ライフサイエンスコーパス: QD

1 extract after oral administration (50 mg/kg, qd).

2 apy: ticagrelor 90 mg BID plus aspirin 81 mg QD).

3 nducting CdSe quantum dots on Si channel (Si-QD).

4 (30 mg/kg, PO, QD) or INT-767 (10 mg/kg, PO, QD).

5 oquinone preserves the cubic phase of CsPbI3 QD.

6 eract with the core electronic states of the QD.

7 of the electron wavefunction over the entire QD.

8 on of FRET as the dye diffuses away from the QD.

9 ats, and a predicted human dose of 120 mg of QD.

10 both shell thickness and number of NDIs per QD.

11 ith ab initio molecular dynamics of a single QD.

12 wice daily [BID], 1.5% once daily [QD], 0.5% QD, 0.15% QD), vehicle, or triamcinolone cream (0.1% BID

13 UX (1.5% twice daily [BID], 1.5% once daily [QD], 0.5% QD, 0.15% QD), vehicle, or triamcinolone cream

14 week induction), followed by 10 mg QD, 30 mg QD, 100 mg once weekly, or placebo (8-week maintenance).

15 lacebo (4-week induction), followed by 10 mg QD, 30 mg QD, 100 mg once weekly, or placebo (8-week mai

16 randomized to PF-06700841 30 mg once daily (QD), 60 mg QD, or placebo (4-week induction), followed b

17 k area ratio computation and the theoretical QD:Ab molar ratios assayed, which internally validates t

18 the different bioconjugate mixtures studied (QD:Ab molar ratios ranging from 0.27 to 4.6).

19 t bioconjugation mixtures (1:1, 2:1, and 3:1 QD:Ab molar ratios were assessed).

20 The resulting weighted QD:Ab ratio computed in this way for each bioconjugate p

21 matches well with both the global (average) QD:Ab ratio experimentally obtained by the simpler peak

22 roviding not only the limits of the range of QD:Ab ratios in the different bioconjugate species resul

23 l quantum dot:rat monoclonal IgG2a antibody (QD:Ab) conjugate mixtures in a single run without any pr

24 itons (95 +/- 5%) via a low concentration of QD acceptors, followed by the emission of IR photons.

25 e controlled via tuning the concentration of QD acceptors.

26 ssue penetration of visible light needed for QD activation, and concern over trace heavy metals, have

27 e an ultrathin freestanding ZnO quantum dot (QD) active layer with nanocellulose structuring, and its

28 icipated and suggest promising potential for QD administration.

29 nced by various factors such as cell damage, QD aggregation or the level of reactive oxygen species,

30 ld of photoinduced charge transfer between a QD and a molecular probe to even low-affinity binding ev

31 nd toxicity of intravesically instilled free QD and anti-CD47-QD in mice.

32 Ctrough levels were slightly lower with DRV QD and BID.

33 In turn, the sum of the QD and dye PL intensities, when adjusted for quantum yie

34 s in ultrafast electron transfer between the QD and FeTPP, enabled by formation of QD/FeTPP complexes

35 ion pairing between the ligand shell of the QD and NR4(+) results from a combination of electrostati

36 As proof of concept, we show that the MNP@QD and SIP pairing is able to selectively isolate, fluor

37 ction by a factor of 2.4 by colocalizing the QD and the Pd-complex.

38 of this review is the colloidal quantum dot (QD) and specifically the interaction of the QD with prox

39 noparticles include a spherical quantum dot (QD) and three differing lateral areas of 4-monolayer-thi

40 acid (MPA)-capped CdSe quantum dot (MPA-CdSe QD) and visible light.

41 ate (MHA) ligand shell of a PbS quantum dot (QD) and water.

42 ploiting the spectral features of Tb(3+) and QD, and the high binding affinity of the streptavidin-bi

43 in doubling time on exposure to 25 mg/L CdTe QD ( approximately 4 nm) as compared to control.

44 The assemblies (MNP@QD) are magnetic iron oxide nanoparticles surrounded by

45 physical properties of a doped quantum dot (QD) are strongly influenced by the dopant site inside th

46 Coherent QD arrays have a spatial distribution which is neither r

47 can be coupled to light or to other spins in QD arrays.

48 to position single QDs and to create ordered QD arrays.

49 ransfer and the use of the ligand shell of a QD as a semipermeable membrane that gates its redox acti

50 energy transfer (FRET) between quantum dot (QD) as a donor and graphene oxide (GO) as an acceptor.

51 the QDs, and (iii) structural components of QD assemblies that dictate QD-QD or QD-molecule interact

52 r rates between quantum dots (QDs) in chiral QD assemblies.

53 des were assembled around a central CdSe/ZnS QD at different ratios, tuning the relative rates of FRE

54 HNC-SLs) self-assembled from quantum-dot-Au (QD-Au) satellite-type HNCs.

55 detrimental to the operation of quantum dot (QD) based semiconductor qubits.

56 e useful in tuning ET processes for advanced QD-based applications.

57 rovide important and useful design rules for QD-based light harvesting applications using the exciton

58 Similarly, we prepared QD-based NPs densely decorated with an isatoic anhydride

59 achieved, which is among the most effective QD-based photocathode water-splitting systems.

60 , we have demonstrated the deposition of the QD-based wavelength shifting material on a large area PD

61 ate that contains a carboxylic acid, a known QD-binding group, is accelerated by more than a factor o

62 , we show that the photoluminescence (PL) of QD bioconjugates can also be modulated by a combination

63 used to capture bacteria, and quantum dots (QD) bound to a second aptamer were utilized to quantify

64 e not only the excited state dynamics of the QD but also, in some cases, its ground state electronic

65 We find that the QD can rectify electrical charges generated from the pie

66 eft unprotonated, serves as a poison for the QD catalyst by adsorbing to its surface.

67 T-cell-regulated B cell IgG production, and QD-CD19-PKM2-null T cell EVs hold high potential to trea

68 electronic transport of one-dimensional (1D) QD chains (QDCs) is theoretically investigated.

69 t charge spins and light particles in future QD circuits.

70 correlates with the strength of the acceptor QD circular dichroism (CD) spectrum.

71 +) or Eu(3+) doped luminescence glass or CdS-QD coated glass lenses provide additional visible light

72 doped borate glasses or CdS-quantum dot (CdS-QD) coated lenses efficiently convert UV light to 542 nm

73 Neither HL6 nor HL6/QD complexes are cytotoxic to A549 or HeLa cells.

74 The mechanism of cellular uptake of HL6/QD complexes is primarily direct membrane translocation

75 ts (QDs) noncovalently to generate stable L6/QD complexes that enter cells by endocytosis.

76 r accelerate the synthetic path discovery of QD compositions, by at least twofold.

77 Single-QD conductance measurements reveal that there are multip

78 opical (i.e. intravesical) administration of QD-conjugated anti-CD47.

79 , -20.0 to -14.6]) was observed in the 30-mg QD continuous treatment group.

80 te that both the chemical composition of the QD core (InP vs CdSe) and the shell play a crucial role

81 The modularity and tunability of the QD core and surface make it a convenient and effective c

82 mbination of the electronic structure of the QD core and the chemistry at its surface to use the ener

83 the yield of electron transfer (eT) from the QD core to AQ, increases as the steric bulk of NR4(+) in

84 romotes the incorporation of <1% Ag into the QD core where it causes p-type doping behavior.

85 e states or to the delocalized states of the QD core, (ii) energy or electron donors or acceptors for

86 Quantum dot (QD) coupling in nanophotonics has been widely studied fo

87 pared across the 3 drugs (rivaroxaban: 20 mg QD, dabigatran: 150 mg BID, or warfarin) using 3-way pro

88 by more spatially regular nucleation as the QD density increases.

89 Freedom in QD design to isolate and control the quantum mechanical

90 e new insights should be significant for the QD design, characterization, and applications, the metho

91 perties of QD surfaces and the interfaces in QD devices are of particular importance, and these enabl

92 antum efficiency over single-bottom graphene/QD devices, overcoming the known restriction that the di

93 onic dynamics in an ensemble of quantum dot (QD) dimers are presented.

94 y, 2) use of high-boiling-point solvents for QD dispersion, and 3) limitations associated with one-st

95 llows us to realize a regime of nearly ideal QD doping when incorporation of magnetic ions occurs sol

96 occupancy attained by BID dosing relative to QD dosing compounded over time to augment downstream bio

97 24 months of 87.2% (95% CI, 57.2-96.7) with QD dosing.

98 more potent pathway inhibition compared with QD dosing.

99 e estimated half-life supporting once-daily (QD) dosing.

100 ublet in motif 1 of family 4 UDGa and in the QD doublet in motif 1 of family 1 UNG.

101 let in family 4 Thermus thermophilus UDGa to QD doublet increases the catalytic efficiency by over on

102 DT/oleate ligand shell of a PbS quantum dot (QD) dramatically reduces the permeability of the ligand

103 plasma HIV-1 RNA suppression on once-daily (QD) DRV-containing ART at screening.

104 er they received vehicle, OCA (30 mg/kg, PO, QD), ELA (3, 10 mg/kg, PO, QD), or combinations (OCA + E

105 ehicle (PO, QD), liraglutide (0.4 mg/kg, SC, QD), elafibranor (30 mg/kg, PO, QD) or INT-767 (10 mg/kg

106 This results in enhanced QD emission and dye quenching.

107 Analysis of the QD emission enhancement as a function of distance reveal

108 ent mechanism for the temporal modulation of QD emission intensity at constant optical pumping rate.

109 nstrated electrical control of the colloidal QD emission provides a new approach for modulating inten

110 te the excitation by X-rays of quantum-dots (QD) emitting in the near-infrared (NIR), using a clinica

111 For each QD-ET mechanism, a working explanation of the appropriat

112 stry at its surface to use the energy of the QD excited state to drive chemical reactions.

113 e findings imply that the CD strength of the QD exciton transition(s) may be used as a predictor for

114 ions between the magnetic ions and intrinsic QD excitons that have been exploited for color conversio

115 a promising strategy to enhance coupling of QD excitons with proximate molecules, ions, or other QDs

116 en the QD and FeTPP, enabled by formation of QD/FeTPP complexes.

117 Herein, we suggest a new protocol for QD film deposition using electrical double-layered PbS Q

118 rs distributed in an orderly manner inside a QD film is studied.

119 ilver resonators, excitation wavelength, and QD film thickness.

120 reparing a dense, smooth, 5.3-mum-thick PbSe QD film via doctor-blading.

121 QD film with increased thickness shows efficient charge

122 The patterned QD films maintain ~75% of original PLQY and the electrol

123 ission behaviors from single- and multilayer QD films on silver resonators are described quantitative

124 eposition process yields high-quality n-type QD films quickly (within 1 min) while minimizing the amo

125 the construction of conductive and intact Pe-QD films to maximize their functionality.

126 d was used to define fluorescent patterns on QD films, allowing for further applications in biosensin

127 d allows for facile hole extraction from the QD films, resulting in a power conversion efficiency of

128 and allow for efficient charge transport in QD films.

129 cal reactions and in situ ligand exchange in QD films.

130 Controlling the thickness of quantum dot (QD) films is difficult using existing film formation tec

131 tionic GNPs efficiently quenched the anionic QD fluorescence by forming nanoparticle hybrid.

132 V-vis absorption and ORF, but it reduces the QD fluorescence depolarization.

133 The brightness of the QD fluorescence is greatly enhanced on resonance with th

134 QD-GNP pair was unlocked by NADH leading to QD fluorescence turn-on.

135 Quantum dot (QD) fluorescence emission in a low background window all

136 2 molecular and 6 semiconductor quantum dot (QD) fluorophores.

137 able signs of toxicity up to 200 mg/kg dosed QD for 7 days.

138 able signs of toxicity up to 300 mg/kg dosed QD for 7 days.

139 be efficacious at 8 mg/kg dosed once daily (QD) for 5 days with no observable signs of toxicity up t

140 The QD formation occurs after anneal of Bismuth droplets und

141 owth intermediates during III-V quantum dot (QD) formation.

142 ight and photostable terbium-to-quantum dot (QD) Forster resonance energy transfer (FRET) nanoprobe w

143 This work establishes QD FRET as a rapid, sensitive technique for probing stru

144 Typically, the QD-FRET constructs have made use of labeled targets or h

145 QD functionalization with beta-cyclodextrin molecular ba

146 ocking and unlocking the interaction between QD-GNP pair leading to differential fluorescent properti

147 Quenching interaction between QD-GNP pair was unlocked by NADH leading to QD fluoresce

148 they provide pivotal clues in understanding QD growth mechanisms.

149 leading to monomer formation and subsequent QD growth.

150 investigation of single TiO(2)-nanowire/CdSe-QD heterojunction solar cell (QDHSC) using a custom-desi

151 the efficiency of light conversion by the PM-QD hybrid material under two-photon excitation is up to

152 hieved by employing Stark effect into the Si-QD hybrid system.

153 mistry and the band edge positions of ligand/QD hybrid systems.

154 framework (MOF) and perovskite quantum dot (QD) hybrid single crystal ZJU-28 MAPbBr(3) is shown via

155 travesically instilled free QD and anti-CD47-QD in mice.

156 The optical properties of the single QD in the devices are characterized.

157 LBN 0.024% QD in the evening was noninferior to timolol 0.5% BID ov

158 0 mg twice daily (BID) or 200 mg once daily (QD) in 48 patients with relapsed/refractory or high-risk

159 rovskite phase when the concentration of the QD increases.

160 min) while minimizing the amount of the PbS QD ink used to less than 5 mg for one device (300-nm-thi

161 ent and the subsequent deposition of the PbS QD ink without requiring a post-deposition annealing tre

162 iques, which employ pre-ligand-exchanged PbS QD inks, because of several issues: 1) poor colloidal st

163 position using electrical double-layered PbS QD inks, prepared by solution-phase ligand exchange usin

164 The QD integration into the bR-containing PMs significantly

165 that are still not fully understood such as QD interactions with gold and other metal nanoparticles

166 magneto-photonic devices containing a single QD is performed on a hybrid material consisting of collo

167 f this novel quintuple detector ThFFF (ThFFF-QD) is documented for three important fields of applicat

168 ts dominate charge transport in these single-QD junctions.

169 We show that QD labeling does not affect major biophysical properties

170 usion chromatography improved specificity of Qd labeling.

171 -based quantum dots (QDs), respectively, the QD labels are dissolved releasing Pb(II) and Cd(II) in t

172 sing device platform for realizing colloidal QD laser diodes.

173 scence quantum yield (PLQY) of the patterned QD layers.

174 Precise patterning of quantum dot (QD) layers is an important prerequisite for fabricating

175 ently thick CdSe shells to impart new single-QD-level photostability, as evidenced by suppression of

176 ind that in addition to ligand dipole, inter-QD ligand shell inter-digitization contributes to the ba

177 inued development of such systems containing QD light absorbers and molecular catalysts for H2 format

178 is an important prerequisite for fabricating QD light-emitting diode (QLED) displays and other optoel

179 oceeded, evolution from uni-molecule-like to QD-like characters was observed.

180 The QD limits of quantification (QD-LOQ) in each matrix were

181 treated for 8 weeks with either vehicle (PO, QD), liraglutide (0.4 mg/kg, SC, QD), elafibranor (30 mg

182 cle tracking of Gal3- or STxB-functionalized QD-loaded DNA icosahedra allows us to monitor compartmen

183 ch a MOF strategy not only results in a high QD loading concentration, but also significantly diminis

184 The QD limits of quantification (QD-LOQ) in each matrix were calculated according to the

185 of environmental concentrations (3.4 ppt <= QD-LOQs <= 2.5 ppb).

186 In aquatic matrices, the QD-LOQs increase 10-, 130-, and 250-fold for Zn, Cd, and

187 An initial discussion of QD materials along with key concepts surrounding their p

188 etically different RE breed, using the novel QD measure of quantitative proteomic distance.

189 confinement of a waveguided mode within the QD medium, which allows for demonstrating low-threshold

190 Netarsudil QD met the criteria for noninferiority to timolol BID.

191 l reaction intermediates of CdS quantum dot (QD):MoFe protein nitrogenase complexes under photochemic

192 Illumination of CdS QD:MoFe protein complexes led to redox changes in the Mo

193 nents of QD assemblies that dictate QD-QD or QD-molecule interactions.

194 Nuclear magnetic resonance analysis of the QD-molecule systems shows that the photoproduct aniline,

195 d lasing even with an ultrathin (about three QD monolayers) active layer.

196 synthetic methods to directly react to form QD monomers, but rather they can generate in situ the sa

197 ticular, spin relaxation rate peaks when the QD motion is in the transonic regime, which we term a sp

198 verlayers as well as the bottom monolayer of QD multilayers exhibit significant PL enhancement mainly

199 The ultrathin ZnO QD-nanocellulose composite is obtained by hydrogel trans

200 This work provides a pathway for advancing QD nanotherapeutics to combat MDR superbugs.

201 Our results identify QD nuclei as a potential quantum information resource, w

202 g the systematic preparation of high-quality QD of any sizes and materials.

203 he QD (where it exchanges electrons with the QD) of 154 J/mol upon introduction of each additional ch

204 orescent nanoparticles such as quantum dots (QD) offer superior optical characteristics compared to o

205 n states and thus the energy and dynamics of QD optical transitions.

206 icant effects on ECD, CV, or %HEX when dosed QD or BID for 3 months in eyes with OHTN or OAG.

207 ients were randomized to maintain DRV 800 mg QD or switch to twice-daily (BID) DRV 600 mg; all receiv

208 4 mg/kg, SC, QD), elafibranor (30 mg/kg, PO, QD) or INT-767 (10 mg/kg, PO, QD).

209 CA (30 mg/kg, PO, QD), ELA (3, 10 mg/kg, PO, QD), or combinations (OCA + ELA) for eight weeks.

210 to PF-06700841 30 mg once daily (QD), 60 mg QD, or placebo (4-week induction), followed by 10 mg QD,

211 ge, there was no significant accumulation of QD outside of the bladder, although in some mice we dete

212 g/mL) using both QD-Ox-Cyt-c (R(2)=0.93) and QD-Ox-Co-Q (R(2)=0.96).

213 Two probes were designed, QD-Ox-Cyt-c and QD-Ox-Co-Q, which were found to quench the fluorescence

214 1-100,000ng/mL (LOD of 0.01ng/mL) using both QD-Ox-Cyt-c (R(2)=0.93) and QD-Ox-Co-Q (R(2)=0.96).

215 Two probes were designed, QD-Ox-Cyt-c and QD-Ox-Co-Q, which were found to quench t

216 to tune the optimized structure of the CdSe QD-peptide-AuNP nanostructures for the application.

217 ligand properties of colloidal quantum dot (QD) perovskites now enable unprecedented device architec

218 e of tunable photocurrent on/off ratio in Si-QD photodetector (ranging from 2.7 to 562) by applying s

219 elds <250 mT, resulting in an enhancement of QD photoluminescence (PL).

220 ribes the design of a colloidal quantum dot (QD) photosensitizer for the Pd-photocatalyzed Heck coupl

221 were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.

222 Quantum dot (QD) photovoltaic devices are attractive for their low-co

223 eatly improves the performance of perovskite QD photovoltaics.

224 Notably, the dye/QD PL intensity ratio reflected changes in the relative

225 ium(II) phenanthroline complex that quenched QD PL through electron transfer.

226 with either a fluorescent dye that quenched QD PL through FRET or a ruthenium(II) phenanthroline com

227 This design yields QD platforms with distinct chemoselectivities that are g

228 d from the thiolate anion adsorbed on a CdSe QD plays a key role by abstracting the hydrogen atom fro

229 ized to netarsudil ophthalmic solution 0.02% QD (PM) or timolol ophthalmic solution 0.5% BID.

230 Netarsudil QD (PM), a first-in-class IOP-lowering medication, was n

231 ows similar effects when applied to other Pe-QD PV systems like CsPbBr(3) and FAPbI(3) (FA = formamid

232 ral components of QD assemblies that dictate QD-QD or QD-molecule interactions.

233 Raman spectra confirm the QD quality.

234 action variables including the new-ligand-to-QD ratio, the size of the particles, and the original li

235 on transition by an average of 1 carrier per QD requires that approximately 10% of the Pb be replaced

236 scent immunolabeling utilizing quantum dots (Qd) resulted in reproducible detection of individual flu

237 By combining compositional grading of the QD's interior for hindering Auger decay with postsynthet

238 r stage in the growth, independently of each QD's surroundings.

239 a built-in signal amplification mechanism), QD-SABER provides an additional 7.6-fold signal amplific

240 d signal amplification by exchange reaction (QD-SABER), for sensitive and multiplexed imaging of endo

241 reports the fabrication of CdSe quantum dot (QD)-sensitized photocathodes on NiO-coated indium tin ox

242 leading to the construction of various CdSe QD-sensitized photocathodes.

243 The QD size and interdot distance in the dimer are used to p

244 high Mn contents, considerable broadening of QD size dispersion during the doping procedure, and larg

245 guideline for combining the chain length and QD size distributions for high-mobility electron transpo

246 The effect of inhomogeneous quantum dot (QD) size distribution on the electronic transport of one

247 Vs, which is one of the highest among all Pe-QD solar cells.

248 ically conductive and structurally intact Pe-QD solids for efficient optoelectronic devices.

249 ngineer the surface and packing states of Pe-QD solids is demonstrated by a mild thermal annealing tr

250 ting interparticle electrical interaction of QD solids.

251 h, using less than 210 mL of total starting QD solutions, and without user selection of experiments.

252 e to even low-affinity binding events at the QD/solvent interface.

253 an electrostatic double-layer model for the QD/solvent interface.

254 ow that LED emission from randomly polarized QD sources can be polarized and directed at will.

255 ck-functional multidentate polymers, the VIR-QD spectral series has high quantum yield in the SWIR (1

256 the QDs, resulting in the modulation of the QD spontaneous emission rate, far-field emission intensi

257 spin-coating method was used to deposit CdSe QD stock solution onto the surface of NiO/ITO electrodes

258 ot (QD), we apply the thick-shell or "giant" QD structural motif to this notoriously environmentally

259 In addition, the QD structure is further optimized to fully exploit the d

260 we detected extravesical biodistribution of QD suggesting a route for systemic exposure under some c

261 e majority of incorporated Ag remains at the QD surface and does not interact with the core electroni

262 Characterization of the QD surface by nuclear magnetic resonance (NMR) spectrosc

263 ns, we establish clear relationships between QD surface chemistry and the band edge positions of liga

264 r interactions of substrate molecules on the QD surface in a syn-precursor structure followed by dime

265 d shell and its subsequent adsorption to the QD surface is well-described with an electrostatic doubl

266 Model QD surface slabs with different possible surface termina

267 Replacing only 21% of the oleates on the QD surface with PFDT reduces the yield of photo-oxidatio

268 elf-assembly of the reagent molecules on the QD surface, but these experiments did not reveal the pre

269 permeate the ligand shell and adsorb to the QD surface.

270 oriented attachment directed by quantum dot (QD) surface chemistry.

271 The chemical and physical properties of QD surfaces and the interfaces in QD devices are of part

272 coverage of these capping agents on the CdSe QD surfaces reveal that they affect system activity and

273 ms are generalizable to other metal-enriched QD surfaces that have a similar surface structure as tha

274 ntraparticle coalescence of Au satellites at QD surfaces transforms individual HNCs into heterodimers

275 These ligands were introduced onto the QD surfaces using a combination of photochemical ligatio

276 ic double layer on electronic passivation of QD surfaces, which we find can be explained using the ha

277 that were used in some of the original II-VI QD syntheses decades ago, i.e., hydrogen chalcogenide ga

278 rtificial Chemist, eleven precision-tailored QD synthesis compositions are obtained without any prior

279 vestigate the reaction mechanism behind CdSe QD synthesis, the most widely studied QD system.

280 uncontrolled impurities participating in the QD synthesis.

281 be isolated as intermediates in quantum dot (QD) synthesis, and they provide pivotal clues in underst

282 r per absorbed unit of photon energy) of the QD system is a factor of 18 greater than that of an anal

283 d CdSe QD synthesis, the most widely studied QD system.

284 established and widely applicable to various QD systems, the structural characteristics of QDs, such

285 n reactions of alkenes photocatalyzed by the QD through self-assembly of the reagent molecules on the

286 oxygen is used, the structure of the CsPbI3 QD transforms from cubic to orthorhombic, while usage of

287 with injecting a free charge carrier into a QD under equilibrium conditions, including a bleach of t

288 with 93% tumor growth inhibition at 50 mg/kg QD upon oral dosing.

289 [BID], 1.5% once daily [QD], 0.5% QD, 0.15% QD), vehicle, or triamcinolone cream (0.1% BID for 4 wee

290 slide through different lattice sites of the QD via Au-halogen coupling.

291 BP) >140/90 mm Hg; hydrochlorothiazide 25 mg QD was added after 1 month if AOBP >=160/110 mm Hg).

292 In vivo biodistribution of anti-CD47-QD was assessed with inductively coupled plasma mass spe

293 Toward a truly photostable PbSe quantum dot (QD), we apply the thick-shell or "giant" QD structural m

294 AQ from bulk solution to the surface of the QD (where it exchanges electrons with the QD) of 154 J/m

295 t is critical to engineer the surface of the QD with a triplet transfer ligand and that bimolecular d

296 high delivery efficiency and specificity of QD with chemical cargoes to chloroplasts in plant cells

297 (QD) and specifically the interaction of the QD with proximate molecules.

298 spin qubit confined in a moving quantum dot (QD), with our attention on both spin relaxation, and the

299 bited researchers' attempts to fully control QD-WL interactions in these hybrid 0D-2D quantum systems

300 As such, we can now modify QD-WL interactions, with future benefits that include mo