ライフサイエンスコーパス: deflection

1 , using CFAE mean (the mean interval between deflections).

2 tical sensors to measure the microindenter's deflection.

3 sed to detect tension induced by hair bundle deflection.

4 reme individual particle forces causing root deflection.

5 mounts of information about columnar whisker deflection.

6 heir internal compass, to compensate for the deflection.

7 ndomization of Adelta-LTMR responses to hair deflection.

8 le actuation, low-cost fabrication and large deflection.

9 uscle and produces a graded ipsilateral tail deflection.

10 ctive responsiveness of Adelta-LTMRs to hair deflection.

11 pport these movements, including a bell-like deflection.

12 ct the amplitude of the cantilevers vertical deflection.

13 d as a nonlinear function of the hair-bundle deflection.

14 not cause significant differences in cuspal deflection.

15 area increased with the frequency of whisker deflection.

16 layer, resulted in an increase in cantilever deflection.

17 eurons whose firing is suppressed by whisker deflection.

18 ientations of adjacent crystals induce crack deflection.

19 ion to the whole organ in situ by transverse deflection.

20 lified fivefold by stress-induced structural deflection.

21 ngle mechanism for slab stagnation and plume deflection.

22 physiological correlates to these mechanical deflections.

23 sensitive current evoked by negative bundle deflections.

24 sistance changes upon compressive or tensile deflections.

25 ntaneous activity and in response to whisker deflections.

26 ividual stereocilia during small hair-bundle deflections.

27 to push stereocilia tips together for small deflections.

28 tive and neighboring L2/3 neurons to whisker deflections.

29 eir integrity against continuous stimulatory deflections.

30 opagation perpendicular to the LB (9.4+/-2.4 deflections; 14.4+/-5.2-ms intervals).

31 tively expressed VT fractionation (7.6+/-1.2 deflections; 16.3+/-8.9-ms intervals) was similar to mod

32 ed to modulate the amplitude of the negative deflection~230 to 280 ms post-stimulus during explicit j

33 nt propagation parallel to the LB (6.7+/-3.1 deflections; 7.1+/-3.8-ms intervals).

34 Fractionation during sinus rhythm (5.9+/-1.8 deflections; 9.2+/-4.4-ms intervals) was similar to mode

35 Moreover, the amplitude of the negative deflection-a hallmark of neuronal bistability according

36 ovides a weak microstructural path for crack deflection, accounting for the crack patterns and delami

37 he resonance frequency (mass) and cantilever deflection (adsorption stress).

38 be to our knowledge a new technique-constant-deflection AFM-in which the compliance of the AFM cantil

39 origin has long stayed at the level of crack deflection along the biopolymer interface between aragon

40 s are attributed to brick pull-out and crack deflection along the ceramic/metal interfaces.

41 ractionation was defined as an EGM with >/=4 deflections, although, in AF, CFE-mean <80 ms was consid

42 shows a good linear relationship between the deflection amplitude and the OTC concentration in the ra

43 ng the probabilistic distribution of whisker deflection amplitudes systematically while measuring the

44 upon awakening, TMS evoked a larger negative deflection and a shorter phase-locked response compared

45 echanisms of pull-out, crack bridging, crack deflection and crack tip shielding were found to be resp

46 ral laser ablation of vSPNs reduces the tail deflection and cycle period specifically during the firs

47 The relationship between cupula deflection and glutamate release demonstrated maximum se

48 tial for direction sensitivity to mechanical deflection and hearing.

49 the metallic particles, together with crack deflection and interfacial debonding, which is compatibl

50 ared-perceiving rats respond to both whisker deflection and intracortical microstimulation, suggestin

51 mensional parameters that govern the central deflection and the choking of the cell, respectively.

52 crack reorientation at the nanoscale; crack deflection and twisting by characteristic features such

53 rd it, movement consistent with the tympanum deflections and suggestive of a monaural mechanism of au

54 d duration of both very weak stimuli (~40 nm deflections) and strong stimuli (~1 mum), underlying the

55 ed to constant stretching during hair-bundle deflection, and accordingly are well designed to prevent

56 tomography has imaged slab stagnation, plume deflection, and changes in large-scale structure and off

57 changes in the threshold voltage, electrode deflection, and frequency shifts.

58 d at the end of the QRS, J wave as an upward deflection, and slur as a conduction delay on the QRS do

59 s, the longitudinal space constant for point deflection, and the deformation of the organ of Corti fo

60 ilia moved by approximately the same angular deflection, and the same motion was observed at 1, 20, a

61 us solution, independent of large mechanical deflections, and demonstrated high pH sensitivity.

62 fracture and crack arrest, reduction of back deflections, and resistance to bending and tensile loads

63 ntal-enamel junction and enamel tufts, crack deflections, and the initiation of new cracks within the

64 Increased alterations in thickness, deflections, and tortuosity were observed in stromal cor

65 e system and identify the singularity of the deflection angle at the photon sphere.

66 Since the deflection angle of the deflector is proportional to the

67 hybrid simulations shows the control of the deflection angle with different number of coils, forming

68 The changes in trident deflection angle with velocity suggest that trident whis

69 nitude and latency depended on the whisker's deflection angle.

70 tasurfaces to steer visible light to a large deflection angle.

71 esigns of metasurfaces were limited to small deflection angles and small ranges of the angle of incid

72 using approaches that are optimal for small deflection angles and their performance for designing hi

73 Remarkably, deflection angles decrease with increasing ground veloci

74 pple mapping (RM) displays every electrogram deflection as a bar moving from the cardiac surface, res

75 ween tracheids, although the extent of torus deflection as a function of applied pressure is not well

76 cells polarized to be activated by posterior deflections, as would occur during forward motion.

77 Measurement of this deflection at multiple epochs allowed us to determine th

78 er crack-initiation toughness and less crack deflection at osteonal boundaries than that of bisphosph

79 ect, weighted with the percentage of voltage deflection at steady state) was 1.69 in basket cells and

80 ; 2- torsion effects on the shaft and needle deflection at tissue boundaries lead to difficulty in co

81 ian cells exhibit voltage-induced mechanical deflections at nanometre scales, but AFM measurements ca

82 We identified large deflections at single MEG sensors and combined them into

83 lation (simultaneous light flash and whisker deflection) augmented the somatosensory-evoked response

84 be preceded by a slow negative-going voltage deflection beginning well before the interruption itself

85 rack growth) through mechanisms (e.g., crack deflection/bridging) generated at larger structural scal

86 This resulted in little angular deflection but high RET to both partners, a very unusual

87 aintain a zero amplitude harmonic cantilever deflection by CL control of a subsample piezo.

88 Such directed deflections can be triggered by a lateralized source of

89 on respond to different directions of arista deflection caused by air flow and project to different r

90 s) and in the amplitude of the late positive deflection component (peaking approximately 230-330 ms p

91 w that the pneumatically controlled membrane deflection/compression method not only generates highly

92 er surfaces correlated to negative curvature deflections, consistent with the induction of negative c

93 We find that the deflection critically depends on the applied frequency a

94 tic increase found in measured stiffness vs. deflection curves under point loading, while for pressur

95 l analyses of pillar elasticity confirm that deflection, deformation force, and mechanical energies a

96 ound that performance in detecting vibrissal deflections degraded with adaptation while performance i

97 Further analyses show that the interfacial deflection depends predominantly on cortical tension, wh

98 n during evoked responses induced by whisker deflection did not differ between the two groups.

99 adhesion site, but the amount of microneedle deflection did.

100 ad of the usual mode of recording cantilever deflection driven by sample expansion, the principle of

101 ed as an elastic beam that may undergo large deflection due to the hydrodynamic load.

102 tion measurement, such as optical flow, post deflection, edge-detection systems, or manual analyses.

103 The deflection efficiency is around 45% due to the material

104 The timed pulsing of a deflection electrode, in conjunction with the release of

105 Single whisker deflection elicited low-probability spikes in highly dis

106 40 mV resulted in a linear upward cantilever deflection equivalent to an increase in membrane tension

107 We found that a whisker deflection evoked abnormal sensory responses in the barr

108 In time-resolved photothermal beam deflection experiments, we monitored apparent volume cha

109 All key features of the force-dependent deflection fluctuations could be reproduced: SD, skewnes

110 s, nose motion is rhythmic and has a maximum deflection following the onset of inspiration.

111 face stimuli produced greater late positive deflections for old items in anterior compared to poster

112 We use mean deflection from baseline when comparing to prior single-

113 iple cantilevers, to isolate and record beam deflection from individual cantilevers using distinct wa

114 as utilised to determine the extent of torus deflection from pressure applied to the torus and margo.

115 10 min after restoration to determine cuspal deflection from the buccal and lingual volume change/are

116 We find a deflection from the cancer phenotype, significantly redu

117 in mean particle forces but does not prevent deflections from 5% of most extreme individual particle

118 much smaller than the amplitude of waves and deflections from interacting wind streams(8).

119 Hair bundle deflection generates a force by pulling on tip-link prot

120 measuring the local cantilever activity and deflection in a feedback generation-collection configura

121 rsistent rotational behavior and interfacial deflection in a simulated cell cluster.

122 n at 100 GHz, offering up to 44 degrees beam deflection in both horizontal and vertical directions.

123 two populations of hair cells, activated by deflection in either the anterior or posterior direction

124 otential classically manifests as a negative deflection in medial frontocentral EEG contacts followin

125 igh-speed imaging technique to quantify this deflection in rat cochlear hair cells.

126 uasi-steady state response of the cantilever deflection in terms of Fourier analysis.

127 ry suggests that this frontocentral negative deflection in the ERP 230-270 ms after the delivery of a

128 people, as revealed by a sustained positive deflection in the event-related potential (ERP) over the

129 ncreasing glutamate release in response to a deflection in the positive direction or by reducing rele

130 um deflection index (the time to the maximum deflection in the precordial leads/QRS duration) was the

131 uron responses were preceded by a global LFP deflection in the theta range.

132 response, we show that electric fields cause deflections in both antennae and hairs.

133 ns but remained in bundles, leading to small deflections in direction of travel.

134 ed with electrogram amplitude, duration, and deflections in linear mixed-effects multivariable models

135 s allows simultaneous imaging via cantilever deflections in normal AFM force feedback mode as well as

136 word stimuli produced greater late positive deflections in posterior compared to anterior regions.

137 In contrast, hair deflections in response to an electric field elicited ne

138 ess the characteristics of dendritic voltage deflections in response to Na/K action potentials in int

139 the linear response function observed under deflections in the inhibitory direction.

140 cordings in cat visual cortex revealed small deflections in the membrane potential of neurons, termed

141 requency power spectrum of the potential and deflections in the raw potential trace (event-related po

142 on the other hand, was signaled by positive deflections in the stimulus-locked local field potential

143 tion was annotated at the sharpest intrinsic deflection including late potentials and compared with 6

144 Torus deflection increased in nonlinear fashion with applied p

145 The magnitude of deflections increases with pressure but they assemble in

146 The maximum deflection index (the time to the maximum deflection in

147 ms, precordial transition >/=V1, and maximum deflection index of >/=0.55.

148 image: the spatiotemporal pattern of voltage deflections induced by spikes on a large-scale, high-den

149 figuration, we demonstrate prominent whisker deflection-induced fLDI hemodynamic responses from micro

150 We observe that the deflection is influenced by electrostatic and intermolec

151 on, its thin wall deflects considerably; the deflection is measured with an optical profilometer and

152 In both reactions, the cantilever deflection is qualitatively detected from the SECM tip c

153 he corresponding change in the gate shape or deflection is reflected in the drain current of FET.

154 imuli, the magnitude of responses to whisker deflections is highest in the presence of optic flow goi

155 The relation between the laser deflection length and the peak positive pressure is deri

156 evealing how the bundle bulk modulus and the deflection length of filaments in the bundles depend on

157 lation-based local field potential transient deflections (LFP spikes) whose rate determined the magni

158 Membrane-deflection measurements at the single-layer level show t

159 ble to high-pressure environments, the laser deflection method exhibits a great potential for measuri

160 cousto-optic interaction, we propose a laser deflection method for rapidly, non-invasively and quanti

161 Then the laser deflection method is assessed by comparing it with the h

162 rophones is always underestimated, the laser deflection method is assumed to be more accurate than th

163 the peak positive pressure measured by laser deflection method is little higher than that obtained by

164 Additionally, the laser deflection method provides a rapid way for measuring the

165 Using force deflection method, we quantify the Young's modulus of th

166 anisms: (i) a simple drag model; (ii) a seed deflection model; and (iii) a 'wear and tear' model.

167 Unit activity and negative LFP deflections (nLFP) consistently changed in rate at singl

168 eased from the ALPHA trap finds a mean axial deflection of 4.1 +/- 3.4 mm for an average axial electr

169 We relate the observed deflection of a cantilever to the changes in the surface

170 s designed to assess the effect of G: on the deflection of a predicted response to selection away fro

171 ties evoked in the whisker system of mice by deflection of a single whisker in vivo.

172 Ripple mapping displays every deflection of an electrogram, thereby providing fully in

173 escribe a model that accurately predicts the deflection of an electron beam trajectory in the vicinit

174 ine Adelta-LTMRs are preferentially tuned to deflection of body hairs in the caudal-to-rostral direct

175 The deflection of cantilever systems may be performed by an

176 ne chondrocytes, stretch of the membrane and deflection of cell-substrate contacts points, respective

177 Upon deflection of distal upstream DNA over the RNA polymeras

178 This work demonstrates selective and tunable deflection of DNA using alternating current (AC) insulat

179 were confined within the PMBSF region during deflection of either single or all whiskers.

180 of cells was carried out through the cyclic deflection of flexible, translucent silicone membranes b

181 anced turbulent intensity and the transverse deflection of flow around individual cylinders.

182 In the inner ear, the deflection of hair bundles, the sensory organelles of ha

183 the glacier's horizontal flow and a downward deflection of its terminus.

184 We combined two-photon calcium imaging with deflection of many whiskers to map whisker receptive fie

185 y gated ion channels that open following the deflection of mechanoreceptive hair bundles that reside

186 Inner ear hair cells detect sound through deflection of mechanosensory stereocilia.

187 its positive polarity represents a southward deflection of moist, westerly monsoon flow from the Arab

188 del surfaces, i.e., velocity, smoothness and deflection of movement, determined via in vitro motility

189 xplants to ectopic Netrin1 caused attractive deflection of post-crossing axons.

190 o infer geometric curvature by measuring the deflection of quantum trajectories in the curved space o

191 Stagnation of subducting slabs and deflection of rising plumes in Earth's shallow lower man

192 More surprisingly, the elasto-inertial deflection of small particles can be even greater than t

193 Gravitational deflection of starlight around the Sun during the 1919 t

194 ia.Inner ear hair cells detect sound through deflection of stereocilia that harbor mechanically-gated

195 Inner ear hair cells detect sound through deflection of stereocilia, the microvilli-like projectio

196 er (BW) and lower magnitude responses to the deflection of surrounding whiskers.

197 ctrical excitation and measuring the maximum deflection of the actuated cantilever electrode.

198 with the principal activation cluster during deflection of the C1 whisker were used as a reference to

199 allowed us to unequivocally assign steps in deflection of the cantilever to membrane states during t

200 CaMiRi is measured and calculated using the deflection of the cantilevers.

201 ne and tetracycline do not cause significant deflection of the cantilevers.

202 e two mechanisms for enhanced uptake: first, deflection of the cell membrane inducing endocytotic upt

203 rotation is often accompanied by a sigmoidal deflection of the cell-cell interface.

204 ed glutamate release in response to a steady deflection of the cupula and others generating transient

205 ransmit mechanical information by converting deflection of the hair bundle into synaptic release of g

206 xerts a force on the fluid, which leads to a deflection of the Lorentz force-driven main flow.

207 molecules can be detected by monitoring the deflection of the microcantilever.

208 By monitoring the deflection of the microcantilevers, real-time free energ

209 Interestingly, the elasto-inertial deflection of the peanut particles can be either greater

210 e feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intrac

211 The vertical deflection of the sheet's center induced by impact draws

212 hiral winding of the spin texture leads to a deflection of the skyrmion trajectory, characterised by

213 is that the swirls are formed as a result of deflection of the solar wind by local magnetic fields.

214 n auditory sensory hair cells depends on the deflection of the stereocilia hair bundle which opens me

215 The mutants also displayed a dorsal-ward deflection of the sternum akin to human PE.

216 ntion decreases the magnitude of the initial deflection of the stimulus-evoked LFP.

217 es, both bend and stretch dominated, elastic deflection of the structure was observed ahead of the co

218 ultiple images of distant sources due to the deflection of their light by the gravity of intervening

219 footprint, i.e. forming an oil slick origin, deflection of which with wind and surface current leads

220 ctivity evoked in the thalamic barreloids by deflection of whiskers in vivo.

221 which are accompanied by significant normal deflections of a cell monolayer (i.e., the endothelium)

222 Mechanical deflections of both hairs and antennae increase with the

223 erformance in discriminating among vibrissal deflections of different velocities was enhanced, a tren

224 In hair cells, TMC1 is gated by small deflections of microvilli that produce tension on extrac

225 s of passive antennal movements: small tonic deflections of the antenna and rapid oscillations at win

226 he wing beat frequency, but not to the tonic deflections of the antennae.

227 amate using the reporter iGluSnFR as well as deflections of the cupula.

228 ortex in the anesthetized rat in response to deflections of the facial vibrissae and electrical or op

229 electrical transducer channels are opened by deflections of the hair bundle about a resting position

230 erlying channels were opened not directly by deflections of the hair bundle but by deformation of the

231 ccompanied by prominent lateral and vertical deflections of the nose, i.e., twitches, which are drive

232 Deflections of the PDMS membrane above the main microflu

233 tation atop soft pillars induces significant deflections of the pillars on the receding edge of the d

234 ves, plasma instabilities result in multiple deflections of the propagation direction, mimicking the

235 Encounters with UvrA2 led to deflections of the whole nanoprobe structure, which were

236 the organ of Corti, which convert mechanical deflections of their actin-rich stereociliary bundles in

237 mechanical stimuli by converting very small deflections of their hair bundle into changes in the rel

238 Cochlear hair cells normally detect positive deflections of their hair bundles, rotating toward their

239 However, stereocilia remained cohesive for deflections of up to +/-35 degrees, ruling out rootlet p

240 eptide 18-4 (WxEAAYQrFL), showed significant deflection on cancer cell (MCF7 and MDA-MB-231) binding

241 To assess the effects of such a deflection on mechanically decoupled hair bundles, compa

242 FN400 effect (a significantly less negative deflection on the second presentation) was observed rega

243 gram bipolar/unipolar voltage, duration, and deflections on electroanatomic mapping.

244 states, which are triggered by a temperature deflection or a temporary application of hydrostatic pre

245 ic stimulation by repetitive sounds, whisker deflection or motor activity led to a near arrest of ang

246 waves were measured at the peak of an upward deflection or notch at the end of QRS, and QRS slurs wer

247 tics and functional properties suggest these deflections originate from a single, nearby cell.

248 phology at 1/10 scale and captured basic fin deflection patterns of batoid fish.

249 The approach produces accurate beam deflection predictions in the fringe field region as wel

250 nner ear hair cells responds to subnanometer deflections produced by sound or head movement.

251 methodology for the calculation of the full deflection profile from video recordings of bending test

252 at the piezo voltage used to maintain a null deflection provides a reliable measure of the local IR a

253 ing a droplet curvature to conventional beam deflection, providing a framework for engineering pressu

254 The magnitude of the vertical ice-shelf deflection reaches maxima of ~1 m at the lake centres, d

255 mation were identified: (1) receptivity, (2) deflection/rejection, (3) emotion, (4) characterization

256 stic-mechanical theory to establish how root deflections relate to particle forces and thickening of

257 rd prediction error) also yielded a negative deflection relative to unexpected pain delivery.

258 rd prediction error) yielded a more negative deflection relative to unexpected reward delivery.

259 use action potentials are too sparse and the deflection response to drifting grating stimuli (e.g. tu

260 sensors exhibit nearly synchronous pressure-deflection responses with a very high sensitivity (89.3

261 Deflection seemed most related to the combination of pos

262 onent ~100 ms post-stimulus), N170 (negative deflection sensitive to faces) and a posterior-occipital

263 he uncertainties in the determination of the deflection sensitivity and subsequently cantilever's spr

264 ates those errors by calculating the correct deflection sensitivity based on spring constants determi

265 ation might come from investigation of large deflections (sharp-waves) in the hippocampal local field

266 euronal responses to BW and surround whisker deflection showed comparable latencies in short-tailed o

267 mpression, and storage of the raw cantilever deflection signal in its entirety at high sampling rates

268 ignal the amplitude and duration of stronger deflections.SIGNIFICANCE STATEMENT Hair cells transmit i

269 solar cell blends, measured by photothermal deflection spectroscopy, is directly proportional to the

270 l excitation and detected by an optical beam deflection system using two laser beams of different wav

271 measured signal in the popular optical beam deflection technique (OBDT).

272 e elicited a stronger negative frontocentral deflection that peaked approximately 60 ms after the res

273 al of neurons, but small unipolar or bipolar deflections that are termed spikelets.

274 al lead as the total number of low-amplitude deflections that deviated from their respective naive QR

275 ces were maximal within the narrow region of deflections that elicited significant channel gating, pl

276 ponses of VPM neurons to sequences of caudal deflections that generated an apparent motion in eight d

277 In such experiences-which we will call gaze deflection-the "deflected" gaze is not directed at anyth

278 g (90%) that is in good agreement with Odijk deflection theory, and we have mapped genomic features u

279 Deflection therefore occurs at low crack speeds, leading

280 short-latency excitatory response to whisker deflection, those having a long-latency response, and ne

281 than 5% to ~50% for the ratio of the bending deflection to the original length of the pillars is real

282 load or by the application of a steady-state deflection to the resting position of the bundle.

283 gle neuron recordings and controlled whisker deflections to examine responses of thalamocortical neur

284 tage, ionomer membranes display a consistent deflection toward the cathode.

285 Occasional, far deflections toward the incorrect target were most likely

286 extension curves were identified: one with a deflection transition (Type I) and another with a discon

287 involve alternated crack tip blunting, crack deflection, twinning/detwinning and slip transmission ac

288 e was measured by monitoring the microneedle deflection using an optical microscope.

289 ediated growth cone advance, the mean needle deflection was 1.05 +/- 0.07 mum.

290 By contrast, the mean deflection was significantly lower (0.48 +/- 0.06 mum) w

291 magnitude and time course of the hair bundle deflection, we developed a high-speed imaging technique

292 For the onset of deflection, we find a critical value kappac congruent wi

293 sing 3D laser vibrometry to measure tympanum deflection, we show that female lesser waxmoths (Achroia

294 ps annotated to the latest local electrogram deflection were created with high-density multielectrode

295 f the initial oscillations of the cantilever deflection when an impulsive excitation is given (as in

296 bruary 2009 in accordance with gravitational deflection, whereas H dominated after 26 March 2009, con

297 ion by hair cells commences with hair-bundle deflection, which is postulated to tense filamentous tip

298 combiner/splitter and independent multibeam deflections with up to 4 incident angles are numerically

299 on was observed in their dynamic state under deflection, with qualitative changes in the oscillation

300 le; DV p95), or late DV changes (A wave [the deflection within the venous waveform signifying atrial