ライフサイエンスコーパス: topologically

1 We have defined these steps topologically.

2 ure-function model is that the cortex, while topologically a two-dimensional surface, is curved.

3 thy volunteers, but they were typically less topologically abnormal than the patients' networks and d

4 formance liquid chromatography (HPLC)) and a topologically achiral figure eight knot (18% by HPLC), c

5 modelling other physical systems exhibiting topologically analogous phenomena.

6 one-way edge states near-zero frequency, is topologically analogous to the 2D topological p+ip super

7 This process is topologically analogous to well-studied apical constrict

8 ing sub-graph isomorphism problem, producing topologically and biologically accurate alignments remai

9 RAAL and NATALIE, regularly produce the most topologically and biologically coherent alignments.

10 ve the film quality, both electronically and topologically, and enhance the photoluminescence intensi

11 sine 9 methyltransferase), including a large topologically associated 1.2-Mb domain conserved in huma

12 The cPcdh topologically associated domain (TAD(cPcdh)) in neurons

13 organization: chromatin interaction hubs and topologically associated domain (TAD) boundaries.

14 ced detection of structural features such as topologically associated domain boundaries.

15 There are 6 genes in a topologically associated domain of chromatin with GPR98,

16 r-level organization of chromosomes, such as Topologically Associated Domains (TAD), i.e., locally pa

17 g sites are interwoven with enhancers within topologically associated domains (TADs) and a positive c

18 genic genomic imbalances, and 7.3% disrupted topologically associated domains (TADs) encompassing kno

19 Our analysis has identified a subset of topologically associated domains (TADs) that are signifi

20 er on lamina-associated domains (LADs) or on topologically associated domains (TADs), defined by pref

21 The genome is organized into repeating topologically associated domains (TADs), each of which i

22 so correspond to boundaries of X-chromosomal topologically associated domains (TADs).

23 an genomes are organized into megabase-scale topologically associated domains (TADs).

24 he location of regulatory chromatin domains (topologically associated domains [TADs]).

25 Distal QTLs are enriched within topologically associated domains and exhibit largely con

26 ization discussed include chromatin looping, topologically associated domains, chromosome territories

27 ture estimation accuracy and preservation of topologically associated domains.

28 pression to its chromatin environment within topologically associated domains.

29 and whose span in many cases coincides with topologically associated domains.

30 ulatory fine structure within megabase-sized topologically associated domains.

31 rgenic and intragenic enhancers found inside topologically associated regulatory domains (TADs) expre

32 interaction networks and be associated with topologically associating domain (TAD) borders, while dC

33 ic lethal (MSL) complex, are enriched around topologically associating domain (TAD) boundaries on the

34 SMARCA4 binding was enriched at topologically associating domain (TAD) boundaries, and S

35 additional interacting elements and defined topologically associating domain (TAD) boundaries, enric

36 nding across several megabases surrounded by topologically associating domain (TAD) boundaries.

37 vely broaden but are ultimately delimited by topologically associating domain (TAD) boundaries.

38 5C identified a topologically associating domain (TAD) over the Shh/ZRS

39 detects significant interactions at the sub-topologically associating domain level, identifying pote

40 eous chromatin folding that lacks detectable topologically associating domains (TADs) and chromatin c

41 genomic organization including compartments, topologically associating domains (TADs) and loops are p

42 multi-megabase compartments to sub-megabase topologically associating domains (TADs) and sub-TAD con

43 ug-induced epigenetic states involving large topologically associating domains (TADs) and the activat

44 ression based on division of the genome into topologically associating domains (TADs) and then model

45 e-conformation-capture studies have revealed topologically associating domains (TADs) as a conserved

46 gation and maintenance of XCI, coincide with topologically associating domains (TADs) as present in t

47 m to identify 3D spatial associations within topologically associating domains (TADs) from 1D maps of

48 ell-type invariant, evolutionarily conserved topologically associating domains (TADs) in a broad spec

49 on, predicting the boundaries of hundreds of topologically associating domains (TADs) in human and Dr

50 The organisation of vertebrate genomes into topologically associating domains (TADs) is believed to

51 regulatory contacts to another, between two topologically associating domains (TADs) located on eith

52 The mammalian HoxD cluster lies between two topologically associating domains (TADs) matching distin

53 Epigenetic alterations cluster to gene-dense topologically associating domains (TADs) that already sh

54 Eukaryotic chromosomes are partitioned into topologically associating domains (TADs) that are demarc

55 insulated neighborhoods, which in turn form topologically associating domains (TADs) that are largel

56 ructure within chromatin compartments called topologically associating domains (TADs) that are largel

57 e genome of metazoan cells is organized into topologically associating domains (TADs) that have simil

58 B-CTCF-cohesin sites flank the boundaries of topologically associating domains (TADs) with TOP2B posi

59 s are spatially organized into compartments, topologically associating domains (TADs), and loops to f

60 Topologically associating domains (TADs), CTCF loop doma

61 at chromosomes of animals are organized into topologically associating domains (TADs), evolutionary c

62 omains of self-interacting chromatin, called topologically associating domains (TADs), in many organi

63 ntra-chromosomal interaction, referred to as topologically associating domains (TADs), interspersed w

64 Topologically associating domains (TADs), typically seve

65 A new level of chromosome organization, topologically associating domains (TADs), was recently u

66 ion capture (Hi-C) has revealed sub-megabase topologically associating domains (TADs), which are the

67 omatin structures including compartments and topologically associating domains (TADs), which may serv

68 that mammalian genomes are partitioned into topologically associating domains (TADs), within which t

69 s ( approximately 1 Mb) resembling mammalian topologically associating domains (TADs).

70 oned in the interphase nucleus into discrete topologically associating domains (TADs).

71 conformation by diminishing the formation of topologically associating domains (TADs).

72 between CTCF target sites and insulation of topologically associating domains (TADs).

73 s are organized into structural units called topologically associating domains (TADs).

74 rge-scale changes in the number and sizes of topologically associating domains (TADs).

75 NAs, gene expression data and information on topologically associating domains (TADs).

76 electively altered boundary strength between topologically associating domains and A/B compartmentali

77 of higher-order domains at different scales: topologically associating domains and nuclear compartmen

78 teraction mapping studies have revealed that topologically associating domains and subdomains are fun

79 xture model And Proportion test, to identify topologically associating domains and subdomains in Hi-C

80 Topologically associating domains are shown to be crucia

81 ds in mitosis and by which cohesin generates topologically associating domains during interphase.

82 CTCF creates boundaries between topologically associating domains in chromosomes and, wi

83 e that these clusters coincide with distinct topologically associating domains in humans and Drosophi

84 These structures, far shorter than topologically associating domains in mammals, typically

85 PRC1 domains differ from topologically associating domains in size and boundary c

86 ide information on the timescales over which topologically associating domains might be restructured.

87 The topologically associating domains of the interphase chro

88 ts to give networks resembling those seen in topologically associating domains, as switching markedly

89 actor (CTCF) that binds to the boundaries of topologically associating domains.

90 on encompasses larger chromatin loops termed topologically associating domains.

91 find large genomic compartments and smaller topologically-associating domains (TADs) that undergo en

92 her network resilience to targeted attack on topologically central nodes in the SF group compared to

93 t the vulnerable set consists of a small but topologically central portion of the network and that la

94 Thus, the biogenesis of large and topologically challenging IgM complexes is dictated by a

95 ed by ring-closing olefin metathesis to form topologically chiral molecular trefoil knots of single h

96 nt species of the library were assigned as a topologically chiral Solomon link (60% of the library, a

97 s, periodically driven quantum matter can be topologically classified by topological invariants, whos

98 to significantly accelerate research in the topologically complex and vast five-dimensional phase sp

99 Borromean rings or links are topologically complex assemblies of three entangled ring

100 r pentafoil knot [2.Cl](PF6)9), making these topologically complex host molecules some of the stronge

101 ing realized and the number of proteins with topologically complex knotted structures has risen.

102 Surface modification of these topologically complex macrostructures ( approximately 3

103 These mesostructures are among the most topologically complex morphologies identified to date an

104 has emerged as a novel technique to produce topologically complex nanoporous and nanocomposite struc

105 propose importin alpha3 evolved to recognize topologically complex NLSs that lie next to bulky domain

106 se of selective imine exchange to generate a topologically complex product.

107 e and high-affinity recognition of large and topologically complex protein surfaces.

108 cation of a trace amount of drugs sitting on topologically complex real-world surfaces.

109 Protein chains are known to fold into topologically complex shapes, such as knots, slipknots o

110 folds for the rational construction of other topologically complex structures.

111 Brain connectomes are topologically complex systems, anatomically embedded in

112 earch for wearable power harvesters based on topologically complex, low-dimensional nanoassemblies.

113 The fold of the molecule is topologically complex, with the first beta-sandwich and

114 els requires methods that can create defined topologically-complex neuronal networks.

115 The C=C linkages topologically connect pyrene knots at regular intervals

116 tion paths to reveal new structures that are topologically connected to but distinctly different from

117 In lipoxygenases, the topologically conserved C-terminal domain catalyzes the

118 er eukaryotic chromosomes are organized into topologically constrained functional domains; however, t

119 egions (rich club and hubs within it) form a topologically continuous band extending through two of t

120 the information loss and thus realize novel topologically-controlled access memory (TAM).

121 dal nanostructures (MCNs) exhibit intriguing topologically dependent chemical and physical properties

122 This fusion is topologically different to that mediated by the membrane

123 of the DNA linking number-that is, they are topologically different.

124 elical conformations that would otherwise be topologically disallowed.

125 chanisms interact to yield a rich variety of topologically disconnected and connected structures.

126 as supercooled liquids, whose structures are topologically disordered like a liquid, but nevertheless

127 in central network positions, have a strong topologically disruptive effect and touch complexes with

128 tence of robust edge states at interfaces of topologically dissimilar systems is one of the most fasc

129 authors present a framework for identifying topologically distinct band-structures for all 3D space

130 ic topological surface-state arcs connecting topologically distinct bulk states in a chiral hyperboli

131 also show that materials can be divided into topologically distinct classes requiring different optim

132 f the large-intestinal core microbiota where topologically distinct co-occurrence networks were const

133 ase of two coupled modes generates a host of topologically distinct dynamics over the parameter space

134 e, nontrivial Fermi arcs, connecting between topologically distinct Fermi surfaces, play vital roles

135 n adopts an open decameric structure that is topologically distinct from other ferritins.

136 Several foldamer helices featuring topologically distinct H-bonds have been discovered, but

137 mechanistic similarities in the formation of topologically distinct multicellular and intracellular l

138 d insulators, these produce a total of eight topologically distinct phases.

139 nalyze the thermodynamics of two families of topologically distinct polymorphs of zinc zeolitic imida

140 t are localized at the interface between two topologically distinct PT-symmetric photonic lattices.

141 bfields of simple cells in layer 2/3 exhibit topologically distinct relationships with the maps of vi

142 magnetic field, a reliable switching between topologically distinct textures can be achieved at reman

143 pping interfaces to form compositionally and topologically diverse oligomers.

144 3-PC, and 4-PC) is demonstrated for a set of topologically diverse, zirconium-based (porphinato)zinc

145 Topologically efficient and biologically expensive hubs

146 t with Rentian scaling: wiring diagrams were topologically efficient because they minimized wiring wi

147 inding, biotin-streptavidin binding, and the topologically enhanced cell-substrate interaction on a 3

148 tron reflectivity experiments to demonstrate topologically enhanced interface magnetism by coupling a

149 The ring-shaped cohesin complex topologically entraps chromosomes and regulates chromoso

150 simple folds and less so if the fold is more topologically entwined.

151 conservation of the machineries involved in topologically equivalent mitotic membrane remodelling ev

152 of a nonaxial His into sperm whale Mb at the topologically equivalent position and in close proximity

153 rt (ESCRT) machinery play essential roles in topologically equivalent processes at both the endosome

154 rectangular unit cell, the band structure is topologically equivalent to that of strongly distorted g

155 Zr8 cluster with a smaller Zr6 cluster in a topologically identical framework.

156 se transition (C2/c to Fdd2) to a denser but topologically identical polymorph.

157 This study identified topologically important genes in interwoven network comm

158 , which encodes ERK1 MAP kinase, as the most topologically important hub in protein-protein interacti

159 Then HubAlign aligns topologically important proteins first and gradually ext

160 information, based upon the observation that topologically important proteins in a PPI network usuall

161 result, MtNadD is rendered inactive as it is topologically incompatible with substrate binding and ca

162 The copper centers are topologically independent of the weaving within the COF

163 Here we realize a topologically induced defect state in a chain of dielect

164 We demonstrate explicitly the topologically induced spatial localisation of quantum st

165 nter-ring penetrations and realizes a novel, topologically induced, glass transition.

166 profiling near surfaces or at interfaces of topologically inequivalent materials.

167 ry aims of which is providing nonmetric, but topologically informative, preanalyses of data which mak

168 estering negative supercoils and stabilizing topologically isolated loops in the DNA.

169 eractions between MukB dimers that stabilize topologically isolated loops in the DNA.

170 naphthalene (DNP) and two TTF units) that is topologically isomeric with the doubly interlocked [2]ca

171 ynamically less stable, less structured, and topologically less rigid compared to ApoE3.

172 within, while binding and hydrolyzing ATP to topologically link the clamp and ptDNA.

173 cillus subtilis, SMC-condensin complexes are topologically loaded at centromeric sites adjacent to th

174 ce than the strongest connections, which are topologically more clustered and shorter distance (spati

175 These extremely weak connections are topologically more random and longer distance than the s

176 hat, in quasi-static sense, the system shows topologically non-trivial band-gaps.

177 invariants, the predicted NaSn2 may display topologically non-trivial behavior and the known BaSn2 c

178 from protected surface states arising from a topologically non-trivial bulk band structure having str

179 eration where the role of the insulating yet topologically non-trivial bulk becomes explicit: an exte

180 d defects leads to knotted, linked and other topologically non-trivial field configurations.

181 x)Se(Te) grown along the (001) direction are topologically non-trivial in a wide range of film thickn

182 ed on Floquet analyses that one can generate topologically non-trivial insulators by periodically dri

183 tures may be captured by a planar graph, the topologically non-trivial knots and catenanes represent

184 an twist the quantum phase of electrons into topologically non-trivial knots-producing protected surf

185 including optomechanical metamaterials with topologically non-trivial properties.

186 of T c in MoTe2 by disorder, we suggest that topologically non-trivial s (+-) state is more likely to

187 Topologically non-trivial spin textures form a fundament

188 d displays information about protein links - topologically non-trivial structures made by up to four

189 ced bandgaps are discussed as candidates for topologically non-trivial surface states.

190 tworks are found to be non-polar (but with a topologically non-trivial texture for the square) and, h

191 ivity in T d-MoTe2, which was proposed to be topologically non-trivial, is of eminent interest.

192 om local atomic orbitals, and show which are topologically non-trivial.

193 Many topologically nontrivial 3D solitonic fields have been p

194 ersal symmetry is broken, it may introduce a topologically nontrivial bandgap.

195 l molecules, so that they generate a host of topologically nontrivial field and defect structures in

196 (3D) topological solitons are continuous but topologically nontrivial field configurations localized

197 Topologically nontrivial field excitations, including so

198 ui-Frequency Contour surfaces (EFCs) to form topologically nontrivial gaps in k space.

199 e studies enrich the theoretical research on topologically nontrivial phases in the Q1D lattice syste

200 gnetic-flux FISDW state, the system exhibits topologically nontrivial phases, which can be characteri

201 se portrait with a single equilibrium into a topologically nontrivial regime characterized by an expo

202 d facilitate identifying naturally occurring topologically nontrivial RNA molecules.

203 ple of a thermodynamically stable phase with topologically nontrivial solitonic field configurations

204 Here we report our finding that a topologically nontrivial spin texture known as a skyrmio

205 a novel quantum state of materials, possess topologically nontrivial valence and conduction bands th

206 The emergence of a topologically nontrivial vortex-like magnetic structure,

207 Insulating states can be topologically nontrivial, a well-established notion that

208 of a lasso peptide isopeptidase revealing a topologically novel didomain architecture consisting of

209 ange of novel phenomena which can arise in a topologically ordered state in the presence of strong in

210 nsulators is the bulk metallicity underneath topologically ordered surface states and the appearance

211 to determine how these various processes are topologically organized across medial frontal anatomy.

212 ss and two cellular component GO terms to be topologically orthologous for the two organisms.

213 in PINs of different species, which we term topologically orthologous functions.

214 Instead, topologically-partitioned atomic energies are trained by

215 f aromaticity have long been associated with topologically planar conjugated macrocyclic systems.

216 These metallic states are topologically protected against backscattering in the ab

217 rs owing to a set of gapless states that are topologically protected against backscattering.

218 n be classified by the dimensionality of the topologically protected band degeneracies.

219 tems with non-equilibrium fluxes can support topologically protected boundary modes that resemble sim

220 leads to a new mechanism to optically induce topologically protected chiral edge modes, facilitating

221 f angular momentum, finite Chern numbers and topologically protected chiral fermionic zero modes boun

222 Skyrmions are topologically protected continuous field configurations

223 Furthermore, they host topologically protected corner states carrying fractiona

224 l spectrum displays a sonic gap populated by topologically protected edge modes that propagate in onl

225 e electrons travel ballistically through the topologically protected edge states even in the presence

226 l captures many aspects of the phenomenon of topologically protected edge states for 2D bulk structur

227 numbers, indicating that the system can host topologically protected edge states.

228 ffect materials feature edge states that are topologically protected from backscattering.

229 , the gapless surface states of DSMs are not topologically protected in general, except on time-rever

230 Quantum braiding operations are topologically protected insofar as these modes are pinne

231 n to phononic crystals has made a remarkable topologically protected interface transport of sound, wh

232 More practically, we have built a topologically protected mechanism that can perform basic

233 ass of materials with an insulating bulk and topologically protected metallic surface states.

234 Such topologically protected one-dimensional chiral states at

235 resulting energy gap becomes populated with topologically protected one-way modes, which travel at t

236 ials where three-dimensional bands develop a topologically protected point-like crossing, a so-called

237 rm for the creation of coherent circuits and topologically protected quantum bits.

238 result opens new directions in the study of topologically protected quantum dynamics.

239 Magnetic skyrmions are topologically protected spin textures that exhibit fasci

240 Magnetic skyrmions are topologically protected spin textures with attractive pr

241 effects of random noise, showing that these topologically protected states are very robust against t

242 onstration of a photonic delay line based on topologically protected surface electromagnetic waves (T

243 he influence of light a single electron in a topologically protected surface state creates a surface

244 onse unambiguosly points out the presence of topologically protected surface states in the nanowires

245 e oscillations is attributed to transport in topologically protected surface states in the Sb2Te3 nan

246 Weyl semimetals host topologically protected surface states, with arced Fermi

247 Interestingly, these EFCs support topologically protected surface states.

248 optics, in which one-way edge propagation in topologically protected two-dimensional materials is ach

249 l behaviour, negative refractive indexes and topologically protected wave motion.

250 ators (TIs) are bulk insulators with exotic 'topologically protected' surface conducting modes.

251 a topologically trivial phase, give rise to topologically protected, dispersionless boundary states.

252 , including broadband acoustic isolation and topologically protected, nonreciprocal acoustic emitters

253 cal phase, implying that its dynamics may be topologically protected.

254 ace is given by the Witten index and thus is topologically protected.

255 eviation from a linear dispersion but remain topologically protected.

256 pursued in electronic systems, resulting in topologically-protected flat edge states.

257 Here we address the breakdown of the topologically-protected stability of such defects driven

258 This can lead to the appearance of topologically-protected surface modes at material interf

259 ophan residue at position 316 and with other topologically proximal sites in the V1V2 domain.

260 hich the quadrupole and octupole moments are topologically quantized electromagnetic observables.

261 s community detection, which finds groups of topologically related nodes.

262 When compared with a topologically related oxo-iron(IV) complex bearing an eq

263 bodies in the endocytic pathway and for the topologically related processes of viral budding and cyt

264 a macrocyclic tetracarbene ligand, which is topologically reminiscent of tetrapyrrole macrocycles th

265 However, how the rat whole-brain network is topologically reorganized to support persistent pain-lik

266 We identify topologically replicable gene networks enriched for dive

267 These novel AuNP frames topologically resemble NP nanorings and cyclic polymer c

268 We show that certain QSLs host distinct, topologically robust boundary types, some of which allow

269 technique, we demonstrate experimentally the topologically robust propagation of electromagnetic wave

270 The basal hypothalamic region is topologically rostral to the basal diencephalon and is c

271 chieved through hydro-dynamically smooth but topologically rough micropillars.

272 ions are intermodular, linking elements from topologically separable subsystems, and localize to know

273 o-oligomeric machines that catalyze multiple topologically similar membrane-remodeling processes.

274 s of how well the method can group (cluster) topologically similar networks.

275 report that DNs contain both RTN3 and REEPs, topologically similar proteins that can shape tubular en

276 ](+) where X = Li, Na, K, and Cs, versus the topologically similar structures of the protonated molec

277 sase with a DD(E/D) catalytic domain that is topologically similar to RNase H.

278 forin adopts a dimeric quaternary structure, topologically similar to the prototypical dual specifici

279 eedom with the effect being most apparent in topologically simple folds and less so if the fold is mo

280 on-native contacts in a conformation that is topologically simpler than the native state.

281 PAT to the periplasmic space are coupled and topologically split across the plasma membrane.

282 etic material in which a long-range order of topologically stable spin vortices known as skyrmions wa

283 Magnetic skyrmions are topologically stable whirlpool-like spin textures that o

284 ith pyramidal axons but apart from the (more topologically symmetric) axons of perisomatic-targeting

285 These are topologically tagged as low-degree nodes surrounded by h

286 Topologically, these flow states are a limit cycle and a

287 nin facilitates unfolding of kinetically and topologically trapped intermediates or (b) the chaperoni

288 n-trivial insulators by periodically driving topologically trivial ones.

289 stem experiences an abrupt transition from a topologically trivial phase portrait with a single equil

290 , when interfaced with one another or with a topologically trivial phase, give rise to topologically

291 ley-dependent spin-split bulk bands, even in topologically trivial photonic crystals.

292 In addition to the topologically trivial rotaxanes, whose structures may be

293 more likely to be realized in MoTe2 than the topologically trivial s (++) state.

294 nature is not, converting the system into a topologically trivial state even in the weak scattering

295 First, we show that a topologically trivial superconductor can be driven into

296 le the superconducting state of BiPd appears topologically trivial, consistent with Bardeen-Cooper-Sc

297 The multi-band edge states are topologically valley-protected and are obtained by simul

298 Topologically, we find that loops are strongly related t

299 a plasma that, unlike the general family, is topologically well defined in the form of a coherent tor

300 Flp recombination after first assembling the topologically well defined Tn3 resolvase synapse, it is