ライフサイエンスコーパス: polyhedral

1 Six of these genomes could be attributed to polyhedral and filamentous viruses that were observed by

2 Coassembling polyhedral and spherical NPs with complementary DNA yiel

3 morphology with spherical granules having a polyhedral angular shaped morphology packed tightly with

4 anions give high conductivities in isolated polyhedral anion structures such as the apatites.

5 ty to native caveolae and reveals a possible polyhedral arrangement of caveolin oligomers.

6 ins and phospholipids can self-assemble into polyhedral arrangements suitable for structural analysis

7 he shell protein domain)] assemble to form a polyhedral barrier that encapsulates the enzymatic conte

8 bly of metal-organic framework (MOF) faceted polyhedral BBs (i.e., cubes instead of spheres) into 3D

9 f clusters and lattices in which anisotropic polyhedral blocks coordinate isotropic spherical nanopar

10 We show that these polyhedral blocks--cubes and octahedrons--when mixed wit

11 the thin sheets that form the facets of the polyhedral BMCs.

12 Carboxysomes are polyhedral bodies consisting of a proteinaceous shell fi

13 Carboxysomes are organelle-like polyhedral bodies found in cyanobacteria and many chemoa

14 addition, it is shown that S. enterica forms polyhedral bodies that are involved in the degradation o

15 The specific function of these unusual polyhedral bodies was not determined, but some possibili

16 s a sensitive screen for form (appearance of polyhedral bodies) and function (ability to grow on air)

17 Bacterial microcompartments (BMCs) are polyhedral bodies, composed entirely of proteins, that f

18 e homologues of genes that are implicated in polyhedral body formation in Salmonella enterica.

19 hat genes of the pdu operon are required for polyhedral body formation, and immunoelectron microscopy

20 r a B(12)-dependent enzyme associated with a polyhedral body.

21 g (as in diborane) or completely delocalized polyhedral bonding (as in B(12)H(12)(2)(-)).

22 interstitial arrangements of boron atoms and polyhedral bonding.

23 owing liposomal delivery of a (10)B-enriched polyhedral borane and a carborane against mouse mammary

24 iated by liposomes containing (10)B-enriched polyhedral borane and carborane derivatives for the trea

25 urally similar tetraphenylporphyrins bearing polyhedral borane anions have been synthesized and their

26 sue, a value analogous to the most promising polyhedral borane anions investigated for liposomal deli

27 Polyhedral boranes and heteroboranes appear almost exclu

28 for excited states calculations of aromatic polyhedral boranes and related systems.

29 The incorporation of polyhedral boranes into novel photoluminescent materials

30 Here, we present polyhedral boron clusters (carboranes) as strongly bindi

31 able synthetic tool for the incorporation of polyhedral boron into novel organic structures.

32 pressures, the dominant species are silicon-polyhedral bound carbonates, tetrahedral coordination, a

33 nides, halides, carbon networks, and even to polyhedral bubbles in foams.

34 (P2(1)/m), where an alternate arrangement of polyhedral building blocks maximizes favorable bonding i

35 Network-forming oxides with rigid polyhedral building blocks often possess significant cap

36 with (K(X)/nu(i)) delta nu(i)/ delta P] uses polyhedral bulk moduli (K(X)) appropriate to the particu

37 reported nanocrystals are isotropic cubes or polyhedral; but anisotropic nanostructures with controll

38 er of distinct "synaptic units" comprising a polyhedral cage and a corona of approximately seven vesi

39 en copper sites confined within a nanoscopic polyhedral cage has been achieved, and the packing of th

40 , have been predicted to possess interesting polyhedral cage structures, which may serve as ideal mol

41 An unprecedented nanoscopic polyhedral cage-containing metal-metalloporphyrin framew

42 n contributes to two connecting edges of the polyhedral cage.

43 try, results in assembly of the mixed-ligand polyhedral cages [M12(mu(3)-L(1))4(mu-L(2))12](24+).

44 athrate hydrates, with solutes surrounded by polyhedral cages composed of tetrahedrally hydrogen-bond

45 The assembly of clathrin triskelia into polyhedral cages during endocytosis is regulated by adap

46 The polyhedral cages measured approximately 60 nm in diamete

47 Barium cations are trapped inside the large polyhedral cages of the gold-phosphorus tetrahedral fram

48 (known as a triskelion) that assembles into polyhedral cages principally made up of pentagonal and h

49 ich molecules are arranged in a hierarchy of polyhedral cages that encapsulate guest molecules and io

50 Proteins that self-assemble into enclosed polyhedral cages, both naturally and by design, are garn

51 3D Zn-Sb framework hosting K(+) ions inside polyhedral cages, some of which are reminiscent of known

52 oligomer containing two trimers into active polyhedral cages, typically containing four or eight tri

53 e guest/host framework compounds composed of polyhedral cages, yet despite their prevalence among tet

54 ron-dense spacers that are precursors of the polyhedral calyx.

55 NA) segments, L, S, and M, packaged within a polyhedral capsid along with RNA polymerase.

56 Polyhedral capsids and closed spherical capsids were fou

57 kedly in structure and stability from mature polyhedral capsids but can be converted to the mature fo

58 In contrast to closed spherical capsids, polyhedral capsids exhibited distinct facets and vertice

59 ndish "procapsids", which mature into robust polyhedral capsids in a transition similar to that under

60 artial capsids, closed spherical capsids and polyhedral capsids were all found to contain VP5, VP19C,

61 ed spherical capsids were disassembled while polyhedral capsids were unaffected.

62 rified closed spherical capsids matured into polyhedral capsids, indicating that the latter arise by

63 artial capsids, closed spherical capsids and polyhedral capsids.

64 Our self-assembled polyhedral capsules, characterized by NMR and electrospr

65 Polyhedral catenanes, such as a cube or a truncated octa

66 tain two predominant cell types: mononuclear polyhedral cells and multinucleated cells (MNCs).

67 ude dendritic, stellate, neuronal, and small polyhedral cells.

68 Polyhedral ceria and nanorods were more effective than c

69 d is characterized by pseudo-one-dimensional polyhedral chains of four face-sharing RhO6 octahedra fo

70 ce, can also initiate the assembly of normal polyhedral clathrin coats on dense lysosomes under physi

71 It is characterized by a polyhedral clathrin lattice that coats budding membranes

72 n+2 (5 <or= n <or= 8) family adopts n-vertex polyhedral closo-structures with two extra hydrogen atom

73 adopt unusual self-assemblies consisting of polyhedral clusters of chloride and pyridinium ions.

74 The number of Zintl phases containing polyhedral clusters of tetrel elements that are accessib

75 complex aggregates that include polygonal or polyhedral clusters, linear or zigzag chains, and circul

76 n resonances of different arrangements of Ag polyhedral clusters.

77 As a result, Co-Fe-P nanorods (from the polyhedral Co-Fe-O nanoparticles) and sea-urchin-like Co

78 he clathrin triskelion self-assembles into a polyhedral coat surrounding membrane vesicles that sort

79 t chains form triskelia, which assemble into polyhedral coats of membrane vesicles that mediate trans

80 clathrin, assembling triskelia into regular polyhedral coats.

81 The shape of olein nanoparticles was more polyhedral compared to the stearin.

82 ration of luminophores within supramolecular polyhedral compartments of a crystalline zeolite-like hy

83 itrogen-doped carbon (H-CoNiSe(2)/NC) hollow polyhedral composite structure using ZIF-67 as a precurs

84 and coordination number (6-9) and different polyhedral compressibilities, together with the observat

85 Convex isogonal polyhedral concepts allow certain combinations of polygo

86 re to an amorphous state, an analysis of the polyhedral connection network reveals that the rotation

87 recisely patterned nano- to centimeter scale polyhedral containers, scaffolds for cell culture and re

88 A polyhedral continuum of states is also found in spleen d

89 hysical and biochemical constraints define a polyhedral convex set of feasible flux vectors.

90 extend the range of accessible topologies of polyhedral coordination cages.

91 ectra result from both the deviations in the polyhedral coordination/site-symmetry within the 4-fold

92 herical morphology, the heterostructure with polyhedral core and shell was presented with the truncat

93 cks such that they come together to create a polyhedral core when the chain folds.

94 offers a general route to fabricate oriented polyhedral crystal arrays of potential interest for new

95 , previously unobserved phase transitions in polyhedral crystallization behavior, and an unexpected s

96 uble-tipped pyramids, which we call graphite polyhedral crystals (GPCs), have been discovered.

97 ide nanomaterials which can adopt spherical, polyhedral, cubic, rod, wire, plate shapes and possibly

98 nt to maintain oligomerization as defined by polyhedral distortion of the caveolar membrane.

99 This reduces metal-oxide polyhedral distortion, thereby increasing the electron m

100 leads to discovery of a general switching of polyhedral distortions at symmetry-disallowed transition

101 he small round precursor capsid into a large polyhedral DNA-containing mature phage.

102 eport a new structure, mesoporous structured polyhedral drum and spherical cages and shells formed by

103 ium molecules yield more regular layers with polyhedral edge-sharing that show substantially delocali

104 ain disordered but spatially correlated with polyhedral edges and corners.

105 , which interact to allow the formation of a polyhedral edifice.

106 were porous, had a low content of compressed polyhedral erythrocytes (polyhedrocytes) and an even dis

107 gher proportion of tightly packed compressed polyhedral erythrocytes than those that developed in WT

108 lose-packed, tessellated array of compressed polyhedral erythrocytes within.

109 Such close-packed arrays of polyhedral erythrocytes, or polyhedrocytes, were also ob

110 Herein, we report a polyhedral expansion protocol to construct a neutral der

111 protein, an STV protein became bound to each polyhedral face, thus resulting in well-structured DNA p

112 t sense and chirality is communicated across polyhedral faces, edges, and vertices.

113 tains an {IrFeCB7} cluster core, with an exo-polyhedral {Fe(CO)3} moiety bridging a {BIrFe} triangula

114 -helices, many were clearly derived, such as polyhedral folds in the all-alpha class and beta-sandwic

115 from a fragile, spherical state to a robust polyhedral form resembles the prohead maturation events

116 apsids only after they have matured into the polyhedral form.

117 led by introduction of the corresponding DNA polyhedral frames.

118 y connecting them through designed DNA-based polyhedral frames.

119 In this context, we describe a more general polyhedral framework for describing virus capsid structu

120 e-sized supramolecular cage compounds with a polyhedral framework is prepared by self-assembly from t

121 and NiSe(2) nanoparticles embedded in the NC polyhedral framework offer a wealth of active sites for

122 hree of their four vertices connected in the polyhedral framework, imparting a potential low-energy m

123 Polyhedral frameworks with central elements exhibiting v

124 lar three-dimensional particles adopting the polyhedral geometry of a non-uniform square antiprism.

125 ocks that offer multiple reactive sites in a polyhedral geometry.

126 s an unprecedented D2d-symmetric 3-connected polyhedral geometry.

127 Rice starch showed polyhedral granule shapes and differences in their mean

128 ased on topological features of an extracted polyhedral graph (PG).

129 These polyhedral groups are separated by Li(+) cations.

130 These polyhedral groups are separated by the A(+) cations.

131 uth Andes, preserve dendritic, skeletal, and polyhedral growth textures.

132 urvature, the regular subunit packing in the polyhedral head cannot be mapped onto the procapsid.

133 The bacteriophage has a polyhedral head with a diameter of 55 nm and appears to

134 they were found to be spherical rather than polyhedral in shape, and they disassembled at 0 degrees

135 ggesting that they are spherical rather than polyhedral in shape.

136 Carboxysomes are polyhedral inclusion bodies that play a key role in auto

137 th a 50% lethal concentration of 1.2 x 10(5) polyhedral inclusion bodies/ml of diet, which is similar

138 In 6, an exo-polyhedral {IrPh(CO)(PPh3)} moiety is attached to a {clo

139 rin and the AP-2 adaptor complex, assemble a polyhedral lattice at plasma membrane bud sites with the

140 Clathrin self-assembly into a polyhedral lattice mediates membrane protein sorting dur

141 molecular resolution in the visualization of polyhedral lattice of clathrin-coated pits in situ.

142 cytoplasmic protein that polymerizes into a polyhedral lattice on intracellular membranes to form pr

143 t triskelia then pack together to assemble a polyhedral lattice that progressively invaginates, buddi

144 elion shape of clathrin allows assembly into polyhedral lattices during the process of clathrin-coate

145 flexible, net-like protein mesh able to form polyhedral lattices on phosphatidylserine-containing ves

146 they interact to form a cage with two nested polyhedral layers.

147 gs that are stacked alternately with lithium polyhedral layers.

148 The structure consists of polyhedral lead centers connected by doubly and triply b

149 formation to polyhedral (polyhedrocytes) and polyhedral-like cells, altogether comprising pressure-de

150 (NMII) assemble into previously undescribed polyhedral-like lattices around the vesicle membrane.

151 ntial of this approach to study variation in polyhedral macromolecular structures.

152 anionic frameworks based on condensation of polyhedral main group non-metal anions offer a wide rang

153 rature, tsProt.A procapsids transformed into polyhedral, mature capsids, providing further confirmati

154 ed tools now exist that can convert an input polyhedral mesh into a DNA origami nanostructure, greatl

155 escribes the self-assembly of small objects--polyhedral metal plates with largest dimensions of 10 to

156 Recently, polyhedral metal-organic framework (MOF) particles have

157 perstructure via coassembly of two colloidal polyhedral metal-organic framework (MOF) particles havin

158 Monodisperse polyhedral metal-organic framework (MOF) particles up to

159 embles with a transition-metal-ion to form a polyhedral metal-organic host with a structure that conf

160 d crystal habits), as opposed to the typical polyhedral microcrystals obtained under bulk crystalliza

161 strate a droplet microfluidic method to form polyhedral microparticles with controlled concavity.

162 es to globular proteins, we believe that the polyhedral models will, with continued development, be h

163 The preparation of synthetic polyhedral molecular assemblies represents a challenging

164 ers consistently assume spherical or regular polyhedral morphologies rather than high-aspect-ratio st

165 A perfect polyhedral morphology can be developed in a thin surface

166 The starch granules showed the irregular polyhedral morphology with spherical granules having a p

167 one obtains structures expectedly containing polyhedral motifs, and geometries are governed by Wade-M

168 Polyhedral nano- and microstructures with shapes of face

169 t distinguished from bulk ices by containing polyhedral nano-cages to accommodate small gas molecules

170 nization of the cavin coat corresponded to a polyhedral nano-net held together by coiled-coil segment

171 se control of the heteroepitaxy of colloidal polyhedral nanocrystals enables ordered grain growth and

172 Superlattices of polyhedral nanocrystals exhibit emergent properties defi

173 Going beyond one facet, herein, different polyhedral nanocrystals of CsPbBr(3) are explored for fa

174 model protein, we prepared membrane protein polyhedral nanoparticles (MPPNs) with uniform radii of a

175 an analytic theory for the self-assembly of polyhedral nanoparticles (NPs) based on their crystal st

176 tand and map the crystallization behavior of polyhedral nanoparticles assembled via the interaction o

177 des consisting of these and related hydrogen polyhedral networks may represent new classes of potenti

178 e represented as closed surfaces rendered as polyhedral networks of parallel DNA duplexes, which enab

179 Polyhedral nitrogen containing molecules such as prismat

180 ere both components order, and another where polyhedral NPs form a periodic lattice, while spherical

181 mbly scheme, we produced planar lattices and polyhedral objects.

182 rous materials containing organic linkers or polyhedral oligomeric siloxane covalently bonded to zeol

183 ock copolymer tail tethered to a fluorinated polyhedral oligomeric silsesquioxane (FPOSS) cage in 1,4

184 iant surfactants consisting of a fluorinated polyhedral oligomeric silsesquioxane (FPOSS) head and fl

185 tant to generate mesopores, and cross-linked polyhedral oligomeric silsesquioxane (POSS) as the silic

186 ctionalization of perylene core with several polyhedral oligomeric silsesquioxane (POSS) cages achiev

187 tetrahedra constructed by placing different polyhedral oligomeric silsesquioxane (POSS) molecular na

188 ass-forming glycerol mixed with 1.1 nm sized polyhedral oligomeric silsesquioxane (POSS) molecules us

189 f organic-inorganic hybrid peptoids by using polyhedral oligomeric silsesquioxane (POSS) nanoclusters

190 prepared by coordination-driven assembly of polyhedral oligomeric silsesquioxane (POSS) with metal-o

191 ferent types of MNPs based on derivatives of polyhedral oligomeric silsesquioxane (POSS), [60]fullere

192 Amine-functionalized polyhedral oligomeric silsesquioxane (POSS), the smalles

193 a series of precisely defined, nonspherical, polyhedral oligomeric silsesquioxane (POSS)-based molecu

194 rolactone urea)urethane backbone integrating polyhedral oligomeric silsesquioxane (POSS-PCLU) with va

195 -dimensional monolayer of Trisilanolisobutyl Polyhedral Oligomeric SilSesquioxane (TBPOSS) on water s

196 are prepared by a facile one-pot reaction of polyhedral oligomeric silsesquioxane and poly(ethylene g

197 e assembly of MXene and amine-functionalized polyhedral oligomeric silsesquioxane at the oil-water in

198 es that comprise a triphenylene core and six polyhedral oligomeric silsesquioxane cages grafted onto

199 lengths between the core and the peripheral polyhedral oligomeric silsesquioxane cages, and exhibits

200 pe memory polymer network constructed from a polyhedral oligomeric silsesquioxane nanoparticle core f

201 controlled functionalization of fluorinated polyhedral oligomeric silsesquioxanes (F-POSS), which ar

202 Herein, organosiloxane and polyhedral oligomeric silsesquioxanes (POSS) compounds a

203 (II) terpyridine complex functionalized with polyhedral oligomeric silsesquioxanes (POSS) moieties ha

204 However, only two families-carboranes and polyhedral oligomeric silsesquioxanes (POSS)-have been w

205 of a giant molecular network of alternating polyhedral oligomeric silsesquioxanes and aromatic imide

206 fonated polyether ether ketone embedded with polyhedral oligosilsesquioxane as a coating layer on cop

207 sitional gradients where high Fo-Ni cores of polyhedral olivines (Fo(92.5), Ni ~3500 ppm) contrast wi

208 shell, leading to formation of capsids with polyhedral or conical morphology.

209 ity to the shell proteins of carboxysomes (a polyhedral organelle involved in autotrophic CO(2) fixat

210 Salmonella enterica forms polyhedral organelles during coenzyme B(12)-dependent gr

211 These results suggest that the polyhedral organelles formed by S. enterica during growt

212 Bacterial microcompartments (BMCs) are polyhedral organelles found in an increasingly wide vari

213 In this report, the polyhedral organelles involved in B(12)-dependent 1,2-PD

214 shell protein required for the formation of polyhedral organelles involved in coenzyme B(12)-depende

215 Salmonella enterica forms polyhedral organelles involved in coenzyme B(12)-depende

216 elated to those involved in the formation of polyhedral organelles known as carboxysomes, and two enc

217 of bacteria package much of the enzyme into polyhedral organelles, the carboxysomes.

218 e PduA protein localized to the shell of the polyhedral organelles.

219 AXS features related to reversible shifts in polyhedral packing on the atomic scale.

220 l particles-very little is known about dense polyhedral packings.

221 rge volume asymmetry between its constituent polyhedral particle motifs.

222 guidelines for predicting phase behaviour of polyhedral particles are proposed: high rotational symme

223 erical particles with tunable attraction and polyhedral particles with anisotropic shape, and exclude

224 t, for up to [Formula: see text] constituent polyhedral particles.

225 Polyhedral plant cells can display complex patterning in

226 thrombi, undergo compressive deformation to polyhedral (polyhedrocytes) and polyhedral-like cells, a

227 or partial product space which arises as the polyhedral product functor described below.

228 he stable homotopy type of the values of the polyhedral product functor.

229 ifs to direct the metal-mediated assembly of polyhedral protein architectures and 3D crystalline prot

230 Our cages closely resemble natural polyhedral protein architectures(7,8) and are, to our kn

231 lase/oxygenase (RubisCO) is sequestered into polyhedral protein bodies called carboxysomes.

232 uilding blocks for modular de novo design of polyhedral protein cages that efficiently self-assemble

233 The carboxysome uses a polyhedral protein shell made of hexamers, pentamers, an

234 -fixing enzyme, Rubisco, within a virus-like polyhedral protein shell.

235 by building not a lipid membrane but a thin polyhedral protein shell.

236 es can be extended to construct higher-order polyhedral RNA architectures for various applications su

237 ography, implying that the various different polyhedral RNA cages observed in experiment are largely

238 rocarbon-capped nanocrystals with spherical, polyhedral, rod, plate, and branched inorganic core shap

239 We show how to compute the shape of a convex polyhedral room from its response to a known sound, reco

240 choes provide a unique description of convex polyhedral rooms.

241 via controlled assembly of initially formed polyhedral seed nanoparticles, which themselves originat

242 s approach to a variety of other types of Pd polyhedral seeds that contained Pd{111} and Pd{100} face

243 rm through selective overgrowth of spherical polyhedral seeds.

244 The granules exhibited a polyhedral shape and, with increased intensity of combin

245 However, structures of similar polyhedral shape are being discovered in an ever-increas

246 % of the object missing, suggesting accurate polyhedral shape classification is possible from individ

247 Cryo-TEM displays a polyhedral shape for eLNPs compared to spherical LNPs, w

248 stand how pavement cells morph from a simple polyhedral shape into highly lobed and interdigitated ce

249 Here, we report a new approach that uses the polyhedral shape of metal-organic-framework (MOF) partic

250 The polyhedral shape of the self-organized supramolecular de

251 , the [111] facets grow, thus facilitating a polyhedral shape.

252 to enable the design of protein cages in any polyhedral shape.

253 Polyhedral-shaped plant cells have faces, corners, and e

254 We propose a classification method for polyhedral shapes from incomplete individual cryo-ET rec

255 ructures dynamically adapt to non-spherical, polyhedral shapes under continuous deposition, ultimatel

256 nded water droplets can spontaneously assume polyhedral shapes, in spite of their concave interface.

257 r colloidal stability, size-tunability, rich polyhedral shapes, porosity and multifunctionality.

258 mine the self-assembly of protein cages into polyhedral shapes, such as the tetrahedron, triangular p

259 pramolecular columns and vesicles exhibiting polyhedral shapes.

260 les with discrete populations of volumes and polyhedral shapes.

261 Proteins that self-assemble into polyhedral shell-like structures are useful molecular co

262 hat most likely constitute the facets of the polyhedral shell.

263 hexamers assemble to form flat facets of the polyhedral shell.

264 many observations, predicts a new family of polyhedral shells, and provides the principles for desig

265 ere we demonstrate the bottom-up assembly of polyhedral silver nanocrystals into macroscopic two-dime

266 d iron moieties have exchanged exo- and endo-polyhedral sites with respect to the 10-vertex metallaca

267 ies can be understood in terms of underlying polyhedral skeletal electron pair theory (PSEPT) concept

268 The formation of these polyhedral--slightly distorted boron cuboctahedra--appea

269 hain is agitated, it will fold into a stable polyhedral structure about the size of a hand.

270 All three compounds have the same unique polyhedral structure having an approximate Cs symmetry a

271 ustness of the cages while maintaining their polyhedral structure, but also enables the incorporation

272 Various macromolecular structures possess polyhedral structure.

273 rease in particle size and loss of internal "polyhedral" structure of the MVLs over the duration of r

274 , which facilitates the synthesis of complex polyhedral structures and their post-assembly modificati

275 Self-assembled polyhedral structures are common in biology.

276 d double-stranded RNA genomes into preformed polyhedral structures called procapsids or inner cores.

277 d double-stranded-RNA genomes into preformed polyhedral structures called procapsids or inner cores.

278 erotrophic bacteria have the ability to make polyhedral structures containing metabolic enzymes that

279 blocks and topological principles to design polyhedral structures distinct from those of natural glo

280 Boranes with closed polyhedral structures feature peculiar bonding and struc

281 lastic hexamers associate to form the unique polyhedral structures found in retroviral cores.

282 f a new class of subcomponent self-assembled polyhedral structures having bimetallic vertices, as opp

283 f-planar gold particles with rose-shaped and polyhedral structures were prepared on the silica partic

284 when present, were typically poorly defined polyhedral structures with at least one curved region co

285 have been employed to form micrometer-sized polyhedral supercrystals by both the droplet evaporation

286 onvex polyhedron with equal edge lengths and polyhedral symmetry--tetrahedral, octahedral, and icosah

287 classes of convex equilateral polyhedra with polyhedral symmetry.

288 do-Ih Pt-centered six-shell successive nu(1) polyhedral system, each with radially equivalent vertex

289 )N(+)F(-) in THF to form mixed-functionality polyhedral T(10) and T(12) silsesquioxane (SQ) cages in

290 S(6) ](6-) , which functions as an intricate polyhedral template with abundant surface O and S atoms

291 s change the shape of CeO2 nanocrystals from polyhedral to spherical.

292 s of state and analyzed the evolution of the polyhedral units under compression.

293 mean diameters of the MVLs and their inner "polyhedral" vesicles were found to be 23.6 +/- 11.5 mum

294 m resolution the structure of the Sulfolobus polyhedral virus 1 (SPV1), which was originally isolated

295 Ten polyhedral viruses, of which nine are in the family Tomb

296 s only accounts for occupancy within regular polyhedral water cages.

297 locations other than the interior of regular polyhedral water cages.

298 s have recently been discovered which render polyhedral water-suspended droplets of several oils.

299 by encapsulating NPs into self-assembled DNA polyhedral wireframe nanocages, which serve as guiding a

300 The starch granules are polyhedral, with a diameter of 2.8 to 5.6mum and average