ライフサイエンスコーパス: stimulation

1 ith many beneficial actions arising from D1R stimulation.

2 on of its downstream ERK cascade without EGF stimulation.

3 n frequency, reaching steady state 1 d after stimulation.

4 oked potentials associated with visual field stimulation.

5 rove performance further during intermittent stimulation.

6 d responsiveness to continuous or repetitive stimulation.

7 subthreshold depolarization preceding mAChR stimulation.

8 r Smad3 was a more precise outcome of ligand stimulation.

9 ices which are capable of more precise point stimulation.

10 ipid mediators in response to subsequent TLR stimulation.

11 oad conditions and/or at higher frequency of stimulation.

12 nce at 24 h post-transcranial direct current stimulation.

13 xternalization during surgery for deep brain stimulation.

14 n innate response to isolation or mechanical stimulation.

15 conductances can be activated with stronger stimulation.

16 regulated genes in patient T cells upon IL-2 stimulation.

17 ve T cells unresponsive to further antigenic stimulation.

18 the ability to induce rapid gravity or light stimulation.

19 e duration of inhibition resulting from, LHb stimulation.

20 ion potentials in the absence of presynaptic stimulation.

21 lf the energy of conventional high frequency stimulation.

22 air of distinctive neuronal responses to the stimulation.

23 s, and HNECs within 15 minutes of local TLR7 stimulation.

24 he net stimulatory effect of beta-adrenergic stimulation.

25 tivation and sterol biosynthesis after M-CSF stimulation.

26 DA ratio is observed following in vivo light stimulation.

27 and produced pro-inflammatory cytokines upon stimulation.

28 secretion in response to lipopolysaccharide stimulation.

29 nhuman primates induced by paired electrical stimulation.

30 tralized rotors by optical S1-S2 cross-field stimulation.

31 r to 3 initial months of VIM-only or VO-only stimulation.

32 both 6 months and 12 months of ongoing brain stimulation.

33 HCV inhibited the recall reaction to antigen stimulation.

34 less interferon-gamma in response to T-cell stimulation.

35 the anti-inflammatory role of MCL after PGN stimulation.

36 equences of transcranial alternating current stimulation.

37 code distinct stimulation patterns as massed stimulation.

38 ectrode and several types of multi-electrode stimulation.

39 nflammatory cytokines in response to ex vivo stimulation.

40 iquitinated targets of LUBAC following TRAIL stimulation.

41 on cocaine locomotion produced by peripheral stimulation.

42 duals in response to M. tuberculosis antigen stimulation.

43 re dramatic glycolytic responses to hormonal stimulation.

44 pression after interleukin-1 beta (IL-1beta) stimulation.

45 straint stress or optogenetic C1 neuron (C1) stimulation (10 min) protected mice from ischemia-reperf

46 nces in LV mechanics with altered adrenergic stimulation achieved through post-handgrip-exercise isch

47 between eating performance and environmental stimulation, adjusting for resident characteristics (i.e

48 activity predominant in early windows and DN stimulation affecting the network in later windows.

49 ing cell; those episomes that did respond to stimulation, aggregated within large domains that appear

50 trol of initiation and assembly of CCPs, EGF stimulation also elicited a Ca(2+)- and PKC-dependent re

51 Cell stimulation and activation did not mobilize CD33m to the

52 mals were divided into three groups based on stimulation and body weight (i.e., lean nonstimulated, o

53 receptors play important roles in T-cell co-stimulation and co-inhibition.

54 hex as a direct target of RUNX1 and FLT3-ITD stimulation and confirmed high HHEX expression in FLT3-I

55 Treg percentage before and after stimulation and FOXP3mRNA expression ex vivo decreased f

56 e use a novel paradigm of repetitive whisker stimulation and in vivo calcium imaging to assess tactil

57 exhibit a similar suppressive effect on TLR-stimulation and inflammatory cytokine expression from ma

58 oinflammatory cytokine response to bacterial stimulation and less human leukocyte antigen - antigen D

59 (RMTg) regions were activated by peripheral stimulation and LHb lesions reversed the inhibitory effe

60 ts link to conscious experience, and reviews stimulation and patient studies of the cortical basis of

61 ecreted more inflammatory cytokines with LPS stimulation and showed more phagocytic activity.

62 ecursor cells and was regulated by antigenic stimulation and signals from the kinase mTOR.

63 ipids in human fibroblasts upon inflammatory stimulation and subsequent treatment with dexamethasone,

64 The interval between the auditory stimulation and the following R peak was significantly s

65 fects dependent on the relative phase of the stimulation and the internal cognitive processing state.

66 istic firing accommodation during maintained stimulation, and reduced membrane channel density causes

67 gnaling blockade upon myostatin or activin A stimulation, and this leads to only a small increase in

68 of real or sham transcranial direct current stimulation applied to the left frontal cortex.

69 ic signals in the absence of a task or overt stimulation are used to infer neural activity.

70 r pressure-time-product were achieved during stimulation assisted breaths in all 22 paced subjects (r

71 inal prostheses), and for closed-loop neural stimulation at a much larger scale than currently possib

72 alhm1 knockout cultures following mechanical stimulation at a pressure of 55 mmHg for 50 milliseconds

73 We show that targeted optogenetic stimulation based on analysis of AT morphology may be a

74 erformance in animals impaired by continuous stimulation but did not improve performance further duri

75 both their basal peptidase activity and the stimulation by ATPgammaS.

76 a fusion clamp, making release dependent on stimulation by Ca(2+)SIGNIFICANCE STATEMENT Syntaxin 1A

77 that both ATPase sites are required for the stimulation by DNA.

78 esynaptic cholinergic synapses to respond to stimulation by elevating presynaptic choline uptake and

79 Acute or chronic stimulation by IL-4 modified expression of more than 100

80 We also show that tension stimulation can be translated to a human cell source to

81 it remains unknown whether electrical brain stimulation can be used to create a sense of ownership o

82 reduction in superoxide production after PMA stimulation compared with non-CF MDMs.

83 gical batteries were administered under four stimulation conditions: VIM on, VO on, both on, and both

84 ion was aversive, and instrumentally pausing stimulation could reinforce lever-pressing.

85 ir axon terminals in the EB, and optogenetic stimulation coupled with electrophysiological recordings

86 tudies of the efficacy of 'awake' deep brain stimulation (DBS) for Parkinson's disease (PD) under loc

87 Deep brain stimulation (DBS) has been used to treat a variety of br

88 cal lesions or the application of deep brain stimulation (DBS) within circuits that modulate motor fu

89 Moreover, we also found that PA stimulation decreased the mitochondrial membrane potenti

90 this study, we used gene signatures of CD40L stimulation derived from human immature dendritic cells

91 The selective glial stimulation did not affect transmural ion conductance or

92 Patterns associated with stimulation did not show an additional risk for seizures

93 Furthermore, deep brain stimulation directed to the interposed cerebellar nuclei

94 olution sensory prostheses based on tailored stimulation (e.g., retinal prostheses), and for closed-l

95 tment vs. neurostimulation by electric field stimulation (EFS) in bovine tracheal smooth muscle.

96 cts as a crucial sensor for electrical field stimulation (EFS)-enhanced osteogenic response in osteop

97 m and local field potentials from deep brain stimulation electrodes in 9 Parkinson's disease patients

98 s involved in beta-arrestin-dependent Erk1/2 stimulation elicited by other GPCRs such as beta2-adrene

99 Amygdala stimulation elicited no subjective emotional response bu

100 otspots in cortex, where mu opioid or orexin stimulations enhance the hedonic impact of sucrose taste

101 Across seven patients, odor stimulation enhanced theta power in human piriform corte

102 Electrical stimulation (ES) is known to promote cutaneous healing;

103 t optogenetic activation of D1R-SPNs reduces stimulation-evoked dopamine release and that bath applic

104 port was obtained by a transcranial magnetic stimulation experiment, where subjects whose frontal con

105 etic follow-up of less-publicized electrical stimulation findings.

106 synaptic currents that were evoked by visual stimulation (flashing dark spots).

107 e, we use 180 pairs of transcranial magnetic stimulation for approximately 30 min over the hand repre

108 However, the modulatory effects of stimulation frequency are not only determined by its abs

109 reased in a saturating manner with increased stimulation frequency; average [Ca(2+) ]i was a linear f

110 face (ALI) and subjected to light mechanical stimulation from an air puff.

111 ot AMPA receptor blockade, prevents synaptic stimulation from facilitating D2R-induced ADPs, suggesti

112 umors overexpress cell migration and stromal stimulation gene signatures compared with their SOX11(-)

113 is known, however, how transcranial current stimulation generates such effects, and the search for b

114 ormance, but the transcranial direct current stimulation group demonstrated significant improvement i

115 cation accuracy of the transcranial magnetic stimulation-guided regions was validated in a second sam

116 The 6 week long stimulation had no residual adverse effects on the elect

117 of the brain employing transcranial magnetic stimulation has convincingly demonstrated a presymptomat

118 ion of neural synchrony through phase-locked stimulation has the potential to both increase the effic

119 The beneficial effects of parasympathetic stimulation have been reported in left heart failure, bu

120 ew methods for precisely controlling retinal stimulation, here we show that covert attention flexibly

121 ively activated by high-threshold mechanical stimulation (HTMRs).

122 We conclude that chronic vagal stimulation improves insulin sensitivity substantially i

123 yogenic MEPs after transcranial motor cortex stimulation in 6 lambs aged 1-2 days.

124 now used to investigate adaptive closed-loop stimulation in first studies.

125 Conditioning stimulation in iPMd induced more frequent and powerful i

126 gle-synapse level after distinct patterns of stimulation in motoneurons of Drosophila We found that t

127 xamine this issue, we used single glomerular stimulation in mouse olfactory bulb slices to measure th

128 -regulation of miR-34c-5p in response to TCR stimulation in naive CD4 T cells.

129 EL) display diminished responsiveness to HEL stimulation in presence of soluble anti-HEL IgM antibodi

130 eatures using SPN type-specific chemogenetic stimulation in rodent models of PD (PD mice) and L-DOPA-

131 lar mechanism by which c-MPL mediates immune stimulation in T cells.

132 logic effects that diverge from those of RAS stimulation in the kidney and vasculature.

133 Remarkably, TCR stimulation in the presence of monensin phenocopied the

134 cus, suggesting a pivotal role of deep brain stimulation in the treatment response.

135 Fluvoxamine stimulation in these cells also activated nitric oxide p

136 ent combination of psychotherapy and somatic stimulation in treating symptoms of endometriosis.

137 t me signal) on cardiac MSCs after both TLR4 stimulation in vitro and transplantation into the infarc

138 Following TCR-driven stimulation in vitro, CXCR5+ but not CXCR5- CD8 T cells

139 requency relationship and in beta-adrenergic stimulation, including decreasing and increasing firing

140 ow that ownership, but not mere visuotactile stimulation, increases the dominance of the hand percept

141 Furthermore, TLR7 or TLR8 stimulation, independent of HCV, caused monocyte differe

142 Rapid optogenetic silencing and electrical stimulation indicated that short-latency pathways linkin

143 s a selective defect in POLA2-binding and PP stimulation, indicating that these activities are critic

144 Mechanistically, TCR stimulation induced rapid sodium influx in Napa(hyh/hyh)

145 O animals exhibit a deficit in low-frequency stimulation-induced NMDAR-dependent long-term depression

146 se the efficiency of therapy and to minimize stimulation-induced side effects.

147 We revealed that altering T-cell receptor stimulation influenced recruitment of mRNAs to heavy pol

148 e is a lack of evidence on how environmental stimulation influences individuals' eating performance a

149 ion in human primary CD4(+) T cells upon TCR stimulation, inhibiting NF-kappaB signaling via its effe

150 During IFNgamma stimulation, integrin beta3 signaling enhanced STAT1-med

151 imulation with short latencies regardless of stimulation intensity, MC latencies correlate negatively

152 sity, MC latencies correlate negatively with stimulation intensity.

153 looks at both nutrition and early childhood stimulation interventions as part of an integrated life

154 ch is of particular interest for bone growth stimulation is achievable by this assembly.

155 or receptor superfamily molecule GITR, whose stimulation is closely linked to thymic Treg cell develo

156 This stimulation is mediated by a FOXO1 induced TGFbeta1/CTGF

157 ffector cytotoxic T lymphocytes upon antigen stimulation is necessary for successful antiviral, and a

158 mporal dynamic using closed-loop optogenetic stimulation is sufficient to increase movement in the TS

159 We paired cVNS with kilohertz electrical stimulation (KES) nerve block to preferentially activate

160 ng to record responses to concurrent thermal stimulation (left forearm) and visual attention tasks of

161 , it is not yet known whether or how sensory stimulation might trigger abnormal sensory processing at

162 Upon ex vivo stimulation, monocytes of sepsis patients were less capa

163 role in the response to beta-adrenoreceptor stimulation occurring during acute exercise.

164 nce and long term stability under electrical stimulation of a new electrode material fabricated from

165 They were exclusively obtained after stimulation of a relatively delimited zone of insula, lo

166 NM myosin II is regulated during contractile stimulation of airway SM tissues by RhoA-mediated NM myo

167 sodium-restricted conditions, physiological stimulation of aldosterone was blunted with older age (b

168 ranscriptome profile, while the antagonistic stimulation of alpha7nAChR will achieve the opposite.

169 es ATP hydrolysis at both sites, as does the stimulation of ATM kinase activity.

170 mpanied by increased ROS generation, and the stimulation of autophagy by rapamycin (Rap) remarkably s

171 Moreover, optogenetic stimulation of axon collaterals of double-projecting vCA

172 raumatic brain injury (TBI), suggesting that stimulation of BDNF signaling pathways may facilitate fu

173 the membrane bound GC receptor, followed by stimulation of beta-catenin and c-myc pathways.

174 13B5 target sequence resulted in the robust stimulation of binding antibodies and, in a subset of im

175 rylation sites in alpha1C in beta-adrenergic stimulation of CaV1.2, and show that phosphoregulatory s

176 Direct stimulation of complex component CD40 on DCs leads to ac

177 Stimulation of cumulative 6-year GPP by warming (29%, P

178 Neither phasic nor tonic stimulation of dopaminergic VTA-PFC projections elicited

179 ChR activation increased responses evoked by stimulation of excitatory corticothalamic and inhibitory

180 in-1 small interfering RNA prevented hnRNP F stimulation of Foxo3alpha and downregulation of acetylat

181 hodiesterase inhibitors, and most notably by stimulation of G protein-coupled receptors (GPCR).

182 Stimulation of glutamatergic median preoptic area neuron

183 ates HER2 at p1248 in PDAC cells, leading to stimulation of HER2 signaling cascade, including ERK1/2,

184 This effect can be partially mimicked by stimulation of Hmox1(+/+) SCs with monocyte chemoattract

185 -6R) alone had no effect on VEGF production, stimulation of HPMCs with IL-6 in combination with sIL-6

186 ficking of Nav1.5 to the plasma membrane and stimulation of INa.

187 eved to be triggered exclusively from visual stimulation of individual RF subregions.

188 In vivo stimulation of iNKT cells by alpha-galactosyl-ceramide w

189 Opioid stimulation of JNK also inactivates dopamine D2 receptor

190 rrets that were conditioned using electrical stimulation of mossy fiber and climbing fiber afferents

191 We find that optogenetic stimulation of mouse zona incerta (ZI) gamma-aminobutyri

192 The current study found that ACh stimulation of nicotinic receptors comprised of alpha4 a

193 roteinases (MMPs) and selective chemogenetic stimulation of nNOS interneurons recapitulated MMP activ

194 Stimulation of normal-weight bone explant with recombina

195 ia, an anomalous blending of senses in which stimulation of one sensory modality produces sensation i

196 We show that stimulation of OXPHOS, inhibition of the PTP, or deletio

197 sal oxytocin administration and chemogenetic stimulation of oxytocin neurons render males sensitive t

198 he same time to mimic the synergistic immune-stimulation of pathogens, while being safe.

199 ncrease feeding during chemogenetic-mediated stimulation of PBN CGRP neurons.

200 stglacial increase in Ca , which matched the stimulation of photosynthesis, suggesting that increases

201 4A or H54Y substitution in 3A interrupts the stimulation of PI4KB and ACBD3.

202 Indeed, optogenetic stimulation of PPN axons reliably evoked spiking in SNc

203 Stimulation of primary OA osteoblasts with recombinant r

204 Stimulation of rat segmental dorsal cutaneous nerves (DC

205 tivate astrocytes through ephrin-B1-mediated stimulation of signal transducer and activator of transc

206 In vascular smooth muscle cells (VSMCs), stimulation of SOCs composed of canonical transient rece

207 y of HLA class II/peptide, further enhancing stimulation of T-cell proliferation.

208 results indicate that selective optogenetic stimulation of TH(VTA) neurons enhanced cerebral blood v

209 for RecN function that includes presynaptic stimulation of the bacterial repair pathway perhaps by c

210 r mechanical conditioning or pharmacological stimulation of the cGMP pathway and by using direct modu

211 Stimulation of the gastrocnemius nerve and sural nerve r

212 Stimulation of the MAPK pathway results in mitogen- and

213 investigated this using transcranial current stimulation of the rat (all males) motor cortex consisti

214 e a new axis for thymic emigration involving stimulation of the thymic microenvironment via type 2 cy

215 Moreover, insulin stimulation of their phosphorylation was significantly s

216 herosclerosis in response to pharmacological stimulation of thermogenesis linked to increased HDL lev

217 Next, we studied how optogenetic stimulation of these projections affects behavior using

218 We found that stimulation of this pathway not only cancelled licking b

219 The stimulation of tissue with phorbol-12-myristate-13-aceta

220 expression was increased and sustained after stimulation of TLRs.

221 Contractile stimulation of tracheal smooth muscle tissues stimulates

222 iation protein treslin in vitro Furthermore, stimulation of treslin phosphorylation does not occur by

223 otein, SHPS-1, resulting in pathophysiologic stimulation of vascular smooth muscle cell (VSMC) migrat

224 Stimulation of vestibular efferent neurons excites calyx

225 k, suppressing Ena activity in parallel with stimulation of WAVE.

226 tudy, we investigated the effect of synaptic stimulation on Tau pathology and synapses in in vivo and

227 ls in response to a novel form of mechanical stimulation, or a pulsed wave at the frequency of 1.5 MH

228 his we used transcranial alternating current stimulation over the left dorsolateral prefrontal cortex

229 ed with CD44(-/-) macrophages following TLR2 stimulation (p < 0.01).

230 Our results indicate that stimulation paired with a particular stimulus increases

231 er understanding of the relationship between stimulation parameters and physiological effects.

232 Later attempt to reduce stimulation parameters resulted in immediate relapse of

233 ng effect and led neurons to decode distinct stimulation patterns as massed stimulation.

234 Experiments show that spike-triggered stimulation performed with Bidirectional Brain-Computer-

235 Following subthreshold electrical stimulation, postsynaptic sodium entry is almost entirel

236 nd nucleotide-binding oligomerization domain stimulation promote ATG16L1 stabilization via IKKalpha-d

237 clusion These results suggest LIP ultrasound stimulation protects against brain injury in the hippoca

238 The stimulation protocol often produced increases in global

239 +) /Ca(2+) exchanger current that followed a stimulation protocol was significantly prolonged in PMCA

240 ates such effects, and the search for better stimulation protocols proceeds largely by trial and erro

241 d to females during reductions to adrenergic stimulation, providing preliminary evidence that LV twis

242 2 receptor agonist treatment with rM3Ds-dSPN stimulation reproduced all symptoms of LID.

243 nucleus accumbens DA, locomotion, and brain-stimulation reward.

244 trated that lumbosacral spinal cord epidural stimulation (scES) and activity-based training can progr

245 local populations driven by different visual stimulation showed different gamma frequencies.

246 y provoke VF if, and only if, the mechanical stimulation site overlaps the repolarization wave edge.

247 The impaired response propagation from the stimulation site was associated with lower expression of

248 raded emergence of gamma oscillations at the stimulation site while retaining propagating waves of ga

249 Age at surgery, regardless of stimulation status, may be related to cognitive outcome

250 nd C fibers, respectively, based on required stimulation strengths, and shows segmental differences i

251 -CML stem cells were MHCI+ without IFN-gamma stimulation, suggesting that IFN-gamma sensitizes these

252 different clinical indications of deep brain stimulation surgery.

253 Transcranial alternating current stimulation (tACS) uses sinusoidal, subthreshold, electr

254 ch is 20 Hz transcranial alternating current stimulation (tACS).

255 processing with transcranial direct current stimulation targeting the FPC while 141 healthy particip

256 gery (MI-BCI) or transcranial direct current stimulation (tDCS) has been used in stroke rehabilitatio

257 d in humans with transcranial direct current stimulation (tDCS) over the right dorsolateral prefronta

258 hypothesis: in humans, transcranial electric stimulation (tES) with a time course that mimics the end

259 stemic immunity by providing tonic microbial stimulation that can functionally replace intestinal bac

260 dict responsiveness to transcranial magnetic stimulation therapy (n = 154).

261 In response to mechanical stimulation, these IS cells differentially express osteo

262 mbining the FCM with a transcranial magnetic stimulation (TMS) intervention that transiently perturbe

263 Transcranial magnetic stimulation (TMS) of human occipital and posterior parie

264 ossibility by means of transcranial magnetic stimulation (TMS) over the hand area of the primary moto

265 ss by combining online transcranial magnetic stimulation (TMS) with computational modeling of behavio

266 Sustained locking of deep brain stimulation to a particular phase of tremor afforded cli

267 inhibitory repetitive transcranial magnetic stimulation to a subject-specific frontal-cingulate rewa

268 crucial intermediary processes that link TLR stimulation to DC maturation and the subsequent developm

269 rimary cilia are sensors of electrical field stimulation to induce osteogenesis of human adipose-deri

270 Using transcranial magnetic stimulation to inhibit the right frontopolar cortex, we

271 se results provide evidence that noninvasive stimulation to MDC nodes can enhance learning rates, the

272 Applications of transcranial direct current stimulation to modulate human neuroplasticity have incre

273 ymptom suppression is achieved by delivering stimulation to the ventrolateral thalamus, timed accordi

274 rate that transcranial static magnetic field stimulation (tSMS) over the somatosensory parietal corte

275 This stimulation was aversive, and instrumentally pausing sti

276 mechanism for reduced plateau [Ca(2+)]i upon stimulation was due to increased sarco/endoplasmic retic

277 Selection of contacts for chronic stimulation was made by matching the post-operative prob

278 ticipants compared with control subjects and stimulation was provided approximately 90 ms prior to mo

279 and perfusion MRI, and transcranial magnetic stimulation were used to study structural connectivity,

280 Electro-acupuncture (EA) stimulations were performed at acupoints of either Stoma

281 sformed into a type II medium by optogenetic stimulation which predominantly targets inhibitory neuro

282 Stimulation with ACh caused NM myosin filament assembly,

283 he production of inflammatory cytokines upon stimulation with aminobisphosphonate-treated cells.

284 er vector increased luciferase activity upon stimulation with an anti-TREM2 antibody, which induces t

285 cells proliferated vigorously in response to stimulation with anti-CD3/CD28 beads and gave rise to CD

286 dilation of the hP2X7R channel on sustained stimulation with ATP(4).

287 naling and via direct cannabinoid receptor 1 stimulation with Delta(9)-tetrahydrocannabinol.

288 dividual showed loss of kinase activity upon stimulation with fibroblast growth factor.

289 Mechanistically, stimulation with FPR2 ligands resulted in down-regulatio

290 same extent as crypts from Cd44(+/+) mice on stimulation with HGF, but had the same response to EGF.

291 oscillation became more entrained by visual stimulation with higher frequencies (>10 Hz).

292 f either FcgammaRIV or FcgammaRIIB following stimulation with IFNgamma or IL-4, respectively.

293 [Ca(2+) ]i was increased by beta-adrenergic stimulation with isoprenaline and increased in a saturat

294 After 1 h of stimulation with ligands, 87, 138, 1013, and 22 genes we

295 significantly reduced cell damage, allowing stimulation with light.

296 ith uric acid for 24 h and then subjected to stimulation with lipopolysaccharide (LPS) in the presenc

297 Cs respond to olfactory sensory neuron (OSN) stimulation with short latencies regardless of stimulati

298 Ps were immediately rescued by pairing mAChR stimulation with subthreshold depolarization ( approxima

299 We demonstrate that stimulation with trophic forms downregulated the express

300 to-toxicity and to allow for long-term photo-stimulation without causing cellular damage, we formulat