ライフサイエンスコーパス: at rest

1 emand during repetitive spike conduction and at rest.

2 from task-independent measurements collected at rest.

3 ves feels notably more slippery than it does at rest.

4 nous anastomoses (QIPAVA ) in healthy humans at rest.

5 e-supplementary motor area (pre-SMA) with M1 at rest.

6 IHCs and do not show correlated spike timing at rest.

7 cited by emotional stimuli and when measured at rest.

8 EF were similar to those in control subjects at rest.

9 nt; and (3) tasks reconfigure networks found at rest.

10 spike rate autocorrelation structure whilst at rest.

11 us arterial CO2 fluctuations in awake humans at rest.

12 tivity between early and late visual regions at rest.

13 ity and respiratory coupling were equivalent at rest.

14 harmonic oscillator can never be completely at rest.

15 es to the maintenance of store Ca(2+) levels at rest.

16 g the absence of relevant myocardial hypoxia at rest.

17 emental prognostic value beyond GLS measured at rest.

18 f life and with a trend toward improved pain at rest.

19 m a single vendor under adenosine stress and at rest.

20 t local neuronal activity determines BOLD FC at rest.

21 on, in contrast to their quasi-helical order at rest.

22 creasing heights even if they were initially at rest.

23 s with pulmonary arterial hypertension (PAH) at rest.

24 human subjects measured non-invasively while at rest.

25 luding effects observed both during task and at rest.

26 patially constrained than local correlations at rest.

27 eus and the rest of the default mode network at rest.

28 exhibit spontaneous action potential firing at rest.

29 a temporally coordinated manner in task and at rest.

30 the visual cortex and sensory-motor networks at rest.

31 ory receptor cells maintain high sensitivity at rest.

32 /min/g; these were significantly higher than at rest (0.9 +/- 0.5 mL/min/g, P < 0.05) and were not di

33 o, except for hepcidin and ferritin with ABI at rest [-0.27 (SE 0.34) and -0.22 (SE 0.35), respective

34 rkload in AS patients compared with controls at rest (12,721 vs. 9,707 mm Hg/min(-1); p = 0.003) and

35 whole-body DEE was approximately 150 kcal/d at rest (149 +/- 52 kcal/d), which decreased to approxim

36 oprusside, SNP), or potassium chloride (KCl) at rest; (2) mild or moderate intensity handgrip exercis

37 ents who could exercise and passed screening at rest, 31 (44%) had 1 vector safety, 16 (23%) had 2 ve

38 uction in pulmonary capillary wedge pressure at rest, 34 (58%) of 59 had a lower pulmonary capillary

39 phase vs. 10 +/- 10 bursts min(-1) ML phase at rest; 34 +/- 15 EF phase vs. 36 +/- 16 bursts min(-1)

40 nd decreased mean pulmonary artery pressures at rest (-7+/-4 versus -3+/-4 mm Hg; P=0.007) and with e

41 At rest, a CS over the occiput significantly (P < 0.001)

42 form computer simulations of SVs near the PM at resting active zones, and the results show that the d

43 tening and lengthening of the macromolecules at resting active zones.

44 out (ATF3-KO) and control mice were analyzed at rest, after exercise, and after training.

45 er flow velocity measurements were performed at rest, after intracoronary adenosine, and during incre

46 euglycemic-hyperinsulinemic clamps performed at rest and 3 h after exercise.

47 lity (grade A) TR Doppler was present in 68% at rest and 34% at peak exercise.

48 Thus, BK and Kv were mostly closed at rest and activated by depolarization.

49 c (10% O2) trial with measurements performed at rest and after 30 minutes of cycling at 70% of maxima

50 lates normal desmosomal reorganization, both at rest and after acute barrier perturbation.

51 ood and muscle biopsy samples were collected at rest and after exercise during primed continuous infu

52 ish mice overexpressing UCP3 in muscle, both at rest and after exercise regimens that challenged musc

53 drin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16 degrees C) t

54 drin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16 degrees C) t

55 SPECT acquisitions using (99m)Tc-tetrofosmin at rest and after vasodilator stress were performed usin

56 rmittent claudication or ischemic pain while at rest and angiographically significant atherosclerotic

57 V) global longitudinal strain (GLS) measured at rest and at dobutamine stress echocardiography on the

58 d flow velocity were simultaneously assessed at rest and at maximal hyperemia in an unobstructed coro

59 Dynamic muscle ultrasonography at rest and at stress is often used for the diagnosis.

60 Although GABA depolarizes neurons at rest and at the onset of population bursts, it transi

61 ization, by the concentration of metabolites at rest and by the temporal dynamics of NADH upon activa

62 , or modules, that are functionally coherent at rest and collectively activated by distinct task requ

63 using functional magnetic resonance imaging at rest and diffusion-weighted imaging tractography.

64 Imaging was performed at rest and during 6-min hypercapnic plateaus (baseline;

65 HF-HRV was assessed at rest and during a cognitive task protocol designed to

66 We also evaluated brain activity at rest and during a hippocampal-dependent pattern separ

67 d frontostriatal reward system activity both at rest and during a sequential risky decision making ta

68 in six migraineurs and six control subjects at rest and during acute glyceryl trinitrate-induced mig

69 ces in left ventricular (LV) mechanics exist at rest and during acute physiological stress.

70 Cardiovascular physiology at rest and during acute stress (Montreal Imaging Stress

71 CBV at rest and during an intravenous glucose tolerance test

72 (Ve), renal SNA (RSNA) and ECG were measured at rest and during CBC activation in sham and CHF rabbit

73 Hence, measurement of GLS at rest and during dobutamine stress echocardiography ma

74 effects of long-duration spaceflight on CBT at rest and during exercise are clearly lacking.

75 ation with simultaneous expired gas analysis at rest and during exercise before and after treatment w

76 mum), and ventilation were higher (P < 0.05) at rest and during exercise in both patients with ILD an

77 ing pressures and pulmonary artery pressures at rest and during exercise in HFpEF.

78 PCWP was higher at rest and during exercise in patients with LA volume i

79 study compared indices of arterial stiffness at rest and during exercise in subjects with HFpEF and h

80 ization studies were prospectively conducted at rest and during exercise in subjects with invasively

81 Rates of EGP and GLY both at rest and during exercise were significantly lower in

82 s the human cerebral and femoral circulation at rest and during exercise, an ideal model system chara

83 Echocardiography at rest and during exercise, and selected biomarkers wer

84 ation with simultaneous expired gas analysis at rest and during exercise, before and 15 min after tre

85 terization and radionuclide ventriculography at rest and during exercise.

86 dysfunction is common in patients with ePVH at rest and during exercise.

87 EGCG) are known to improve energy metabolism at rest and during exercise.

88 th diastolic anterior leaflet (AL) tethering at rest and during exercise.

89 Skeletal muscle generates ROS at rest and during exercise.

90 accompanied by impaired coronary blood flow at rest and during exercise.

91 dentified that autonomic heat loss responses at rest and during fixed-intensity exercise in well-trai

92 33 patients with HCM and 20 control patients at rest and during hyperemia, allowing calculation of wa

93 ed in IPAH (n=9) and SSc-PAH (n=15) patients at rest and during incremental atrial pacing or supine b

94 erfusion is lower in older individuals, both at rest and during incremental dynamic exercise.

95 ng of the MRF using extracellular recordings at rest and during locomotion in a nonhuman primate (NHP

96 th extracellular recordings in behaving NHPs at rest and during locomotion.

97 ic fetuses compared to control fetuses, both at rest and during maximal flow, suggesting reduced micr

98 analyzed detailed cardiac and pulmonary data at rest and during maximal incremental cardiopulmonary e

99 t also exhibit relatively normal ventilation at rest and during other conditions, similar to multiple

100 on in cerebral blood flow PET scans acquired at rest and during task performance.

101 Glucose kinetics were measured at rest and during the final 30 min of exercise by infus

102 YT1 dystonia and 10 healthy control subjects at rest and during the perception of 'natural' and 'unna

103 nd within (intracortical inhibition) the iS1 at rest and during tonic index finger voluntary activity

104 ed frequent dyskinesia and studied them both at rest and during voluntary movement.

105 tion of BP via the Modified Oxford technique at rest and during VRCE.

106 Reduced pulmonary diffusing capacity at rest and excessively high ventilation during exercise

107 at exercise; n = 118), and C3 (E/e' >13 both at rest and exercise; n = 26) HF.

108 olic mitral annular velocity [E/e'] <13 both at rest and exercise; n = 63), C2 (E/e' >13 only at exer

109 sea level (344 m) and high altitude (3800 m) at rest and following both maximal exercise and 30 min o

110 sea level (344 m) and high altitude (3800 m) at rest and following both maximal exercise and 30 min o

111 ar outflow tract obstruction was absent both at rest and following physiological exercise (<30 mm Hg;

112 relationships between ADSCT and both HF-HRV at rest and HF-HRV reactivity.

113 We performed echocardiography at rest and immediately post-cardiopulmonary exercise te

114 o, nitrite decreased aortic wave reflections at rest and improved arterial compliance and elastance a

115 of catecholamines, or absent/decreased, e.g. at rest and in all conditions with alveolar hyperoxia (F

116 erapies improve cardiac contractile function at rest and in response to adrenergic stimulation in obe

117 rucial determinant of arterial diameter both at rest and in response to endogenous vasodilators.

118 tomic, hemodynamic, and physiologic behavior at rest and in response to renal insults.

119 Cardiac performance was assessed at rest and in response to sympathomimetic challenge (do

120 f endogenous CD40L in unedited T cells, both at rest and in response to T-cell stimulation.

121 interact with higher cortical centres, both at rest and in the context of breathlessness threat.

122 d an attached, spread morphology in PMN both at rest and in the presence of chemotactic stimuli.

123 e of CMICE-013 was 1.5% of the injected dose at rest and increased more rapidly with increased blood

124 Resting end systolic volume was 129+/-60 mL at rest and increased to 158+/-66 after mental stress (P

125 ular end diastolic dimension was 179+/-65 mL at rest and increased to 217+/-71 after mental stress an

126 ary pressure and flow velocity were measured at rest and maximal hyperemia in undiseased vessels in 1

127 investigate the causes of screening failure at rest and on exercise to inform optimal S-ICD ECG vect

128 r sudden death underwent S-ICD ECG screening at rest and on exercise.

129 e measurement of pulmonary arterial pressure at rest and peak exercise were simultaneously obtained.

130 AL opening angles were measured at rest and peak exercise.

131 The connections are inhibitory at rest and possibly mediated by inhibitory interneurone

132 phe nuclei led to excitation of tufted cells at rest and potentiation of their odor responses.

133 The increased connectivity at rest and reduced neural activation during task perfor

134 s (SGs) docked onto the plasma membrane (PM) at rest and reduced SG recruitment to the PM after gluco

135 span (20-89 years), we measured correlations at rest and related the functional connectivity patterns

136 e volume of possible activity configurations at rest and reliably settling into a confined stimulus-d

137 pinal cords of anesthetized squirrel monkeys at rest and show that the strength of connectivity withi

138 multaneously with the radiotracer injections at rest and stress to measure blood flow.

139 The uptake at rest and stress was compared with microsphere flow me

140 and the decay-corrected ratio of the signals at rest and stress was used to separate the well-counter

141 oscillations in children (3-5 years; N = 65) at rest and tested our hypotheses that this temporal asy

142 t calsequestrin is polymerized within the SR at rest and that it depolymerized as [Ca(2+)] went down:

143 ocaine did not affect neurovascular coupling at rest and that the reduction in resting CBF reflected

144 the topology of areal connectivity measured at rest and the functional recruitment of these areas du

145 ar-arterial O2 tension gradient was elevated at rest and throughout exercise in COPD (P<0.05).

146 of LE-PAD is the ankle-brachial index (ABI) at rest and typically an ABI </= 0.90 is used to define

147 ns were derived to correlate VMHDVCG with BF at rest and validated using real-time phase-contrast.

148 ls with PTSD underwent functional MRI (fMRI) at rest and while completing three tasks assessing emoti

149 use mitochondrial oxidative phosphorylation at rest and with short-term activation.

150 hout obstruction to left ventricular outflow at rest and/or under physiological exercise and to exami

151 htly interconnected network during tasks and at resting and that lower gray matter in this network wa

152 calpain activation, increased SR Ca(2+) leak at rest, and depressed force production due to impaired

153 -free ratio, distal pressure/aortic pressure at rest, and FFR were measured in 763 patients from 12 c

154 include pain on walking (claudication), pain at rest, and loss of tissue integrity in the distal limb

155 ongestive heart failure, paraplegia, dyspnea at rest, and reoperation are associated with the highest

156 ains of BTN3A1 adopt a V-shaped conformation at rest, and that locking them in this resting conformat

157 more noisy) 1/f power spectral density, even at rest, and that visual cortical 1/f noise statisticall

158 spectral resolution (31)P-MRS data, acquired at rest, as a marker of oxidative metabolism.

159 urn resulted in a high level of PNS activity at rest, as well as strong PNS activity withdrawal in re

160 sis of oscillatory activity and connectivity at rest, based on high-density electroencephalographic (

161 the room air and three levels of hypoxic gas at rest before (control) and after CaO2 was reduced by 1

162 d intensity for 20 min and TMS was performed at rest (before, during, and after tACS) and during move

163 re, PE-mediated vasoconstriction was blunted at rest (blockade: -20 +/- 5 vs. CONTROL: -31 +/- 3% vs.

164 At rest, blood samples and microdialysates from adipose

165 At rest, broadband gamma (50-200 Hz) power in the primar

166 riphosphate (ATP) and phosphocreatine levels at rest but cannot maintain normal ATP levels in the vis

167 responses or spontaneous neural fluctuations at rest but no prior study has concurrently probed both

168 can be induced by exercise or be persistent at rest, but many patients are asymptomatic.

169 izing pFL neurons produced active expiration at rest, but not when inspiratory activity was suppresse

170 perpolarizing pFV neurons affected breathing at rest by decreasing inspiratory-related activity, atte

171 functional consequences of oxygen limitation at rest by measuring myocardial energetics before and af

172 f which are populated, at least transiently, at resting Ca(2+) conditions.

173 onstrate that the brain's intrinsic coupling at rest can be selectively modulated by choosing appropr

174 graphy, collected from 104 patients measured at rest, can provide valuable information about brain co

175 with respect to how T1D affects spontaneous at-rest connectivity in young developing brains.

176 ifferent patterns of functional connectivity at rest (coupling with the "default mode network" and "f

177 At rest, DCVs are captured bidirectionally as they circu

178 Liquid-like at rest, dense suspensions of hard particles can undergo

179 VRCs were assessed at rest, during 30 min of induced limb ischaemia and dur

180 alculated forearm vascular conductance (FVC) at rest, during steady-state stimulus conditions (pre-ph

181 ive orifice area 0.7 cm(2)) and 38 controls, at rest, during supine bicycle exercise, and during hype

182 ntrol) underwent right heart catheterization at rest, during supine exercise, and with acute saline l

183 myocardium was twice that of control fetuses at rest, during vasodilatory hyperaemia, and during hype

184 in which the carotid bodies are hyperactive at rest, e.g. essential hypertension, obstructive sleep

185 We examined the hypotheses that (1) at rest, endothelial function would be impaired at high

186 BSTRACT: We examined the hypotheses that (1) at rest, endothelial function would be impaired at high

187 Our findings were: (1) at rest, FMD remained unchanged between sea level and hi

188 nance imaging data from forty healthy humans at rest for the investigation of the basal scaffold of t

189 plifying NMDA receptor-driven Ca(2+) signals at rest for the maintenance of synaptic homeostasis.

190 a raised pulmonary capillary wedge pressure at rest (>15 mm Hg) or during exercise (>25 mm Hg).

191 of body mass but consumes 20% of body energy at rest, has a limited capacity to store energy and is t

192 However, almost 40% of athletes die at rest, highlighting the need for complementary prevent

193 that can be observed even when the brain is at rest, i.e. not engaged in any particular task.

194 matic stress disorder that is in action even at rest, implicating dysregulated triangular sensory-pre

195 tudy, 21 healthy adult subjects were exposed at rest in a randomized, balanced order to diesel exhaus

196 ricular outflow tract obstruction is present at rest in about one third of the patients and can be pr

197 ations between subregions of the spinal cord at rest in humans, similar to those found in the brain,

198 ith the changes (ie, post-training increase) at rest in ipsilesional intrahemispheric connectivity in

199 moglobin formation (venous>arterial; P<0.05) at rest in normoxia, during hypoxia (P<0.05 versus normo

200 BK/Kv were mostly closed at rest in normoxia.

201 7- to 8-month-old wild-type and rTg4510 mice at rest in their home cage.

202 nts show abnormalities in brain connectivity at rest, including hyperconnectivity within the default

203 of this network is present in brain activity at rest, independently of any stimulus and of any paroxy

204 tribution of contact areas recovered to that at rest, indicating the extent of a VM-PM contact area i

205 heart failure, daytime oscillatory breathing at rest is associated with a high risk of mortality.

206 cal network generating the alpha oscillation at rest is different in people with epilepsy and visual

207 either sex) evoked by steady depolarization at rest is replaced by irregular firing during functiona

208 pothesis that GABAergic inhibition, measured at rest, is reduced by deprivation, as demonstrated by a

209 o be important in top-down executive control at rest (left dlPFC), which, in turn, is associated with

210 connectivity indicates that the human brain, at rest, lies in a dynamical state that reflects the lar

211 sis' that rundown of inhibitory SK responses at resting membrane potentials (RMPs) reflects depletion

212 endent potassium channels that are activated at resting membrane potentials and therefore provide a p

213 ellular calcium stores, and run down rapidly at resting membrane potentials when calcium stores becom

214 CaV3.1 mediated a substantial current at resting membrane potentials, and its deficiency had n

215 ely 75% and approximately 95%, respectively, at resting membrane potentials, and only activate apprec

216 With no difference between age groups at rest, Mn(2+) quench of Fura-2 fluorescence revealed 2

217 in the primary visual cortex (V1), measured at rest, modulates the susceptibility of ocular dominanc

218 rt failure, paraplegia, reoperation, dyspnea at rest, nongastric band surgery, age >/=60 years, male

219 t differ between sea level and high altitude at rest, nor following maximal exercise.

220 ites, whereas Esco2 is infrequently enriched at REST/NRSF target genes.

221 e demonstrate that hydrogel drops, initially at rest on a surface, spontaneously jump upon rapid heat

222 monary capillary wedge pressure (>/=15 mm Hg at rest or >/=25 mm Hg during supine bicycle exercise) p

223 r without a 5 wk endurance training protocol at rest or after an acute exercise bout (EB).

224 oxidation (CHOx) rates, were measured either at rest or during 40 min of exercise (0.5 W/kg).

225 ding on whether the antibody uptake occurred at rest or during depolarization.

226 was detected in rates of GNG between groups at rest or during exercise (Exercise: LCHF, 2.8 +/- 0.4

227 otice difficulty with their breathing either at rest or even during heavy exercise.

228 n-dependent mechanisms in aged rats, whether at rest or following a learning challenge.

229 nally moved target (while keeping their hand at rest or not).

230 CLI) is a clinical syndrome of ischemic pain at rest or tissue loss, such as nonhealing ulcers or gan

231 ffectiveness was defined as changes in pain (at rest or with activity) greater than 13 mm on a 100-mm

232 ndrome, elevated left atrial pressure-either at rest or with exertion-is a common factor among all fo

233 izing pFL neurons had no effect on breathing at rest, or changes in inspiratory activity induced by h

234 bility and GABA concentrations were measured at rest, outside a task context, providing assays of int

235 l intensity was 78% less with adenosine than at rest (P < .001), but unchanged with regadenoson (4% r

236 ventricular outflow tract gradient reduction at rest (P=0.883) or during Valsalva maneuver (P=0.885).

237 near the mid-point of the adjustment ranges at resting PaO2 where sensitivity is maximum.

238 At rest, patients with mitochondrial disease exhibit ele

239 At rest, PCWP was <12 mm Hg in 11 patients (44%) with LA

240 At rest, postprandial EE and CHOx, as well as adipose ti

241 At resting potential (-63.7 +/- 0.6 mV), approximately 9

242 attention, models based on network strength at rest predicted attention-deficit/hyperactivity disord

243 cm(2) and 68 +/- 10 degrees , respectively, at rest (r = 0.4; p = 0.014).

244 measured pulmonary capillary wedge pressure at rest (r=0.63, P<0.0001) and during exercise (r=0.57,

245 ed reasonably well with invasive measurement at rest (r=0.72, P<0.001; bias, -2.9+/-8.0 mm Hg) and pe

246 nectional topology of brain areas quantified at rest relates to the functional activity of those area

247 At rest, respiratory chemoreflexes initiated at peripher

248 with medium supplemented with serum obtained at rest (RestTx) or 15 min post-exercise (ExTx), before

249 maximal sensitivity, tip links are tensioned at rest, resulting in a continuous influx of Ca(2+) into

250 Analysis of the FRET quenching at rest revealed an unexpected result that can be interp

251 owing evidence has shown that brain activity at rest slowly wanders through a repertoire of different

252 impaired evoked release, whereas HRP uptake at rest solely potentiated spontaneous release.

253 frequency, [Na(+)]sm is bounded between 9 mM at resting state and 11.5 mM; and 3) the cells can maint

254 y is shown to enhance mPFC/ACC activity even at resting state and improve cognitive function in patie

255 , numerous studies have found that the brain at resting state displays many features characteristic o

256 Immunocytochemical staining revealed that, at resting state, p47phox colocalizes with NOX2, whereas

257 ivity in left ventricular of adult offspring at resting state.

258 er working state and functional connectivity at resting state.

259 the hHv1 dimer based on the Ci-VSD structure at resting state.

260 At rest, striatal CMRO2 of R6/2 mice was equivalent to t

261 Imaging the brain at rest ('task-free') provides the opportunity to examin

262 g (phase lag index) that was more widespread at rest than during walking.

263 ng exercise-induced ischemia and reperfusion at rest that are associated with endothelial dysfunction

264 as the pFL is a conditional oscillator quiet at rest that, when activated, e.g., during exercise, dri

265 tic resonance imaging have demonstrated that at rest the brain exhibits coherent activity within a nu

266 At rest the lPAG was functionally correlated with cortic

267 At rest, the %ID in the liver decreased from a maximum o

268 At rest, the brain is traversed by spontaneous functiona

269 For terminals fixed at rest, the contact area between the VM of docked vesic

270 stimuli and to delineate functional circuits at rest, the extent to which BOLD signals correlate spat

271 that are strongly correlated and segregated at rest: the visual (VIS) network and the dorsal attenti

272 At rest there was no difference in [Ca(2+) ]i between ag

273 At rest, there was binding of (11)C-dihydroergotamine in

274 tion that causes the opening of HCN channels at rest, thereby increasing VSN excitability.

275 ry MR and LVEF >/=60% using echocardiography at rest; they were evaluated at our center from 2005 to

276 is that they can transform from liquid-like at rest to solid-like under sudden impact.

277 vity recruits a separate mechanism than used at rest to stimulate additional synaptic capture of DCVs

278 xpected, whereas ventilation and blood gases at rest under normoxia were normal.

279 lls and bone marrow-derived basophils (BMBs) at rest, upon an adaptive-type activation (IgE cross-lin

280 Pulmonary diffusing capacity at rest was a significant predictor of dead space ventil

281 y, we found that brain network configuration at rest was already closer to a wide variety of task con

282 Additionally, elevated HC connectivity at rest was associated with reduced HC neural recruitmen

283 Median MBF at rest was comparable between CZT and PET (0.89 [interq

284 CBF at rest was quantified on a voxelwise basis using arteri

285 Greater insula-dACC coupling at rest was significantly correlated with enhanced smoki

286 Higher HF-HRV at rest was significantly related to both more severe AD

287 While mitral cells at rest were also excited by raphe activation, their odo

288 rger motor-evoked potentials (MEPs) measured at rest were associated with faster RTs.

289 o systematically interrogate these disorders at rest, when muscle symptoms are typically minimal, and

290 t in the lumen of the sarcoplasmic reticulum at rest, whereas Ca(2+) concentrations similar to those

291 The vlPAG showed fronto-limbic correlations at rest, whereas during breathlessness anticipation, red

292 NK cell efficiently kills malignant targets at rest, whereas the less mature CD56(bright) NK cells c

293 a generic excitatory drive to breathe, even at rest, whereas the pFL is a conditional oscillator qui

294 iability of connection strengths across time at rest, while there was a selective inversion of this e

295 oxygenation level-dependent signals measured at rest with functional magnetic resonance imaging.

296 We measured corticospinal excitability at rest with transcranial magnetic stimulation, local co

297 k would decrease pain at 8 h, 16 h, and 24 h at rest, with coughing and upon standing.

298 umerical rating scale at 8 h, 16 h, and 24 h at rest, with coughing, and upon standing.

299 th increased strength of neural connectivity at rest, with the magnitude of these specific neurophysi

300 d that activation of the muscle metaboreflex at rest would cause hyperpnoea.