D-DNP) assisted by cross-polarization (CP) provides a reli

77 dissolution dynamic nuclear polarization (D-DNP) has emerged as a technique for enhancing NMR signal

78 dissolution dynamic nuclear polarization (D-DNP) technique provides an important breakthrough to ove

79 dissolution dynamic nuclear polarization (D-DNP) usually involves saturating the ESR transitions of

80 dissolution dynamic nuclear polarization (D-DNP), both in in vivo and in vitro contexts.

81 dissolution dynamic nuclear polarization (D-DNP).

82 dissolution dynamic nuclear polarization (D-DNP).

83 dissolution dynamic nuclear polarization (D-DNP).

84 We show that D-DNP can be performed efficiently with hybrid polarizing

85 dition of the electroporation pulse to the D-DNP experiment increases the signals of the downstream m

86 axation and concentration gradients in the D-DNP experiment, the subtractive process for Hadamard rec

87 7 intermediate during the timescale of the D-DNP NMR experiment.

88 determination of binding mechanisms using D-DNP RD.

89 for membrane permeabilization for use with D-DNP in cell cultures.

90 Two-dimensional DNP MAS NMR of the silica-bound peptide and solution NMR

91 -dibenzo- (DBP) and syn-dinaphthoporphyrins (DNP), lowers the symmetry of the porphyrin skeleton.

92 rphyrins (DBPs) and syn-dinaphthoporphyrins (DNPs) were synthesized by [2 + 2] condensation of the co

93 itochondrial protonophore 2,4 dinitrophenol (DNP) has beneficial effects on NAFLD, insulin resistance

94 The chemical uncoupler 2,4-dinitrophenol (DNP) was an effective and widely used weight loss drug i

95 ased PCr recovery from either dinitrophenol (DNP) or azide in L6 cells.

96 f the mitochondrial uncoupler dinitrophenol (DNP) were compared using 16.4 T in isoflurane anesthetiz

97 ilizing surface-patterned 2,4 dinitrophenyl (DNP) ligands.

98 ained antibody-recruiting 2,4-dinitrophenyl (DNP) groups and iodine were synthesized and screened in

99 We report that addition of a dinitrophenyl (DNP) moiety to the C7 end of ciprofloxacin (Cip-DNP) red

100 olyether incorporating 1,5-dioxynaphthalene (DNP) and tetrathiafulvalene (TTF) units along with a 4,4

101 lyether containing two 1,5-dioxynaphthalene (DNP) and two TTF units) that is topologically isomeric w

102 ne) (CBPQT(4+)), and a 1,5-dioxynaphthalene (DNP) guest.

103 h viologen (V(2+)) and 1,5-dioxynaphthalene (DNP) recognition units using click chemistry.

104 electron relaxation times by studying direct DNP of (13)C using SA-BDPA and trityl radical, and achie

105 ce imaging (MRI) sensitivity and dissolution DNP can be used to perform in vivo real-time (13)C MRI.

106 approach may be best suited for dissolution DNP and for studies of (1)H depleted biological and othe

107 analysis into two steps, making dissolution DNP an attractive method to study polymerization reactio

108 The recent development of rapid dissolution DNP methods has facilitated previously impossible in vit

109 nuclear polarization achieved by dissolution-DNP is observed with full intensity and then returned to

110 osing an adequate solvent, (1)H cross effect DNP enhancements of over 80 can be obtained at 240 K.

111 at over a 2-fold improvement in cross-effect DNP enhancements can be achieved in MAS experiments on f

112 Here we report solid-state Overhauser effect DNP enhancements of over 100 at 18.8 T.

113 we demonstrate the possibility of efficient DNP transfer in polycrystalline samples of [Co(en)3Cl3]2

114 This charge reversal eliminates DNP attachment to model membranes containing the highest

115 To enable DNP experiments without major modifications of the formu

116 ing distance in solution, allowing favorable DNP subsetCBPQT(4+) host-guest interactions to overcome

117 kes it a very efficient polarizing agent for DNP, yielding unprecedented proton enhancements of over

118 niform for DNP-SLB and edge-concentrated for DNP-BSA.

119 l bTUrea, is used as a polarizing matrix for DNP NMR experiments of solutions containing alanine and

120 mental setup offers an attractive option for DNP-enhanced solid-state NMR on ordered membranes and pr

121 g at the cryogenic temperatures required for DNP.

122 new approach for preparation of samples for DNP experiments.

123 alternative sample preparation strategy for DNP MAS ssNMR studies of lipid membranes and integral me

124 g highly efficient polarization transfer for DNP.

125 shows distinctive distributions: uniform for DNP-SLB and edge-concentrated for DNP-BSA.

126 desirable and which would also benefit from DNP signal enhancement.

127 ecover the expected signal enhancements from DNP, we explored time domain experiments such as NOVEL w

128 ensing platform preparation (DNPs/Au and GOx/DNPs/Au systems) by atomic force microscopy (AFM), field

129 ts, lead to large and relatively homogeneous DNP enhancements throughout the lipid bilayer and to an

130 ment of TRPM7 kinase function suppressed IgE-DNP-dependent exocytosis, slowed the cellular degranulat

131 extracellular Mg(2+) assured unperturbed IgE-DNP-dependent exocytosis, independently of TRPM7.

132 olved in low viscosity solvents to implement DNP in liquids.

133 ter-soluble and shows significantly improved DNP performance compared to the commonly used DNP agent

134 angiotensin-converting enzyme inhibition in DNP.

135 evels could contribute to podocyte injury in DNP.

136 nsor for lactate determination that includes DNPs as nanomaterial.

137 phages, some DCs, and myeloid cells ingested DNPs, but CD11b(+) DCs were the only cells to express IF

138 To investigate DNP action, mice fed a high fat diet and housed at 30 de

139 64)Cu-L19K-FDNB to VEGF, whereas (64)Cu-L19K-DNP and (64)Cu-L19K did not bind covalently.

140 with (64)Cu-L19K-FDNB than with (64)Cu-L19K-DNP and (64)Cu-L19K, with mean standardized uptake value

141 (64)Cu-L19K-(2,4-dinitrophenyl) ((64)Cu-L19K-DNP) and (64)Cu-L19K.

142 ion studies of (64)Cu-L19K-FDNB, (64)Cu-L19K-DNP, and the native (64)Cu-L19K were compared in HCT-116

143 fluoro-2,4-dinitrobenzene, resulting in L19K-DNP.

144 hermogenesis) were treated with 800 mg/liter DNP in drinking water.

145 ut employing the enzyme lactate oxidase (LOx/DNPs/Au).

146 onstrated that substrates containing ACC/Lys(DNP) exhibit 7 to 10 times higher sensitivity than conve

147 We therefore propose that the ACC/Lys(DNP) pair can be considered a novel and sensitive scaffo

148 luorophore and 2,4-dinitrophenyl-lysine (Lys(DNP)) as the quencher.

149 -methoxy-coumarin-4-yl acetic acid (MCA)/Lys(DNP) substrates; thus, substantially lower amounts of su

150 polarization under magic angle spinning (MAS-DNP) could be used to dramatically increase the sensitiv

151 ly demonstrates the possibility of using MAS-DNP to greatly facilitate the acquisition of 2D (29)Si-(

152 Lung inflation did not alter mean DNP within the slice (P = 0.10).

153 endritic cells (DCs) after DNA nanoparticle (DNP) treatment.

154 lectrode with undoped diamond nanoparticles (DNPs) and its applicability to the fabrication of electr

155 kinetic properties of diamond nanoparticles (DNPs) functionalized with the polycation poly(allylamine

156 Diamond nanoparticles (DNPs) were incorporated into matrix-assisted laser desor

157 ophan-phenylalanine dipeptide nanoparticles (DNPs) that can shift the peptide's intrinsic fluorescent

158 Rationally designed DNA nanoparticles (DNPs) have emerged as facile delivery vehicles because t

159 esis of proteinuria in diabetic nephropathy (DNP).

160 Here, we demonstrate new DNP-based measurements that extend (17)O solid-state NMR

161 Hybrid PET/MRI with a 13-nm DNP enables noninvasive assessment of inflammation in ex

162 c nuclear polarization surface enhanced NMR (DNP-SENS), Mossbauer spectroscopy, and computational che

163 ization of a biradical dopant to the nuclei, DNP allowed selective detection of (13)C spin diffusion

164 ctly observed at natural abundance by (17) O DNP surface-enhanced NMR spectroscopy (SENS).

165 We observe DNP enhancement factors epsilon > 40 at a magnetic field

166 protonated samples investigated, we observed DNP signal enhancements of ~10 at 400 MHz using only 4-6

167 his work represents the first application of DNP-enhanced ssNMR to the characterization of peptide or

168 will pave the way for future applications of DNP in paramagnetically doped materials or metalloprotei

169 onses of M. spretus living in three areas of DNP (the reference) and surrounding areas (El Partido an

170 wever, treatments with low concentrations of DNP or azide reversibly decreased ATP concentration.

171 abundance, thereby extending the concept of DNP surface-enhanced NMR spectroscopy to the (17)O nucli

172 This first demonstration of DNP transfer from one paramagnetic metal ion to its diam

173 Furthermore, the beneficial effects of DNP suggest that chemical uncouplers deserve further inv

174 Micron-sized features of DNP are presented as densely immobilized conjugates of b

175 ped a controlled-release oral formulation of DNP, called CRMP (controlled-release mitochondrial proto

176 s after thymidine (dT)-induced inhibition of DNP dCTP synthesis by switching to NSP-mediated dCTP pro

177 However, the physiology of DNP has not been studied in detail because toxicity, inc

178 Our work also demonstrates the power of DNP-enhanced solid-state NMR at low temperatures for the

179 cle of PR and also demonstrates the power of DNP-enhanced solid-state NMR to bridge the gap between f

180 tion really opens new avenues for the use of DNP-enhanced solid-state NMR as an on-cell investigation

181 ng can be facilitated tremendously by use of DNP-enhanced solid-state NMR spectroscopy.

182 Herein, we constructed a number of DNPs of rectangular and tubular shapes with varied dimen

183 {1+1} macrocycles (each containing also one DNP unit) of the isomeric [3]catenane exhibit slightly d

184 studied using MD simulations and Overhauser DNP-enhanced NMR.

185 Our results demonstrate that Overhauser DNP at high field provides efficient polarization transf

186 However, paramagnetic DNP polarizing agents can have deleterious effects on NM

187 ant ecological area of Donana National Park (DNP) and surrounding areas (SW Spain), where many migrat

188 In particular, DNP SENS provides molecular-level information about the

189 can be produced both by the de novo pathway (DNP) and by the nucleoside salvage pathway (NSP).

190 Density-normalized perfusion (DNP) magnetic resonance imaging data were obtained in he

191 high-frequency dynamic nuclear polarization (DNP) and (1)H-detected MAS techniques.

192 vity-enhancing dynamic nuclear polarization (DNP) and differential isotopic labeling of expansin and

193 angle spinning dynamic nuclear polarization (DNP) at temperatures around 100 K.

194 ancements from dynamic nuclear polarization (DNP) at temperatures below 30 K.

195 Dynamic nuclear polarization (DNP) can dramatically enhance the sensitivity of nuclear

196 Dynamic nuclear polarization (DNP) can enhance NMR sensitivity by orders of magnitude

197 ng dissolution dynamic nuclear polarization (DNP) enable the detection of NMR spectra from low-gamma

198 Dynamic nuclear polarization (DNP) enhanced solid-state NMR spectroscopy at 9.4 T is d

199 Dynamic nuclear polarization (DNP) enhanced solid-state nuclear magnetic resonance (NM

200 ontinuous wave dynamic nuclear polarization (DNP) experiments decreases at the high magnetic fields u

201 Dynamic nuclear polarization (DNP) has recently emerged as a tool to enhance the sensi

202 DNMR) based on dynamic nuclear polarization (DNP) in a quantum Hall ferromagnet (QHF) is a highly sen

203 efficiency of dynamic nuclear polarization (DNP) in solid-state NMR studies.

204 Efficient dynamic nuclear polarization (DNP) in solids, which enables very high sensitivity NMR

205 cement through dynamic nuclear polarization (DNP) increases the sensitivity of metal detection to aff

206 ss-effect (CE) dynamic nuclear polarization (DNP) is a rapidly developing technique that enhances the

207 (HP MRS) using dynamic nuclear polarization (DNP) is a technique that has greatly enhanced the sensit

208 Dynamic nuclear polarization (DNP) is generally capable of enhancing NMR signals by tr

209 larization via dynamic nuclear polarization (DNP) is pivotal for boosting magnetic resonance imaging

210 Dynamic nuclear polarization (DNP) magic-angle spinning (MAS) solid-state NMR (ssNMR)

211 feasibility of dynamic nuclear polarization (DNP) magic-angle-spinning NMR techniques, along with a j

212 or solid-state dynamic nuclear polarization (DNP) NMR experiments.

213 me, the use of dynamic nuclear polarization (DNP) NMR for characterizing zeolites containing ~2 wt %

214 g schemes with dynamic nuclear polarization (DNP) NMR.

215 Dissolution dynamic nuclear polarization (DNP) of monomers provides a sufficient signal-to-noise r

216 Dynamic nuclear polarization (DNP) potentially offers significant improvements in this

217 on sources for dynamic nuclear polarization (DNP) solid-state NMR at 9.4 T and with ca. 100 K sample

218 Dynamic nuclear polarization (DNP) solid-state NMR was used to obtain natural abundanc

219 gands, through dynamic nuclear polarization (DNP) surface enhanced NMR spectroscopy.

220 ished by using dynamic nuclear polarization (DNP) surface-enhanced solid-state NMR techniques.

221 tion using the dynamic nuclear polarization (DNP) technique has emerged as a powerful means to improv

222 nterest in the Dynamic Nuclear Polarization (DNP) technique to improve the signal to noise ratio of s

223 using standard dynamic nuclear polarization (DNP) techniques and their (15)N chemical shifts were fou

224 MR enhanced by dynamic nuclear polarization (DNP) through which a 19-fold signal enhancement was achi

225 ate the use of dynamic nuclear polarization (DNP) to elucidate ligand binding to a membrane protein u

226 enhancement by dynamic nuclear polarization (DNP) was applied to determine precisely the retinal stru

227 ts provided by dynamic nuclear polarization (DNP), and in particular if the theoretical maximum enhan

228 ty enhanced by dynamic nuclear polarization (DNP), provide direct evidence of shared covalent (29) Si

229 abundance with dynamic nuclear polarization (DNP), Pruski et al. were able to measure oxygen-proton d

230 rom the use of dynamic nuclear polarization (DNP), which in some cases allowed us to shorten the data

231 plicability of dynamic nuclear polarization (DNP), which leads to sensitivity enhancements of 2 order

232 mensional (2D) dynamic nuclear polarization (DNP)-enhanced NMR techniques.

233 Dynamic nuclear polarization (DNP)-enhanced solid-state NMR spectroscopy has been show

234 n the basis of dynamic nuclear polarization (DNP)-enhanced solid-state NMR, we were able to analyze t

235 ng dissolution dynamic nuclear polarization (DNP).

236 lved in the biosensing platform preparation (DNPs/Au and GOx/DNPs/Au systems) by atomic force microsc

237 At higher NOM-to-DNP ratios, DNP charge is reversed, and DNP aggregates remain stable

238 At low NOM-to-DNP ratios, DNPs aggregate to a limited extent but retain a positive

239 Registered DNP images were normalized by the mean to estimate perfu

240 lumina with the acquisition of well-resolved DNP surface-enhanced (27)Al cross-polarization spectra.

241 he electrochemical behavior of the resulting DNPs/Au platform was studied.

242 ted in liposomes containing SL-lipids reveal DNP enhancement values over two times larger for KL4 com

243 of cells isolated from excised aortas showed DNP uptake predominantly in monocytes and macrophages (7

244 In sedimented solute DNP (SedDNP), the biradical polarizing agent is co-sedim

245 We study the solvent DNP enhancement of both TEKPol and BDPA in OTP in the ra

246 Specifically, DNP MAS ssNMR experiments at 600 MHz/395 GHz on KL4 reco

247 arization surface-enhanced NMR spectroscopy (DNP SENS) allows the unambiguous description of the coor

248 arization surface enhanced NMR spectroscopy (DNP SENS) and density functional theory (DFT) calculatio

249 ion surface-enhanced (89)Y NMR spectroscopy (DNP SENS).

250 C isotope, this experiment demonstrates that DNP NMR is sufficiently sensitive to observe spin system

251 adipose tissue activity, demonstrating that DNP-mediated heat generation substituted for brown adipo

252 They further show that DNP-enhanced solid-state NMR fills the gap for challengi

253 nce for the proposed mechanism and show that DNP-induced cross-relaxation is a robust feature within

254 We show that DNPs are photostable, biocompatible and have a narrow em

255 This study suggests that DNPs are effective tools for the systemic delivery of th

256 The DNP-containing M12L24 molecular flasks are effectively "

257 The DNP-NMR results corroborate the presence of MWW layers a

258 Additionally, the DNP sensitivity-enhanced two-dimensional (13)C/(13)C che

259 oss-effect are the main determinants for the DNP enhancements we obtain.

260 d (13)C-substrates can be extracted from the DNP apparatus in the solid form, while maintaining the e

261 be described as emergent because neither the DNP subsetCBPQT(4+) nor the M12L24 assemblies exhibit th

262 splitting, as well as the dependence of the DNP enhancement factor on the external magnetic field an

263 by simple filtration in the cryostat of the DNP polarizer, and a pure hyperpolarized solution is col

264 This review presents the basics of the DNP technique, identification of appropriate DNP substra

265 Pharmacological co-targeting of the DNP with dT and the NSP with DI-39 was efficacious again

266 kly tuned on-resonance with electrons on the DNP polarizing agent.

267 Surprisingly, we find that the DNP enhancement decreases only relatively slowly for tem

268 icate that the microwave field (and thus the DNP enhancement) is inhomogeneous in the sample, and we

269 he TTF unit, the CBPQT(4+) ring moves to the DNP unit, producing a red color.

270 The DNPs optimize the MALDI sample morphology and thermalize

271 The visible emission signal allows the DNPs to act as imaging and sensing probes.

272 The siRNA delivered by the DNPs inhibited cell growth both in vitro and in vivo, wh

273 ned peaks were observed corresponding to the DNPs oxidation/reduction at the underlying gold electrod

274 temperature that is below thermoneutrality, DNP treatment had no effect on body weight, adiposity, o

275 This DNP MAS NMR approach allows efficient, high-throughput c

276 Hall phases; however, the mechanism of this DNP and, in particular, the role of quantum Hall edge st

277 Thus, DNP makes structural studies of proteins at endogenous l

278 Suwannee River NOM induces changes to DNP hydrodynamic diameter and apparent zeta-potential in

279 The NOM-induced changes to DNP properties alter subsequent interactions with model

280 the contributions of bulk and edge states to DNP in QHF.

281 HCl) in a manner that depends on the NOM-to-DNP concentration ratio.

282 Diamond nanoparticles at low NOM-to-DNP ratios attach to model membranes to a larger extent

283 At higher NOM-to-DNP ratios, DNP charge is reversed, and DNP aggregates r

284 At low NOM-to-DNP ratios, DNPs aggregate to a limited extent but retai

285 es and provides a general perspective toward DNP at ambient temperatures.

286 de, which demonstrate that, although undoped DNPs have an insulating character, they show electrochem

287 NP performance compared to the commonly used DNP agent TOTAPOL.

288 Nonetheless, few studies have used DNPs to deliver siRNAs in vivo, and none has demonstrate

289 results demonstrate the feasibility of using DNP-enhanced NMR techniques to measure and assess dilute

290 ddressed are the biochemical events to which DNP-NMR has been applied, with descriptions of several p

291 At 600 MHz and with DNP, we measured a distance between the drug and the pro

292 n decoupling experiments in conjunction with DNP and magic-angle-spinning NMR spectroscopy.

293 WT mice were similar after immunization with DNP-keyhole limpet hemocyanin.

294 on of a small number of specific labels with DNP NMR enables determination of architectural informati

295 re demonstrated to be readily performed with DNP and provide the bonding motifs between the QD surfac

296 everse micelle encapsulation technology with DNP offers a route to a significant increase in the sens

297 Without DNP, no (119)Sn resonances were detected after 10 days o

298 PET/MRI revealed high uptake of (89)Zr-DNP in the aortic root of apolipoprotein E knock out (Ap

299 with short-interfering RNA decreased (89)Zr-DNP plaque signal (P<0.05) and inflammatory gene express

300 amine for zirconium-89 radiolabeling ((89)Zr-DNP) and a near-infrared fluorochrome (VT680) for micros