ライフサイエンスコーパス: mechanical stimulation

1 g of hairy skin, but not by noxious punctate mechanical stimulation.

2 with no change in their response to noxious mechanical stimulation.

3 doses of morphine showed hypersensitivity to mechanical stimulation.

4 ing capacity display compromised response to mechanical stimulation.

5 persensitive hindlimb withdrawal response to mechanical stimulation.

6 in response to direct activation or noxious mechanical stimulation.

7 s are generated independently by thermal and mechanical stimulation.

8 cord neurons in response to noxious heat and mechanical stimulation.

9 y expressed were up-regulated in response to mechanical stimulation.

10 cally required for habituation to repetitive mechanical stimulation.

11 combination with pharmacological probes and mechanical stimulation.

12 hannel acts to induce neuronal adaptation to mechanical stimulation.

13 ses of dorsal root ganglion (DRG) neurons to mechanical stimulation.

14 anifested as hypersensitivity to thermal and mechanical stimulation.

15 role in the osteoblast anabolic response to mechanical stimulation.

16 at are thought to bend at their ankle during mechanical stimulation.

17 he dlPAG had no effect on MAP or HR during a mechanical stimulation.

18 hat exhibit seizures and paralysis following mechanical stimulation.

19 anal responses to angular motion, sound, and mechanical stimulation.

20 imulation, and enhanced responses to noxious mechanical stimulation.

21 cells to touch, particularly after repeated mechanical stimulation.

22 kin of the hindlimb and responded to noxious mechanical stimulation.

23 activation and the anti-apoptotic effect of mechanical stimulation.

24 glutamate and GABA values (P>0.05) during a mechanical stimulation.

25 urons responded to both gastric and duodenal mechanical stimulation.

26 sistant to rapamycin in muscles subjected to mechanical stimulation.

27 llular fibroblast aging and a lower level of mechanical stimulation.

28 n velocity and defects in their responses to mechanical stimulation.

29 e of renal epithelial cells to fluid flow or mechanical stimulation.

30 root growth is affected by both gravity and mechanical stimulation.

31 during the early stages of gravitropism and mechanical stimulation.

32 receptor inhibited chondrocyte responses to mechanical stimulation.

33 d may be co-released with nucleotides during mechanical stimulation.

34 in's cytoskeletal recruitment in response to mechanical stimulation.

35 neurons or their in vivo responses to harsh mechanical stimulation.

36 dels have previously focused on responses to mechanical stimulation.

37 d by chondrocytes at rest and in response to mechanical stimulation.

38 on of traction forces and the application of mechanical stimulation.

39 genes; double mutants were nonresponsive to mechanical stimulation.

40 ined the responses of hair bundles to direct mechanical stimulation.

41 ge tissues and show that caveolae respond to mechanical stimulation.

42 m signaling attenuated the response to acute mechanical stimulation.

43 apeutic potential for magnetically modulated mechanical stimulation.

44 sed the amount of bone formed in response to mechanical stimulation.

45 g mice is an innate response to isolation or mechanical stimulation.

46 mice, tendons failed to respond to the same mechanical stimulation.

47 determines the linearity and sensitivity to mechanical stimulation.

48 ins on a millisecond time scale triggered by mechanical stimulation.

49 mode TB-ATC for both subcellular probing and mechanical stimulation.

50 the exquisite sensitivity of the sacculus to mechanical stimulation.

51 tilage as an alternative to bioreactor-based mechanical stimulation.

52 adopt different orientations in response to mechanical stimulation.

53 PER2 expression was also sensitive to mechanical stimulation.

54 be required for Cx43 hemichannel opening by mechanical stimulation.

55 zation of peripheral nociceptor terminals to mechanical stimulation.

56 nuclear translocation or survival induced by mechanical stimulation.

57 the mouse in response to graded thermal and mechanical stimulation.

58 position that underlies their sensitivity to mechanical stimulation.

59 ections describing biochemical, physical and mechanical stimulations.

60 Placebo or low-magnitude, high-frequency mechanical stimulation (0.3 g; 32-37 Hz) for 2 sessions

61 cultured for 4 days in the CCCM under cyclic mechanical stimulation (10 mmHg, 8-15% stretch, 2 Hz fre

62 injection of histamine in the rostral back, mechanical stimulation 7 mm from the injection site elic

63 f the native extracellular matrix, providing mechanical stimulation, activating cell-driven matrices,

64 Previous studies in vitro have shown that mechanical stimulation also can affect axon growth; howe

65 Mechanical stimulation also evoked release of ATP that w

66 In mid-density BALB/cByJ mice, mechanical stimulation also increased BFR, whereas disus

67 These findings suggested that mechanical stimulation altered the mechanical properties

68 two distinct regimes develop in cells under mechanical stimulation: an initial event of increased in

69 afferent neurones are activated by punctate mechanical stimulation and acid but are unresponsive to

70 ant of bone strength and is promoted by both mechanical stimulation and activation of the Wnt signali

71 ty-eight percent of VLF neurons responded to mechanical stimulation and all responded to noxious chem

72 g times (minutes), and the energy levels for mechanical stimulation and chemical stimulation were com

73 n the left or right ventricle initially with mechanical stimulation and confirmed with a stimulating

74 ptive-specific neurons in response to graded mechanical stimulation and decreased the relative number

75 nd slamdance (sda) epileptic flies following mechanical stimulation and electroconvulsive shock.

76 on in linking the aberrant responsiveness to mechanical stimulation and extracellular matrix accumula

77 high significance during plant responses to mechanical stimulation and is associated with specific g

78 but the sensory fibres responded normally to mechanical stimulation and joint movement.

79 fter gravity stimulation (reorientation) and mechanical stimulation and monitored transcript levels o

80 However, responses to punctate mechanical stimulation and nocifensive responses to ther

81 on; mechanothermal nociceptors responding to mechanical stimulation and noxious heat; and mechanochem

82 es and periosteal osteoblasts in response to mechanical stimulation and parathyroid hormone (PTH).

83 , acts as a scaffold to regulate DG-mediated mechanical stimulation and pathway bifurcation.

84 s we mechanically strained the cells via our mechanical stimulation and polymer surface chemical modi

85 nadequate processing of signals derived from mechanical stimulation and that PTH might be an effectiv

86 tory events could enhance type I response to mechanical stimulation and thereby increase symptoms of

87 le of integrin signaling in IVD cells during mechanical stimulation and to determine whether RGD inte

88 imals exhibited novel responses to innocuous mechanical stimulation, and enhanced responses to noxiou

89 depolarization without AP generation during mechanical stimulation, and no increase in max. dAP/dDel

90 s bone resorption and bone loss with reduced mechanical stimulation, and receptor activator of NF-kap

91 cle delivery of growth factors, simultaneous mechanical stimulation, and the delivery of microRNA.

92 anscripts occurred in response to gravity or mechanical stimulation, and these transcript level chang

93 CBF was observed in wild-type ALIs following mechanical stimulation, and this increase was significan

94 and not on the magnitude or duration of the mechanical stimulation applied.

95 ion and beta-catenin accumulation induced by mechanical stimulation are abolished by either pharmacol

96 translocation and anti-apoptosis induced by mechanical stimulation are abolished by the Wnt antagoni

97 s mediating osteoblast anabolic responses to mechanical stimulation are incompletely understood.

98 y benefit from low-magnitude, high-frequency mechanical stimulation as a novel and safe intervention

99 ular dialysis or to increased sensitivity to mechanical stimulation as a result of microtubule disrup

100 perineal skin, genital, rectal, and urethral mechanical stimulation, as well as to determine the peri

101 nuated in Calhm1 knockout cultures following mechanical stimulation at a pressure of 55 mmHg for 50 m

102 In this study, we found that mechanical stimulation at the acupoint of Yanglingquan (

103 n rats that is markedly enhanced by repeated mechanical stimulation at the site of administration.

104 ensitizing its release of ATP in response to mechanical stimulation; ATP in turn acts at the nocicept

105 that intervene in the response of muscle to mechanical stimulation, being central to myofibril homeo

106 neurons were recorded, in response to graded mechanical stimulation (brush, pressure, and pinch) at t

107 neurons were recorded in response to graded mechanical stimulation (brush, pressure, and pinch) at t

108 ally required for neural responses to gentle mechanical stimulation, but do not affect the basic phys

109 Of the PSDC neurons, 43% responded to mechanical stimulation, but only one responded to noxiou

110 In mechanoreceptors, mechanical stimulation by external forces leads to the r

111 rs for thrombin or acetylcholine, and during mechanical stimulation by hypotonic stress.

112 Mechanical stimulation by rotational shaking released 5-

113 Direct mechanical stimulation by shear loading of articular car

114 was measured after a 4-h period of localized mechanical stimulation, by using a behavioral assay base

115 of cell cultures have shown that damage and mechanical stimulation can activate changes in intracell

116 l rate approximately 0.01 fmol/s, and gentle mechanical stimulation can increase this to 50 fmol/s.

117 Mechanical stimulation can prevent adipogenic and improv

118 Our findings indicate that mechanical stimulation causes up-regulation of genes tha

119 By identifying pathways involved in mechanical stimulation, chemical equivalents that mimic

120 -HT release was investigated under basal and mechanical stimulation conditions, no changes were detec

121 weak interactions, sensitive to voltage and mechanical stimulation, confer prestin with a unique cap

122 B4) binding] generated distinct responses to mechanical stimulation consistent with their predicted i

123 Mechanical stimulation contributes to the health of alve

124 rologically healthy human adults to localize mechanical stimulation delivered to the same skin region

125 cement of actin stress fibers in response to mechanical stimulation depends on a posttranslational me

126 We show that the speed of ramp-like mechanical stimulation determines the dynamics of mechan

127 cebo device or low-magnitude, high-frequency mechanical stimulation device, which was used at home.

128 ted a hypothesis that osteoblasts respond to mechanical stimulation differently on titanium with diff

129 displaced handle condition) were tested with mechanical stimulation during quiet stance, and 98% resp

130 ne, thrombin, or lysophosphatidic acid or by mechanical stimulation evoked hyperpolarizing responses

131 Spontaneous discharges and mechanical stimulation-evoked responses were recorded in

132 Our data indicate that trigger-hair mechanical stimulation evokes APs.

133 Secondary cartilage requires mechanical stimulation for its induction and maintenance

134 odeled tissue that requires gravity-mediated mechanical stimulation for maintenance of mineral conten

135 iquid interface (ALI) and subjected to light mechanical stimulation from an air puff.

136 However, the mechanical stimulation had no effect on cardiovascular r

137 e opening of osteocytic Cx43 hemichannels by mechanical stimulation had similar inhibitory effects on

138 ar calcium (Ca(2+)) signaling resulting from mechanical stimulation has been widely studied in osteoc

139 mmetric responses to the onset and offset of mechanical stimulation has eluded understanding for deca

140 molecular weight HA increases sensitivity to mechanical stimulation, high molecular weight HA reduces

141 are selectively activated by high-threshold mechanical stimulation (HTMRs).

142 on acts as a second messenger in response to mechanical stimulation, hydrogen peroxide, NaCl, and col

143 nstructs and subject them to chemical and/or mechanical stimulation in an attempt to develop a functi

144 on via beta1 integrin signaling initiated by mechanical stimulation in cells grown on native type I c

145 r strain, and cell viability under prolonged mechanical stimulation in cells lacking both lamins A an

146 A reduction in mechanical stimulation in chronologically aged skin was

147 nd with adaptable sensitivity as a sensor of mechanical stimulation in diverse cellular contexts.

148 cal second messenger in sensitization toward mechanical stimulation in models of neuropathic (diabete

149 ehavioral responses to chemical, thermal and mechanical stimulation in rats.

150 both cellular fibroblast aging and defective mechanical stimulation in the aged tissue contribute to

151 utaneous receptive fields and sensitivity to mechanical stimulation in the first weeks of life sugges

152 e tissue engineering by combining effects of mechanical stimulation in the form of fluid shear stress

153 We demonstrate that mechanical stimulation in vitro, without ligament-select

154 ons were generated and neuronal responses to mechanical stimulation in vivo before and after subcutan

155 ye does not block the electrical response to mechanical stimulation, in contrast to its effect on the

156 f the cultured cells to increasing levels of mechanical stimulation, in the form of fluid shear stres

157 red in emerin-deficient cells, and prolonged mechanical stimulation increased apoptosis in emerin-def

158 Mechanical stimulation increased SLV recycling, increasi

159 ated visceromotor response, referred pain to mechanical stimulation, increased spinal Fos expression,

160 These experiments revealed that mechanical stimulation increases the concentration of di

161 43 and that this interaction is required for mechanical stimulation-induced opening of the Cx43 HC.

162 channels are those predominantly involved in mechanical stimulation-induced rCBF changes and thus may

163 Mechanical stimulation induces opposite behavioral respo

164 These results show that mechanical stimulation induces segmental opioid release,

165 The ability of cells to respond to external mechanical stimulation is a complex and robust process i

166 Thus, our work reveals that mechanical stimulation is a critical regulator of lympha

167 The biomechanical behavior of tissues under mechanical stimulation is critically important to physio

168 These results suggest that mechanical stimulation is crucial in regulating periodon

169 Differently, mechanical stimulation is known to trigger healing (rege

170 This ER Ca(2+) release upon mechanical stimulation is mediated not only by the mecha

171 Mechanical stimulation is recognized as a potent modulat

172 ormation, the sensitivity of hair bundles to mechanical stimulation is reduced.

173 entral to understanding cellular response to mechanical stimulation is the organization of the cytosk

174 nown about how the Cx43 molecule responds to mechanical stimulation leading to the opening of the HC.

175 Thus, mechanical stimulation likely elicits Ca(2+)-dependent a

176 Mechanical stimulation likewise elicited an apoplastic a

177 lipids recruited to the invasion junction by mechanical stimulation may be remodeled by the malaria p

178 We show that mechanical stimulation may promote PIP2 activation of TR

179 As a source of mechanical stimulation, mouse skeletal muscles were subj

180 Three types of mechanical stimulations, namely, proprioception, touch a

181 Mechanical stimulation of 1321N1 human astrocytoma cells

182 perception is the sensation arising from the mechanical stimulation of a bone-anchored prosthesis.

183 ow-cost electronic system to standardise the mechanical stimulation of a rat's hindpaw.

184 or Ca(2+) wave activity following micropipet mechanical stimulation of a single cell.

185 Mechanical stimulation of airway epithelial cells causes

186 nit responses elicited by focal chemical and mechanical stimulation of antennular hooded sensilla.

187 Mechanical stimulation of astrocyte somata evoked Ca(2+)

188 nists of these respective channels following mechanical stimulation of B cells.

189 verlap between rhythms and cycles suggests a mechanical stimulation of bioluminescence, as organisms

190 Moreover, inhibition of miR-365 abolishes mechanical stimulation of chondrocyte differentiation.

191 RECENT FINDINGS: Mechanical stimulation of conventional outflow cells due

192 NFATc1 knockdown prevented mechanical stimulation of COX2, implicating NFATc1 signa

193 The responses to noxious mechanical stimulation of deep paraspinal muscles increa

194 ic tweezing cytometry (ATC), for subcellular mechanical stimulation of disassociated single hESCs to

195 Mechanical stimulation of DM skin or DM skin graft trans

196 Direct mechanical stimulation of duck TG neurons evokes high-am

197 phosphorylation has been observed following mechanical stimulation of EC but its role in mechanosens

198 These results demonstrate that early mechanical stimulation of embryonic cardiac tissue is ne

199 cold, osmotic and hydrostatic pressure, and mechanical stimulation of exposed dentine and to drying

200 hase-locked action potentials in response to mechanical stimulation of hair cells.

201 Furthermore, direct mechanical stimulation of hairs on the patella of the fo

202 Light mechanical stimulation of hairy skin can induce a form o

203 ulation of the caudal Vme or masseter nerve, mechanical stimulation of jaw muscles and jaw opening.

204 alpha increased spinal neuronal responses to mechanical stimulation of knee and ankle joints.

205 ticle, we demonstrate a new strategy for the mechanical stimulation of large cell clusters, taking ad

206 of brain activity in response to nociceptive mechanical stimulation of normal skin and capsaicin-indu

207 Mechanical stimulation of one receptive field increased

208 These data explain how mechanical stimulation of osteoblasts leads to increased

209 dy was to evaluate the extent to which focal mechanical stimulation of osteocyte cell body and proces

210 Mechanical stimulation of plants triggers a cytoplasmic

211 f pressure overload and an in vitro model of mechanical stimulation of primary cardiomyocytes, we ide

212 A recent study links the mechanical stimulation of sensory hair cells with short-

213 into cells, however, focus predominantly on mechanical stimulation of single cells, affect cell inte

214 Third, mechanical stimulation of skeletal muscle with intermitt

215 ch to dynamic elastography using non-contact mechanical stimulation of soft media with precise spatia

216 rapid, local conformation switching upon the mechanical stimulation of specific cadherin bonds.

217 Mechanical stimulation of stretch-activated calcium chan

218 ithdrawal threshold and did not escape/avoid mechanical stimulation of the afflicted paw.

219 Mechanical stimulation of the artery, by increased intra

220 It is hypothesized that the mechanical stimulation of the corneal surface, due to th

221 Mechanical stimulation of the cultured CM using the CCCM

222 F), ongoing discharge, and responsiveness to mechanical stimulation of the dura were studied after ei

223 Sensitisation of mechanical stimulation of the FRF could also not be obse

224 g their release from epithelial cells during mechanical stimulation of the gut, and from immune cells

225 nal cord were recorded in response to graded mechanical stimulation of the hind paws (brush, pressure

226 nor changes were observed in the response to mechanical stimulation of the hind paws and face.

227 Mechanical stimulation of the hindpaw consisted of repea

228 recurrent laryngeal nerves were elicited by mechanical stimulation of the intrathoracic trachea.

229 of A-889425 on neuronal responses to intense mechanical stimulation of the knee and on the spontaneou

230 eripheral nervous system responds to electro-mechanical stimulation of the limb, will help to inform

231 The mechanical stimulation of the outer hair cell hair bundl

232 injection of bile acids caused analgesia to mechanical stimulation of the paw by an opioid-dependent

233 difference in the threshold for response to mechanical stimulation of the paw in rats injected with

234 Low-threshold mechanical stimulation of the skin normally does not eli

235 We discover that mechanical stimulation of the skin with ultrasound can o

236 ocuous and/or noxious convergent inputs from mechanical stimulation of the stomach and duodenum.

237 Cough was evoked by electrical or mechanical stimulation of the tracheal or laryngeal muco

238 tized male rats were tested for responses to mechanical stimulation of the urinary bladder, urethra,

239 IV) attenuated the CBF increase produced by mechanical stimulation of the vibrissae.

240 er-discharges, and/or increased responses to mechanical stimulation of their receptive fields, compar

241 Because direct mechanical stimulation of tip links has not been experim

242 closes the Venus flytrap upper leaf without mechanical stimulation of trigger hairs.

243 heless responded to specific types of gentle mechanical stimulation on hairy skin.

244 eatures are consistent with a lower level of mechanical stimulation on the cells in old versus young

245 osteoblastic differentiation is promoted by mechanical stimulation on titanium, and that the promoti

246 f algal cells in response to a novel form of mechanical stimulation, or a pulsed wave at the frequenc

247 ctors such as innervation, endolymph, normal mechanical stimulation, or an intact organ of Corti.

248 dothelial cells releasing ATP in response to mechanical stimulation, P2X(2/3) receptor antagonists el

249 local osteogenesis in response to increased mechanical stimulation, perhaps via releasing the local

250 Mechanical stimulation prevents OA-induced cartilage deg

251 studies demonstrate that electric pacing and mechanical stimulation promote maturation of the structu

252 Mechanical stimulation promotes osteocyte (and osteoblas

253 ased mineral deposition, suggesting that the mechanical stimulation provided by fluid shear forces in

254 isplay paralysis and seizures in response to mechanical stimulation, providing a complementary excita

255 The frequency of mechanical stimulation, rather than its amplitude, seeme

256 exhibited significantly lower thresholds to mechanical stimulation relative to wild-type neurons.

257 We demonstrate that local mechanical stimulation reliably triggers PVEM at the con

258 induced by normally innocuous low-threshold mechanical stimulation, represents a cardinal feature of

259 In WT mice, responses to mechanical stimulation returned to baseline 3 weeks afte

260 can reliably provoke VF if, and only if, the mechanical stimulation site overlaps the repolarization

261 found: fast adapting receptors responding to mechanical stimulation; slowly adapting receptors respon

262 n the activation of DNIC by noxious heat and mechanical stimulations, substance P release was measure

263 the body but do not habituate to repetitive mechanical stimulation such as tapping on the side of th

264 s and elicit a calcium influx in response to mechanical stimulation, such as fluid flow across the ap

265 enhanced the sensitivity of CD afferents to mechanical stimulation, suggesting that mAChR activation

266 was only 1.1 h and remained unchanged after mechanical stimulation, suggesting that rapid responses

267 le cell micro-manipulation and 2D cell sheet mechanical stimulation techniques.

268 T mice were significantly more responsive to mechanical stimulation than B6 control mice, as assessed

269 r stress provided a physiologically relevant mechanical stimulation that significantly promoted insul

270 are triggered to flux calcium by chemical or mechanical stimulation, the signal can be propagated wit

271 s exhibited a slow burst of exocytosis under mechanical stimulation; the expression of SNAP25B did no

272 In response to mechanical stimulation, these IS cells differentially ex

273 The method imposes localized mechanical stimulation through indentation of an elastom

274 When we imposed specific mechanical stimulation through the substrate, the stretc

275 We introduced a local mechanical stimulation to human umbilical vein endotheli

276 In this study we used mechanical stimulation to induce oligemia and hyperemia,

277 function in Abeta-LTMRs cause low-intensity mechanical stimulation to produce pain behavior.

278 measuring these relationships is to deliver mechanical stimulations to individual hair bundles with

279 estigated whether podocytes release ATP upon mechanical stimulation using a fluorometric approach.

280 latation (PD) was produced by vaginocervical mechanical stimulation (VCMS) in intact rats, and in rat

281 reased and afferent discharge in response to mechanical stimulation was attenuated.

282 release was measured in resting cells; then mechanical stimulation was delivered by injection of an

283 Sensitization to mechanical stimulation was found in 24.2% of silent noci

284 Mechanical stimulation was highly associated with sustai

285 Purely mechanical stimulation was not sufficient; the exogenous

286 Transmembrane dye flux evoked by mechanical stimulation was potentiated by low Ca(2+) and

287 logue D-NAME, peak [Ca(2+)](i) transients to mechanical stimulation were increased more than 2-fold.

288 Behavioral pain responses to noxious mechanical stimulation were inhibited in a reversible, d

289 ehavioral responses to innocuous and noxious mechanical stimulation were tested using calibrated von

290 phosphorylation indicated that CCL increased mechanical stimulation, while a higher number of Pax7(+)

291 functional data support the hypothesis that mechanical stimulation with a brush releases nucleotides

292 calcium levels and transients increased upon mechanical stimulation with a hydrogel, and single cells

293 cribes how to combine magnetic-field-induced mechanical stimulation with confocal fluorescence micros

294 rized by recording their responses to graded mechanical stimulation with controlled forces of 10-120

295 bearing cells in these clusters responded to mechanical stimulation with currents that were reminisce

296 ibroblasts and kidney cells upon chemical or mechanical stimulation with high specificity, high sensi

297 Here, we observed that podocytes respond to mechanical stimulation with increased intracellular calc

298 This conductance develops very rapidly upon mechanical stimulation with its latency and activation t

299 f an elastomeric substrate and combines this mechanical stimulation with whole-cell patch clamp recor

300 firing frequency with increased strength of mechanical stimulation, with evidence of response satura