ライフサイエンスコーパス: human volunteer

1 was estimated by whole-body PET of a single human volunteer.

2 ced antigen-specific CD8+ T cells in healthy human volunteers.

3 orrelated with AEA concentrations in healthy human volunteers.

4 artially attenuated for pustule formation in human volunteers.

5 ole for these sites in semantic cognition in human volunteers.

6 obacterial growth following BCG challenge in human volunteers.

7 rus-like particle (VLP) candidate vaccine in human volunteers.

8 assessed with dynamic PET scans of 6 healthy human volunteers.

9 ies in guinea pigs, chimpanzees, and healthy human volunteers.

10 artially attenuated for pustule formation in human volunteers.

11 d with subsequent clinical investigations in human volunteers.

12 tration-grade LPS injection (1 ng/kg) in 294 human volunteers.

13 n social and emotional processing in healthy human volunteers.

14 analysis to answer this question in healthy human volunteers.

15 (18)F-FEOBV scans were obtained in 3 healthy human volunteers.

16 ced sputum macrophages isolated from healthy human volunteers.

17 imetry profiles of (18)F-D4-FCH in 8 healthy human volunteers.

18 mics of the response to viral vaccination in human volunteers.

19 and infarcted mice (n=6) as well as healthy human volunteers.

20 ng a cross-neutralizing antibody response in human volunteers.

21 mg and 600 mg administered in healthy adult human volunteers.

22 30 lowered Abeta in the CSF of healthy human volunteers.

23 metry profiles of (18)F-ICMT-11 in 8 healthy human volunteers.

24 reting cells in the circulation of immunized human volunteers.

25 n direct ophthalmoscopy using simulators and human volunteers.

26 GLP-1 on resting EE and glycemia in healthy human volunteers.

27 venous injection of (18)F-CP-18 in 7 healthy human volunteers.

28 rter, and tested the mutant for virulence in human volunteers.

29 mutant was fully attenuated for virulence in human volunteers.

30 eas (A1 and R) within the "auditory core" of human volunteers.

31 duced levels of Neu5Ac, is fully virulent in human volunteers.

32 ated excellent pharmacokinetic properties in human volunteers.

33 elative humidity) on particle emissions from human volunteers.

34 tional magnetic resonance imaging in healthy human volunteers.

35 PET scans were obtained for 7 adult human volunteers.

36 mice and LSA-NRC-vaccinated HLA-DR1-positive human volunteers.

37 ing obtained for the same three compounds in human volunteers.

38 ated further by dietary nitrate ingestion in human volunteers.

39 5000HP for their ability to cause disease in human volunteers.

40 ibacumab (40 mg per kilogram) in 333 healthy human volunteers.

41 testing of vaccines that cannot be tested in human volunteers.

42 ication to cloth patches worn on the arms of human volunteers.

43 storm and multiorgan failure in six healthy human volunteers.

44 rved following TGN1412 administration to the human volunteers.

45 hepcidin in normal C57Bl/6 mice and healthy human volunteers.

46 s in peripheral blood white cells of healthy human volunteers.

47 lemic hypotension in spontaneously breathing human volunteers.

48 m parasites in experimental rodent hosts and human volunteers.

49 ses to HuNoV that are difficult to assess in human volunteers.

50 ovirus infection in 24 healthy and asthmatic human volunteers.

51 P, FX517 does not cause pustule formation in human volunteers.

52 sessed with MRI in a large sample of healthy human volunteers.

53 on and virus load in experimentally infected human volunteers.

54 y of 11C-raclopride was performed in healthy human volunteers.

55 body and has been tested in pilot studies in human volunteers.

56 , and informed consent was obtained from the human volunteers.

57 f the triceps surae was tested in 14 healthy human volunteers.

58 e, 15 rats, 6 rabbits, 8 mongrel dogs and 38 human volunteers.

59 Subjects were eight healthy human volunteers.

60 gh cell culture, infectivity surrogates, and human volunteers.

61 over- or underestimate global OEF in healthy human volunteers.

62 ate PET was therefore performed on 6 healthy human volunteers.

63 protons, to investigate acid-induced pain in human volunteers.

64 estimate its radiation dosimetry in healthy human volunteers.

65 ich has undergone several clinical trials in human volunteers.

66 rebral OEF in local brain tissues of healthy human volunteers.

67 emia (3.0 +/- 0.3 mmol/liter) in nine normal human volunteers.

68 iates across a large cohort of young healthy human volunteers.

69 hagocytosis during experimental infection of human volunteers.

70 tion technique for estimating OEF in healthy human volunteers.

71 attenuated strains were still reactogenic in human volunteers.

72 ation of marrow Tregs to peripheral blood in human volunteers.

73 H MR spectra from the gallbladder bile of 10 human volunteers.

74 ed in studies with a respiratory phantom and human volunteers.

75 luid collected from the conjunctival sacs of human volunteers.

76 compared to the results obtained for normal human volunteers.

77 vascular integrity; 3K3A-APC proved safe in human volunteers.

78 ive field locations in visual cortex (V1) of human volunteers.

79 growth of BCG in whole blood from healthy UK human volunteers.

80 anel and in vivo retention of sodium ions in human volunteers.

81 ay inflammation in animal models and healthy human volunteers.

82 shown to increase renal perfusion in healthy human volunteers.

83 elicited cross-neutralizing antibodies from human volunteers.

84 cted patients and in experimentally infected human volunteers.

85 at least one facial skin site of 17 healthy human volunteers.

86 robed over time, and recorded EEG in healthy human volunteers.

87 to the behavioral differences of free-living human volunteers.

88 y in normal mice, rats, monkeys, and healthy human volunteers.

89 s in the blood transcriptome of IAV-infected human volunteers.

90 gle-pulse TMS to the motor cortex of healthy human volunteers (10 females and 7 males) during electro

91 d a double-blind sham-controlled study on 20 human volunteers (10 females) using a sequential neurofe

92 Twenty-nine human volunteers (13 females) participated in this study

93 PET studies of 6 healthy human volunteers (3 male, 3 female) were acquired after

94 cans were performed in 10 healthy nonsmoking human volunteers (34 +/- 13 years old); the two PET scan

95 dependent, gender-mixed sample of 57 healthy human volunteers (36 female, 21 male).

96 Thirty-five healthy, nonsmoking human volunteers 70 years or older were enrolled and und

97 imal studies when administering 1 to healthy human volunteers, a phase I clinical trial was conducted

98 ma metabolome in metabolically characterized human volunteers across a spectrum of insulin resistance

99 l responses to amphetamine in 99-162 healthy human volunteers (ADORA2A, SLC6A3, BDNF, SLC6A4, CSNK1E,

100 tates Inventory) were measured in 24 healthy human volunteers after a normal night's sleep and after

101 histamine administration to the forearms of human volunteers after Nanopatch(R) treatment, although

102 Vitreous Po(2) was imaged in three human volunteers (age range, 26-28 years) in multiple se

103 ossover, placebo-controlled trial in healthy human volunteers also revealed that the NSAID drug celec

104 cal interventions in a sample of 128 healthy human volunteers and a hierarchical Bayesian learning mo

105 In vivo studies in healthy human volunteers and animal models indicated that angiot

106 f these new measurements has been studied in human volunteers and clinical trials.

107 ted anatomically defined neck fat from adult human volunteers and compared its gene expression, diffe

108 required for virulence in orally challenged human volunteers and for the localized adherence and aut

109 inhibitor, reduced triglycerides in healthy human volunteers and in homozygous familial hypercholest

110 investigated simultaneously in healthy adult human volunteers and in interferon-gamma knockout (GKO)

111 sing nitrite infusion protocols in 20 normal human volunteers and in nonhuman primates to answer thes

112 t to affect reversal learning in monkeys and human volunteers and measures of impulsivity in rats.

113 NETosis of neutrophils collected from normal human volunteers and naive mice in an exchange protein a

114 f direct gaze to visual awareness in healthy human volunteers and show that with increasing neural ac

115 Ethyl pyruvate has been tested in human volunteers and shown to be safe at clinically rele

116 Healthy human volunteers and subjects hospitalized with bacteria

117 h control of mycobacterial growth in vivo in human volunteers and supports the use of BCG challenge a

118 ) were optimized for imaging at 3.0 T in two human volunteers and then used to image 10 porcine knees

119 ine responses in historically BCG-vaccinated human volunteers and to assess the contribution of vacci

120 A panel of 10 healthy HLA-A*02 human volunteers and two kidney transplant recipients we

121 as isolated from the blood of adult rats and human volunteers and was analyzed by protein marker expr

122 Tears were collected from healthy human volunteers and were studied in vivo in mice.

123 meat modulates biomarkers of cancer risk in human volunteers and whether specific agents can suppres

124 esulted in a short plasma half-life (5 h) in human volunteers, and a backup program was initiated to

125 studies linking research with animal models, human volunteers, and clinical populations are greatly e

126 te was taken from the iliac crest of healthy human volunteers, and hMSCs were isolated as previously

127 distribution and pharmacokinetics in healthy human volunteers, and show its ability to detect multipl

128 acy over PLS when measurements from multiple human volunteers are employed in the calibration set.

129 ch lipoprotein (TGRL) particles derived from human volunteers are nondestructively analyzed by laser

130 ible blood is potentially lethal, studies on human volunteers are not ethical.

131 through the lung, spleen, and bone marrow of human volunteers are significantly different.

132 tracer quantities of (45)Ca was measured in human volunteers as a part of an otherwise low-calcium t

133 temporarily lower brain serotonin in healthy human volunteers as they completed a novel task designed

134 Importantly, antisera from NV-infected human volunteers, as well as from mice inoculated with p

135 d as an intravenous bolus in 7 healthy adult human volunteers at </=2 mg/kg to provide circulating CR

136 motional and neutral faces were presented to human volunteers at cardiac systole, when ejection of bl

137 med high-resolution 7 Tesla fMRI while adult human volunteers attended either to the numerosity or an

138 Human volunteers bearing the (T) allele of PDYN (prodyno

139 n magnetic resonance spectroscopy studies in human volunteers before and after vigorous exercise (>/=

140 the potential of this technique on a healthy human volunteer breathing along different respiratory pa

141 In vivo bioavailability was determined in human volunteers by (14)C urinary excretion following to

142 ding cardiovascular collapse were induced in human volunteers by applying progressive lower body nega

143 nt in the lower gastrointestinal tract of 12 human volunteers by determining 48 billion bases of vira

144 uphoric response to d-amphetamine in healthy human volunteers by identifying enrichment between SNPs

145 cid levels were quantified in serum from 161 human volunteers by LC/MS.

146 s were isolated on 2 separate occasions from human volunteers by using Current Good Manufacturing Pra

147 eumonia, 3) the endotoxin response of normal human volunteers can be mapped at the level of gene expr

148 ainst life-threatening cholera diarrhea in a human volunteer challenge model.

149 randomized, double-blind, placebo-controlled human volunteer cholera challenge model.

150 Treatment of non-human primates and healthy human volunteers confirmed NSAID-mediated egress in othe

151 dly reactive hMAbs by vaccination in healthy human volunteers confirms the value of the polyvalent fo

152 In human volunteers, cooling damaged sebaceous glands and r

153 that have been observed after vaccination in human volunteers coupled with low mosquito infectivity,

154 Studies in animals and human volunteers demonstrate that antibodies against the

155 Studies in human volunteers demonstrate that hpre-CDCs are a dynami

156 BOLD neuroimaging in human volunteers demonstrates rigid representations of r

157 inary results from our first measurements in human volunteers demonstrating the potential of the tech

158 rcing, and analgesic effects of oxycodone in human volunteers diagnosed with opioid dependence (equiv

159 00 mg (approximately 7 mg/kg) VCV in healthy human volunteers did not suppress HSV-1 DNA shedding in

160 plored the dynamics and function of FGF21 in human volunteers during a 10-day fast.

161 ion (directional motion vs. motion noise) of human volunteers during fMRI experiments.

162 xamined behavioral pain responses in healthy human volunteers during mindfulness meditation and a non

163 sonance imaging (fMRI) was used while normal human volunteers engaged in simple detection and discrim

164 e the humoral immune response in a subset of human volunteers enrolled in a phase 1 rVSV-ZEBOV vaccin

165 In healthy human volunteers experimentally infected with RSV, a pot

166 , bronchoalveolar lavage fluid obtained from human volunteers exposed to O3 contained elevated levels

167 llular memory responses could be recalled in human volunteers exposed to P. falciparum parasites in a

168 Seven normal human volunteers (five men, two women; age range, 27 to

169 combination, or placebo was infused into 13 human volunteers for 120 min.

170 (135 nmol/min) was infused into six healthy human volunteers for 120 minutes and blood collected at

171 was also prospectively evaluated in healthy human volunteers (from January 2017 to September 2017).

172 In 20 human volunteers, from the ON to the apex of lateral rec

173 ethanol solution to the forearms of healthy human volunteers has been a reliable predictor of their

174 ies in rats and functional neuroimaging with human volunteers have led to the suggestion that the amy

175 termates, as well as those of obese and lean human volunteers have revealed that obesity is associate

176 olated a panel of monoclonal antibodies from human volunteers immunized in a clinical vaccine trial o

177 Sera from ten human volunteers immunized with a multivalent NoV VLP va

178 tiated rats (47% meat diet for 100 d) and to human volunteers in a crossover study (180 g/d for 4 d).

179 ansfusion of autologous red cells to healthy human volunteers increased extravascular hemolysis, satu

180 dies in human liver cell cultures, mice, and human volunteers indicate that IL-6 is the necessary and

181 The use of this technique in human volunteers indicates that cardiomyocyte fat correl

182 In human volunteers infected with 35000HP, the ratio of mye

183 When normal human volunteers ingested Neu5Gc, a portion was absorbed

184 With human volunteers inoculated at two sites with Haemophilu

185 ieved with pooled immune gamma globulin from human volunteers inoculated with live vaccinia virus.

186 of NV RNA, isolated from stool samples from human volunteers, into human hepatoma Huh-7 cells leads

187 , ingestion of calcitriol (1alpha25VitD3) by human volunteers led to an increase of both IL-10 and TL

188 Metformin administered to healthy human volunteers led to significant downregulation of ge

189 In two experiments, human volunteers made binary judgments about images of e

190 phase of a verbal memory task where healthy human volunteers made Remember, Know, or New judgments t

191 ring risky decision making such that healthy human volunteers moved from defending against losses to

192 Human volunteers (n = 10) were fed almonds for 7 d and t

193 sing freshly isolated monocytes from healthy human volunteers (n = 10).

194 t range, 20-25 kg; mongrel dogs) and healthy human volunteers (n = 10; age range, 22-53 years; seven

195 d from magnetic resonance imaging of healthy human volunteers (n = 11, male, 30 +/- 9 y).

196 effects using MEG data acquired from healthy human volunteers (N = 13, 7 female).

197 RESEARCH DESIGN AND Healthy human volunteers (n = 14) were treated with intravenous

198 In healthy human volunteers (n = 24), we found that the same reliab

199 then applied to blood samples collected from human volunteers (n = 6, healthy controls; n = 14, peanu

200 In non-allergic human volunteers, nasal symptoms were positively correla

201 Healthy human volunteers occasionally elect to undergo surgical

202 Intravenous administration to human volunteers of a commercial preparation of recombin

203 model to single-trial EEG data from healthy human volunteers of either sex who received the NMDAR an

204 hods (direct ophthalmoscopy on simulators or human volunteers, or use of fundus photographs) and reco

205 ction after influenza vaccination in healthy human volunteers (P=0.017 and 0.014, respectively).

206 While human volunteers performed a modified double-step task,

207 Healthy human volunteers performed a motor task by pressing a pi

208 Fifteen human volunteers performed a single (Flanker or Simon) c

209 Here, healthy human volunteers performed an auditory spatial localisat

210 Twenty-three female and male healthy human volunteers performed two probabilistic cueing task

211 of simultaneously recorded data from healthy human volunteers performing unilateral finger tapping at

212 mPFC concentrations of GABA and glutamate in human volunteers predict both behavioral performance and

213 Healthy human volunteers produced leftward AS during three diffe

214 fMRI in healthy human volunteers revealed that activity fluctuations in

215 Our investigation in normal human volunteers revealed the presence of 2 to 4 distinc

216 Healthy human volunteers showed a surprising improvement in moti

217 Human volunteers showed increased myocardial T2 at stres

218 Dosing ETX0914 in human volunteers showed sufficient exposure and minimal

219 after collection by bronchial brushing of a human volunteer) showed dephosphorylation rates ranging

220 In 12 human volunteers, single-pulse TMS of the primary motor

221 A dietary origin was suggested by human volunteer studies and by observing that free Neu5G

222 Next, human volunteer studies were performed, and motion estim

223 In human volunteer studies, motion estimates were obtained

224 used in several research projects including human volunteer studies.

225 icroarray chips assaying 12,023 genes of 151 human volunteer subjects under 4 different inoculation r

226 Furthermore, human monocytes isolated from human volunteers, subsequently preconditioned with HSP-7

227 Studies of patients and healthy human volunteers suggest that even relatively small volu

228 as recently reported to be well tolerated in human volunteers, suggesting a role for Hap in reactogen

229 Wild-type mice or human volunteers taking cyclooxygenase-2 inhibitors also

230 e was consistent with functional MRI data in human volunteers that revealed an association of the DUS

231 In experimentally infected human volunteers, the cutaneous immune response to Haemo

232 Among human volunteers, the majority of experimentally infecte

233 In pustules obtained from infected human volunteers, there was an enrichment of CD56bright

234 om placebo, we randomly assigned 75 healthy, human volunteers to 4 d of the following: (1) mindfulnes

235 h field, we performed (1)H-MRS in 60 healthy human volunteers to asses age-related differences in met

236 t Bald's eyesalve could be tested further on human volunteers to assess safety for topical applicatio

237 We administered Imprime to healthy human volunteers to assess the necessity of ABA for Impr

238 Here, we instructed human volunteers to classify words with lateralized hand

239 n the present study, we used fMRI in healthy human volunteers to determine the neural mechanisms supp

240 direct DA agonist, on willingness of healthy human volunteers to exert effort for monetary rewards at

241 ell banks were administered to malaria-naive human volunteers to explore infectivity.

242 In the present fMRI study, we exposed human volunteers to sequentially presented object stimul

243 gnetic resonance imaging (fMRI) with healthy human volunteers to study how the processing of threat-r

244 multivariate pattern analysis in 15 healthy human volunteers to test whether spatial information of

245 idates can be obtained by exposing immunized human volunteers to the bites of laboratory-reared P. fa

246 in saliva-derived metagenomic DNA of healthy human volunteers, two novel variants of genes encoding a

247 d fMRI responses, despite being invisible to human volunteers: under crowding conditions , areas V3A,

248 A study with human volunteers undergoing glucose tolerance tests indi

249 Twelve overweight or obese human volunteers underwent a randomized, double-blinded,

250 Healthy human volunteers underwent a training period of voluntar

251 Three macaque monkeys and 13 healthy human volunteers underwent diffusion tensor MRI with a 3

252 designed and executed such a disturbance in human volunteers using a dense longitudinal sampling sch

253 ural processes of memory encoding in healthy human volunteers using a visual task.

254 and spatial arrangement were examined in two human volunteers using an intraoral stent containing ret

255 ) in cell-free serum and plasma samples from human volunteers using deep sequencing of barcoded small

256 lacebo over 1-6 weeks in scars created in 62 human volunteers using quantitative noninvasive devices,

257 ons on brain and behavior in male and female human volunteers, using two matched visual-motor tasks t

258 e CD8(+) T-cell response in flavivirus-naive human volunteers vaccinated with 2 doses of TDV 90 days

259 lood from patients with scleritis or healthy human volunteers was analyzed for SOCS expression by RNa

260 uated S. typhimurium previously evaluated in human volunteers was further deleted for uvrAB genes and

261 Venous blood from human volunteers was stimulated with LPS, MPLA or vehicl

262 The task of the participants (male/female human volunteers) was to discriminate the pointing direc

263 iameter nociceptive-specific laser pulses to human volunteers, we discovered that (1) the spatial acu

264 magnetoencephalography recordings in healthy human volunteers, we dissociated brain activities underl

265 magnetic resonance imaging (fMRI) data from human volunteers, we found evidence implicating the vent

266 In 10 healthy human volunteers, we found that the sympathomimetic ephe

267 agnetic resonance imaging study with healthy human volunteers, we manipulated subjects' requirement t

268 In female and male human volunteers, we recorded EEG in a motor adaptation

269 In a delayed-movement paradigm, human volunteers were asked to plan and execute three ty

270 Ten healthy human volunteers were enrolled in this study; 6 complete

271 mportant for bacterial survival in vivo, six human volunteers were experimentally infected with 35000

272 Fifteen human volunteers were experimentally infected with both

273 Human volunteers were imaged using high specific absorpt

274 Healthy human volunteers were instrumented to record BP, ECG, re

275 ic fingerprint of Gc sensitivity 100 healthy human volunteers were polarized into the 10% most Gc-sen

276 Twenty-two healthy human volunteers were randomly assigned to either a high

277 Healthy human volunteers were scanned with functional magnetic r

278 To test this prediction, 32 human volunteers were trained to a coarse orientation di

279 Ten human volunteers were used to determine the horizontal r

280 Ten human volunteers where administered a dietary relevant d

281 We confirmed this link in healthy human volunteers, where injection of natural glucagon in

282 port a behavioral study performed on healthy human volunteers, where we demonstrate that spatial prio

283 To test this hypothesis, we scanned healthy human volunteers while they performed a probabilistic in

284 We prospectively studied 14 healthy human volunteers who donated standard leuko-reduced, dou

285 tional magnetic resonance imaging in healthy human volunteers who were exposed to faces with direct o

286 Prospective study of human volunteers who were tested on 2 consecutive days,

287 Using blood samples from human volunteers, whose diet was supplemented by a soy-b

288 After experimental infection of human volunteers with a gonococcal variant incapable of

289 l T cell clonal lineages upon vaccination of human volunteers with a single dose of YF-17D.

290 nthase (plasma tHcy, 93 +/- 16 microM) or in human volunteers with acute hyperhomocysteinemia (plasma

291 tron emission tomography approach in healthy human volunteers with amphetamine and the D2/D3 ligand [

292 e genomes of two input strains isolated from human volunteers with asymptomatic infection, and the ge

293 curs rapidly in nature, whereas infection of human volunteers with bacteria grown in vitro is difficu

294 nd quantitative changes in the microbiota of human volunteers with CeD prior to and following infecti

295 We inoculated human volunteers with either influenza A (A/Brisbane/59/

296 ial of MSP-1(19), immunization of nonexposed human volunteers with either of the two allelic forms of

297 Intranasal vaccination of human volunteers with live influenza virus also increase

298 investigated whether controlled infection of human volunteers with N. lactamica prevents colonization

299 In particular, we assessed 43 young human volunteers with normal hearing thresholds for thei

300 s caused neutrophilic airway inflammation in human volunteers, with GSTM1 null genotype being associa