ライフサイエンスコーパス: resting

1 tivities, including desk work, cleaning, and resting.

2 Hg versus 8.4+/-2.6 mm Hg; P=0.96) and mean resting (3.2+/-1.9 mm Hg versus 3.1+/-1.1 mm Hg; P=0.67)

3 The study employs a three-state resting-active-desensitized model to link radioligand bi

4 y analyzed in the framework of a three-state Resting-Active-Desensitized model.

5 nial magnetic phosphene data show that lower resting activity and excitability levels in early visual

6 Resting affinities for PIP(2) differ for Kv7.4 and Kv7.5

7 ent our standard procedures involving both a resting and 12-lead ambulatory ECG, an exercise stress t

8 xpression dynamics of nascent transcripts in resting and activated CD4+ T cells.

9 Resting and activated sGC enzyme converts guanosine trip

10 TF binding, and gene expression patterns in resting and activated subsets of Treg cells, conventiona

11 glycolysis and mitochondrial respiration in resting and activated T cells, along with markers relate

12 ity of integrated HIV DNA was intact in both resting and activated T cells.

13 Resting and activated TILC2s express the inhibitory chec

14 The number of eosinophils (both resting and activated) and chemoattractant receptor homo

15 , quantitative framework for predicting both resting and active metabolic rate and hence aerobic scop

16 is study determined the mechanism of altered resting and maximal flow in CMD endotypes.

17 bitory effects on the whole transcriptome of resting and PAR2-activated COLO-357 cells, which tended

18 of a single bolus of mycoprotein stimulates resting and postexercise muscle protein synthesis rates,

19 ore, we investigated T-cell signatures under resting and stimulated conditions to assess cluster spec

20 ter when cells are unstimulated and finally, resting and stimulated samples can be combined to levera

21 tivity, variability, and correlations during resting and task states.

22 ted flight, area-restricted search (ARS) and resting-and model the probability of transitioning betwe

23 P=0.002), yielding no difference in overall resting ATP delivery (obese 2.5+/-0.9 umol.g(-1).s(-1) v

24 In normal resting B cells, IFITM3 was minimally expressed and main

25 Moreover, during resting behavior, coactivation of hippocampal cells in s

26 malaria vector host choice over 3 years and resting behaviour over 4 years following a mass long-las

27 ified longitudinal shifts in host-choice and resting behaviour that are consistent with adaptation to

28 eloped prediction models revealing potential resting blood-based biomarkers of peak oxygen consumptio

29 ans, ketamine has been demonstrated to raise resting BP, although it has not been studied with the co

30 anisms for the observed diurnal variation in resting brain activity and the importance of accounting

31 and EMRE subunits to inhibit ion flow under resting Ca(2+) conditions.

32 c efficacy and neuronal signalling, neuronal resting Ca(2+) signals warrant further mechanistic analy

33 nally more than V O(2) max but did not alter resting cardiac output.

34 Persistent HIV infection of long-lived resting CD4 T cells, despite antiretroviral therapy (ART

35 VOR treatment in HCT116, Jurkat, and primary resting CD4 T cells, yet return to baseline levels after

36 rences in the frequency of persistent HIV in resting CD4 T cells.

37 HIV+, stably treated participants in whom resting CD4(+) T cell-associated HIV RNA (rca-RNA) incre

38 Long-lasting, latently infected resting CD4(+) T cells are the greatest obstacle to obta

39 Analysis of resting CD4(+) T cells from tissues after AZD5582 treatm

40 ver, HIV-1 persists in a latent reservoir in resting CD4(+) T cells, and rebound viremia occurs follo

41 ne activation status, increasing the pool of resting CD4(+) T cells; and impair CD8(+) T cell functio

42 l HIV viremia, rca-RNA, and the frequency of resting CD4(+) T-cell infection (RCI) was measured at ba

43 on from latency in both cell line models and resting CD4(+)T cells isolated from aviremic infected in

44 t and sequenced HIV-1 outgrowth viruses from resting CD4+ T cells.

45 Biological degradation was investigated in resting cell suspensions of Geobacter metallireducens st

46 state organization of the plasma membrane in resting cells that is poised to orchestrate assembly of

47 ed viral sequences formed more frequently in resting cells, likely due to lower deoxynucleoside triph

48 In resting cells, RIP of CREB3L1 is blocked by transmembran

49 self-clusters that did not associate well in resting cells.

50 magnetic resonance spectroscopy measures of resting CK flux suggest that ATP delivery is reduced ear

51 roscopy structures of human PAC in a high-pH resting closed state and a low-pH proton-bound non-condu

52 Resting CMV-specific CD8 T cells were terminally differe

53 h the pFRG restrain abdominal activity under resting conditions and contribute to abdominal expirator

54 t NPY3-36 is the main circulating peptide in resting conditions and that NPY and catecholamines are s

55 Only some RVLM neurons are active under resting conditions due to significant, tonic inhibition

56 synaptic communication and signalling under resting conditions independently of activity.

57 Resting coronary blood flow (CBF) (24.6 +/- 2.0 cm/s vs.

58 indings suggested inhibitory effects of even resting cytosolic [Ca(2+)] on I(Na).

59 wer on the exercise day as compared with the resting day due to decreased (~37%) insulin-stimulated g

60 se playbacks the mother's proportion of time resting decreased by 30%, respiration rate doubled and s

61 creased ATP that causes elevated cytoplasmic resting (diastolic) Ca(2+) concentration and reduced mec

62 tem, we trained a DNN with 1,169,662 12-lead resting ECGs obtained from 253,397 patients, in which 99

63 information to the interpretation of 12-lead resting ECGs, even in cases that are interpreted as norm

64 In fourteen male volunteers, resting EEG and TEPs from prefrontal (PFC) and parietal

65 itory steady-state response (40 Hz ASSR) and resting EEG.

66 Secondary endpoints included resting energy expenditure (REE), plasma metabolites, an

67 ations tend to either over- or underestimate resting energy expenditure at different phases.

68 ion by dual-energy X-ray absorptiometry, and resting energy expenditure by indirect calorimetry.

69 Degree of agreement between resting energy expenditure calculated by predictive equa

70 None of the resting energy expenditure calculated from predictive eq

71 Although none of the resting energy expenditure calculated from predictive eq

72 Pairwise comparison showed mean resting energy expenditure measured by indirect calorime

73 iture calculated by predictive equations and resting energy expenditure measured by indirect calorime

74 edictive equations differing by +/- 10% from resting energy expenditure measured by indirect calorime

75 d respiratory data had better agreement with resting energy expenditure measured by indirect calorime

76 Resting energy expenditure values calculated from predic

77 ss three phases and could be used to predict resting energy expenditure when indirect calorimetry is

78 sistance [HOMA-IR]), trunk-to-leg fat ratio, resting energy expenditure, respiratory quotient, and fa

79 protein and energy at 1.7 times the measured resting energy expenditure.

80 patic lipid (IHL) content, body composition, resting energy metabolism, blood pressure, plasma marker

81 reby becomes rate-limited by slow IET to the resting enzyme.

82 Functional CMD is characterized by elevated resting flow that is linked to enhanced NOS activity.

83 sticity, suggesting a critical role for this resting form of signalling in regulation of synaptic eff

84 ediate (NI), which only slowly decays to the resting form.

85 CD4+ and CD8+ T cells had impaired resting glycolysis.

86 e decay and the initial delay in recovery of resting head configuration, and this could facilitate su

87 ADHD medications cause modest elevations in resting heart rate and blood pressure.

88 ood biomarkers were systolic blood pressure, resting heart rate and body mass index.

89 hancer exhibit significant associations with resting heart rate in human populations.

90 d on the occurrence of extreme elevations in resting heart rate relative to the individual baseline.

91 y the integrative physiological parameter of resting heart-rate variability (HRV); low resting HRV in

92 However, SNA, resting HR, HRV, and atrial (p = 0.03) and ventricular (

93 showed consistent individual differences in resting HRV across years.

94 of resting heart-rate variability (HRV); low resting HRV indicating proactive coping styles, while hi

95 gest correlations to HRR therefore, averaged resting HRV measures do not strengthen the prediction of

96 er 5 successive breeding seasons we measured resting HRV of 57 lactating grey seals.

97 dicating proactive coping styles, while high resting HRV typifies reactive individuals.

98 three presumptive functional states, high-pH resting, low-pH desensitized, and toxin-stabilized open,

99 phocytes in vitro and in vivo, while sparing resting lymphocytes.

100 omoter-proximal RNA polymerase II pausing in resting macrophages is marked by co-localization of the

101 Resting MBF in the remote zones was quantified using Fer

102 MBF values were consistent with those (mean resting MBF range, 1.0-1.2 mL/min/g) reported by two pri

103 rom glucose toward other sources and reduced resting MBF.

104 scular parameters, grafting RN-NSCs restored resting mean arterial pressure to normal levels and rema

105 tive interaction between STAT2 and IFNAR2 in resting MEFs, an interaction that is dependent on the as

106 hyperactivity and chronic depolarization of resting membrane potential (RMP) that is maintained by c

107 reased plasma membrane permeability, reduced resting membrane potential and accelerated protein catab

108 tle, but not significant, differences in the resting membrane potential and action potential characte

109 They play a crucial role in setting the resting membrane potential and regulating cellular excit

110 The calcium deficit was related to resting membrane potential changes that led to abnormal

111 onsequence of SCI (chronic depolarization of resting membrane potential) decrease sensitivity to opio

112 teps to varying voltages 0-80 mV positive to resting membrane potential.

113 ge, IHCs retained a normal KCNQ4 current and resting membrane potential.

114 reshold sodium conductance that controls the resting membrane potentials of neurons.

115 iciency virus (HIV) reservoir is composed of resting memory CD4(+) T cells, which often express the i

116 ine if metabolic adaptation, at the level of resting metabolic rate (RMR), is modulated by participan

117 nce of metabolic adaptation, at the level of resting metabolic rate (RMR), remains highly controversi

118 slowly, contributing to the muscle's overall resting metabolic rate.

119 uatic organisms and restricts predictions to resting metabolism, which is less affected by oxygen lim

120 l membrane potential; a subset had increased resting mitochondrial mass.

121 aily sessions over 5 consecutive days at 90% resting motor threshold (adjusted for cortical depth).

122 yosin heads were extended closer to actin in resting muscle.

123 udies have demonstrated that manipulation of resting neuronal Ca(2+) signalling yielded pronounced ho

124 Pt NPs and linker-deficient Zr(6)O(8) nodes resting on the Pt NP surface.

125 usjacksoni to move its eyes extensively when resting on the sea floor.

126 No difference was found in resting or sleeping energy expenditure, normalised to le

127 The participants had similar resting peak (8.3+/-4.4 mm Hg versus 8.4+/-2.6 mm Hg; P=

128 Resting perfusion scans were performed in 10 patients wi

129 basal activity of the NF-kappaB signaling in resting peripheral T cells.

130 constitutive activity of these channels at a resting pH.

131 r-calmodulin retains affinity for eNOS under resting physiological calcium concentrations.

132 is, after acidification, decoupled from the resting position and inserted into an acidic pocket that

133 tantly, no changes were observed in membrane resting potential, AP amplitude, or the inward K(+) curr

134 e shown that crypsis reduces attack rates on resting prey, predation risk increases with increased pr

135 RRC8A channels are key cGAMP transporters in resting primary human vasculature cells and universal hu

136 84.2 and 95.8% of participants showed resting pupil asymmetry of <=0.5 mm and <= 1.0 mm, respe

137 The strong overlap between QT dynamics and resting QT interval loci suggests common biological path

138 oci did not overlap with previously reported resting QT interval loci; candidate genes included KCNQ4

139 according to systolic BP (SBP): G1 (n = 16), resting SBP <110 mmHg and G2 (n = 14), resting SBP betwe

140 16), resting SBP <110 mmHg and G2 (n = 14), resting SBP between 120-110 mmHg.

141 Forty-two participants (54 +/- 11 y, resting SBP/DBP 137 +/- 9/86 +/- 6 mmHg) were randomly a

142 PE caused robust vasoconstriction in resting skeletal muscle during control vasodilator infus

143 Resting SNA (p = 0.002) and VNA (p = 0.04), exercise SNA

144 sin layer line (MLL1) and restoration of the resting spacing of the third and sixth order of meridion

145 tential importance of microbial dormancy and resting stages in the formation of a "buffer" against el

146 Microbial resting stages might heavily contribute to microbial bio

147 al connectivity (FC), even during interictal resting state (RS).

148 uscle and myosin heads return to an ordered, resting state after contraction more quickly.

149 ; (2) phosphetane 1 represents the catalytic resting state as observed by (31)P NMR spectroscopy; (3)

150 he following study design: phase I, 2-minute resting state at baseline (room air); phase II, 6-minute

151 These findings demonstrate that resting state connectivity can be leveraged to produce g

152 ound that human peripheral blood Th cells in resting state do not show surface expression of IL-3R; h

153 We recorded the resting state EEG (rsEEG), the visual evoked potentials

154 lly with oral water ingestion, (2) examining resting state fMRI (rs-fMRI) which is more natural since

155 roup of healthy participants across baseline resting state fMRI as well as two distinct levels of pro

156 Resting state fMRI data of 130 individuals (65 melanchol

157 y and an ability to differentially influence resting state fMRI studies.

158 e relationship between these target-enriched resting state functional connectivity (FC) maps and inte

159 ctural magnetic resonance imaging (MRI), and resting state functional connectivity (rs-fc) were colle

160 Cross-sectional resting state functional connectivity (rsFC) studies in

161 In the present study, we used resting state functional connectivity (rsFC) to investig

162 As such, we investigated dACC activity using resting state functional connectivity (rsFC) with functi

163 e in migraineurs as seed regions to generate resting state functional connectivity network maps from

164 1-site consortium study in order to identify resting state functional connectivity patterns that pred

165 in network information derived from both the resting state functional magnetic resonance imaging (rs-

166 used as seeds in a high-resolution normative resting state functional magnetic resonance imaging temp

167 droxyphenyl-l-alanine PET (18F-DOPA-PET) and resting state functional MRI (rs-fMRI).

168 In this study, we used dynamic resting state functional MRI analyses to increase tempor

169 We compared resting state functional MRI data during chronic stimula

170 Static resting state functional MRI studies have already furthe

171 iously reported ones originating from static resting state functional MRI studies post-stroke.

172 During resting state functional MRI, similar eigenvector centra

173 l-coordinated M(4+) carbonate species as the resting state in all cases.

174 yl bromide oxidative addition complex is the resting state intermediate, and transmetalation is turno

175 atory tolerance" in which BBB opening in the resting state is sufficient to stimulate a protective ba

176 In contrast, the Ni-Ga resting state is the Ni(eta(2)-H(2)) species, and Ni-Sc

177 t sex differences in prefrontal and striatal resting state networks that may contribute to difference

178 We find the dominating resting state of the catalyst as a Co(IV) species CoO(2)

179 bound by the catalyst, point to a plausible resting state of the catalyst-substrate complex predispo

180 is equipotent in a protocol that favors the resting state of the channel, a protocol that favors the

181 iscontinuation in patients, and obtained two resting state scans from matched healthy volunteers to a

182 t influences on fMRI signals during 440 h of resting state scans in 440 healthy young adults, both ca

183 The resting state structure reveals a new out active site co

184 orphological transition from a monitoring or resting state to an altered morphological state, by exhi

185 e transitions that accompany the switch from resting state to perceptual immersion in an ecologically

186 r and provides a gradual transition from the resting state to the oscillatory regime, as observed in

187 om highly inflammatory cell subsets toward a resting state upon demethylase inhibition.

188 ile the return of myosin heads to an ordered resting state was initially slower, then became more rap

189 hat emerged intermittently during a wakeful "resting state" and that had comparable electrophysiologi

190 d SidA without NADP(H) or l-ornithine bound (resting state).

191 itioning of macrophages is primed during the resting state, dependent on cumulative history of cell d

192 ng enantioinduction, reaction rate, catalyst resting state, enolate crossover experiments, water tole

193 In the resting state, high GSCORR was observed mainly in the pr

194 be suppressed by trapping the linker in the resting state, indicating that isomerization of the beta

195 iration mimicked the topography of GS in the resting state, whereas both differed during the task sta

196 d phosphate release launch the return to the resting state, which facilitates nucleotide exchange and

197 hydrolysis per se does not reset MRP1 to the resting state.

198 nctional connectivity, especially during non-resting state.

199 lso when BBB integrity is compromised in the resting state.

200 ceptor in the open, desensitized, and closed/resting state.

201 oxygen; and phase III, 5.6-minute return to resting state.

202 isms that regulate channel activation from a resting state.

203 s revealed that the correlations between the resting-state absolute EEG powers and wisdom scores were

204 In a sample of combat veterans, we examined resting-state alpha (8-12 Hz) oscillatory activity (in b

205 Using resting-state and reward-related functional MRI data fro

206 trinsic neuronal activity was assessed using resting-state blood oxygen level-dependent functional MR

207 tivity to pain is reflected in the pain-free resting-state brain activity and functional connectivity

208 t reflect brief activations of components of resting-state brain networks.

209 s study was to determine whether patterns of resting-state connectivity between brain regions predict

210 d loss of symmetry in measures of hand motor resting-state connectivity compared with control subject

211 emisphere yielded less asymmetric hand motor resting-state connectivity than seeding the tumor hemisp

212 IHM region, loss of symmetry in strength of resting-state connectivity was correlated with tumor per

213 Conclusion Hand motor resting-state connectivity was less symmetrical in a tum

214 nts, based on diffusion-weighted imaging and resting-state connectivity, localized those task-defined

215 P = .01) and strength (R = 0.33, P = .03) of resting-state connectivity.

216 riance, followed by language aptitude (17%), resting-state EEG power in beta and low-gamma bands (10%

217 Behavioral and neural (resting-state EEG) indices of language aptitude were use

218 Here we report an analysis of resting-state FC using magnetic resonance imaging data f

219 nd in healthy controls, using a simultaneous resting-state fMRI and (18)F-FDG PET.

220 ate networks (RSNs) in awake marmosets using resting-state fMRI and then compared these networks with

221 We studied in humans of either sex resting-state fMRI connectivity associated with performa

222 is (intrinsic connectivity contrast, ICC) to resting-state fMRI data acquired in 108 individuals (n =

223 s humans, non-human primates, and mice using resting-state fMRI data in all species.

224 Graph theoretic analyses of 7.0-Tesla resting-state fMRI data revealed that CA3 damage disrupt

225 tive connectivity between brain regions from resting-state fMRI data.

226 Using resting-state fMRI in the youngest sample of newborn hum

227 s were similarly consistent between task and resting-state fMRI, improved age-based classification an

228 % female) completed 7 days of actigraphy and resting-state fMRI.

229 tral nervous system such that structural and resting-state functional activity changes occur in the b

230 Here, we collected resting-state functional and diffusion-weighted MRI data

231 The effects of age on static resting-state functional brain integration were assessed

232 Finally, the number of significant resting-state functional connections across the brain in

233 into large-scale networks identifiable using resting-state functional connectivity (RSFC).

234 ressive disorder is associated with aberrant resting-state functional connectivity across multiple br

235 ified on the basis of a participant-specific resting-state functional connectivity analysis with a hi

236 In addition, patients with MDD had higher resting-state functional connectivity between hippocampu

237 Resting-state functional connectivity data were obtained

238 Resting-state functional connectivity findings highlight

239 Resting-state functional connectivity is used throughout

240 Here we decompose resting-state functional connectivity using a temporal u

241 Resting-state functional connectivity was largely unalte

242 Resting-state functional connectivity was quantified via

243 d morphometry, diffusion tensor imaging, and resting-state functional connectivity.

244 ol network activity as the primary driver of resting-state functional connectivity.

245 aging was characterized by decreased static resting-state functional integration and dynamic stabili

246 ted intrinsic functional connectivity during resting-state functional magnetic resonance imaging (fMR

247 unctional connectivity and dynamics based on resting-state functional magnetic resonance imaging (rs-

248 al brain connectivity (GBC), as assessed via resting-state functional magnetic resonance imaging (rsf

249 Resting-state functional magnetic resonance imaging (rsf

250 Resting-state functional magnetic resonance imaging data

251 Resting-state functional magnetic resonance imaging scan

252 In this study, we used resting-state functional magnetic resonance imaging to e

253 The probabilistic reward task and resting-state functional magnetic resonance imaging were

254 cipants using diffusion spectrum imaging and resting-state functional magnetic resonance imaging.

255 Recent resting-state functional MRI (fMRI) studies have reveale

256 diffusion magnetic resonance imaging (MRI), resting-state functional MRI (fMRI), and sensory-evoked

257 stratification models based on single visit resting-state functional MRI (rs-fMRI) data that assess

258 nal connectivity using daily 30-min scans of resting-state functional MRI (rs-fMRI).

259 Background Resting-state functional MRI holds substantial potential

260 tanding of how tumors exert local effects on resting-state functional MRI readings.

261 Here, using resting-state functional MRI, we show that the timescale

262 This study aims to compare resting-state functional properties of these networks be

263 bic exercise (MAE) on inhibitory control and resting-state heart rate variability (HRV) in children w

264 ty-insensitive k-means clustering to segment resting-state high-density (128-channel) EEG data into m

265 s (20-hour time-in-bed) of recovery sleep on resting-state hippocampal connectivity and episodic memo

266 e complex formed post-transmetalation is the resting-state intermediate, and loss of SO(2) from this

267 In resting-state MEG recordings from healthy participants (

268 ationship between baseline brain morphology, resting-state network connectivity and clinical response

269 However, whether such resting-state networks (RSNs) are interconnected across

270 ns of subcortical connectivity with cortical resting-state networks (RSNs) in awake marmosets using r

271 anonical variates did not relate to specific resting-state networks but comprised edges interconnecti

272 _INST group (i.e. Peak VOR > 2.0); canonical resting-state networks preferentially engaged by EL_INST

273 y maps, which were compared with established resting-state networks to identify potential networks pr

274 identified reproducible and highly symmetric resting-state networks, with overall connectivity streng

275 sed to strong connections encompassing known resting-state networks.

276 al change in functional connectivity (FC) of resting-state oscillations between pairs of 330 cortical

277 sive re-experiencing symptoms and attenuated resting-state posterior->frontal alpha connectivity, whi

278 -wide association studies (MTAG) on parietal resting-state theta (3-7 Hz) EEG coherence, which previo

279 ed voxel-based morphometry (VBM) studies and resting-state voxel-based pathophysiology (VBP) studies

280 otomimetic effects and their relationship to resting-state whole-brain magnetoencephalography (MEG) g

281 e widely used as an fMRI-based surrogate of "resting-state" neuronal activity.

282 s measured by an increase in HRV, versus the resting-state.

283 hibition by altering the equilibrium between resting states (with D4S4 in the inner position) and ina

284 mployed iridium photocatalyst, determine the resting states of both iridium and nickel catalysts, and

285 uted set of brain regions coactivated during resting states that is vulnerable to brain disorders.

286 ic reactions and were identified as catalyst resting states.

287 Mechanistic studies revealed two catalyst resting states: an arylpalladium(II) hydroxide and arylp

288 ress stimulus for vasodilatation and reduced resting steady-state nitric oxide levels in the blood Co

289 34 degrees C water and completed two trials resting supine in a 28.5 +/- 0.4 degrees C environment.

290 T cells stimulated for 5 days as compared to resting T cells.

291 In CD4(+) myeloid lineage and resting T-cells, SAMHD1 blocks HIV-1 and other viral inf

292 ntervention had no significant effect on non-resting time use (RR = 1.00 [CI: 0.96, 1.05, p=0.93]) or

293 findings shed light on the genetic basis of resting Tpe and Tpe response to exercise and recovery, u

294 fteen and one single-nucleotide variants for resting Tpe and Tpe response to exercise, respectively,

295 In a full dataset GWAS, 13 further loci for resting Tpe, 1 for Tpe response to exercise and 1 for Tp

296 t deficits in WT alphaS mice and the PD-like resting tremor and progressive motor decline of 3K alpha

297 aspase-3 and -9 are basally persulfidated in resting (unstimulated) cells and become depersulfidated

298 a (CH) produces a time-dependent increase of resting ventilation and the hypoxic ventilatory response

299 male crew (age: 40-years; BMI: 26.5-kg/m(2); resting VO(2) and VO(2max): 3.3- and 43.4-mL/kg/min) on

300 oesophageal temperature of 2 degrees C above resting was reached.