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1 ize regime (1-3 nm in diameter, often called nanoclusters).
2 1.25 eV are calculated for the Au25(SH)18(-) nanocluster.
3 y reported four-shell Au133(SC6H4-p-Bu(t))52 nanocluster.
4 of a platinum atom into a molecule-like gold nanocluster.
5 ated by varying cation substitution to these nanoclusters.
6 ls of the frontier orbitals of Au25(SR)18(-) nanoclusters.
7 m earth-abundant phosphorescent metal halide nanoclusters.
8 in situ monitoring of the formation of gold nanoclusters.
9 by the decreased fluorescence of both metal nanoclusters.
10 ureus with and without labeling by gold (Au) nanoclusters.
11 densities of endogenous antigen-loaded CD1d nanoclusters.
12 rface of the target cell and internalized as nanoclusters.
13 sis was employed to characterize the surface nanoclusters.
14 as observed to be transiently trapped in the nanoclusters.
15 otected gold, silver, and bimetal (or alloy) nanoclusters.
16 irs, leading to the unusual stability of the nanoclusters.
17 dynamics and stability of H-Ras lipid-anchor nanoclusters.
18 l-chains are required for forming GPI-anchor nanoclusters.
19 commonly used to test the raft-preference of nanoclusters.
20 KRas leads to formation of higher order Ras nanoclusters.
21 ted with the accumulation of low-order CXCR4 nanoclusters.
22 pid domains and thereby the stability of the nanoclusters.
23 and operation of spatially segregated K-Ras nanoclusters.
24 itting (Ag9:HSA) and red-emitting (Ag14:HSA) nanoclusters.
25 in compromised signal output from H-RasG12V nanoclusters.
26 ly an obligate structural component of K-Ras nanoclusters.
27 ion of a regular array of ice-like hexameric nanoclusters.
28 r CdTe quantum dots, free NIR dyes, and gold nanoclusters.
29 stable, atomically precise, colloidal metal nanoclusters.
30 ctrical conductivity of the entrapped copper nanoclusters.
31 ise to growth of monodisperse, size-tailored nanoclusters.
32 electronic and optical properties of the 58e nanoclusters.
33 imaging revealed that FLS2 and BRI1 form PM nanoclusters.
34 s up to 3 nm, the size regime referred to as nanoclusters.
35 structural polymorphism in these archetypal nanoclusters.
36 easons of the dimensional transition in gold nanoclusters.
37 osphatidylserine, in turn undergoes enhanced nanoclustering.
38 cholesterol restores K-Ras4A but not K-Ras4B nanoclustering.
39 brane to the endomembrane and inhibits their nanoclustering.
42 cular dynamics study of a test system-a gold nanocluster adsorbed on free-standing graphene clamped b
43 tmospheric aerosol characterization to cover nanocluster aerosol (NCA) particles and show that a majo
45 d across all sub-regions, PSD95 packing into nanoclusters also varied between sub-regions determined
49 anization: in CAV1-deficient cells K-RasG12V nanoclustering and MAPK activation were enhanced, wherea
50 ostulate that caveolae remotely regulate Ras nanoclustering and signal transduction by controlling PM
52 achieved by chemical coupling of active CoO nanoclusters and high-index facet Mn3 O4 nano-octahedron
53 ng chemistry for tailoring the structures of nanoclusters and is expected to open new avenues for des
56 rials, nanoscale photonic devices, plasmonic nanoclusters and surface-enhanced Raman scattering (SERS
57 tin-1 affect both the number and lifetime of nanoclusters and thus determine the specific Raf effecto
59 c performance of Au25(SPh)18 and Au36(SPh)24 nanoclusters, and on the basis of their crystal structur
60 Pd164-xPtx(CO)72(PPh3)20 (x approximately 7) nanoclusters, and within the recently reported four-shel
64 inated surface gold atoms in the Au22(L(8))6 nanocluster are unprecedented in atom-precise gold nanop
65 ffects of caveolin and cortical actin on Ras nanoclustering are similarly mediated through regulation
66 vacancies in facilitating the nucleation of nanoclusters are a long-standing puzzle, due to the expe
67 rticle tracking revealed that diffusing CD1d nanoclusters are actively arrested by the actin cytoskel
68 s absorption and PLE spectra of the reported nanoclusters are consistent with previously established
71 m, indicating that the means by which Nav1.6 nanoclusters are maintained in the soma is biologically
76 ddress stability of thiolate-protected metal nanoclusters as a function of the number of metal core a
77 stability of these 'magic-number' colloidal nanoclusters as a function of their atomic-level structu
78 port the application of protein-templated Ag nanoclusters as a luminescent photoswitch for the detect
80 toward the application of luminescent metal nanoclusters as potential metal sensors since by tuning
81 e and energetically low structures of BenH2n nanoclusters as predicted using density functional theor
82 for selective self-assembly of molecules or nanoclusters, as well as for the functionalization of th
84 phore-tagged apamin and monitored SK channel nanoclustering at the single molecule level by combining
85 microscopy, we show that CD1d molecules form nanoclusters at the cell surface of APCs, and their size
87 The luminescence property of thiolated gold nanoclusters (Au NCs) is thought to involve the Au(I)-th
88 s of progress in synthesizing thiolated gold nanoclusters (Au NCs), the knowledge of their growth mec
90 e-sensitive incorporation of a gold-thiolate nanocluster, Au133(SR)52, selectively in the bMOF-102/10
93 characterization of a new DNA-templated gold nanocluster (AuNC) of approximately 1 nm in diameter and
95 noglobulin E (IgE) in human serum using gold nanoclusters (AuNCs) as fluorescent label was developed.
96 escence (ECL) is detected from dithiolate Au nanoclusters (AuNCs) in aqueous solution under ambient c
98 uminescent near-infrared (NIR)-emitting gold nanoclusters (AuNCs) using bovine serum albumin (BSA) as
100 y slow down renal clearance of few-atom gold nanoclusters (AuNCs) with the same surface ligands but d
101 tudy, we generated protein encapsulated gold nanoclusters (AuNCs@ew) with bright photoluminescence by
103 ry and isolation of a range of new molecular nanoclusters based on [Mo(2)O(2)S(2)](2+)-based building
106 cluster probe, termed methyladenine-specific NanoCluster Beacon (maNCB), which can detect single m(6)
107 VP-AuNPs) and fluorescent BSA-protected gold nanoclusters (BSA-AuNCs) were used as an IFE absorber/fl
109 dylserine is a common constituent of all Ras nanoclusters but is only an obligate structural componen
110 e ability to control the atomic structure of nanoclusters by systematically varying the gas-phase for
112 nd that the saturated polymeric forms of the nanoclusters cannot retain molecular hydrogen, in contra
114 ervation of a body-centered cubic (bcc) gold nanocluster composed of 38 gold atoms protected by 20 ad
115 to the preparation of arrays or ensembles of nanoclusters containing a dominant or single isomer, thu
116 is and structure determination of a new Au22 nanocluster coordinated by six bidentate diphosphine lig
117 a cyclohexanethiolate-capped [Au23(SR)16](-) nanocluster (counterion: tetraoctylammonium, TOA(+)).
118 dope single atoms of Ag or Cu into hollow Au nanoclusters, creating precise alloy nanoparticles atom-
119 ch was developed for the synthesis of copper nanoclusters (Cu NCs) and used as a fluorescent probe fo
122 uding bovine serum albumin (BSA) template Cu nanoclusters (CuNCs@BSA) and single-walled carbon nanotu
125 ation of the polymer in acidic solution, the nanoclusters dissociated into primary ~5 nm Au nanospher
126 ers (Hb/AuNCs) and aptamer-stabilized silver nanoclusters (DNA/AgNCs) for analysis of Cyt c are prese
127 thesis of the enzyme DNase 1 stabilized gold nanoclusters (DNase 1:AuNCs) with core size consisting o
128 ering from the generation of p-LAT and p-SLP nanoclusters driving TCR signal amplification and divers
131 Supported sub-monolayers of [Mo3S13](2-) nanoclusters exhibited excellent HER activity and stabil
135 20 and Au18(SR)14 nanoclusters, forms a "4e" nanocluster family, which illustrates a trend of shrinka
136 ano-based materials, as well as their use as nanocluster fillers, in nanocomposites, mouthwashes, med
140 sful application of an aptamer bioconjugated nanoclusters for the detection of apoptosis based on rel
141 sis reveals that the thiolate ligands on the nanocluster form local tetramers by intracluster interac
142 bout the evolutionary paths of molecular and nanocluster formation and its relation to laser plume hy
143 dynamic development leading to molecular and nanocluster formation remain one of the most important t
144 cability of the "critical nucleus" of CNT to nanocluster formation systems such as the Ir(0)n one stu
146 an effective template for fluorescent silver nanoclusters formation without any chemical modification
147 together with the Au24(SR)20 and Au18(SR)14 nanoclusters, forms a "4e" nanocluster family, which ill
148 the structure determination of a large gold nanocluster formulated as Au130(p-MBT)50, where p-MBT is
149 eport the crystal structure of an ultrasmall nanocluster formulated as Au20(TBBT)16 (TBBT = SPh-t-Bu)
156 ion spatial mapping shows that different Ras nanoclusters have distinct lipid compositions, indicatin
157 e assays based on hemoglobin-stabilized gold nanoclusters (Hb/AuNCs) and aptamer-stabilized silver na
160 between two thiolate-protected 28-gold-atom nanoclusters, i.e. Au28(S-c-C6H11)20 (where -c-C6H11 = c
161 currently focuses on thiolate-protected gold nanoclusters, important progress has also been achieved
162 ncentrations of vacancies in Y-Ti-O-enriched nanoclusters in a nanostructured ferritic alloy using a
163 h implications for the symmetry of rafts and nanoclusters in cell membranes, which have similar repor
164 ollowing the emergence of conformer-specific nanoclusters in the plasma membrane of mammalian cells,
165 s show that the (100) surface breaks up into nanoclusters in the presence of CO2 at 20 Torr and above
166 talyst (supported thiomolybdate [Mo3S13](2-) nanoclusters) in which most sulfur atoms in the structur
167 ng into the [Au23(SR)16](-) (R = cyclohexyl) nanocluster, in which two neighboring surface Au atomic
168 d that antioxidant (glutathione) chiral gold nanoclusters induce a decrease of 5-hydroxymethylcytosin
170 ZrOCo(II) group coupled to an iridium oxide nanocluster (IrO(x)) was assembled on an SBA-15 silica m
173 ferent doping modes when the [Au23(SR)16](-) nanocluster is doped with different metals (Cu, Ag), inc
176 ogenation of the aldehyde group catalyzed by nanoclusters is a surprise because conventional nanogold
177 hway of terminal alkynes by "ligand-on" gold nanoclusters is identified, which should follow a deprot
178 a single crystal containing uranyl peroxide nanoclusters is reported for pyrophosphate-functionalize
181 and 1.51 V vs RHE) potentials of these metal nanoclusters make them suitable for driving the water-sp
184 materials such as metal nanoparticles, metal nanoclusters, metal oxide nanoparticles, metal and carbo
185 d-pulsed laser irradiation and magnetic gold nanoclusters (MGNCs) as the etching agents is described.
186 and suggests that ion channel topography and nanoclustering might be under the control of second mess
187 ver, the observation that TCRs assemble into nanoclusters might allow for homotropic allostery, in wh
188 )12(TPP)4, an atomically precise tetravalent nanocluster (NC) (BDT, 1,3-benzenedithiol; TPP, tripheny
190 ure determination of a large box-shaped Ag67 nanocluster (NC) protected by a mixed shell of thiolate
196 ous synthesis and assembly of Au, Pt, and Pd nanoclusters (NCs; with sizes </=3 nm) into mesoscale st
197 rgent monolayer-protected gold quantum dots (nanoclusters, NCs) composed of 25 Au atoms by utilizing
198 eading to a self-assembled superparamagnetic nanocluster network with T2 signal enhancement propertie
201 ture of ultra-stable Au144(SR)60 magic-sized nanoclusters obtained from atomic pair distribution func
204 ll as mathematical modeling, we investigated nanoclustering of H-ras helix alpha4 and hypervariable r
206 via a processing route that creates distinct nanoclusters of atoms that pin grain boundaries within t
207 of osteopontin is their ability to sequester nanoclusters of calcium phosphate to form a core-shell s
209 for the generation of cholesterol-dependent nanoclusters of GPI-anchored proteins mediated by membra
210 gammaRII, are constitutively associated with nanoclusters of SIRPalpha, within 62 +/- 5 nm, mediated
212 III-nitride nanowires decorated with Ru sub-nanoclusters offer controlled surface charge properties
214 GTPases form transient, spatially segregated nanoclusters on the plasma membrane that are essential f
215 is able to self-assemble into colloidal gold nanoclusters or membranes in a controlled and reversible
216 e isomer, thus enabling the investigation of nanocluster (or nanoparticle) properties as a function o
217 atomically precise, thiolate-protected metal nanoclusters, our understanding of the driving forces fo
219 We report a new method to identify metallic nanoclusters (polyoxometalate structures) in solution at
220 m the previously reported Au30 S(S-(t) Bu)18 nanocluster protected by 18 tert-butylthiolate ligands a
222 talytic activity of the resulting bimetallic nanocluster, PtAu24(SC6H13)18, for the hydrogen producti
225 ance of signals favors activation, FcgammaRI nanoclusters reorganize into periodically spaced concent
231 ts show that mutations in Ras can affect its nanoclustering response and thus allosterically effector
232 ls, we found that conformers impart distinct nanoclustering responses depending on the cytoplasmic le
235 hatidylserine spatiotemporal dynamics, K-Ras nanoclusters set up the plasma membrane as a biological
237 ations from Au103 and Au102 include (i) both nanoclusters show similar HOMO-LUMO gap energy (i.e., Eg
239 a nucleation inhibitor and Au size-selected nanoclusters (SSNCs) as catalytic particles for which th
242 ates a ligand-based strategy for controlling nanocluster structure and also provides a method for the
244 ers, particularly 17, were used to stabilize nanoclusters such as Pd/Au for the catalytic asymmetric
245 PPh3)10(C identical withCPh)5X2 (X = Br, Cl) nanoclusters supported on oxides for the semihydrogenati
247 lyst leads to the in situ formation of Rh(I) nanoclusters that catalyze stereoselective tautomerizati
249 gions revealed they comprised discrete PSD95 nanoclusters that were spatially organised into single a
251 wn to be associated with the Y-Ti-O-enriched nanoclusters, the roles of vacancies in facilitating the
252 of monodisperse [Cd54Se32(SePh)48(dmf)4](4-) nanoclusters; the second is a unique porous CdSe crystal
253 HC injecting electron density into the metal nanocluster thus lowering the barrier for bromobenzene a
255 , Ca(2+) membrane territories, and signaling nanoclusters to modulate T cell signaling and function.
256 re of the phenomenon ensures eruption of the nanoclusters towards a much colder region, giving rise t
258 -shaped Au25(PPh3)10(C identical withCPh)5X2 nanoclusters under conditions similar to the catalytic r
259 u25(SR)18(-) (R = H, CH3, CH2CH3, CH2CH2CH3) nanoclusters upon photoexcitation are discussed using ti
261 tability and decomposition pathways of LiBH4 nanoclusters using grand-canonical free-energy minimizat
262 track the seeded growth of atom-precise gold nanoclusters using mass spectrometry, revealing that the
264 e intermediacy of heterogeneous catalysis by nanoclusters was confirmed by mercury poisoning, tempera
265 peroxidase-like catalytic activity of these nanoclusters was exploited for colorimetric detection of
274 eveal a host of new structures for water-ice nanoclusters when adsorbed on an atomically flat Cu surf
275 ently discovered icosahedral Au133(p-TBBT)52 nanocluster (where p-TBBT = 4-tert-butylbenzenethiolate)
276 elaxation of Au144(SR)60(q) ligand-protected nanoclusters, where SR = SC6H13 and q = -1, 0, +1, and +
277 ons in the number/size of emissive graphenic nanoclusters wherein multiscale modelling captures essen
278 we can eliminate completely all icosahedral nanoclusters, which are commonly found under other condi
279 Ras proteins are organized into membrane nanoclusters, which are necessary for Ras-MAPK signaling
280 catalyst (or "a cocktail of catalysts") into nanoclusters, which in turn catalyze and control the ste
281 een the stabilities of lipid domains and Ras nanoclusters, which is supported by our finding that C60
282 y the treatment with glutathione chiral gold nanoclusters, which may inhibit the activity of TET prot
285 nd crystal structure determination of a gold nanocluster with 103 gold atoms protected by 2 sulfidos
286 We report the X-ray structure of a gold nanocluster with 30 gold atoms protected by 18 1-adamant
287 mainly through the side entry.Doping a metal nanocluster with heteroatoms dramatically changes its pr
289 egated to sort subsets of phospholipids into nanoclusters with defined lipid compositions that determ
290 e set of nanoparticles can be used to create nanoclusters with different chiroptical activities.
291 cally inhibited intermediate phase, (LiBH4)n nanoclusters with n </= 12 are predicted to decompose in
293 s expected to open new avenues for designing nanoclusters with novel surface structures using differe
295 report a family of atomically precise ceria nanoclusters with ultra-small dimensions up to 1.6 nm (
296 on for the future exploration of other metal nanoclusters with well-controlled numbers of metal atoms
297 homogeneously decorated with palladium (Pd) nanoclusters with well-defined shape and size (2.3 +/- 0
298 phage surfaces but are organized in discrete nanoclusters, with a mean radius of 71 +/- 11 nm, 60 +/-
299 x microstructures containing numerous Y-Ti-O nanoclusters within grains and along grain boundaries.
300 -poor liquid phases, nucleation of amorphous nanoclusters within the metal-rich liquid phase, followe
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