ライフサイエンスコーパス: stimulation

1 scious perception of auditory near-threshold stimulation).

2 otein activation resulting from dopaminergic stimulation.

3 and decrease its activity under chemogenetic stimulation.

4 R were profiled by qRT-PCR after aldosterone stimulation.

5 following TNF (tumor necrosis factor)-alpha stimulation.

6 ction on the cellular response to mechanical stimulation.

7 s without any hand manipulation and electric stimulation.

8 blasts (MEFs), and human HeLa cells upon IFN stimulation.

9 and remain in their state for seconds after stimulation.

10 a disintegrin and metalloproteinase-17 upon stimulation.

11 RC1 activity in the absence of growth factor stimulation.

12 d were specific to active compared with sham stimulation.

13 cells that have recently received antigenic stimulation.

14 n of alpha oscillations by tVNS than by sham stimulation.

15 actors that occur during and after antigenic stimulation.

16 lesions of VLO abolished the effects of SubM stimulation.

17 in mouse and human neutrophils upon integrin stimulation.

18 sic increase of RhoA activity upon histamine stimulation.

19 Associates problems before, during and after stimulation.

20 e behaviors and aversive learning to noxious stimulation.

21 1) or tumor necrosis factor alpha (TNFalpha) stimulation.

22 creased IL-2 expression after tetanus toxoid stimulation.

23 on with the effect depending on the phase of stimulation.

24 les elicited using transcutaneous electrical stimulation.

25 e and was perturbed by indiscriminate global stimulation.

26 responses and reduced inhibitory input to CC stimulation.

27 y in the somatosensory cortex during sensory stimulation.

28 a less invasive alternative than subthalamic stimulation.

29 countering the high levels of environmental stimulation.

30 single human cells to process repetitive IFN stimulation.

31 ow a hair bundle is desensitized by efferent stimulation.

32 cytolytic function were restored after IL-2 stimulation.

33 ve times larger than those evoked by sensory stimulation.

34 o the plasma membrane in response to insulin stimulation.

35 icroglia in response to interleukin-4 (IL-4) stimulation.

36 ory and excitatory currents that persists on stimulation.

37 in differentiated VSMCs in response to serum stimulation.

38 h was unrelated to the procedure, device, or stimulation.

39 ir modulation during a sensory-task, whisker stimulation.

40 ng waves) similar to that elicited by visual stimulation.

41 tal inputs and fail to depress with repeated stimulation.

42 to controls at baseline and following IL-33 stimulation.

43 nse to both unspecific and pathogen-specific stimulations.

44 cKO mice were unresponsive to high frequency stimulation (100 Hz), while the NMN-treated cKO mice res

45 increases B-cell signaling following antigen stimulation-a mechanism conferring selective advantage d

46 actography to parcellate the total volume of stimulation across all patients to identify local region

47 ver, across conditions with identical visual stimulation, activation shifted the decision criterion s

48 P2X7 stimulation affected cell cycling of effector T cells an

49 p = 0.0001) for patients receiving bilateral stimulation after excluding one patient with pleural eff

50 plying that pDCs were refractory to in vitro stimulation after IFNalpha production in vivo.

51 Upon cold or beta-adrenergic stimulation, Aifm2 associates with the outer side of the

52 l-stimulation, in bright environments, photo-stimulation also contributes to the afterglow emission a

53 f GA, were driven by continuous choroidal MC stimulation and activation in a slow release fashion in

54 ysis of human fibroblasts undergoing LTbetaR stimulation and affinity-purification mass spectrometry

55 Membrane-bound ligands for stimulation and co-stimulation of T-cell receptors are p

56 stocysts naturally conceived without hormone stimulation and developed in vivo prior to transfer can

57 ll responses to antigen in the absence of co-stimulation and do so, in part, by repressing the expres

58 adening of the AP(syn) during high-frequency stimulation and eliminated synaptic facilitation without

59 calcium influx resulting from acetylcholine stimulation and G-protein activation resulting from dopa

60 We refined ovarian stimulation and in vitro fertilization (IVF) methods est

61 in diameter, and allowed chronic electrical stimulation and monitoring for 2 months without disrupti

62 Here, we show that both IFN-gamma stimulation and murine norovirus (MNV) infection induce

63 n nuclear (TAN) lines are induced by stretch stimulation and nuclear envelope (NE) proteins including

64 rmal System, Korea, where detailed hydraulic stimulation and on-site seismicity monitoring data provi

65 A neurons produced optical intracranial self-stimulation and place preference.

66 of DHHC5 can be palmitoylated in response to stimulation and such modification is important for its d

67 der to form heme that is required for growth stimulation and survival in vivo Consequently, B. fragil

68 in retinal blood flow in response to flicker stimulation and systemic hyperoxia in mice using a laser

69 of retinal blood flow in response to flicker stimulation and systemic hyperoxia may be useful indexes

70 < 0.05) when the interval between trigeminal stimulation and transcranial magnetic stimulation (TMS)

71 Approaches such as deep brain stimulation and treatment with levodopa-carbidopa entera

72 how little depression in response to tetanic stimulation and, therefore, can be distinguished other E

73 s-eQTLs are largely specific to cell type or stimulation, and 31% and 52% of genes with cis-eQTLs hav

74 switching, without involving any additional stimulation, and a relation between the switching magnit

75 that combines both mechanical and electrical stimulation, and as such, we foresee it finding applicat

76 bring antisense oligonucleotides, deep brain stimulation, and gene therapy into the clinic within the

77 ted form of repetitive transcranial magnetic stimulation, and it is an effective add-on intervention

78 ulation paradigms, closed-loop and on-demand stimulation, and sensing technologies are expected to en

79 e hyperplasia through Wnt-mediated paracrine stimulation, and suggest that this tumor suppressor can

80 e produced by noninvasive transcranial brain stimulation, and therefore possibly able to modulate neu

81 ic, and rectal distension, cutaneous thermal stimulation, and vulvar pressure) to establish and valid

82 alian lymphocytes following antigen receptor stimulation are Ca(2+) release-activated Ca(2+) (CRAC) c

83 The anti-inflammatory effects of vagus nerve stimulation are well known.

84 nsient stimulation pulse shaping, we reduced stimulation artifact on miniSTAR muLED optoelectrodes to

85 We found that stimulation at 1 Hz for 1 hr resulted in an almost compl

86 -of-plane for highly controlled photothermal stimulation at subcellular precision without the need fo

87 ced nicotinic receptor affinity using NS9283 stimulation at the unorthodox alpha-alpha nicotinic bind

88 IL-6 stimulation augmented mTOR activation in iMCD patients,

89 Additionally, electrical stimulation based on drawn-on-skin electronics demonstra

90 4 reduces T cell proliferation upon weak TCR stimulation but does not significantly affect phosphoryl

91 eir subcellular redistribution and autocrine stimulation by cellular ATP release and was perturbed by

92 Yet the motivational effects of paired CeA stimulation can be reversed to negative valence in a Pav

93 The high-bandwidth optical-stimulation capacity of the device might facilitate the

94 ptotic cellular response, whereby mechanical stimulation causes those cells near the crack to die, as

95 tle cue on MEPs elicited by cervicomedullary stimulation (CMEPs) on biceps and triceps brachii in mal

96 hich successfully classified three different stimulation conditions with a test accuracy of 94.66%, a

97 of two TMS sessions, continuous theta-burst stimulation (cTBS) was applied to either a control site

98 Upon IL8 stimulation, cytosolic NADP(+) is transported to acidifi

99 nsensus has yet to emerge whether deep brain stimulation (DBS) for treatment-refractory obsessive-com

100 Deep brain stimulation (DBS) is a treatment option for refractory c

101 Deep brain stimulation (DBS) is an effective treatment option for p

102 ced Parkinson's can be treated by deep brain stimulation (DBS) of the subthalamic nucleus (STN).

103 In the presence of co-stimulation-deficient T cell activation, anergy is a dom

104 nce includes tactile, thermal, and olfactory stimulation delivered to the young via contact with the

105 entified transcription factors that regulate stimulation-dependent E-P interactions.

106 TGFbeta stimulation downregulated SOX2 and induced epithelial-to

107 We found that this "electro-haptic" stimulation dramatically improved sound localisation.

108 ed vascular endothelial growth factor (VEGF) stimulation due to a reduced capacity to re-synthesize p

109 memory consolidation is affected by sensory stimulation during sleep.

110 Empirical studies found that sensory stimulation during SWS can selectively enhance memory co

111 ected by tDCS, confirming the specificity of stimulation effects to movement sensations.

112 Electrical field stimulation (EFS) in the presence of L-NNA and MRS 2500

113 iability in the spatiotemporal parameters of stimulation employed to date notwithstanding, it is like

114 Agonist stimulation enhanced PDEV release, but did not alter the

115 nt inhibition of face M1, while facial nerve stimulation evoked LAI but not SAI.

116 Over up to 29 days, stimulation evoked sensory percepts in consistent locati

117 It was found that mechanical stimulation-evoked Ca(2+) responses in astrocytes of the

118 Neural responses arise from stimulation-evoked, temporally dynamic excitatory (E) an

119 Reversely, upon growth factor stimulation, Exo70 is phosphorylated by ERK1/2, which in

120 ntly upregulated MRGPRX2 expression in both, stimulation for 24 hours with anti-IgE, C5a, fMLP, and I

121 ene applying Easi-CRISPR followed by BMP-4/7 stimulation for 72 h.

122 ulosa cells and cultured in vitro with BMP-4 stimulation for three different durations In addition, t

123 matergic system, leading to excessive, toxic stimulation, have been associated with AD.

124 as recently demonstrated that high-frequency stimulation (HFS) of cortical inputs induced long-term d

125 Intracranial electrical stimulation (iES) of the human brain has long been known

126 ed for several months after the cessation of stimulation, illustrating long-term benefits.

127 Here, we show that persistent antigenic stimulation impaired ADP-coupled oxidative phosphorylati

128 continuous theta-burst transcranial magnetic stimulation in a randomized, sham-controlled design.

129 thereby abrogated an anergic response to BCR stimulation in CLL cells.

130 in response to dopamine and acetylcholine co-stimulation in living flies.

131 proinflammatory cytokines after FcepsilonR1 stimulation in mast cells, implicating a role in allergy

132 beta3 adrenoceptor (beta3 AR) mediates pump stimulation in myocytes.

133 ay narrowing in response to electrical field stimulation in precision cut lung slices (PCLS) were ass

134 multielectrode array recordings during light stimulation in retinas of adult guinea pigs of either se

135 ent neuronal dynamics arise from optogenetic stimulation in the primate brain.

136 lts upregulated PD-1 following P. falciparum stimulation in vitro Additionally, functional in vitro s

137 l response to Abeta peptide 1-42 (Abeta(42)) stimulation in vitro, in aging-associated microgliosis i

138 Besides thermal-stimulation, in bright environments, photo-stimulation a

139 ulation in the retina when exposed to visual stimulation, in our case flicker.

140 active IL1beta or pharmacologic inflammasome stimulation increased HSPC number as assessed by in situ

141 e loading experiments showed that mechanical stimulation increased open probability of carboxyfluores

142 ubpopulations showed different basal and BCR stimulation-induced phosphorylation levels of downstream

143 troencephalographic recording and electrical stimulation integrated and synchronized with virtual rea

144 pairing CS presentation with BLA-ChR2 photo-stimulation intensified responding for the CS.

145 lized therapies (e.g., transcranial magnetic stimulation, intracerebral stem/progenitor cells) that c

146 ies of the physical environment from retinal stimulation is a distinct and more challenging computati

147 ing and genetic-engineering-assisted optical stimulation is a powerful tool for the study of neuronal

148 se control nodes, it is theorized that brain stimulation is able to selectively target difficult-to-r

149 plexity three months after peripheral immune stimulation is accompanied by impairment in long-term po

150 If the cell stimulation is mediated by piezomechanical SAWs, we obse

151 hould be a primary consideration if auditory stimulation is used to enhance slow-wave activity.

152 ceptor II (TbetaRII), in response to TGFbeta stimulation, is a prerequisite for TGF signaling, we inv

153 Intermittent theta-burst stimulation (iTBS) is a noninvasive brain stimulation tr

154 troconvulsive therapy, transcranial magnetic stimulation, ketamine infusions, and, more recently, gla

155 In vivo imaging revealed that behavioral stimulation likewise elicited focal synaptic responses w

156 We tested the hypothesis that A2AR stimulation maintains or enhances mitochondrial function

157 developed a mobile deep brain recording and stimulation (Mo-DBRS) platform that enables wireless and

158 y (n = 35), repetitive transcranial magnetic stimulation monotherapy (n = 35), or sham stimulation (n

159 ic stimulation monotherapy (n = 35), or sham stimulation (n = 35).

160 ypical spike detection threshold, at optical stimulation of >50 mW mm(-2) irradiance.

161 resistance to chemotherapy and indicate that stimulation of A3B expression by activation of DNA repai

162 rther, within the PVN, selective optogenetic stimulation of afferents that arise from these lamina te

163 hetamine depresses neurotransmission through stimulation of astrocytes and the consequent A(1) recept

164 Here, we show that adrenergic stimulation of BAT activates a PKA-dependent mitochondri

165 Responses to chemogenetic and pharmacologic stimulation of beta-cells were blocked by a 5-HT(3)R ant

166 In this study, we show that stimulation of CD4 T cells from C57BL/6 mice not only de

167 and they suggest a therapeutic potential of stimulation of ChIs to restore gait and balance, and to

168 Selective stimulation of cholinergic axons was sufficient to induc

169 Striatal field recordings and electrical stimulation of corticostriatal afferents revealed that h

170 Thus, our results suggest that stimulation of D1 receptors in the dentate gyrus is a po

171 The Pif1-dependent stimulation of DNA synthesis across strong protein barri

172 unds and thereby delays healing, whereas the stimulation of dopamine D1 receptors promotes angiogenes

173 The stimulation of dopamine D2 receptors negatively regulate

174 We used optogenetic stimulation of either glutamatergic or cholinergic affer

175 We asked whether pharmacological stimulation of endogenous neural precursor cells (NPCs)

176 s to test a novel neuromodulation therapy of stimulation of epicardial cardiac nerves passing along t

177 uction and secretion of matrix proteins upon stimulation of fibroblasts by transforming growth factor

178 Optogenetic stimulation of GAD65(+) TBCs increased chorda tympani ne

179 Optogenetic stimulation of GAD65(+) TBCs on the anterior tongue had

180 le of simultaneous electrical and mechanical stimulation of human induced pluripotent stem cells in 6

181 Ligand stimulation of IGF1R promotes its clathrin-dependent end

182 d changes in tissue impedance in response to stimulation of individual fascicles (tibial, peroneal an

183 se components affect the direct and indirect stimulation of iNKT cells, we used mice deficient for ei

184 s inhibited Ca(2+) transients in ICC-SS, and stimulation of intrinsic nerves activated nitrergic resp

185 One hypothesis suggests that cholinergic stimulation of islets by pancreatic ganglia resets these

186 uron-glial cultures and macrophage under the stimulation of lipopolysaccharide (LPS), KCl and oxygen/

187 e results suggest that presynaptic mu-opioid stimulation of local PV(+) interneurons induces a long-l

188 Stimulation of low threshold afferents in the trigeminal

189 Stimulation of mDCs with PN also induced a 7-fold increa

190 Here, we used ex vivo stimulation of memory T cells and screening of naive and

191 der high temperature reversed the short-term stimulation of metabolic rates, resulting in increased r

192 hat opioid reward is more likely mediated by stimulation of MORs in GABA afferents from other brain r

193 eals significant influence of MoS(2) and NIR stimulation of MoS(2) on integrins, cellular migration,

194 The interaction of MoS(2) and NIR stimulation of MoS(2) with human stem cells is investiga

195 nstrate direct and spatially confined neural stimulation of mouse brain and modulation of motor activ

196 Intersectional optogenetic stimulation of MPOA neurons that express ESR1 and vesicu

197 threshold for dendritic spikes), and (3) the stimulation of neighboring synapses.

198 h-clamp recording, we found that optogenetic stimulation of nigrostriatal dopamine axons rapidly and

199 ethyl-d-aspartate (NMDA) receptors following stimulation of non-motor regions.

200 In support of this, stimulation of nonlesional explants with IL-1beta result

201 used a novel rat model in which cholinergic stimulation of PFC produced wakefulness despite continuo

202 Stimulation of plasma membrane receptor tyrosine kinases

203 e useful for the treatment of CUD, likely by stimulation of PPARalpha and PPARgamma in the mesolimbic

204 Optogenetic stimulation of projections from these neurons to the par

205 isease, where cell type-specific optogenetic stimulation of PV(+) neurons over other neuron populatio

206 We observe diverse SNr responses to stimulation of SNr-projecting striatal and GPe neurons,

207 Mechanistically, stimulation of specific bone marrow cell populations in

208 Antigen stimulation of T cells in ex vivo vaginal tissue culture

209 embrane-bound ligands for stimulation and co-stimulation of T-cell receptors are presented via the fl

210 TCR stimulation of T-PLL cells evoked higher-than-normal cel

211 ex in response to repeated brief optogenetic stimulation of thalamocortical afferents.

212 Mice also acquired operant self-stimulation of thalamostriatal terminals when ChR2 expre

213 nwound ssDNA product, resulting in a ~5-fold stimulation of the apparent DNA-unwinding rate.

214 plex nerve network in response to electrical stimulation of the CN, which was clearly differentiated

215 ed by the muscle twitch evoked by electrical stimulation of the facial nerve.

216 nia may respond differentially to deep brain stimulation of the globus pallidus pars interna (GPi DBS

217 drug intake, are primarily mediated through stimulation of the GLP-1 receptor.

218 Stimulation of the membrane Na(+)-K(+) pump should lower

219 Stimulation of the metabotropic GABA(B) receptor by gamm

220 upper limb muscles were first measured after stimulation of the primary motor cortex (M1), corticospi

221 s are consistent with the theory that anodal stimulation of the rTPJ increases the precision of value

222 orts the view that transcutaneous electrical stimulation of the spinal cord (TESS) promotes functiona

223 nstrate that clinically effective deep brain stimulation of the subthalamic nucleus differentially mo

224 Stimulation of the terminals in simulated models of infl

225 Stimulation of this colonic intestinalization process by

226 We further showed that stimulation of this population of vHC-PrL projectors sup

227 Stimulation of trigeminal afferents induced short-latenc

228 ults identify the involvement of PKCdelta in stimulation of TRPC1-based SOCs and highlight that store

229 llagen expression, that were associated with stimulation of tumour growth by DDRs and collagen I.

230 ly been shown that low-level, transcutaneous stimulation of vagus nerve at the tragus (LLTS) reduces

231 mall spots of light produced with electrical stimulation of visual cortex (phosphenes) will combine i

232 Notably, we report the novel finding that stimulation of VLPO glutamatergic neurons causes a stron

233 mediating the clinical effects of deep brain stimulation on motor symptoms in Parkinson's disease.

234 porary percutaneous electrical phrenic nerve stimulation on user-specified inspiratory breaths while

235 during and after 3 min flicker light (12 Hz) stimulation; on day 2, retinal blood flow was measured e

236 g seismicity corresponding to the sequential stimulation operations in Pohang, South Korea.

237 itis by partial duct ligation with caerulein stimulation or intraperitoneal injection of l-arginine i

238 sured in isolated cardiomyocytes under field stimulation or patch clamp.

239 er outcomes involved reward gain, electrical stimulation, or reward loss.

240 als (MEPs) elicited by transcranial magnetic stimulation over the arm representation of the primary m

241 akthroughs in electrode and battery designs, stimulation paradigms, closed-loop and on-demand stimula

242 g mice while stimulating MNTB afferents with stimulation patterns that mimicked those present in vivo

243 Prolonged intermittent theta burst stimulation (piTBS) with triple doses of the standard pr

244 Direct pathway stimulation produced a resetting of the internal timing

245 ations by implementing adaptive sampling and stimulation protocols compatible with parameter identifi

246 With transient stimulation pulse shaping, we reduced stimulation artifa

247 The responses of these networks to visceral stimulation rather than their organisation at rest may b

248 include adoptive transfer therapies, direct stimulation, recruitment of NK cells into the tumor micr

249 lasting and marked effects of M(1) receptor stimulation reinforce our interest in this target as pot

250 Chronic optical stimulation revealed normal homeostatic plasticity of Up

251 ) pro-inflammatory or IL-4 anti-inflammatory stimulation revealed the importance of Trem2 in driving

252 RTN stimulation robustly increased breathing frequency and a

253 ippocampus dentate gyrus (DG) in an electric stimulation rodent model which displays classical HS dam

254 idence that repetitive transcranial magnetic stimulation (rTMS) can be used as a treatment for dyspha

255 Glucose stimulation significantly enhances L-DOPA uptake, leadin

256 Every stimulation site activated a distinctive pattern of patc

257 om improvement in an exploratory analysis of stimulation sites from 14 clinical TMS trials.

258 External stimulations such as seafloor hydrocarbon seeps have bee

259 ty and excitability changes from the site of stimulation, such that after active treatment, the dlPFC

260 zed that exercise combined with non-invasive stimulation targeting spinal synapses further promotes f

261 sory cortices by using transcranial magnetic stimulation techniques.

262 Upon ligand stimulation, the endoplasmic reticulum (ER) protein STIN

263 Upon growth factor stimulation, the guanine-nucleotide exchange modulator d

264 ustatory neurons that responded best to NaCl stimulation through a benzamil-sensitive mechanism.

265 Here, we combined transcranial magnetic stimulation (TMS) and fMRI to test the role of awake con

266 re we used fMRI-guided transcranial magnetic stimulation (TMS) and simultaneous electroencephalograph

267 ducer was coupled to a transcranial magnetic stimulation (TMS) coil.

268 ceived left prefrontal transcranial magnetic stimulation (TMS) for treatment of depression (discovery

269 Transcranial magnetic stimulation (TMS) measures of corticospinal excitability

270 eminal stimulation and transcranial magnetic stimulation (TMS) of fM1 was 15-30 ms.

271 plasticity often used transcranial magnetic stimulation (TMS) of hand motor cortex (M1) as a model,

272 e applied paired-pulse transcranial magnetic stimulation (TMS) protocols to evaluate the excitation i

273 levant processes using transcranial magnetic stimulation (TMS).

274 citability (CSE) using transcranial magnetic stimulation (TMS).

275 a coli CheY protein transduces chemoreceptor stimulation to a highly cooperative flagellar motor resp

276 eech and spatial hearing cues through haptic stimulation to augment the electrical CI signal.

277 nstrated the use of in situ electrical field stimulation to deactivate the adhesive property of catec

278 asured after anti-CD3 or vaccinia virus (VV) stimulation to measure T cells elicited after childhood

279 High Definition Transcranial Direct Current Stimulation to the rATL (active and sham condition) or t

280 nal timing process, whereas indirect pathway stimulation transiently paused timing, and proportionall

281 st stimulation (iTBS) is a noninvasive brain stimulation treatment that has been approved by the U.S.

282 ciple, considered inadequate for deep tissue stimulation unless accompanied by optic fiber insertion.

283 IL-23 and IL-1beta stimulation upregulates LAT1 expression and induces mTOR

284 Photothermal stimulation using NW-templated 3D fuzzy graphene (NT-3DF

285 l strategy that uses closed-loop vagus nerve stimulation (VNS) paired with tactile rehabilitation to

286 Transcutaneous electrical stimulation was applied onto the fingertips of teleopera

287 The stimulation was completely abolished by pretreatment wit

288 alpha-Band suppression following tactile stimulation was lateralized relative to the stimulated h

289 fy cysteines that are redox regulated by EGF stimulation, we performed time-resolved quantification o

290 Vibrio casei had the strongest growth stimulation when exposed to all fungi.

291 nals constitutively, independent of IL-1beta stimulation, which was abrogated by deletion of IRAK4.

292 e exclusively increased by contralateral eye stimulation, which was enhanced by expressing tetanus ne

293 ic T-cell responses between groups following stimulation with an EBV-infected cell lysate.

294 Stimulation with cowhage induced a more intensive itch s

295 ansfected with a miR-145a mimic, followed by stimulation with lipopolysaccharide (LPS).

296 Upon stimulation with microbes, monocytes from PSC patients p

297 more intensive itch sensation compared with stimulation with other substances in all patient groups

298 Local soma stimulations with micrometer-sized beads evoke transient

299 ts an insignificant thermal contributions to stimulation, with a predicted increase of 0.03 (o)C for

300 e chip-scale axon and neuron specific neural stimulation, with future applications in neural prosthet