ライフサイエンスコーパス: mechanical stimulation

1 hanotransduction on the cellular response to mechanical stimulation.

2 determines the linearity and sensitivity to mechanical stimulation.

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

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

5 the exquisite sensitivity of the sacculus to mechanical stimulation.

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

7 adopt different orientations in response to mechanical stimulation.

8 PER2 expression was also sensitive to mechanical stimulation.

9 be required for Cx43 hemichannel opening by mechanical stimulation.

10 zation of peripheral nociceptor terminals to mechanical stimulation.

11 nuclear translocation or survival induced by mechanical stimulation.

12 an signal the onset, offset and intensity of mechanical stimulation.

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

14 position that underlies their sensitivity to mechanical stimulation.

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

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

17 doses of morphine showed hypersensitivity to mechanical stimulation.

18 ing capacity display compromised response to mechanical stimulation.

19 persensitive hindlimb withdrawal response to mechanical stimulation.

20 in response to direct activation or noxious mechanical stimulation.

21 s are generated independently by thermal and mechanical stimulation.

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

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

24 cally required for habituation to repetitive mechanical stimulation.

25 hannel acts to induce neuronal adaptation to mechanical stimulation.

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

27 CIRL dampens the response of nociceptors to mechanical stimulation.

28 anifested as hypersensitivity to thermal and mechanical stimulation.

29 role in the osteoblast anabolic response to mechanical stimulation.

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

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

32 hat exhibit seizures and paralysis following mechanical stimulation.

33 imulation, and enhanced responses to noxious mechanical stimulation.

34 cells to touch, particularly after repeated mechanical stimulation.

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

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

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

38 urons responded to both gastric and duodenal mechanical stimulation.

39 sistant to rapamycin in muscles subjected to mechanical stimulation.

40 y of nerve terminal impulse discharges under mechanical stimulation.

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

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

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

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

45 during the early stages of gravitropism and mechanical stimulation.

46 gle group IV fibre activity to a ramp-shaped mechanical stimulation.

47 mic force microscopy (AFM) probes to deliver mechanical stimulation.

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

49 combination with pharmacological probes and mechanical stimulation.

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

51 of efference on the hair bundle response to mechanical stimulation.

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

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

54 m signaling attenuated the response to acute mechanical stimulation.

55 apeutic potential for magnetically modulated mechanical stimulation.

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

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

58 ections describing biochemical, physical and mechanical stimulations.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 proline-rich receptor-1 (IGPR-1) responds to mechanical stimulation and increases the stiffness of en

74 leased from platelets upon activation and/or mechanical stimulation and many of the benefits attribut

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

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

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

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

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

80 ompartments, axons are highly susceptible to mechanical stimulation and predominantly show sustained

81 on for the formation of actin bundles due to mechanical stimulation and provide new insights into the

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 During durotaxis, mechanical stimulation by matrix rigidity leads to direc

106 Direct mechanical stimulation by shear loading of articular car

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

108 Mechanical stimulation can prevent adipogenic and improv

109 Mechanical stimulation can regulate skeletal muscle diff

110 Mechanical stimulations can prevent bone loss, but their

111 robial symbionts in herbivore secretions and mechanical stimulation caused by insects, have illuminat

112 strong apoptotic cellular response, whereby mechanical stimulation causes those cells near the crack

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

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

115 Rostral RB neurons respond to mechanical stimulations close to the soma and produce up

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

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

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

119 Mechanical stimulation contributes to the health of alve

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

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

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

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

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

125 Finally, mechanical stimulation disrupts the assembly of ILK and

126 uted complementary information regarding the mechanical stimulation event.

127 It was found that mechanical stimulation-evoked Ca(2+) responses in astroc

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

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

130 rmal Ca(2+) concentration has been restored, mechanical stimulation facilitates the reconstitution of

131 Secondary cartilage requires mechanical stimulation for its induction and maintenance

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

133 The study supports the benefit of mechanical stimulations for locally and remotely suppres

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

135 nd accuracy for detecting weak physiological mechanical stimulation from diaphragm motions and blood

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 pproaches, cell sources, and biochemical and mechanical stimulation have resulted in constructs exhib

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

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

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

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

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

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

147 A reduction in mechanical stimulation in chronologically aged skin was

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

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

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

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

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

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

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 and 20 minutes of alternating electrical and mechanical stimulations increase the force by 18% and 31

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

158 Dye loading experiments showed that mechanical stimulation increased open probability of car

159 Mechanical stimulation increased SLV recycling, increasi

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

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

162 43 and that this interaction is required for mechanical stimulation-induced opening of the Cx43 HC.

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

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

165 , and a coordinated, combined electrical and mechanical stimulation induces the desired ECM remodelli

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

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

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

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

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

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

172 Mechanical stimulation is recognized as a potent modulat

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

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

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

176 Previously, strikes have been studied using mechanical stimulation like poking or pinching the insec

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

178 Mechanical stimulation likewise elicited an apoplastic a

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

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

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

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

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

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

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

186 elevations, ATP, and vesicular release after mechanical stimulation of a single osteoblast, the model

187 Mechanical stimulation of airway epithelial cells causes

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 With the increased interest in mechanical stimulation of cells and huge potential for c

191 Mechanical stimulation of cells was carried out through

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

193 RECENT FINDINGS: Mechanical stimulation of conventional outflow cells due

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

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

196 Mechanical stimulation of DM skin or DM skin graft trans

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

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

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

200 Mechanical stimulation of fibroblasts induces changes in

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

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

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

204 evice capable of simultaneous electrical and mechanical stimulation of human induced pluripotent stem

205 In this study, we discovered that mechanical stimulation of integrin beta1 leads to the ph

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

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

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

209 Recently, nanoscale mechanical stimulation of mesenchymal stem cells (MSCs)

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

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

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

213 Mechanical stimulation of plants triggers a cytoplasmic

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

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

216 Third, mechanical stimulation of skeletal muscle with intermitt

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

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

219 Mechanical stimulation of stretch-activated calcium chan

220 Mechanical stimulation of the artery, by increased intra

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

222 Mechanical stimulation of the cultured CM using the CCCM

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

224 of mouse refusal to determine thresholds for mechanical stimulation of the face with Von Frey filamen

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

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

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

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

229 we recorded behavioral withdrawal evoked by mechanical stimulation of the hindpaw and, simultaneousl

230 Mechanical stimulation of the hindpaw consisted of repea

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

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

233 The mechanical stimulation of the outer hair cell hair bundl

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

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

236 l and mechanical perturbations, we show that mechanical stimulation of the SAM causes transient chang

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

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

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

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

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

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

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

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

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

246 While the impact of quick mechanical stimulation on molecular changes in cells has

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

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

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

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

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

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

253 Mechanical stimulation prevents OA-induced cartilage deg

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

255 Mechanical stimulation promotes osteocyte (and osteoblas

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

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

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

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

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

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

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

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

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

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

266 reclinical and human study demonstrated that mechanical stimulations, such as knee loading and step a

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

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

269 Bone cells are exposed to dynamic mechanical stimulation that is transduced into cellular

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

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

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

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

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

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

276 These cells are also finely tuned sensors of mechanical stimulation to coordinate with effector cells

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

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

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

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

281 Mechanical stimulation triggers Piezo channels to open,

282 Here we characterize the nuclear response to mechanical stimulation (uniaxial cyclic stretch).

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

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

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

286 This mechanical stimulation was coupled and synchronized with

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

288 Mechanical stimulation was highly associated with sustai

289 Purely mechanical stimulation was not sufficient; the exogenous

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

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

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

293 Given reduction of bone sensitivity to mechanical stimulation with age, these findings may lead

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

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