ライフサイエンスコーパス: polyhedral

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

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

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

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

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

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

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

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

9 Carboxysomes are polyhedral bodies consisting of a proteinaceous shell fi

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

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

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

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

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

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

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

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

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

19 interstitial arrangements of boron atoms and polyhedral bonding.

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

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

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

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

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

25 The incorporation of polyhedral boranes into novel photoluminescent materials

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

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

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

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

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

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

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

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

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

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

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

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

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

39 The polyhedral cages measured approximately 60 nm in diamete

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

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

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

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

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

45 Polyhedral capsids and closed spherical capsids were fou

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

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

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

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

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

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

52 artial capsids, closed spherical capsids and polyhedral capsids.

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

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

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

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

57 Polyhedral ceria and nanorods were more effective than c

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

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

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

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

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

63 n resonances of different arrangements of Ag polyhedral clusters.

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

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

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

67 clathrin, assembling triskelia into regular polyhedral coats.

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

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

70 Convex isogonal polyhedral concepts allow certain combinations of polygo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 led by introduction of the corresponding DNA polyhedral frames.

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

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

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

98 Polyhedral frameworks with central elements exhibiting v

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

126 The preparation of synthetic polyhedral molecular assemblies represents a challenging

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

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

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

130 Polyhedral nano- and microstructures with shapes of face

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

168 Polyhedral plant cells can display complex patterning in

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

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

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

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

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

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

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

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

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

178 choes provide a unique description of convex polyhedral rooms.

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

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

181 rm through selective overgrowth of spherical polyhedral seeds.

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

183 % of the object missing, suggesting accurate polyhedral shape classification is possible from individ

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

185 The polyhedral shape of the self-organized supramolecular de

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

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

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

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

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

191 pramolecular columns and vesicles exhibiting polyhedral shapes.

192 les with discrete populations of volumes and polyhedral shapes.

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

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

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

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

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

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

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

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

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

202 Various macromolecular structures possess polyhedral structure.

203 Self-assembled polyhedral structures are common in biology.

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

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

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

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

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

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

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

211 classes of convex equilateral polyhedra with polyhedral symmetry.

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

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

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

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

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

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

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

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