ライフサイエンスコーパス: vertex

1 n stimulation was applied to a control site (vertex).

2 noise (a constant number of noisy edges per vertex).

3 MS to the left angular gyrus relative to the vertex.

4 projecting from the vertex opposite the tail vertex.

5 enters and exits the capsid through a unique vertex.

6 ctron microscopy density of the phage portal vertex.

7 of symmetry-mismatched layers of the portal vertex.

8 netic seizure therapy (MST) with cap coil on vertex.

9 se, which are located at an especial prohead vertex.

10 t only one Fab fragment occupies each 5-fold vertex.

11 ive and negative in- and out-degrees of each vertex.

12 aging machine situated at a special fivefold vertex.

13 ortion of a line segment (block boundary) or vertex.

14 ation of a portal complex at a unique capsid vertex.

15 or the DNA-packaging machinery at the portal vertex.

16 preassembled capsids through a unique portal vertex.

17 s and the 12-fold portal located at a unique vertex.

18 ctor assemblages embedded at a unique capsid vertex.

19 id are missing in the vicinity of the unique vertex.

20 a stoichiometry of about one per three-fold vertex.

21 ate docking of the terminase with the portal vertex.

22 ng a single prehair initiates at each distal vertex.

23 erful motors assembled at the special portal vertex.

24 sk receiving anodal or placebo tDCS over the vertex.

25 red with females that received tDCS over the vertex.

26 ygdala, compared with TBS delivered over the vertex.

27 th a nanometer scale tip protruding from one vertex.

28 apsid protein gp23 at the special pentameric vertex.

29 by peripentonal hexon trimers at the 5-fold vertex.

30 ngated octahedron; the polyhedra share oxide vertexes.

31 For the isomer with naked vertex 12, a DFT computational search failed to reveal a

32 moted by the carborane substituent in the 13-vertex/12-vertex precursor.

33 with [Ru(eta-arene)Cl2 ]2 results in the 14-vertex/12-vertex species [1-(eta-mes)-9-(1'-1',2'-closo-

34 PDB scale, with either FT-IR (in this case a Vertex 70 V (Bruker)) or an isotope ratio infrared spect

35 five tegument densities capping each penton vertex, a pattern highly similar to that in alphaherpesv

36 the pan-caspase inhibitor VX-166 (6 mg/kg/d; Vertex, Abingdon, UK) or vehicle only and sacrificed at

37 ted two-domain molecule present at a unique, vertex-adjacent site that is not seen at other quasiequi

38 xtended conformation, which seals the portal vertex after genome packaging, and a postejection trimer

39 pes, or entire monolayers-that combines both vertex and contact-inhibition-of-locomotion models to in

40 sembly pathway that initiates at a five-fold vertex and continuously proceeds outwards in a spiraling

41 sing on a more literal comparison, vertex by vertex and edge by edge, the conclusion is the same: the

42 suggests possible models for the particle's vertex and edge organization.

43 ggests a model where key interactions at the vertex and edges are mediated at the inner layer of the

44 ract with PhiX174 at an icosahedral fivefold vertex and induce single-stranded (ss) DNA genome ejecti

45 DNA exits the capsid through the portal vertex and proceeds by way of the nuclear pore complex i

46 initiating the capsid assembly at the portal vertex and propagating its growth on a T = 7 icosahedral

47 growth of a tubular structure from a portal vertex and release of the genome.

48 f aplasia cutis congenita (ACC) of the scalp vertex and terminal limb-reduction defects.

49 face-exposed residue that maps to the 5-fold vertex and that has been implicated in receptor binding.

50 results indicate that it resides at a unique vertex and that there are approximately six to eight IVa

51 h between the fivefold symmetry of the shell vertex and the 12-fold symmetry of the portal protein ha

52 me, which contains a T-rich probe DNA at one vertex and three sulfhydryl groups modified with 10nm Au

53 entameric ring motor on the prohead's portal vertex and uses ATP hydrolysis energy for DNA translocat

54 mbles at a special vertex called the 'portal vertex' and consists of a portal, a DNA packaging ATPase

55 ve indicated that intact capsids, the portal vertex, and all components of a tripartite terminase enz

56 The portion of UL17 nearest the vertex appears to be poorly constrained, which may provi

57 timulation) to the left or right AC, and the vertex as a control.

58 DNA and as a nucleating site for the unique vertex assembly.

59 hedral system, each with radially equivalent vertex atoms: Pt@M(12)(icosahedron)@M(30)(icosidodecahed

60 as indexed by the age at which each cortical vertex attained its peak surface area.

61 probabilistically coalescing vertices, using vertex attributes to determine the probabilities.

62 ose-response relation" between the extent of vertex baldness and prevalent MI.

63 nalysis indicates that frontal plus moderate vertex baldness at age 45 years is associated with an in

64 ared with no baldness, frontal plus moderate vertex baldness at age 45 years was not significantly as

65 del were 1.28 (frontal baldness), 1.02 (mild vertex baldness), 1.40 (moderate vertex baldness), and 1

66 1.02 (mild vertex baldness), 1.40 (moderate vertex baldness), and 1.18 (severe vertex baldness).

67 (moderate vertex baldness), and 1.18 (severe vertex baldness).

68 In particular, vertex baldness, but not frontal baldness alone, was str

69 Both gyral-level and vertex-based analyses revealed significantly thinner cor

70 Vertex-based analyses revealed that damage predominated

71 red between groups in whole brain, lobar and vertex-based analyses.

72 ical thickness estimates were obtained using vertex-based methods.

73 To do this, we use a vertex-based model, implemented on an ellipsoidal surfac

74 In contrast with many vertex-based models, our statistical-mechanical model do

75 r Myosin II polarization that we tested in a vertex-based simulation.

76 FA, its left homolog (leftOFA), rightLO, and vertex (baseline) while participants were discriminating

77 est (ROI) approach as well as on a vertex-by-vertex basis.

78 eins and lipids concentrate in a ring at the vertex between apposing organelle membranes, the encircl

79 uorescein molecule attached at the remaining vertex by an amide linkage.

80 When focusing on a more literal comparison, vertex by vertex and edge by edge, the conclusion is the

81 n of interest (ROI) approach as well as on a vertex-by-vertex basis.

82 By using a general linear model approach, a vertex-by-vertex statistical analysis (P < .01) was used

83 ] with dimorphite (As4S3) gave the closed 11-vertex cage clusters [(Cp'''Sm)3(AsS3)2] (3) and [(Cp*Yb

84 DNA packaging complex assembles at a special vertex called the 'portal vertex' and consists of a port

85 lic acetylide complexes featuring 10- and 12-vertex carboranes embedded within the diethynyl bridging

86 BL/6J background were selected for submental vertex cephalometric imaging.

87 Vertex coloring of graphs, belonging to the class of com

88 Vanadium Dioxide (VO2) to efficiently solve vertex coloring of graphs.

89 intermolecular nonbonded interactions of the vertex complex.

90 We propose that the vertex complexes orchestrate virion assembly by coordina

91 al cluster analysis, k-means clustering, and vertex component analysis.

92 The unique vertex consists of virally coded proteins, some of which

93 ipates in making the fivefold channel at the vertex contacting the LPS.

94 Most viral procapsids possess a special vertex containing a dodecameric portal protein that is u

95 ing terminase docked onto a unique procapsid vertex containing a portal ring.

96 tive right posterior STS (rpSTS) or over the vertex control site.

97 stimulation of PFC without reactivation and vertex (control site) after reactivation.

98 following cTBS targeted at rPoG, rPM, or the vertex (control site).

99 bitory rTMS over right hemisphere S1 and the vertex (control).

100 mography proceeds from the N terminus at one vertex, corresponding to the axis of 3-fold symmetry, to

101 tures in all layers of the multilayer portal vertex could not be resolved simultaneously.

102 These intra- and inter-vertex coupling constants are used to track the degree o

103 sing more modern algorithms based in part on vertex cover and the theory of fixed-parameter tractabil

104 apping particle tracks near the annihilation vertex, creating spatially correlated DNA lesions.

105 born in an ambulance by spontaneous vaginal vertex delivery.

106 In each graph, a vertex denotes a similar subsequence pair.

107 mprises three steps: site-specific (edge and vertex) deposition of Pt, etching of inner Au, and regro

108 ccessfully synthesized through desymmetrized vertex design strategy.

109 coordination polymers (MCPs) are derived by vertex desymmetrization using linkers with symmetry ineq

110 nality of a series of previously reported 14-vertex dicobaltacarboranes.

111 drug delivery system, we used the resulting vertex-differentiated ammonio derivative to construct a

112 Several representative vertex-differentiated icosahedral closo-boranes were pre

113 We report methods for the synthesis of vertex-differentiated icosahedral closo-boranes.

114 part of the trisymmetrons around the unique vertex disassemble, probably in part because two minor c

115 Relative to TMS to a control site (vertex), disruption of the left angular gyrus significan

116 previously confirmed that UL25 occupies the vertex-distal region of the CVSC density by visualizing

117 e) subunit, transiently docked at the portal vertex during genome packaging.

118 , metal polyhedra, M(O,F)(n), linked through vertex, edge, or face-sharing, and mu(2), mu(3), and mu(

119 ear the particle edges in vacuum and surface vertex/edge sites in oxidizing conditions, where it enha

120 ar the ear (e.g., mastoid) in reference to a vertex electrode (Cz).

121 The 12-vertex endohedral cluster [Ru@Ge12](3-) reveals an unpre

122 After both suppressing activity in the vertex (Experiment 2) and sham stimulation (Experiment 1

123 The nine-vertex ferracarborane salt [N(PPh3)2][7,7,7-(CO)3-closo-

124 of the sole two edge-transitive nets with a vertex figure as double six-membered-ring (d6R) building

125 models, among them, node and edge addition, vertex fitness and the deletion of nodes and edges.

126 ractility and tissue stress to multicellular vertex formation and resolution, respectively.

127 The vertex geometry involves four copies of the Sec31 beta-p

128 res: It is based on the stages at which each vertex gets removed from a graph in the standard algorit

129 On random N-vertex graphs, the median number of variables is reduced

130 oso-7,9,1-IrFeCB6H7] (3), in which one {BH}- vertex has formally been subrogated by an {Ir(CO)2(PPh3)

131 prism when connector arm ends attached to a vertex have a strongly correlated twist sense and chiral

132 *Ru)2 C2 B10 H12 ], the first examples of 14-vertex heteroboranes containing 14-skeletal electron pai

133 tor that translocates DNA through the portal vertex in the capsid during DNA packaging.

134 retrieve the structure of the unique portal vertex in the context of the icosahedral capsid and, for

135 e report the first visualization of a unique vertex in the Kaposi's sarcoma-associated herpesvirus (K

136 mputing first the signature vector for every vertex in the network and then the graphlet correlation

137 Our data also suggest that the portal vertex in these viruses is the weakest point in the over

138 her planar or pyramidal with a 109.5 degrees vertex) in a 3:2 ratio to explore the structural require

139 electrode placements) and MST (round coil on vertex) in nonhuman primates.

140 lls established that the spike at the unique vertex initiates binding to the cell wall, which results

141 r, and COPI shares with COPII highly similar vertex interactions involving the axial ends of beta-pro

142 of the herpes simplex virus 1 (HSV-1) portal vertex into the capsid requires interaction with a 12-am

143 esults in the incorporation of the phosphide vertex into the cyclotrisilene scaffold, yielding a cong

144 This unique vertex is also believed to comprise the site with which

145 e viral transmembrane density at the special vertex is assigned to be a hexamer of heterodimer of pro

146 th l is an edge-weighted graph in which each vertex is associated with a string and there is an edge

147 respectively), whereas the HSV type 1 portal vertex is encoded by UL6.

148 ormed protein capsid through a unique portal vertex is essential in the life cycle of a large number

149 nsistent with the hypothesis that the portal vertex is the conduit through which DNA is ejected to in

150 This vertex is the site of assembly of the DNA packaging moto

151 " then it is proved that the genome of every vertex is uniquely determined and can be explicitly reco

152 positions, and sequential order of T7 portal vertex layers, resolving in tandem the 5-fold gene produ

153 e FreeSurfer image analysis suite quantified vertex-level surface area and gyrification.

154 endo-polyhedral sites with respect to the 10-vertex metallacarborane.

155 ucture consists of two incomplete (i.e., one vertex missing) icosahedral Au(12) units joined by five

156 We introduce an Active Vertex Model (AVM) for cell-resolution studies of the me

157 tation is encoded in the ground state of the vertex model and its complexity is reflected in the dyna

158 We constructed a vertex model for cells in a curved environment.

159 The AVM combines the Vertex Model for confluent epithelial tissues with activ

160 FF) was used to restrain the majority of the vertex model in well-defined cryoEM density.

161 We also construct a mapping of the vertex model into the Chimera architecture of the D-Wave

162 We employ a vertex model of an embryonic segment to test hypotheses

163 Experimental validation of 3D vertex model simulations demonstrates that enhanced inte

164 ersible classical computations onto a planar vertex model that exhibits no bulk classical thermodynam

165 In this work, we develop a computational vertex model to investigate the role of the passive mech

166 computer simulations based on a generalized vertex model.

167 related explicitly to the parameters of the vertex model.

168 sults of stability calculations based on the vertex model.

169 Vertex models are a class of such models that consider c

170 Vertex models are used to study cellular processes withi

171 This review summarizes how vertex models have been used to provide insight into dev

172 uestions are explored computationally, using vertex models of epithelial shells assembled from prisml

173 phogenesis can be adequately described using vertex models, in which the two-dimensional arrangement

174 el, but periodic patterns with distinct five-vertex motifs remained elusive.

175 lowing demagnetizing and annealing, specific vertex motifs retain low-energy configurations, which ex

176 resenting cellular interfaces, in which each vertex moves in response to forces due to growth, interf

177 sharing common properties; (2) summarize the vertex neighbor information from the partitioned dataset

178 portal protein complex embedded in a single vertex of a preformed viral protein shell called procaps

179 e recognizes a conformational epitope at the vertex of a three-fold protrusion on the viral surface,

180 of a molecular motor assembled at the portal vertex of an icosahedral head.

181 s of 3D-DX DNA triangle motifs, and to every vertex of bulged-junction DNA triangles.

182 ed 5 nm or 10 nm gold nanoparticles to every vertex of DNA parallelograms, to two or three vertices o

183 one actin-rich wing hair at the distal-most vertex of each cell.

184 single actin-based wing hair from the distal vertex of each cell; in forming unbranched wing hairs; a

185 of DNA-binding proteins is positioned at the vertex of each crossed strand.

186 The portal vertex of herpesvirus capsids serves as the conduit thro

187 At the unique vertex of PRD1, the packaging complex replaces the regul

188 ted asymmetric reconstructions of the portal vertex of T7 and other bacteriophages.

189 study the multilayer structure of the portal vertex of the bacteriophage T7 procapsid, the recipient

190 Each vertex of the BHG is a local minimum, which represents t

191 erved dodecameric portal at a special 5-fold vertex of the capsid.

192 pes located around the icosahedral five-fold vertex of the capsid.

193 We infer that the trimer constitutes the vertex of the COPI cage.

194 ul molecular machine assembled at the portal vertex of the empty prohead.

195 thanol content and decreased in the opposite vertex of the experimental domain.

196 The tail, attached at a unique pentameric vertex of the head, consists of a neck, 12 appendages, a

197 A single B-OH vertex of the icosahedral borane [closo-B(12)(OH)(12)](2

198 wo concentric rings at the special five-fold vertex of the icosahedral capsid.

199 cture of a trimer of receptor dimers at each vertex of the lattice accounts well for the density and

200 the IVa2 protein would be found at a unique vertex of the mature virion.

201 actions of the substituent with the proximal vertex of the other ring.

202 a-barrel shell protein that likely plugs the vertex of the particle.

203 tion of a connector-pRNA complex at a unique vertex of the procapsid conclusively demonstrates the pe

204 inase protein (gp17) assembled at the portal vertex of the prohead, is the fastest and most powerful

205 the head-tail connector at the unique portal vertex of the prohead.

206 assembled at the special head-tail connector vertex of the prohead.

207 elected from significant genes by clustering vertexs of the mutation network.

208 ere made by using two-sample t tests at each vertex on the group surface; statistical results were co

209 isomers, one cage C atom occupies a degree-4 vertex on the short parallel edge of the trapezium.

210 -negative template, a maximum depth for each vertex on the surface models was calculated to avoid ext

211 l slender horn structure projecting from the vertex opposite the tail vertex.

212 and a single novel hornlike structure at the vertex opposite the tail.

213 t stimulation to the left FEF, right FEF, or vertex, participants performed a visual discrimination t

214 tor potentiator, ivacaftor (VX-770/Kalydeco, Vertex Pharmaceuticals, Boston, MA), as a therapeutic st

215 Vertex Pharmaceuticals, Cystic Fibrosis Foundation Thera

216 At each vertex point on the surface tessellation, the diffusion-

217 he AlnHn+2 (5 <or= n <or= 8) family adopts n-vertex polyhedral closo-structures with two extra hydrog

218 common to clathrates along with a unique 22-vertex polyhedron with two hexagonal faces capped by add

219 he carborane substituent in the 13-vertex/12-vertex precursor.

220 double helix with ejection occurring at one vertex presumed to be the portal.

221 posed of the major capsid protein gp23*, the vertex protein gp24*, and the portal protein gp20.

222 ere consistent with roles as facet, edge, or vertex protein, respectively.

223 tions to the core inhibit the release of the vertex proteins and lead to the cell entry defect of Ad2

224 be one step on the way to the release of Ad vertex proteins during cell entry.

225 ic frameworks that addresses the size of the vertex rather than the length of the organic linker.

226 t, preinspiratory potentials were present at vertex recording sites in 12 of the remaining 13 subject

227 ogether glue peripentonal hexons beneath the vertex region and connect them to the rest of the capsid

228 oposed mechanism in which HD5 stabilizes the vertex region of the capsid and blocks uncoating steps r

229 Models were built for the vertex regions of these chimeras with monomeric and dime

230 ncreasing dorsal-ventral tension resulted in vertex resolution perpendicular to the AP direction.

231 local, periodic contractile forces polarize vertex resolution to drive Drosophila axis elongation.

232 and developmental course from the well-known vertex response.

233 After S1 rTMS, but not after vertex rTMS, sensory discrimination was reduced and subj

234 primarily of aplasia cutis congenita of the vertex scalp and transverse terminal limb defects.

235 42%; although pain was also reported in the vertex, second division of trigeminal nerve, neck, nose,

236 aset as a coexpression graph, and search for vertex sets which are frequently densely connected acros

237 x (M1 stimulation) and the parieto-occipital vertex (sham stimulation) to test for dose-dependent iTB

238 would predict a biicosahedral structure via vertex sharing of two icosahedral M13 building blocks as

239 bly of two Pt-centered Ag icosahedra through vertex sharing.

240 ing differences from the previously reported vertex-sharing biicosahedral [Au(25)(PPh(3))(10)(SC(2)H(

241 The structure features a vertex-sharing bitetrahedral Au7 kernel and an unprecede

242 fascinating sodalite-like structure with 24 vertex-sharing cubane-like [Er(4)(mu(3)-OH)(4)](8+) unit

243 ounds like Mo8Ga41 prefer architectures with vertex-sharing gallium clusters, whereas electron-rich c

244 win dimers are connected to single layers of vertex-sharing octahedra, forming infinite chains along

245 Preferential attachment to edge and vertex sites occurs by performing a thiol place-exchange

246 eta-arene)Cl2 ]2 results in the 14-vertex/12-vertex species [1-(eta-mes)-9-(1'-1',2'-closo-C2 B10 H11

247 HSV-1, including distribution of the capsid vertex specific component (CVSC) of HSV-1, which is a he

248 d through the inner nuclear membrane, to the vertex-specific complex of HSV capsids, which comprises

249 hich along with pU(L)17 comprises the capsid vertex-specific complex, or CVSC.

250 pUL17 and pUL25, which form the capsid vertex-specific component (CVSC), particularly contribut

251 5 form a heterodimeric structure, the capsid vertex-specific component (CVSC), that lies on top of th

252 of the capsid vertices as part of the capsid vertex-specific component and implicates the importance

253 ow refer to it more generally as the "capsid vertex-specific component" (CVSC).

254 attern 2, continuous background with narrow, vertex spike-wave discharges in lockstep with myoclonic

255 a general linear model approach, a vertex-by-vertex statistical analysis (P < .01) was used to assess

256 The portal vertex structure of the phage P22 is a 2.8 MDa molecular

257 e energy of the resonant states to the local vertex structure of the quasicrystal.

258 The assembled portal vertex structure represents both a membrane-binding and

259 der to understand the assembly of the portal vertex structure, we have isolated the gene encoding tai

260 l composition and assembly within the portal vertex structure.

261 to gp10, which is thought to plug the portal vertex structure.

262 y of the gp26 assembly into the phage portal vertex structure.

263 the investigator, the study monitor, and the Vertex study team were masked to treatment assignment.

264 with DNA coaxially spooled around the portal vertex, suggesting that newly packaged DNA triggers the

265 hat pUL36 stabilizes other components of the vertex-tegument interface.

266 Strikingly, at the vertex that contacts the pilus, a rod of density that ma

267 a central exocytic zone, tightening it to a vertex that establishes the polarity axis for the ensuin

268 omers in properdin oligomers conform a curly vertex that holds together the AP convertase, interactin

269 (HSV) type 1 capsids contain a single portal vertex that is composed of 12 copies of the U(L)6 gene p

270 ding-are oriented toward the adjacent 5-fold vertex, the entry pathway of ssRNA segments.

271 ains a single "portal" structure at a unique vertex; the portal serves as the hole through which DNA

272 d via an adapter protein to the virus portal vertex, through which the DNA is ejected during infectio

273 virus contacts the pilus at a capsid 5-fold vertex, thus locating the surface-accessible portion of

274 icosahedral viruses use a specialized portal vertex to control genome encapsidation and release from

275 acing regular polygons edge-to-edge around a vertex to fill the plane.

276 and that the genome may escape from a 5-fold vertex to initiate infection.

277 tion fields (from skull base to ischia, from vertex to ischia, from skull base to mid thigh, from ver

278 198.3 +/- 3.3 MBq), 3 successive whole-body (vertex to mid thigh) PET/CT scans at 3 time points (30,

279 Whole-body (vertex to mid thigh) PET/CT scans were acquired at 6 tim

280 Whole-body (vertex to mid thigh) PET/CT scans were acquired at 6 tim

281 o ischia, from skull base to mid thigh, from vertex to mid thigh).

282 ined for the largest acquisition field, from vertex to mid thigh: ICC, 0.994; 95% confidence interval

283 lowed by 4 whole-body PET/CT scans, from the vertex to the mid thigh, at 10, 60, 120, and 240 min aft

284 was performed 5 min after injection from the vertex to thighs at 3 min per bed position.

285 -closo-CoC2B10H12 selectively removes the B5 vertex to yield the dianion [nido-(eta-C5H5)CoC2B9H11](2

286 rative manifest refraction astigmatic error (vertexed to the corneal surface) was 1.29 +/- 0.92 D (P

287 and active cathodal-inhibitory tDCS over the vertex, to exclude any unspecific effect of tDCS.

288 of pi-conjugated dehydrobenzoannulene (DBA) vertex units.

289 ally introduce functional groups at the B(2) vertex using B(9)-bromo-meta-carborane as the sole start

290 12-subunit ring structure at a unique capsid vertex which functions as a conduit for encapsidation of

291 12-subunit ring structure at a unique capsid vertex which functions as a conduit for the encapsidatio

292 symmetry, to the C terminus at the opposite vertex, which forms the prominent 6-fold symmetry axis.

293 ckaged into the procapsid through the unique vertex while the genome terminal protein P8 functions as

294 sing the DNA to exit-probably via the portal vertex-while the capsid, although largely intact, sustai

295 Whole-brain vertex-wise analyses identified three clusters in prefro

296 Vertex-wise analyses revealed significant thinning of ov

297 each native-surface region of interest, and vertex-wise comparisons were made by using two-sample t

298 Vertex-wise group comparisons were performed and cortica

299 Vertex-wise maps of the association between gene express

300 that the quasiicosahedral virus has a unique vertex, with a pocket on the inside and a spike structur