ライフサイエンスコーパス: higher order

1 nd) root orders had lower lignin compared to higher orders.

2 eveal that gC1qR clusters FXII and HK into a higher-order 500-kDa ternary complex.

3 Higher-order aberrations (HOA's) are exaggerated in eyes

4 Corneal higher-order aberrations (SA, coma, trefoil, and corneal

5 root mean square (RMS) postoperative ocular higher-order aberrations were 1.07 +/- 0.34, 0.67 +/- 0.

6 eratometry, thinnest pachymetry, and corneal higher-order aberrations were 60.89 +/- 10.9 D, 396.05 +

7 d surgically induced astigmatism) as well as higher-order aberrations were analyzed.

8 cy, safety, stability, cylinder vectors, and higher-order aberrations were evaluated, together with s

9 regulates the dynamics and the formation of higher-order actin structures, possibly through direct b

10 which is mediated through the recruitment of higher-order activator and repressor complexes, respecti

11 Higher order Ag(i)-MT complexes (i = 7-17) are formed in

12 Active control of higher-order anapoles and multimodal tuning are also inv

13 e that functional interactions between these higher-order and lower-order brain areas contribute to a

14 fficient mean for constructing programmable, higher-order, and complex DNA objects, as well as sophis

15 tics that benefit from target clustering and higher-order antigen-binding valency.

16 es for site-specific self-assembly to create higher ordered architectures.

17 messenger RNA structures, we reveal distinct higher-order architectures between pre-messenger RNAs an

18 e different symmetry elements needed to form higher-order architectures(1,6)-a daunting task for prot

19 ry visual area but amplified in a subsequent higher-order area.

20 ic connections between this region and other higher order areas of the avian pallium.

21 g the global hierarchy from early sensory to higher order areas.

22 sensory information moves through the brain, higher-order areas exhibit more complex tuning than lowe

23 otor area (SMA) is believed to contribute to higher order aspects of motor control.

24 ce lifetime imaging microscopy we identified higher order assemblies containing 40 molecules (median)

25 In this study we investigated whether higher order assemblies of 5-LO and FLAP included cytoso

26 last several years it has become clear that higher order assemblies on membranes, exemplified by sig

27 -lipoxygenase-activating protein (FLAP) into higher order assemblies on the nuclear envelope of mast

28 e associations of cPLA(2), FLAP, and 5-LO in higher order assemblies on the nuclear envelope support

29 However, the architecture of septin higher-order assemblies and their control mechanisms, in

30 r, are unclear, mainly because structures of higher-order assemblies are still lacking.

31 matography shows that trimer 4(F20Cha) forms higher-order assemblies in solution.

32 RADX compacts RPA-coated ssDNA filaments via higher-order assemblies that can capture ssDNA in trans.

33 n of the ribonucleoproteins (RNPs) and their higher-order assemblies were revealed.

34 we propose an alternative perspective: that higher-order associations instead arise from natural err

35 PAC) persisted after LOC, while responses in higher-order auditory regions were variable, with neuron

36 portant for guiding perceptual decisions and higher-order behavior.

37 in structure/function, and mental states and higher-order behaviors) and highlight consistencies acro

38 t that paranoia may be explained by stronger higher-order beliefs about others and increased sensitiv

39 w these channels are processed by first- and higher order brain areas has not been well characterized

40 l associated telencephalons communicate with higher order brain areas such as prefrontal cortex.

41 th the emergence of multisensory evidence in higher-order brain areas.

42 ts that use a self-report to directly engage higher-order brain circuitry.

43 t analog of the mammalian olfactory bulb, to higher-order brain regions in an adult animal brain.

44 Increased activation of higher-order brain regions related to multisensory integ

45 cal circuitry underlying the generation of a higher-order brain response (MMN) versus sensory respons

46 ap states, and we demonstrate the associated higher-order bulk-boundary correspondence.

47 morphs that differ in width and tendency for higher-order bundling.

48 e, we bring to bear recent research into the higher-order capacities that underpin deliberation-parti

49 egy to explore the exotic chemistry of novel higher-order carbenes in the gas phase.

50 nt cargo transfer, and the identification of higher order cell-cell interactions across a wide range

51 polymerization pathways collaborate to form higher-order cellular structures.

52 We also show that these structural and higher-order changes induced by the beta3-subunit do not

53 Higher-order characters that define these body plans wer

54 hemp (Amaranthus tuberculatus) suggests that higher order chromatin interactions contribute to the ge

55 up new avenues for modeling and visualizing higher order chromatin structure.

56 induces temperature-specific changes to the higher-order chromatin and gene expression profiles of h

57 his response is accompanied by compaction of higher-order chromatin and hindrance of mRNPs from engag

58 tics and reveal the rapid timescale by which higher-order chromatin architecture reconfigures during

59 We also demonstrate the potential of imaging higher-order chromatin disruption to detect high-risk pr

60 wide range of eukaryotic organisms fold into higher-order chromatin domains.

61 a gradual decompaction and fragmentation of higher-order chromatin folding throughout all stages of

62 al structures as well as inferred models for higher-order chromatin formation.

63 However, the higher-order chromatin organization in T. thermophila is

64 Here, we explored the higher-order chromatin organization in the two distinct

65 Overall, we demonstrated the distinct higher-order chromatin organization in the two nuclei of

66 states and chromatin marks, and reveal that higher-order chromatin structure after fertilization coi

67 Higher-order chromatin structure and DNA methylation are

68 al gradual decompaction and fragmentation of higher-order chromatin structure as an enabling characte

69 is critical to the functional stability of a higher-order chromatin structure.

70 g and modifying complexes, and disruption of higher-order chromatin structure.

71 i of the T. thermophila and suggest that the higher-order chromatin structures may play important rol

72 ne-related folding features without altering higher-order chromatin structures.

73 ements form specific interactions in dynamic higher-order chromatin structures.

74 ondensin-histone activity is responsible for higher order chromosomal structures, including recently

75 e well documented in cancer, but the fate of higher-order chromosomal structure remains obscure.

76 The revolution in understanding higher order chromosome dynamics and organization derive

77 Mechanisms establishing higher-order chromosome structures and their roles in ge

78 EPTOR KINASE (CIK) family co-receptors, with higher order cik mutant combinations phenocopying clv2/c

79 e can instead be more faithfully emulated by higher-order circuit elements that naturally express neu

80 ous feelings and their downstream effects on higher-order cognition.

81 ssociation networks that are responsible for higher-order cognition.

82 y the orbitofrontal cortex, severely impairs higher order cognitive and executive functions.

83 tion extracted from the visual system in the higher-order cognitive and affective neural systems.

84 This asymmetry suggests that higher-order cognitive and neural processes may be requi

85 Difficulties with higher-order cognitive functions in youth are a potentia

86 owing evidence for cerebellar involvement in higher-order cognitive functions including working memor

87 t is a critical building block for basic and higher-order cognitive functions.

88 t individual-differences in three domains of higher-order cognitive functions: General Ability, Speed

89 dings propose functional couplings among the higher-order cognitive network system as neural correlat

90 Functional couplings among the higher-order cognitive network system including the sali

91 tion networks coincides with improvements in higher-order cognitive processes such as executive funct

92 Predictions can be sourced from higher-order cognitive processes, such as schemas, but t

93 ry areas have been shown to be influenced by higher-order cognitive processes.

94 rsus affective processing and sensory versus higher-order cognitive processing.

95 order perceptual task, and categorization, a higher-order cognitive task, differs across voice gender

96 al networks, particularly those involved in "higher order" cognitive functions.

97 developmental behaviors and the formation of higher-order community structures.

98 kle subunits self-assemble into hexamers and higher-order complexes that can switch between open and

99 bosomes collide and form disome, trisome, or higher-order complexes.

100 In conclusion, LG4s adopt novel, higher-order, composite G4 structures directly contribut

101 How BAX monomers assemble into a higher-order conformation, and the structural determinan

102 amic equilibrium, we introduce a language of higher-order cooperativities and show how it can rigorou

103 This shows that higher-order correlation functions are extremely useful

104 work with primary sequence alone, neglecting higher-order correlations.

105 her this suppressive mechanism was driven by higher-order cortical areas.

106 y, followed by mid-level regions, while some higher-order cortical regions took more than 10 seconds

107 However, higher-order cslc mutants had significantly reduced XyG

108 GTP-binding proteins that self-assemble into higher order cytoskeletal structures.

109 obtain an extended Chern-Simons theory with higher order derivatives as well as two coupled Chern-Si

110 biguities due to potential contribution from higher order diffraction effects or other diffraction pl

111 particulate nitrate (pNO(3)(-))) provides a higher-order dimensional analysis of critical atmospheri

112 ses and APE1 in controlling the formation of higher-order DNA secondary structures to regulate transc

113 a few discrete time-points, ignoring complex higher-order dynamical features.

114 cuit tuned to discrete sensory events, and a higher-order edge subcircuit tuned to temporally distrib

115 macroscales, in mechanics, nonlocality is a higher-order effect that becomes appreciable only at the

116 Cross-module interactions allow for higher-order effects where past experience influences fu

117 ration and concentration system based on the higher-order electric properties.

118 exceptional nexus" (EX), which is not only a higher-order EP but also the cusp singularity of multipl

119 In the last example, higher order epistasis among four SVs affecting three re

120 eatment drives the emergence of pairwise and higher-order epistasis for fitness at loci underlying co

121 Higher-order exchange interactions and quantum effects a

122 ted for the majority of 2D vdW magnets where higher-order exchange interactions are appreciable.

123 ions (1 yeast gene to 2 human genes, 1:2) or higher-order expansions (1:>2) in the human lineage.

124 are due to its potential to polymerize into higher-order fibrillar structures.

125 genetic modifications in cancer, the in-situ higher-order folding of chromatin structure during malig

126 ed structures, which appeared to represent a higher-order form of gI.

127 ed structures, suggesting the formation of a higher-order form.

128 its are critical for the synchronization and higher order function of brain networks.

129 nteractions) forming a hitherto undescribed, higher-order, G4-based secondary structure we term a 'G4

130 The resulting models can capture complex higher-order genetic interactions near the data, but app

131 inding contributes to the establishment of a higher-order genome structure by demarcating the boundar

132 s, yet the mechanisms for establishing these higher order geometries remain poorly understood.

133 -like cell GLP1R expression patterns, reveal higher-order GLP1R organization including membrane nanod

134 nalize the empirically derived syndromes and higher-order groupings for applications to clinical serv

135 From the calculated energies of higher-order groupings of dimers discernible in the latt

136 romes of problems that tend to co-occur plus higher-order groupings such as those designated as inter

137 irac semimetals exhibit one-dimensional (1D) higher-order hinge Fermi arcs (HOFAs) as universal, dire

138 dated at the molecular level and expanded to higher-order homolog carbenes such as butadiynylcyclopro

139 ork from which to investigate more abstract, higher-order human learning and knowledge generalization

140 hylNet can study cellular differences, grasp higher order information of cancer sub-types, estimate a

141 n our complex environment requires continual higher order integrated spatiotemporal information.

142 entral complex (CX) in the insect brain is a higher order integration center that controls a number o

143 robust framework for identifying changes in higher-order interactions among genes.

144 Higher-order interactions appear facilitated by the C-te

145 of scHOT by studying coordinated changes in higher-order interactions during embryonic development o

146 Our results provide a view of higher-order interactions in angiogenesis that has poten

147 g and provides a framework for interrogating higher-order interactions using single-cell data.

148 uch as a discontinuous transition induced by higher-order interactions.

149 rsFC between left fusiform gyrus (L-FG) and higher-order language systems predicts oral reading beha

150 nd neurons in primary visual cortex (V1) and higher-order, lateromedial (LM) and rostrolateral (RL) a

151 ee-dimensional anomalous Hall insulators and higher-order magnetic semimetals.

152 ering has been a long-appreciated feature of higher order mammalian brain structures but the extent t

153 Higher-order many-body errors are small in both SCAN and

154 We, therefore, revisited higher-order Markov models and assessed their performanc

155 Higher-order Markov models have been used with caution,

156 ory or across space and accommodates various higher-order measurements including variability or corre

157 hat low-level multisensory processes predict higher-order memory and cognition already during childho

158 An apparent exception is the higher order middle temporal visual area (MT), which app

159 les that further assemble and transform into higher-order mineral structures.

160 ing recent evidence of better performance of higher order models such as Markov models of order one,

161 Comparative assessment of higher-order models (HOMs, 9th order or higher) with int

162 , potentially in line with counterfactual or higher-order models of confidence formation in detection

163 bled exploitation of the predictive power of higher-order models.

164 of supramolecular receptors and sensors into higher-order molecular analytical devices with advanced

165 ating a substantial barrier to understanding higher-order molecular and biological systems of disease

166 ent interactions for spatial organization of higher-order molecular assemblies that exhibit emergent

167 non-motor proteins crosslink filaments into higher-order motifs, such as overlapping bundles.

168 l system to examine response magnitudes in a higher-order motion processing region [middle temporal a

169 We find that higher-order motion stimuli, gliders, induce optomotor b

170 Early neonate deaths, stillbirths, and higher order multiple births were excluded from analysis

171 However, a higher-order multiplexing dPCR assay for measuring SMN1

172 In summary, presented here is a simple higher-order multiplexing solution on a novel digital PC

173 n situ RCA toward easier sample preparation, higher-order multiplexing, autofluorescence-free detecti

174 ens have the potential to routinely generate higher-order mutant collections and facilitate the chara

175 The higher-order mutants grew with mild tissue-specific phen

176 mers in an effort to realize the prospect of higher-order, nanoscale control over associative cross-l

177 were pooled, but neither mNBH nor preformed higher-order NBH complexes (oNBH) were acutely synaptoto

178 last-mediated species dispersal where we use higher-order network analysis to identify critical shipp

179 Here, we identify changes in higher-order network properties of freely behaving roden

180 nents within vesicles reorganized actin into higher-order networks.

181 might be established more conclusively when higher-order neuronal interactions are mapped to the cho

182 ired paradigm to drive auditory responses in higher-order neurons, our results demonstrate that mouse

183 ns (PNs), providing olfactory information to higher-order neuropils via parallel pathways, and local

184 ne cyclopropanation offers a direct route to higher-order, non-aromatic carbocycles; however, the inh

185 Retroviral integrase forms a higher order nucleoprotein assembly (intasome) to cataly

186 that this repositioning is incompatible with higher-order nucleosome stacking, which involves contact

187 eb to the TSCC, and also hints at functional higher order oligomerisation, which has previously been

188 sembly-disassembly dynamics, persistent Drp1 higher-order oligomerization over membranes is sufficien

189 Higher-ordered oligomerization of this protein forms hex

190 to affect the pathways leading to symmetric higher-ordered oligomerization, and thereby affect cruci

191 Trimers and higher-order oligomers composed of trimers are thought t

192 exist as a mixture of monomers, dimers, and higher-order oligomers in cell membranes and show that o

193 ivity than its ability to insert and to form higher-order oligomers in model membranes.

194 nking, revealing a 1:2 complex that can form higher-order oligomers in solution, and we solved the cr

195 th and truncated arrestin-3 form trimers and higher-order oligomers in the presence of IP(6); we show

196 hrough its transmembrane domain and can form higher-order oligomers that arrange MRAP2 monomers in a

197 antigenic than the E. coli protein, and form higher-order oligomers.

198 exists as non-covalent dimers, trimers, and higher-order oligomers.

199 minantly not only into trimers but also into higher-order oligomers.

200 ers contain structural elements suggesting a higher order organization of their components.

201 nal repression, how H3K9me3 regulates genome higher-order organization and transcriptional activity i

202 the level of single nucleosomes rather than higher-order organization of more than one nucleosome.

203 We also draw attention to the higher-order organization of plant specialized metabolis

204 complex topologies that display features of higher-order organization; 3) IRE1 clusters contain a di

205 accuracy has not been rigorously tested for higher-order oxides.

206 of newly generated NAP acids was mainly from higher-order oxygen species (O(5)-O(6)) with increased h

207 h of 30 nm that is expected from theories of higher order packaging.

208 ults point to the crucial role of excitatory higher-order patterns in sustaining asynchronous activit

209 Higher-order patterns, such as triplet or triangle motif

210 dG(6) at neutral pH, bm-Calpha-PNA 1 forms a higher order pentameric double duplex of a triplex compo

211 anding of the role of sensory uncertainty in higher-order perception.

212 for other flatfishes in that no evidence of higher order periodicity was present.

213 Metaplasticity is a higher order plasticity which regulates cortical respons

214 nal dynamics were dissociated between S1 and higher-order PMv prior to return of consciousness.

215 l vector vortex beams, a particular class of higher-order Poincare sphere beams, are generalized form

216 sported across the epithelium, as dimers and higher-order polymers, by the polymeric immunoglobulin r

217 across the brain, but gradually uncouple in higher-order polysensory areas.

218 Moreover, higher-order power law dependence of photoluminescence i

219 pectral oscillatory responses in visual and 'higher-order' prefrontal cortices.

220 bral cortex, suggesting a prominent role in 'higher order processes'.

221 cent evidence suggests that modifications in higher-order processing centers, and not in retinal comp

222 efficiency in the population code and enable higher-order processing of visual information, such as f

223 nzymatic digestion of nucleic acids, whereas higher-order PrP assemblies derived from pooled mM1000,

224 when needed, they form mixed assemblies for higher-order purposes, as in the case of ribosomal prote

225 ion symmetries, it is challenging to achieve higher-order quantized multipole moments, such as octupo

226 studies focusing on RBP-RNA interactions and higher-order RBP coregulation and describe approaches th

227 However, we found that higher-order regions could rapidly forget prior context.

228 it regulation, while emerging adults recruit higher-order regions involved in the extraction of seman

229 These studies have also shown that higher-order regions such as the prefrontal cortex are c

230 Many empirical networks incorporate higher order relations between elements and therefore ar

231 prefrontal and temporoparietal cortex; these higher-order representations, which were sensitive to se

232 ll-optical tuning of light scattering at the higher-order resonant mode under a low incident light in

233 ed bandgap renormalization, producing strong higher-order resonant modes in single NPs with Q factors

234 We considered a key higher order role: tracking progress throughout an actio

235 ation samples provide norms for syndrome and higher-order scales for each gender, at different ages,

236 his study demonstrates a significant role of higher-order schemas in pain perception and indicates th

237 ortex, combined with diffuse reactivation of higher-order semantic representations.

238 ve visual input and which may be involved in higher order sensorimotor integration.

239 nes likely play in modulating spider vision, higher order sensorimotor processing, and motor patterni

240 th CBS had atrophy connected to a network of higher-order sensorimotor regions beyond perirolandic co

241 f stimulus history, functions carried out in higher-order sensory areas such as the posterior parieta

242 ely resemble multisensory features of other, higher-order sensory areas.

243 provides evidence to suggest that the TMJ in higher order species are in fact vascularized.

244 nts a feasible pathway to glioma modeling in higher order species.

245 een the spike trimers, allowing formation of higher-order spike complexes.

246 is interplay between first-order statistics, higher-order statistics, and configuration space growth.

247 the coordination of enzymatic catalysis with higher-order structural organization of substrate maximi

248 We show the yeast ISW1a remodeler has such higher-order structural specificity, as manifested by la

249 should be a valuable CL reagent for protein higher order structure characterization by MS.

250 ve interactions between neighboring SBPs and higher order structure formation.

251 merged as a premier tool to characterize the higher order structure of protein therapeutics and in pa

252 , thus providing a better overall picture of higher order structure.

253 The higher-order structure (HOS) of proteins plays a critica

254 dor representations is therefore mediated by higher-order structure in the wiring diagram that is ada

255 three such ligands required to guarantee the higher-order structure integrity.

256 in model, can be largely accommodated by the higher-order structure of chromatin.

257 Intuitively, learning the higher-order structure of statistical relationships shou

258 ith the posterior medial thalamic nucleus, a higher-order structure that carries both top-down and bo

259 Genomic DNA is folded into a higher-order structure that regulates transcription and

260 can interactions that drive the formation of higher-order structure within the glycan shield.

261 The organization of chromatin into higher order structures is essential for chromosome segr

262 epigenetic factors, organizes the genome in higher order structures required for transcriptional con

263 ides to the protein induced the formation of higher order structures that may represent biocrystallin

264 Proteins adopt different higher-order structures (HOS) to enable their unique bio

265 Understanding the complexities of protein higher-order structures and dynamics requires integrated

266 homodimerization, a crucial step in forming higher-order structures during assembly of the CSC.

267 termines its intrinsic roles in facilitating higher-order structures in CSCs.

268 Characterization of the higher-order structures in idursulfase (iduronate-2-sulf

269 f-assembly of molecular building blocks into higher-order structures is exploited in living systems t

270 gered, likely important for the formation of higher-order structures of different shapes.

271 ence of the PAR confers unique chromatin and higher-order structures that are crucial for recombinati

272 ary-structure epitopes found on E dimers and higher-order structures that form the viral envelope.

273 diffusion-driven process, while formation of higher-order structures was complex and involved self-te

274 lexes that assemble into filaments and other higher-order structures, such as rings or hourglasses, a

275 complexes that can assemble in filaments and higher-order structures.

276 ve demonstrated that full-length AMELX forms higher-order supramolecular assemblies that regulate ord

277 izability tensor, which captures independent higher-order symmetric-to-symmetric and symmetric-to-ant

278 nergistic mixtures; and (iii) the search for higher-order synergistic interactions.

279 adapt to new tasks, we propose metamappings, higher-order tasks that transform basic task representat

280 tofugal pathway (the entopallium) with their higher order telencephalon, nidopallium caudolateral (NC

281 We describe an approach, scHOT-single-cell higher-order testing-which provides a flexible and stati

282 th the functionally distinct first-order and higher-order thalamic nuclei to form molecularly defined

283 t a model in which L6CTs modulate first- and higher-order thalamus through parallel excitatory and in

284 order thalamus and also sends projections to higher-order thalamus, yet how it engages the full corti

285 etains the PAAR domain is capable of forming higher-order, thermostable complexes with VgrG, yet thes

286 cultural learning, and the attempt to ground higher order thinking in embodied theory.

287 topological crystalline insulator (TCI), and higher order topological insulator.

288 ment task, indicating the importance of this higher-order topological feature for conscious cognition

289 Our work offers a pathway to explore higher-order topological states in 3D classical platform

290 allows for the unambiguous identification of higher-order topology, even without in-gap states, and w

291 Our study uncovers an unrecognized higher-order-translation regulatory mechanism in a metaz

292 niculate nucleus (first-order) and pulvinar (higher-order) using optogenetics and extracellular elect

293 Direct strategies have been sought for a 'higher order' variant of this reaction via the coupling

294 Our results suggest that higher-order visual areas may fill in the missing inform

295 e axon regeneration and correct targeting of higher-order visual centers.

296 ng memory performance, implicating disrupted higher-order visual processing.

297 ing the cerebellum, early visual cortex, and higher-order visual regions spanning occipital and tempo

298 r time-and second-order cues, by correlating higher-order visual statistics.

299 Higher-order visual thalamus communicates broadly and bi

300 an its reported statistics and that n-grams, higher order word combinations that humans have difficul