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

3 shown to increase renal perfusion in healthy human volunteers.

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

5 30 lowered Abeta in the CSF of healthy human volunteers.

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

7 reting cells in the circulation of immunized human volunteers.

8 elicited cross-neutralizing antibodies from human volunteers.

9 n direct ophthalmoscopy using simulators and human volunteers.

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

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

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

13 mutant was fully attenuated for virulence in human volunteers.

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

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

16 ated excellent pharmacokinetic properties in human volunteers.

17 cted patients and in experimentally infected human volunteers.

18 tional magnetic resonance imaging in healthy human volunteers.

19 PET scans were obtained for 7 adult human volunteers.

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

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

22 5000HP for their ability to cause disease in human volunteers.

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

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

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

26 storm and multiorgan failure in six healthy human volunteers.

27 rved following TGN1412 administration to the human volunteers.

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

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

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

31 lemic hypotension in spontaneously breathing human volunteers.

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

33 m parasites in experimental rodent hosts and human volunteers.

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

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

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

37 on and virus load in experimentally infected human volunteers.

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

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

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

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

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

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

44 Subjects were eight healthy human volunteers.

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

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

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

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

49 estimate its radiation dosimetry in healthy human volunteers.

50 ich has undergone several clinical trials in human volunteers.

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

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

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

54 hagocytosis during experimental infection of human volunteers.

55 tion technique for estimating OEF in healthy human volunteers.

56 attenuated strains were still reactogenic in human volunteers.

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

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

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

60 luid collected from the conjunctival sacs of human volunteers.

61 compared to the results obtained for normal human volunteers.

62 s vaccine target, keeping in mind its use in human volunteers.

63 ysis of LPA species in plasma and serum from human volunteers.

64 vioral inhibition and impulsivity in healthy human volunteers.

65 ria in biopsy samples obtained from infected human volunteers.

66 atients with Parkinson's disease and healthy human volunteers.

67 ately 370 MBq (10.0 mCi) 99mTc in 10 healthy human volunteers.

68 rofiles of xenoreactive PBLs from a panel of human volunteers.

69 nd perform radiation dosimetry in 10 healthy human volunteers.

70 2, which has been shown to cause diarrhea in human volunteers.

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

72 ily detected in the nasal washings of normal human volunteers.

73 ts regional cerebral distribution in healthy human volunteers.

74 4 indexes of anticoagulant effect in healthy human volunteers.

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

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

77 artially attenuated for pustule formation in human volunteers.

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

79 obacterial growth following BCG challenge in human volunteers.

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

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

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

83 artially attenuated for pustule formation in human volunteers.

84 d with subsequent clinical investigations in human volunteers.

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

86 ay inflammation in animal models and healthy human volunteers.

87 n social and emotional processing in healthy human volunteers.

88 analysis to answer this question in healthy human volunteers.

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Malarial TCTP was found in lightly infected human volunteers and in heavily infected Malawian childr

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 n, ACC was immunoprecipitated from muscle of human volunteers and its activity assayed in the same in

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

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

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

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

117 examined in monocytes obtained from healthy human volunteers and stimulated with either lipopolysacc

118 Healthy human volunteers and subjects hospitalized with bacteria

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

120 ng of undisturbed intact plaque samples from human volunteers and the viewing of the biofilms in thei

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

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

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

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

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

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

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

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 skin has been investigated in vivo on normal human volunteers as well as on patients with psoriasis a

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

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

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

138 was applied for 24 h with a dermal patch to human volunteers at low (0.167 mg, 6.45 muCi) and high (

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

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

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 virulent V. cholerae O139 4260B for use in a human volunteer challenge model.

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

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

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

153 In human volunteers, cooling damaged sebaceous glands and r

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

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

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

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

158 00 mg (approximately 7 mg/kg) VCV in healthy human volunteers did not suppress HSV-1 DNA shedding in

159 either Flt3-ligand (FL) or G-CSF to healthy human volunteers dramatically increases distinct DC subs

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 oscillations in the electromyogram (EMG) of human volunteers during tasks requiring precision grip o

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

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

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

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

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

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

175 Sera from experimental animals and human volunteers immunized with a virus-like particle va

176 restricted by HLA-A*01 and is recognized by human volunteers immunized with irradiated P. falciparum

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

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

179 rt here that administration of FL to healthy human volunteers increased the number of circulating CD1

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 cytic infiltration in the airways of healthy human volunteers involving neutrophils, lymphocytes, and

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

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

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

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

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

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

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

195 Healthy human volunteers occasionally elect to undergo surgical

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

197 y recirculating heparinized whole blood from human volunteers on a membrane oxygenator.

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

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

200 In healthy human volunteers PEG-rHuMGDF transiently increases megak

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

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

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

204 Here, healthy human volunteers performed an auditory spatial localisat

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

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

207 cyte growth and development factor to normal human volunteer platelet donors increases platelet yield

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

209 imetry, and safety of [(18)F]FHBG in healthy human volunteers, preparatory to imaging patients underg

210 Healthy human volunteers produced leftward AS during three diffe

211 sporozoite cDNA library with the serum of a human volunteer protected experimentally by the bites of

212 fMRI in healthy human volunteers revealed that activity fluctuations in

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

214 Healthy human volunteers showed a surprising improvement in moti

215 Dosing ETX0914 in human volunteers showed sufficient exposure and minimal

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

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

218 case control study in which seven, healthy, human volunteers (skin type II; aged 23-56 y; three male

219 ger increase in renal plasma flow in healthy human volunteers studied on a low salt diet to activate

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

221 virus-like particles-used in the setting of human volunteer studies and large epidemiologic studies.

222 stages: (1) "ancient times (1972-1978), when human volunteer studies prevailed, (2) the "middle ages

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

224 In human volunteer studies, motion estimates were obtained

225 used in several research projects including human volunteer studies.

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

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

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 were compared with those of elderly healthy human volunteers that had been analyzed similarly.

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

232 of [11C]thymidine and [11C]thymine in normal human volunteers, the kinetics of the first labeled meta

233 Among human volunteers, the majority of experimentally infecte

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

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

236 f DE on human airways, we exposed 15 healthy human volunteers to air and diluted DE under controlled

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

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

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

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

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

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

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

244 ng and glucose-loaded sessions in five adult human volunteers, together with published brain paramete

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

246 A study with human volunteers undergoing glucose tolerance tests indi

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

248 Healthy human volunteers underwent a training period of voluntar

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

250 Ten normal human volunteers underwent dilation with tropicamide, ph

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

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

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

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

255 on of radiolabeled 15-A2t-isoprostane into a human volunteer was in the form of a polar conjugate(s).

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

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

258 od mononuclear cells isolated from 8 healthy human volunteers was measured 20 and 60 min after FDG wa

259 umb extension and flexion movements of eight human volunteers was measured using functional magnetic

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

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

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

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

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

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

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

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

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

269 Fifteen human volunteers were experimentally infected with both

270 ssion of PAL is required for virulence, nine human volunteers were experimentally infected.

271 To investigate this, 15 healthy human volunteers were exposed to diluted DE and air on t

272 Human volunteers were imaged using high specific absorpt

273 Two groups of human volunteers were inoculated with 2 doses of live Ha

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

275 Studies on phantoms and healthy human volunteers were performed to determine whether the

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

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

278 Healthy human volunteers were scanned with functional magnetic r

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

280 Ten human volunteers were used to determine the horizontal r

281 Ten human volunteers where administered a dietary relevant d

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

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

284 d pulmonary inflammatory response in healthy human volunteers, which is underestimated by standard lu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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