ライフサイエンスコーパス: vertex

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

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

3 sk receiving anodal or placebo tDCS over the vertex.

4 red with females that received tDCS over the vertex.

5 tion (rTMS) to the right PPC or to the scalp vertex.

6 th a nanometer scale tip protruding from one vertex.

7 apsid protein gp23 at the special pentameric vertex.

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

9 projecting from the vertex opposite the tail vertex.

10 enters and exits the capsid through a unique vertex.

11 ctron microscopy density of the phage portal vertex.

12 of symmetry-mismatched layers of the portal vertex.

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

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

15 ile retaining the local geometry around each vertex.

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

17 aging machine situated at a special fivefold vertex.

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

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

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

21 preassembled capsids through a unique portal vertex.

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

23 he native receptor at any singular threefold vertex.

24 ur, or five edges radiate out from a certain vertex.

25 protein, which is located at a unique 5-fold vertex.

26 ical component of the KSHV virion-the portal vertex.

27 ygdala, compared with TBS delivered over the vertex.

28 ngated octahedron; the polyhedra share oxide vertexes.

29 We show that ERK inhibitors Vertex-11e and SCH772984 exploit the small energetic dif

30 Furthermore, Vertex-11e and SCH772984 show opposite effects on HX nea

31 X-ray structures of 2P-ERK2 complexed with Vertex-11e or GDC-0994 recapitulate this closure, which

32 MS) reveal distinct binding interactions for Vertex-11e, GDC-0994, and AMP-PNP with active vs. inacti

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

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

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

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

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

38 orm dodecameric rings that occupy one capsid vertex and are incorporated during the assembly of capsi

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 PAR-6 is localized to the rosette vertex and dendrite tips, and promotes DYF-7 localizatio

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 -PSMA-11 PET/CT imaging field to include the vertex and lower extremities (total-body acquisition) af

46 normal and miniaturized hair follicles from vertex and occipital region in males with and without an

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

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

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

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

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

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

53 the length of the longest path to any given vertex and we show numerically that the longest path als

54 pendent biotinylated DNA strand in different vertexes and is further assembled via streptavidin to fo

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

56 e complex and pUL25 with pUL17 at the portal vertex, and (vi) packaging of the viral genome results i

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

58 rtex-wise estimates of CV, CT and SA at each vertex, and compared the frequencies of vertices with a

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

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

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

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

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

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

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

66 Vertex-based analyses revealed that damage predominated

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

68 Using a vertex-based mechanical model, we show that key features

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

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

71 Existing vertex-based models for the epithelium are unable to cap

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

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

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

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

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

77 g following cTBS to the angular gyrus versus vertex but not during the nonepisodic control task.

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

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

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

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

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

83 Since each vertex can be individually programmed to move upward or

84 al Au(7)Ag(6) units by sharing one common Au vertex can produce two temperature-responsive conformati

85 first indirect observation and use of boron vertex-centered carboranyl radicals generated by the oxi

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

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

88 eal the composition and the structure of the vertex complex along with new protein conformations that

89 med by the capsomeres is replaced by a large vertex complex in the pseudo T = 25 capsid.

90 The 3D structure of the vertex complex shows interactions with the viral membran

91 intermolecular nonbonded interactions of the vertex complex.

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

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

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

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

96 d capsid defined the structure of the single vertex containing the portal protein.

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

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

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

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

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

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

103 ine-tuning mechanism related to the weighted vertex cover problem.

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

105 born in an ambulance by spontaneous vaginal vertex delivery.

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

107 ccessfully synthesized through desymmetrized vertex design strategy.

108 e building blocks, through the desymmetrized vertex design strategy.

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

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

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

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

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

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

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

116 e symmetrically related alternatives) at one vertex does not correlate with its position at other ver

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

118 rsomedial thalamus and motor cortex near the vertex ECT electrode, as well as decreased CBF within la

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

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

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

122 Finally, our atomic models of portal vertex elements reveal how the fivefold-related capsid a

123 unique cohesive footprint near the threefold vertex, encompassing residues primarily from viral prote

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

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

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

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

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

129 structure of the symmetry-mismatched portal vertex from bacteriophage T4.

130 Now, vertex-functionalized amorphous scrambled porous organic

131 sent in situ structures of the unique portal vertex, genomic termini and ordered dsDNA coils in the c

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

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

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

135 in which directed edges are added to the new vertex in one of two ways: using cumulative advantage (p

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

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

142 This vertex is critical for driving capsid assembly, DNA pack

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

144 be is composed of a single peptide, and each vertex is occupied by a divalent metal ion.

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

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

147 rtal is selectively incorporated at a unique vertex is unclear.

148 plex inserted into a 5-fold-symmetric capsid vertex, is found in numerous icosahedral viruses, includ

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

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

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

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

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

154 Using a vertex model combined with experimental validation, we s

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

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

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

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

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

160 opose a theoretical framework that couples a vertex model of solid confluent tissues with the dynamic

161 Three-dimensional vertex model simulations and a continuum theory of epith

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

163 From theoretical considerations and vertex model simulations, we predict that in anisotropic

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

165 By modifying and calibrating an active vertex model to experiments, we have simulated numerical

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

167 Here, we develop a three-dimensional vertex model to investigate tissue mechanics at the onse

168 experimental results, we propose a modified vertex model with two essential ingredients for junction

169 Using a 3D surface tension-based vertex model, we reproduce the characteristic shapes fro

170 Using an enhanced vertex model, we show this is explained by two effects:

171 computer simulations based on a generalized vertex model.

172 related explicitly to the parameters of the vertex model.

173 sults of stability calculations based on the vertex model.

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

175 Vertex models are an important class of statistical mech

176 Vertex models are used to study cellular processes withi

177 They also significantly expand the class of vertex models available to experiment.

178 ubisostatic 2D spring networks and 2D and 3D vertex models for dense biological tissues.

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

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

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

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

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

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

185 he motor assembles transiently at the portal vertex of an empty precursor capsid (or procapsid) to po

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

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

188 In addition, there is one HS site at the vertex of each q3 and i3 spike (the "axial" sites).

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

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

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

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

193 The pUL6 portal dodecamer is anchored at one vertex of the capsid by interactions with the adjacent t

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

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

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

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

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

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

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

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

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

203 The vertex of the rosette, which becomes the dendrite tips,

204 uctural studies focused on the unique portal vertex of wild-type HSV and packaging mutants provide in

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

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

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

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

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

210 In such a network, each vertex or node corresponds to an individual's genotype a

211 (cTBS) was applied to either a control site (vertex) or to a left angular gyrus target region.

212 e have then used a graph labeling method for vertex ordering in our graph embedding process.

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 that clinically-approved VX-809 (Lumacaftor, Vertex Pharmaceuticals, Boston, MA, USA) and VX-770 (Iva

216 als, Boston, MA, USA) and VX-770 (Ivacaftor, Vertex Pharmaceuticals, Boston, MA, USA) significantly e

217 Vertex Pharmaceuticals, Cystic Fibrosis Foundation Thera

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

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

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

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

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

223 do not possess a visible tail structure, one vertex rearranges after interacting with host lipopolysa

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

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

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

227 virion and a localized reconstruction of the vertex region reveal the composition and the structure o

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

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

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

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

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

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

234 sed network control method from the Feedback Vertex Sets-based control perspective to identify the pe

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

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

237 In 2 and 3, these units are vertex-sharing and are assembled linearly.

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

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

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

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

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

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

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

245 proteins pUL15, pUL28, and pUL33; the capsid vertex-specific component (CVSC) proteins pUL17 and pUL2

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

247 5 form a heterodimeric structure, the capsid vertex-specific component (CVSC), that lies on top of th

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

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

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

251 issociation between LOC and OPA: relative to vertex stimulation, TMS over LOC selectively impaired th

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

253 stly select the desired branch even in multi-vertex structures with reasonably high complexity.

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

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

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

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

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

259 ue and unusually dynamic symmetry-mismatched vertex that is central to building an infectious virion.

260 es and a globular complex capping the portal vertex that is not observed in phages, indicative of her

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

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

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

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

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

266 198.3 +/- 3.3 MBq), 3 successive whole-body (vertex to mid thigh) PET/CT scans at 3 time points (30,

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

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

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

270 f an ATP-driven terminase to a unique portal vertex to recognize, package and cleave concatemeric dsD

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

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

273 nt (68)Ga-PSMA-11 PET/CT scans acquired from vertex to toes for primary staging (n = 93/388, 24%), bi

274 true whole-body (18)F-FDG PET/CT scans from vertex to toes in pediatric lymphoma patients, although

275 Including the total body (from vertex to toes) in (68)Ga-PSMA-11 PET/CT imaging reveale

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

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

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

279 nd alternate orientation of CATC-interacting vertex triplexes, suggest a mechanism whereby the portal

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

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

282 conducted before this "host-induced" unique vertex was discovered and before DNA sequencing became r

283 12-subunit ring structure at a unique capsid vertex which functions as a conduit for the encapsidatio

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

285 scovery rate corrections were applied to all vertex-wide analyses.

286 Vertex-wide cortical thickness was estimated using FreeS

287 ans were processed with CIVET 2.1 to extract vertex-wide CTh and cortical surface area (CSA).

288 Cerebral perfusion was compared vertex-wise according to APOE epsilon4 status and family

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

290 Vertex-wise analyses revealed significant thinning of ov

291 ts, we found progressive cortical atrophy on vertex-wise analysis in TLE before surgery that was bila

292 Whole-brain vertex-wise analysis of LGI was performed for group comp

293 g the post- versus presurgical TLE groups on vertex-wise analysis, the areas of postoperatively reduc

294 te Carlo corrected for multiple comparisons, vertex-wise cluster threshold of 1.3, p < 0.01).

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

296 Using FreeSurfer, we examined differences in vertex-wise estimates of CV, CT and SA at each vertex, a

297 Vertex-wise group comparisons were performed and cortica

298 Vertex-wise linear model tests were conducted across the

299 sed in regions of interest (ROIs) as well as vertex-wise map analyses.

300 Vertex-wise maps of the association between gene express