ライフサイエンスコーパス: deflection

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

2 mounts of information about columnar whisker deflection.

3 heir internal compass, to compensate for the deflection.

4 ndomization of Adelta-LTMR responses to hair deflection.

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

6 uscle and produces a graded ipsilateral tail deflection.

7 ctive responsiveness of Adelta-LTMRs to hair deflection.

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

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

10 not cause significant differences in cuspal deflection.

11 area increased with the frequency of whisker deflection.

12 layer, resulted in an increase in cantilever deflection.

13 eurons whose firing is suppressed by whisker deflection.

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

15 magnetic field is tracked by changes in tip deflection.

16 lified fivefold by stress-induced structural deflection.

17 transduction current during sustained bundle deflection.

18 ngle mechanism for slab stagnation and plume deflection.

19 tical sensors to measure the microindenter's deflection.

20 sed to detect tension induced by hair bundle deflection.

21 sistance changes upon compressive or tensile deflections.

22 ntaneous activity and in response to whisker deflections.

23 ividual stereocilia during small hair-bundle deflections.

24 to push stereocilia tips together for small deflections.

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

26 s faster and is greater with higher velocity deflections.

27 lly decrease responsiveness to brief whisker deflections.

28 s the coding of spatiotemporally distributed deflections.

29 physiological correlates to these mechanical deflections.

30 sensitive current evoked by negative bundle deflections.

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

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

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

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

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

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

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

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

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

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

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 The ratio of the atrial-to-ventricular deflection amplitude was significantly greater in the NC

44 Pre-ablation EGM characteristics (number of deflections, amplitude, and duration) were measured in s

45 ing had the effect of drastically decreasing deflection amplitudes and reducing the effect of the non

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

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

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

49 tial for direction sensitivity to mechanical deflection and hearing.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

68 Remarkably, deflection angles decrease with increasing ground veloci

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

70 nd recording decreases in drain current with deflections as small as 5 nanometers.

71 gruent trials, causing an increased positive deflection (associated with preparation of the incorrect

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

73 els caused 3.5% +/- 5.3 (standard deviation) deflection at MW ablation compared with 26.2% +/- 27.9 a

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

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

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

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

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

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

80 results predict a measurably nonlinear force-deflection behavior at moderate-to-large deformations, w

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

82 lections (by approximately 47%) and downward deflections (by approximately 44%), increased cardiac pa

83 d increased baroreceptor slope during upward deflections (by approximately 47%) and downward deflecti

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

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

86 The percentage deflection caused by local blood vessels (heat-sink effe

87 Although periodic whisker deflection causes a frequency-dependent reduction of the

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

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

90 Whisker deflection conditioned stimuli (CS) were demonstrated to

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

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

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

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

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

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

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

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

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

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

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

102 40 mV resulted in a linear upward cantilever deflection equivalent to an increase in membrane tension

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

104 ) of the rat barrel cortex, a single whisker deflection evokes a stereotyped sequence of excitation f

105 For preferred direction deflections, excitation precedes inhibition, but as the

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

107 ch subregion to measure, by image shift, the deflection faced by each group of rays as they emerge fr

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

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

110 Our unique approach uses laser deflection for high-performance tracking of cell-adhered

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

112 10 min after restoration to determine cuspal deflection from the buccal and lingual volume change/are

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

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

115 ic pattern of pre-ablation sinus rhythm EGM (deflections > or =4, amplitude > or =0.7 mV, and duratio

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

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

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

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

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

121 The error-related negativity is a negative deflection in the event-related potential maximal approx

122 The earliest deflection in the evoked potential ranged from 2 to 10 m

123 The ventricular deflection in the His bundle electrogram was significant

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

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

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

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

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

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

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

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

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

133 to electrode location produced the strongest deflections in the averaged ERP at approximately 90 and

134 Cassini Plasma Spectrometer measured strong deflections in the corotating ion flow, commencing at le

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

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

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

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

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

140 A delayed precordial maximum deflection index > or =0.55 identified epicardial VT rem

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

142 ecognition of a prolonged precordial maximum deflection index and early use of transvenous epicardial

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

144 as quantified by a novel metric, the maximum deflection index, was more useful.

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

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

147 Inner ear hair cells convert hair bundle deflection into mechanical force sensed by ion channels

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 Negative LFP deflections (nLFPs) correlate with neuronal spiking and

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

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

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

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

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

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

171 The deflection of cantilever systems may be performed by an

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

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

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

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

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

177 ly probed through gravitational lensing: the deflection of light from distant galaxies by the gravita

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

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

180 in the superior laryngeal nerve (SLN) or by deflection of mechanoreceptors in the laryngeal mucosa.

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

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

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

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

185 oton source reveals field structures through deflection of proton trajectories, and areal densities a

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

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

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

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

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

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

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

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

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

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

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

197 region accurately predicts the shear-induced deflection of the cell nucleus to be 0.87 +/- 0.03 micro

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

199 Flow-mediated deflection of the cilia axoneme induces an increase in i

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

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

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

203 The maximum amplitudes of deflection of the plant stem were calculated numerically

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

205 orce applied was determined by measuring the deflection of the probes' cantilever arms.

206 AW responses during activation, simultaneous deflection of the PW and AWs produced VPM responses that

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

208 Here we report measurements of the deflection of the solar wind plasma flows in the heliosh

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

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

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

212 The observed approximately 100-meter maximum deflection of the underlying substrate in response to th

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

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

215 Mechanical deflections of both hairs and antennae increase with the

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

217 onically activated by unidirectional, static deflections of larger magnitude.

218 t the vibrissa tip, corresponding to angular deflections of less than 0.2 degrees, drove neural firin

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

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

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

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

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

224 Deflections of the PDMS membrane above the main microflu

225 This can be attributed to the fact that the deflections of the plant, and hence mechanical stresses

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

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

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

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

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

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

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

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

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

235 By contrast, a later positive deflection (onset ca. 500 ms post-stimulus) was enhanced

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

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

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

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

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

241 y (DeltaR/R, lambda = 633 nm) and probe beam deflection (PBD) measurements at solid electrodes in aqu

242 to estimate the elastic modulus from a force-deflection physical model based on the continuous bridge

243 enes also appears to have originated at this deflection point.

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

245 d incongruent trials produced a positive LRP deflection reflecting initial partial activation of the

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

247 proximate analytical solutions for the force-deflection relation of this unique biophysical force pro

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

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

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

251 Furthermore, we show that periodic whisker deflection results in balanced adaptation of the magnitu

252 Deflection seemed most related to the combination of pos

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

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

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

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

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

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

259 method utilizes the second derivative of the deflection signal to recover the tip acceleration trajec

260 use of the highly distorted character of the deflection signal.

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

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

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

264 E), has resulted in a polymer with high heat deflection temperature and greater structural stability

265 The amplitude of a negative-going ERP deflection that onsets around 300 ms post-stimulus varie

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

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

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

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

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

271 We recorded responses to whisker deflections that thoroughly explored the space of tempor

272 Depolarization evoked rapid positive bundle deflections that were reduced by perfusion with the MET

273 A positive-going ERP deflection--the left parietal old/new effect--was sensit

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

275 Deflection therefore occurs at low crack speeds, leading

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

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

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

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

280 fact that most of the information about the deflection trajectory is contained in the higher harmoni

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

282 entations in cortical bone, using both crack-deflection/twist mechanics and nonlinear-elastic fractur

283 l (splitting) direction owing to major crack deflections/twists, principally at cement sheaths.

284 g of the cantilevers that is detected as tip deflection using an array of vertical cavity surface emi

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

286 Employing whisker deflections varying in velocity or frequency and a cross

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

288 uits with torus-margo type pits pit membrane deflection was also modeled and pit aspiration, the disp

289 proximately 40 min; a 40 nm net differential deflection was observed.

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

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

292 tial photoinduced cell damage during optical deflection, we investigated the response of mouse macrop

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

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

295 We measured this deflection, which is on the order of tens of nanometers,

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

297 Modeling this bending as a cantilever deflection with uniform loading requires accurate mechan

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