ライフサイエンスコーパス: modal

1 l activation is associated with a dynamic bi-modal 3D organization, whereby the genes switch autonomo

2 To answer this, we present MODAL: a Modular Overlap-Directed Assembly with Linkers

3 ctigraphy, heart rate) largely lack in cross-modal ability, are inconvenient and/or stigmatizing.

4 the results demonstrate that increased cross-modal activation of auditory brain regions by visual spe

5 The aim of this study was to examine cross-modal activation of auditory brain regions by visual spe

6 which are thought to be the basis for cross-modal adaptation.

7 in the binocular cortex is followed by cross-modal adaptations in the monocular cortex, in which whis

8 d Mie scattering signatures, suggesting that modal aerosol concentrations can be retrieved.

9 sample included 16,332 high school seniors (modal age, 18 years) in the United States.

10 rveys of 8th, 10th, and 12th-grade students (modal ages 13-14, 15-16, and 17-18 years, respectively),

11 Integrative multi-modal analyses generally do not increase predictive sign

12 t, we used our recently developed Green-Kubo modal analysis (GKMA) method to study amorphous silicon

13 the recently developed interface conductance modal analysis (ICMA) method along with a new compliment

14 The waveguiding is revealed through the modal analysis of the periodic patterns observed around

15 Detailed modal analysis reveals the lasing mode matches with the

16 onstrating simultaneous spatial and temporal modal analysis, micrometer vibrations of a metamaterial

17 ber of beeps or the number of flashes in uni-modal and bi-modal conditions.

18 We show that modal and chromatic dispersions in fiber lasers can be c

19 their unique properties while achieving the modal and polarization control that are essential for th

20 We show that the modal and propagation length characteristics of the SPhP

21 analyzed each modality separately using uni-modal approaches based on several state-of-the-art super

22 adult ME mice specifically reduces the cross-modal aspect of reactivation.

23 Here, we wanted to probe whether such cross-modal attention effects also target the vestibular syste

24 In this study we investigate cross-modal attention effects in the human vestibular cortex.

25 ivity in sensory systems is subject to cross-modal attention effects.

26 r the visual or auditory modality in a cross-modal attention task.

27 consequences of this impairment during cross-modal attention tasks, however, are unclear.

28 These findings suggest cross-modal attentional modulation in the vestibular cortex.

29 y or repetition suppression, we used a cross-modal (audiovisual) omission paradigm and used functiona

30 port on a behavioural strategy whereby cross-modal (auditory-visual) training reinstates visuomotor c

31 ction with FBP, ITER and a novel, iterative, modal-based reconstruction (IMR) algorithm.

32 capable of projecting optical beams onto any modal basis.

33 the Met-35 displaying the most complex multi-modal behavior.

34 investigate the cellular mechanism for cross-modal behavioral interactions.

35 flexibility of the flow-diverter with multi-modal bending.

36 Trim28(+/D9) mutant mice exhibit a bi-modal body-weight distribution, with isogenic animals ra

37 l perception and in the absence of any cross-modal boosting.

38 sensory deprivation leads to important cross-modal brain reorganization that is paralleled by enhance

39 This interaction, termed stimulated inter-modal Brillouin scattering, decouples Stokes and anti-St

40 It is shown that the tri-modal CCRW found to describe accurately the movement pat

41 pression corresponded directly with discrete modal changes in polythymidine tract length.

42 The modal characterization of various families of beams is a

43 Then, we applied integrative multi-modal classification techniques.

44 sue, we introduce a novel approach for multi-modal co-registration called Multi-scale Spectral Embedd

45 Prior research on modal cognition asks how humans explicitly and deliberat

46 and reasoning over sets of possibilities, or modal cognition, supports diverse kinds of high-level ju

47 udgements was observed for the learned cross-modal combinations than for new combinations of the same

48 Generally, gestures and multi-modal combinations were more flexibly used to communicat

49 We show that the cross-modal component does not occur in adolescence because of

50 lgorithm was adapted to estimate the aerosol modal concentrations from its hyperspectral extinction s

51 was found to depend on the relative aerosol modal concentrations, especially when there is a substan

52 Crucially, in a cross-modal condition, we replicated previous unimodal finding

53 egration predicts improved reliability in bi-modal conditions.

54 or the number of flashes in uni-modal and bi-modal conditions.

55 Nanoscale modal confinement is known to radically enhance the effe

56 diation pressures, produced by subwavelength modal confinement, yield enhancement of Brillouin nonlin

57 tion information and, under sufficient cross-modal congruence, integrate it into a multisensory repre

58 Additionally, the dual-modal construct was evaluated in an orthotopic murine pa

59 We studied the modal contributions to heat conduction at crystalline Si

60 behavior differently than neurons with high modal controllability, thought to influence the network

61 elf-looping connections to neurons with high modal controllability.

62 Modal copy number was 4 (range 2-7).

63 A genetic cross-modal correlation was seen between the ventral attention

64 Some cross-modal correlations were purely phenotypic, such as that

65 Tuning the modal coupling between the two allows optimization of th

66 However, our understanding of modal coupling is largely restricted to clamped-clamped

67 mpatible mode-division multiplexing with low modal crosstalk and loss.

68 plifiers, lasers, and sensors in which inter-modal crosstalk imposes a fundamental performance limita

69 r modes, which usually results in high inter-modal crosstalk.

70 ultimately sets a fundamental limit on inter-modal-crosstalk for FMFs.

71 ponds to prediction violations using a cross-modal cueing paradigm.

72 roduct to differences in the timing of cross-modal cues than do earlier mechanistic hypotheses based

73 s regular coupling of any given set of cross-modal cues than does the otherwise "impoverished" labora

74 Cross-modal cues that are near-simultaneous are likely to be d

75 We introduce a novel method of multi-modal data analysis that is designed for heterogeneous d

76 While multi-modal data does contain distinct biological information

77 f the method for brain extraction from multi-modal data of 50 newborns is evaluated and compared with

78 ible, the next frontier is to collect "multi-modal" data for the same set of subjects and conduct int

79 co-visualization of the multi-scale or multi-modal datasets the technique promises to provide insight

80 the selective pressures that maintain multi-modal defence mechanisms or that may favour one over the

81 erestingly, our recordings showed also cross-modal dendritic interaction because auditory evoked PSPs

82 drites of the Mauthner cell, we report cross-modal dendritic interactions via backpropagating postsyn

83 o provide a sensitive, dose-dependent, multi-modal description of the response to mechanical insult.

84 We propose to use a high-dimensional multi-modal descriptor that combines multiple texture features

85 owbirds (Molothrus ater) consists of a multi-modal display, including song as well as postural and wi

86 any pair of isolates was nine SNPs, and the modal distance between isolates was two SNPs.

87 gly, WarA influences P. aeruginosa O antigen modal distribution and interacts with the LPS biogenesis

88 es in membranes, whereas PopB displayed a bi-modal distribution with 6 and 12 subunits peaks.

89 sed-phase chromatography, gave rise to multi-modal distributions of data.

90 that infants infer category boundaries from modal distributions of speech sounds along acoustic cont

91 ying sensory selection, we developed a cross-modal divided-attention task in mice that allowed geneti

92 The modal dose of guanfacine at week 8 was 3 mg/day (range:

93 8 was 3 mg/day (range: 1-4 mg/day), and the modal dose was 3 mg/day (range: 2-4 mg/day) for placebo.

94 ons were similar in polydispersity with mono-modal droplet distribution and size of 0.43mum that carr

95 n this study, we present and evaluate a dual-modal, dual-channel light endoscope that allows quantita

96 In 28 unique trials, the modal e-intervention was brief feedback on alcohol consu

97 lectron spin in determining the direction of modal edge propagation.

98 neural mechanisms of attention and of cross-modal effects across visual and auditory processing.

99 ion for many previous failures to find cross-modal effects in experiments where the visual load effec

100 g of V1 diminished but did not abolish cross-modal effects on S1 oscillatory activity, while leaving

101 Drosophila Hx exhibits cross-modal enhancement of visual responses by paired odor, an

102 The amplitude of this cross-modal ERP was predictive of perceptual judgments about t

103 mate is more reliable than the component uni-modal estimates.

104 genetic association studies along with multi-modal evidence for hippocampal dysfunction in schizophre

105 iation cortex mediates the encoding of cross-modal experience in the midbrain.

106 Multisensory neurons in animals whose cross-modal experiences are compromised during early life fail

107 naffected by different combinations of cross-modal feature, suggesting that featural similarity of cr

108 e-learning classifier to recognize the multi-modal 'fingerprint' of each cortical area.

109 ringency, and bitterness intensity via cross-modal flavour interactions.

110 hase showing that informal exposure to multi-modal foreign language leads to foreign language vocabul

111 screte, time-correlated perturbations to all modal frequencies of the device.

112 fording acoustically deprived AAF with cross-modal functionality.

113 halide-capped quantum dots that exhibit high modal gain (1,200 cm(-1)) and an ultralow amplified spon

114 Modal gain and hence laser spectra are highly sensitive

115 Surprisingly, the modal gain in the nanocavity with the externally amplifi

116 es of the effective refractive index and the modal gain is described by the linewidth broadening fact

117 al optical losses of 10-15 cm(-1) and a peak modal gain of 24 cm(-1), corresponding to a material gai

118 in subunits, previous mathematical models of modal gating are coarse grained at the level of whole-ch

119 in the kinetics of individual subunits, then modal gating can arise as an emergent property of channe

120 ing biophysical mechanisms that give rise to modal gating in this and most other channels remain unkn

121 ating to larger pressures, (3) appearance of modal gating of MS channels and small conductance channe

122 responses to changing ligand conditions, and modal gating statistics.

123 Here we propose an origin for modal gating, by modeling the kinetics of ligand binding

124 conformational changes are not required for modal gating.

125 We observe bi-modal gene expression, a previously-described phenomenon

126 ls leads to the appearance of bistable or bi-modal growth behaviors, ultrasensitivity to external gro

127 hotspots, distinguishing hotspots from mono-modal H3K4me1 singletons.

128 Multi-modal image co-registration via optimizing mutual inform

129 mption that intensity distributions of multi-modal images follow a consistent relationship.

130 Using a multi-modal imaging approach, we visualized the NEC in situ fo

131 described nanoplatform as an effective multi-modal imaging enabled PTT agent.

132 ivo multi-photon and magnetic resonance dual-modal imaging probe.

133 Our multi-modal imaging, combined with multivariate statistical mo

134 d-polyaniline nanoparticle (RDLPNP) for dual-modal imaging-guided enhanced PTT efficacy is reported f

135 orescence (NIRF) and photoacoustic (PA) dual-modal imaging-guided synergistic chemo-photothermal ther

136 nd deep penetration via in vivo NIRF/PA dual-modal imaging.

137 (PAI)/magnetic resonance imaging (MRI) dual-modal imaging.

138 strongly indicating the possibility of cross-modal impacts of noise pollution on information use [3].

139 ytical techniques now enable us to use multi-modal information in order to develop complex 'biomarker

140 s and compromised postnatal pruning of cross-modal input.

141 ving the temporal relationship between cross-modal inputs, an important cue for multisensory integrat

142 For multi-modal inputs, we found that larvae linearly combine olfa

143 the events that provide the convergent cross-modal inputs.

144 ts this view, the neural mechanisms of cross-modal integration in primary sensory areas, such as the

145 These data represent a new example of cross-modal integration in the primary sensory thalamus.

146 ANCE STATEMENT The neural substrate of cross-modal integration is not limited to specialized cortical

147 Full or partial cross-modal integration predicts improved reliability in bi-mo

148 ttractor dynamics, temporal coding and multi-modal integration.

149 The degree of cross-modal interaction decreased with age: the youngest obser

150 ur findings demonstrate a value-driven cross-modal interaction that affects perception and stimulus e

151 We also found that the cross-modal interaction was frequency-sensitive at low tempora

152 Cross-modal interactions are very common in perception.

153 Cross-modal interactions between sensory channels have been sh

154 Nonlinear modal interactions have recently become the focus of int

155 that V1 is involved in the encoding of cross-modal interactions in a more versatile way than previous

156 In this work we discuss nonlinear modal interactions in these laser systems under steady s

157 erceptual ambiguity is one function of cross-modal interactions.

158 ng due to instabilities induced by nonlinear modal interactions.

159 de (prGO) film is deposited on a fiber-optic modal interferometer, acting as both the fluorescent que

160 We found that the modal intron length range of 60-70 nt represents a local

161 These results, together with further multi-modal investigations, are warranted to provide important

162 MODAL is accompanied by a custom software tool that desi

163 r neurons are a fascinating product of cross-modal learning.

164 y detection method, CMsearch, based on cross-modal learning.

165 s with a distinct, geometrically determined, modal length.

166 that dissipates heat while offering minimal modal loss.

167 Using multi-modal magnetic resonance images from the Human Connectom

168 In this study, we hypothesized that multi-modal magnetic resonance imaging (MRI) can reveal the ef

169 em by optical coherence tomography and multi-modal magnetic resonance imaging in healthy subjects and

170 generation of new hypotheses regarding cross-modal mapping, particularly whether it occurs via direct

171 ay a critical role in the emergence of cross-modal mappings, the acquisition of language, and the evo

172 erimental evidence demonstrates robust cross-modal matches between music and colors that are mediated

173 al experiments showed similarly robust cross-modal matches from emotionally expressive faces to color

174 The phase and modal matching conditions in this scheme are investigate

175 ol subjects, using a new test based on cross-modal matching of flavours to words and pictures.

176 integrates within the nucleolus via a multi-modal mechanism involving multivalent interactions with

177 ession or functional immaturity of the cross-modal mechanisms.

178 rbate 80 resulted in 3 twofold and 2 twofold modal MIC decreases for Enterobacteriaceae and Pseudomon

179 urements were outside +/-1 dilution from the modal MIC, suggesting enhanced reproducibility.

180 This effect depended on the cross-modal modulation strength and was absent when modulation

181 r results suggest that attention has a cross-modal modulatory effect on the vestibular cortex during

182 Therefore, a multi-modal molecular imaging (MRI & MALDI IMS) approach was e

183 tic domains), quality of life (HRQOL), multi-modal MRI (fMRI go/no-go task, volumetry and MR spectros

184 uronal changes in brain function using multi-modal MRI in patients with cirrhosis.

185 Multi-modal MRI may help evaluate the pathophysiological mecha

186 Multi-modal MRI techniques have identified biomarkers that cou

187 Using longitudinal multi-modal MRI, we monitored hippocampal injury and tissue re

188 rt multiple band-edge modes capable of multi-modal nanolasing at programmed emission wavelengths and

189 for the fabrication of tumor-targeted multi-modal nanotheranostic agents, which enables precision an

190 a novel method for brain extraction of multi-modal neonatal brain MR images, named ALFA (Accurate Lea

191 s paper, we use the data acquired from multi-modal neuroimaging data to diagnose PD by investigating

192 corroborating our previous preliminary multi-modal neuroimaging findings.

193 ual attention tasks in the presence of cross-modal noise distraction.

194 deepening penitentes reproduce both the tri-modal (north-south, east-west and northeast-southwest) o

195 The strongest prognostic factor was the modal number of chromosomes (MNC): the 6-year EFS of 51-

196 Our results show that spontaneous cross-modal object recognition and dynamic weighting of sensor

197 , is capable of performing spontaneous cross-modal object recognition and that the sensory inputs are

198 So far, spontaneous cross-modal object recognition has only been shown in a few ma

199 Furthermore we show that cross-modal object recognition is influenced by a dynamic weig

200 on of auditory and visual streams into cross-modal objects, enabling listeners to better attend the t

201 In comparison with P45, emergent cross-modal participation was demonstrated in P90 animals, alt

202 A bi-modal particle size distribution was found for all mater

203 h visually complex structures, such as multi-modal peaks extended over large genomic regions.

204 positron emission tomography (PET) and dual modal PET-MRI.

205 eport the development of PET, NIRF, and dual-modal (PET/NIRF) imaging agents, using 5B1, a fully huma

206 uropeptide signaling leads to specific cross-modal plastic changes in neural circuit connectivity, en

207 Together these findings suggest that cross-modal plasticity by visual speech does not exert previou

208 ever, neuroscientific understanding of cross-modal plasticity following cochlear implantation has bee

209 We show that the presence of cross-modal plasticity in a higher-order auditory area does no

210 frontoparietal input as a mechanism of cross-modal plasticity in blindness.

211 ABAA receptor alpha1 subunit restricts cross-modal plasticity in P45 mice but is relaxed in adults to

212 Understanding cross-modal plasticity in response to sensory loss is essentia

213 Our results support the idea that cross-modal plasticity in the case of early sensory deprivatio

214 Therefore, cross-modal plasticity in the deaf higher-order auditory corte

215 Therefore, cross-modal plasticity might conflict with restoration of audi

216 According to this view, cross-modal plasticity takes over the unused cortex and reassi

217 Sensory loss induces cross-modal plasticity, often resulting in altered performance

218 the macroscopic mechanisms underlying cross-modal plasticity, only scant information exists about it

219 ite life-long auditory deprivation and cross-modal plasticity.

220 evelopment and deprivation can lead to cross-modal plasticity.

221 c inhibition also regulates ME-induced cross-modal plasticity.

222 may influence the nature and extent of cross-modal plasticity.

223 veral extravisual networks, suggesting cross-modal plasticity.

224 And is it retained despite cross-modal plasticity?

225 ponse to precipitation with a maximum around modal precipitation, whereas rare species peaked at high

226 We propose that this cross-modal predictive facilitation involves multisensory conv

227 is allows us to produce output beams of high modal purity, which are well defined in three dimensions

228 We also show that forward inter-modal Rayleigh scattering ultimately sets a fundamental

229 tentiation is followed by a late overt cross-modal reactivation by whiskers.

230 ME in adulthood also prevents the late cross-modal reactivation component, thereby converting the out

231 nd optical properties being capable of multi-modal readout.

232 period in which gradual recruitment of cross-modal recovery upon long-term ME coincides with the tran

233 on with a cochlear implant (CI) due to cross-modal recruitment of auditory brain regions.

234 eech processing, and negatively by the cross-modal recruitment of the right temporal cortex during an

235 dies suggest that experience-dependent cross-modal regulation of the spared sensory cortices may be m

236 Cross-modal regulation of visual performance by olfactory stim

237 at auditory cortex is known to undergo cross-modal reorganization following deafness, such that behav

238 Cross-modal reorganization following the loss of input from a

239 Cross-modal reorganization in the auditory and visual cortices

240 These results indicate that cross-modal reorganization is less detrimental for neurosensor

241 Such cross-modal reorganization may either compete with or compleme

242 hat higher-order areas involved in the cross-modal reorganization show more auditory deficits than pr

243 processing to DZ may contribute to the cross-modal reorganization that functionally manifests as supe

244 spatial processing following potential cross-modal reorganization.

245 r-order areas is limited to effects of cross-modal reorganization.

246 al correlations potentially related to cross-modal representation.

247 d that learning changes the overlap of cross-modal representations.

248 rience-, and cortical region-dependent cross-modal response to unilateral visual deprivation.

249 Upon learning, both prevalence of cross-modal responsive neurons and their breadth of tuning inc

250 emonstrate spatially scattered visual (cross-modal) responsiveness in the DZ, but show that this did

251 f individual mechanisms and reveal the multi-modal role played by the cardiotonic and scavenging acti

252 ing sponges for signalling purposes in multi-modal sexual displays.

253 focus towards compact cities-that support a modal shift away from private motor vehicles towards wal

254 use urban designs that encourage a transport modal shift away from private motor vehicles towards wal

255 to produce low motorised mobility, namely a modal shift from private motor vehicles to walking, cycl

256 Using WIFE, we developed two modal shift scenarios: one focusing on intraregional fre

257 ity can be synchronized by a congruent cross-modal signal in a frequency-selective way, suggesting th

258 We found that this cross-modal signaling between the mechanosensory and olfactory

259 ature on the roles of neuropeptides in cross-modal signaling, by showing how activity-dependent neuro

260 Social interactions involve multi-modal signaling.

261 suggesting that featural similarity of cross-modal signals may not modulate cross-modal temporal infl

262 The bars were accompanied by different cross-modal signals that onset synchronously or asynchronously

263 n there is a substantial overlap between the modal spectral signatures.

264 only achieved based on the Zeeman effect, or modal splitting in ferromagnetic atoms induced by a magn

265 This study observes increased modal splitting of two plasmon-phonon polariton hybrid m

266 duced event-based model for use with a multi-modal sporadic disease data set.

267 gether, these results demonstrate that cross-modal statistical regularities are used to generate pred

268 w that the gustatory cortex represents cross-modal stimuli according to their sensory identity, and t

269 Indeed, it is poorly understood if cross-modal stimuli evoke unique or overlapping representation

270 oncerning the neural representation of cross-modal stimuli remain open.

271 auditory responses during attention to cross-modal stimuli.

272 auditory responses during attention to cross-modal stimuli.

273 ed equal numbers of flashes and beeps for bi-modal stimuli.

274 the individual and shared features of cross-modal stimulus constituents, such as contrast, frequency

275 h three different assembly technologies, the MODAL strategy gives assembly of both yeast and bacteria

276 evels and reveal the non-trivial topological modal structure exclusive to non-Hermitian systems.

277 : see text] is essentially determined by its modal structure.

278 ximate number system theory, including cross-modal studies, animal studies, and so forth.

279 neurons exhibit the diagnostic form of cross-modal suppression, whereas unisensory neurons in area MT

280 on sources, indicative of regulation by a bi-modal switch, but it is not clear how these switches are

281 at transcription itself is a component of bi-modal switches, facilitating reciprocal expression in ge

282 We present a multi-modal system capable of simultaneously acquiring both si

283 ouse gas emissions, progressively raises the modal temperature threshold of each ENSO cycle.

284 These dynamic cycles and the increasing modal temperatures appear to influence the dynamics of c

285 f cross-modal signals may not modulate cross-modal temporal influences in short time scales.

286 varying radius, while manipulating the cross-modal temporal relationships.

287 Overcoming MDR generally involves multi-modal therapeutic approaches that integrate enhancement

288 We thus propose a multi-modal therapeutic paradigm for colloidal bio-detoxificat

289 todynamic-/ultrasound-/thermo-combined multi-modal therapy by virtue of functionalized hollow/rattle-

290 This cross-modal thermo-tactile interaction could reflect a process

291 Multi-modal three dimensional (3D) optical imaging combining b

292 In bi-modal trials, beeps and flashes differed in number by 0,

293 interference waveguide that allows for multi-modal tuning of waveguide properties through core liquid

294 the same pathway, providing important cross-modal validation of the effective connectivity measures.

295 ributions were unimodal and log normal, with modal values well within the quantifiable range.

296 Thus, CCt is a bi-modal vasodilator.

297 nsions of previously known laws: One gives a modal version of a radiation law for reciprocal objects-

298 The cross-modal versus unimodal responses of the adult monocular a

299 known to be differentially involved in cross-modal (visual) reorganization in deaf cats.

300 rometer incorporating such a 'delay' obtains modal weights in the associated Hilbert space.