ライフサイエンスコーパス: experimental group

1 lus bevacizumab (5 mg/kg every 2 weeks x 26, experimental group).

2 sted for proficiency on days 10, 20, and 30 (experimental group).

3 ontrol group) or FOLFOXIRI plus bevacizumab (experimental group).

4 cerebroventricular and intra-PFC) (n = 10-12/experimental group).

5 least 5 sample replicates were used for each experimental group.

6 ropriate subset of outliers to represent the experimental group.

7 tected in calretinin-positive neurons in any experimental group.

8 oluble CD40 ligand were also observed in the experimental group.

9 ion were divided into a control group and an experimental group.

10 tion time were significantly shorter for the experimental group.

11 at least five animals were assigned to each experimental group.

12 tion response to KCl and endothelin for each experimental group.

13 se bengal, riboflavin, or water according to experimental group.

14 symptoms were also better controlled in the experimental group.

15 ost-test and 3 months after post-test in the experimental group.

16 simultaneously in either the control or the experimental group.

17 neutropenia were significantly higher in the experimental group.

18 e NMDA-DeltaCa(2+) responses between the two experimental groups.

19 ges did not significantly differ between the experimental groups.

20 rol particularly LDL cholesterol observed in experimental groups.

21 levels did not significantly differ between experimental groups.

22 after attaining steady [Ca(2+)](SR) in both experimental groups.

23 essments should be identical for control and experimental groups.

24 y rats were divided among control, sham, and experimental groups.

25 able until the end of the experiment for all experimental groups.

26 ersion of CO(2) has been studied by numerous experimental groups.

27 differences in feed efficiency ratios among experimental groups.

28 /Fet-/- mice that were placed in control and experimental groups.

29 significant differences between control and experimental groups.

30 For this purpose, we first defined four experimental groups.

31 sites after 21 days differed for each of the experimental groups.

32 d XY littermates (n=8) were separated into 5 experimental groups.

33 sponse relationship was not available in all experimental groups.

34 lated OT-1/GFP group compared with all other experimental groups.

35 were present in both hemispheres of all the experimental groups.

36 rformed for comparisons between all pairs of experimental groups.

37 ovascular function compared with the other 3 experimental groups.

38 rs must control for non-random assignment to experimental groups.

39 nesis for cerebellar neurons and glia across experimental groups.

40 d hypertrophied hearts compared to all other experimental groups.

41 changes in impedance between the control and experimental groups.

42 sside induced similar relaxations in the two experimental groups.

43 /80) that are highly expressed in all of our experimental groups.

44 ined equal in other OB-layers throughout all experimental groups.

45 frequency flux noise measurements of various experimental groups.

46 ological analyses in comparison to the other experimental groups.

47 imultaneously classify samples from multiple experimental groups.

48 n of muscle samples did not differ among the experimental groups.

49 behaviors between animals in the control and experimental groups.

50 ccessibility, as compared with that of other experimental groups.

51 mab (5 mg/kg every 2 weeks for 52 weeks [ie, experimental group]).

52 insonian motor symptoms in either of the two experimental groups (1-methyl-4-phenyl-1,2,3,6-tetrahydr

53 Rats were randomly assigned to one of five experimental groups: 1) acutely anesthetized control, 2)

54 olled trial were randomly assigned to 1 of 3 experimental groups: 1) control, 706 mL cow milk/d plus

55 Twenty-one animals were randomized to three experimental groups: 1) Local cooling with water for 20

56 y rats were randomly assigned to one of five experimental groups: (1) control (Con), (2) 6 h of MV, (

57 d in control (group 1, periosteum alone) and experimental (group 2, periosteum with alloplastic graft

58 death occurred in 56 of 257 patients in the experimental group (21.8%), as compared with 58 of 260 p

59 rence in the risk of an unfavorable outcome (experimental group [21.0%] minus control group [17.2%])

60 response (AUC: control group 817 +/- 107 and experimental group 3,445 +/- 573 pg x ml(-1) x 90 min(-1

61 ory T (Treg)-cells was increased only in the experimental group 30 days after infection.

62 was longer, but not significantly so, in the experimental group (31.0 vs. 25.8 months; hazard ratio f

63 e curve [AUC]: control group 240 +/- 261 and experimental group 4,346 +/- 1,259 pg x ml(-1) x 90 min(

64 osis rates in 1, 2, 3, 4, and 5-years in the experimental group (6.9%, 11.5%, 19.1%, 26.0%, and 35.9%

65 In the experimental group, 65 healthy male and female subjects

66 ntly, the 4 and 5-year survival rates in the experimental group (83.2% and 76.3%, respectively) were

67 rticipants dropped out after assignment to 3 experimental groups; 90 participants were assigned to a

68 ed removal and replacement of individuals in experimental groups (a key method in testing for CCE) al

69 randomly assigned into one of the two 4-week experimental groups, a forced exercise group and a non-e

70 itially, 35 tumors were randomized into four experimental groups: (a) conventional monopolar RF (70 d

71 (n=8, each group) were randomized into four experimental groups: (a) conventional monopolar RF alone

72 ed animals performed better than the other 3 experimental groups across 1 year of treatment.

73 group vs 43.1 [95% CI, 42.0 to 44.1] in the experimental group; adjusted difference, 4.9 [95% CI, 2.

74 y arch, were randomly distributed into three experimental groups administered either 1) low-dose flur

75 e-pilocarpine injections and divided into an experimental group (administered by MK-801) and a positi

76 found lower all-cause mortality risk in the experimental group after age 40 [hazard ratio (HR) = 0.9

77 ical pathway proteins did not differ between experimental groups after 3 months of diabetes, while NF

78 Men in the experimental group also rated heavier female bodies as m

79 Participants in experimental groups also received usual care.

80 In parallel experimental groups, an attempt was made to eliminate mi

81 ts of each participant was -2.8 (7.2) in the experimental group and 10.7 (10.8) in the control group.

82 roup, among Hispanic participants (27 in the experimental group and 19 in the control group), there w

83 uction of excess arm volume was 29.0% in the experimental group and 22.6% in the control group (diffe

84 28 days, 277 of 501 patients (55.3%) in the experimental group and 251 of 509 patients (49.3%) in th

85 The objective response rate was 65% in the experimental group and 53% in the control group (P=0.006

86 75.6% (95% CI 73.7-77.5) of patients in the experimental group and 74.3% (72.3-76.2) of controls wer

87 re was a significant interaction between the experimental group and baseline symptom severity.

88 d at euro218.30 (95%CI 150.52-286.08) in the experimental group and euro232.20 (95%CI: 203.80-260.60)

89 o compare disease-free survival between each experimental group and placebo in the intention-to-treat

90 ere not significantly different between each experimental group and the respective control group at 2

91 Patients in the experimental group and their partners received an interv

92 d-type female mice were distributed into six experimental groups and sacrificed at 7, 15, and 30 days

93 ts adhering to a particular blood type diet (experimental group) and participants continuing a standa

94 received 1 mg phylloquinone daily for 12 mo (experimental group), and 21 subjects were treated with a

95 d in the striatum or substantia nigra in any experimental group, and amphetamine-induced behavioral r

96 /lesions over time decreased slightly in the experimental group, and increased slightly in the contro

97 In the second experimental group, animals received a purified diet wit

98 specimens were selected and divided into two experimental groups: animals with tough meat (TO) and an

99 n and puncture, mice were randomized to four experimental groups as follows: 1) sham control; 2) sham

100 nin-immunoreactive cells was similar for all experimental groups as well.

101 ays (interquartile range, 4.0 to 5.0) in the experimental group, as compared with 8.0 days (interquar

102 ression-free survival was 12.1 months in the experimental group, as compared with 9.7 months in the c

103 rvings per day), declined to nearly 0 in the experimental group at 1 year, and remained lower in the

104 n the mean CAL or PD values between the four experimental groups at baseline and 3 or 12 months post-

105 Samples were distributed into experimental groups based on donor age (young [20-39 yea

106 s (Callithrix jacchus) were divided into two experimental groups based on their response to monocular

107 r, both measures of spatial recall separated experimental groups beyond what would be expected based

108 ant differences were noticed between the two experimental groups both for PD (P = 0.03) and clinical

109 n the standard group and 0.1 +/- 0.5% in the experimental group, but the overall time course of %BF d

110 LIMK-1, cofilin-1, and beta-actin in all the experimental groups by semiquantitative and quantitative

111 All quantitative data were compared between experimental groups by using a mixed linear model and t

112 atios (SNRs) were compared between different experimental groups by using the Kruskal-Wallis test and

113 nts were seen in 517 of 2073 patients in the experimental group compared with 539 of 2089 controls (h

114 e Short Form 36 survey, was 69 points in the experimental group compared with 58 points in the contro

115 y significant improvements in outcome in the experimental group compared with control group at both 8

116 Job loss was delayed in the experimental group compared with the control group (P =

117 ere significantly higher at 12 months in the experimental group compared with the control group, and

118 was lower (5.1 versus 6.3; P = 0.02) in the experimental group compared with the control group.

119 m-focused coping (P = 0.03) were seen in the experimental group compared with the control group.

120 alth status, and lower fatigue scores in the experimental group compared with the control group.

121 eactivity was significantly decreased in all experimental groups compared to the control groups (P <0

122 age and after 5 days of attention training (experimental group) compared with different types of no

123 Six participants in the experimental group, compared with one in the control gro

124 All three experimental groups completed a 14-week intervention.

125 Participants undergoing a DBPCFC (experimental group) completed the FAQLQ and Food Allergy

126 luenza viruses, a ferret contact model using experimental groups comprised of one inoculated ferret a

127 Four experimental groups comprising both strains treated thre

128 Experimental groups consist of rats subjected to 2 h of

129 This gave four experimental groups: Control (C), C+ADR, Dose 1+ADR, and

130 Male rats were divided into four experimental groups: Control rats, CONTR-ARG rats, were

131 cFMA improvements in the experimental group correlated with changes in fMRI later

132 assigned 30 Sprague-Dawley rats to one of 5 experimental groups: corticotomy alone, corticotomy-assi

133 The VAS scores for the experimental group decreased during the study (alpha = 0

134 Furthermore, in none of these experimental groups did beta cell proliferation and isle

135 ol group compared with 1.93 +/- 0.37 for the experimental group) did not differ.

136 stereotypies were not observed in any of the experimental groups during the first year of life.

137 p (C; no periodontal therapy) (n = 35) or an experimental group (E; NSPT in the form of scaling and r

138 archers are interested in comparing multiple experimental groups (e.g. tumor size) with a reference g

139 Each rat in the two experimental groups (early, late) was also yoked to a co

140 posure to the solution was contingent on the experimental groups entry into the goal box of the runwa

141 Experimental groups exhibited increases in: 1) total cho

142 e randomly assigned to a control group or to experimental groups exposed to 6 or 12 h of MV with or w

143 l control, atherogenic control and six other experimental groups (fed atherogenic diet supplemented w

144 or to receive a fixed course of antibiotics (experimental group) for 4+/-1 calendar days.

145 In the experimental group (group 1), donor lungs were obtained

146 Those in the experimental group had 1 eye dilated and their optic ner

147 tial proficiency test, while students in the experimental group had a 91.7% pass rate at day 30 (P <

148 After the trial, the experimental group had higher mean scores in knowledge (

149 Thus, the experimental group had lower mortality from causes known

150 After age 40, the experimental group had lower mortality from overall canc

151 After 6 months, the experimental group had statistically significantly less

152 The placebo and experimental groups had significant differences in the 1

153 regulated by infection in the livers of both experimental groups; however, its levels were several-fo

154 t enzymatic degradation was observed for all experimental groups; however, statistically significant

155 ort if significant differences favouring the experimental group in a prespecified primary or secondar

156 r of replicates and the variance within each experimental group in clustering expression data, and pr

157 significant differences between control and experimental groups in both organism transcriptional act

158 ere no significant differences between the 2 experimental groups in radiographic root development ( P

159 , the effect of the person was less than the experimental group (in this case, sampling method) for a

160 Men were randomly assigned to either an experimental group, in which they took part in a task th

161 Experimental groups included non-allergic rats (NA) (n =

162 No other experimental groups, including riboflavin-mediated PDT,

163 Women in the experimental group increased physical activity from 1609

164 In an experimental group, infants were given the possibility t

165 gene expression profiles that differentiate experimental groups is critical for discovery and analys

166 ue at the site of injury was similar in both experimental groups (L2: 79% and T8: 82%).

167 The experimental group learned the discrimination and animal

168 t, compared to controls, participants in the experimental group make more generous choices in an inde

169 ealed enhanced poly(ADP-ribosyl)ation in all experimental groups manifesting neuropathic changes.

170 atomical configurations in all zones of both experimental groups matched the functional circuit stren

171 ansected adult female rats and compared four experimental groups: media-untrained, media-trained, OEG

172 nificantly between the two groups (change in experimental group minus change in control group, -0.3;

173 Mice in the experimental group (n = 10) were administered azoxymetha

174 After the 14-day treatment, the experimental group (n = 35) exhibited significantly lowe

175 The rate of diarrhea was 76.1% in the experimental group (n = 68) and 78.9% in the control gro

176 of rabbits in the control group (n = 6) and experimental group (n = 7), respectively.

177 Animals were randomized into shPHD2 experimental group (n=25) versus shScramble control grou

178 n plus an active impedance threshold device (experimental group, n = 15).

179 t online movements of hand and arm orthoses (experimental group, n = 16).

180 took part in a task that heightened stress (experimental group, n = 41) or in which they did not tak

181 ometrically in adult Brown Norway rats (nine experimental groups; n=4-7 in each; 10-100 mmHg and sham

182 ed to the surface of sound dentin disks in 4 experimental groups: non-antibacterial adhesive and gent

183 [non-inferiority margin] at 5 years for each experimental group; non-inferiority was shown if the upp

184 gp140 trimers was included as a comparative experimental group of NHPs.

185 Four experimental groups of adult male C57BL/J mice were expo

186 Three experimental groups of animals (groups 1 to 3) were sens

187 focused on disease classification, comparing experimental groups of effected to normal patients.

188 n the SI cortices of both hemispheres in all experimental groups of this study suggests that a focal

189 Mice were divided into two major experimental groups, one to examine the effects of cigar

190 Of all three experimental groups, only mice expressing IkappaKca show

191 demic medical centers and randomized into an experimental group or a control group.

192 best respiratory-system compliance (n = 501; experimental group) or a control strategy of low PEEP (n

193 help equally often from an out-group member (experimental group) or an in-group member (control group

194 January 2006 to December 2010, the covered (experimental group) or bare stent (control group) was us

195 oney over the next 4 weeks either on others (experimental group) or on themselves (control group).

196 ral feeding with an immunonutrition formula (experimental group) or standard formula (control group)

197 tients were assigned to the 4-month regimen (experimental group) or the standard regimen (control gro

198 Defects were treated with BPBM/GTR/PRP (experimental group) or with BPBM/GTR (control group).

199 decrease in lung signal was observed in each experimental group over 24 h.

200 ference in histologic findings between the 2 experimental groups ( P > 0.05).

201 pt mean GBI, were significantly lower in the experimental group (P <0.05).

202 ater than in the non-sonicated brain for all experimental groups (p<0.0001), and 1.5-fold higher for

203 umulative results during 24 months show that experimental group participants (359/648 [55%]) were mor

204 The experimental group patients received their local anesthe

205 Moreover, the experimental groups presented enhanced excitability of t

206 id secretion varied, the glands of all three experimental groups produced significant amounts of flui

207 Similarly, patients in experimental group programs (330/648 [51%]) were more li

208 Finally, participants in experimental group programs had significantly higher mon

209 Further analyses showed that men in the experimental group rated a significantly heavier female

210 f the instructive placebo procedure, the two experimental groups reached higher levels of force, beli

211 The experimental group received a 1-year intervention design

212 Participants in the experimental group received a 3-month multidisciplinary

213 andomly assigned to one of three groups: The experimental group received an individualized telephone

214 The experimental group received orally dosed PRT318, whereas

215 The experimental group received the polymeric device inserte

216 Subjects in the experimental group received two 1.5-hour sessions of voc

217 Experimental groups received vehicle, dexamethasone, or

218 Firefighters were randomly divided into 6 experimental groups receiving 1.2, 2.4, or 3.6 g flax oi

219 her maintained or switched resulting in four experimental groups: regular chow (R), high fat diet (H)

220 tes were 0.96% and 0.90% for the control and experimental groups, respectively.

221 sed BH4 in retinas, lungs, and aortas in all experimental groups, resulting in a dose-dependent decre

222 The experimental group showed a decrease in ulceration (alph

223 The DG experimental group showed increased freezing in the orig

224 esults Compared with bare nanoparticles, all experimental groups showed significantly increased negat

225 Both experimental groups showed that aromatase is localized i

226 unt data were analyzed by nested ANOVA for 5 experimental groups, split-mouth controls, 3 levels alon

227 Compared with the control group, the experimental group strategy increased 6-month mortality

228 ilesional lateral geniculate nucleus in both experimental groups, suggesting that postlesion visuomot

229 es in aromatase distribution between the two experimental groups suggests that these localization pat

230 Animals were allocated into two experimental groups: t-extracorporeal cardiopulmonary re

231 The PCB levels were reduced in all of the experimental groups tested, where addition of starter cu

232 r a control group (no thalidomide) or to the experimental group (thalidomide during induction, betwee

233 mpletion, MCP-1 levels remained lower in the experimental group than in the control group (313.88 vs

234 fatigue was also significantly lower in the experimental group than in the control group (P = 0.05).

235 verse event was significantly greater in the experimental group than in the control group (p<0.0001);

236 ents, the increase in BMI was smaller in the experimental group than in the control group after a 1-y

237 l group at 1 year, and remained lower in the experimental group than in the control group at 2 years.

238 MDA levels were higher in all experimental groups than in group C, but significant in

239 es into holes, subjects were assigned to two experimental groups that were given different kinds of e

240 deo was shown on a tablet to children in the experimental group the afternoon preceding a planned sur

241 In participants in the experimental group, the hemodynamic response in the amyg

242 For the experimental group, the largest RMSDs were 1.1 mm in ant

243 For the experimental group, the templates were designed based on

244 Within the experimental groups, the authors found a trend toward di

245 Among the other experimental groups, there was no change in kidney uptak

246 ately after the baseline EGG (5 pigs in each experimental group): thiopental, isoflurane, nitrous oxi

247 opulation precludes experimentation on large experimental groups, those examined in our study indicat

248 s suitable for examining differences between experimental groups, though, as with any method for imag

249 intraperitoneally before suture only in the experimental group to facilitate the fusion of the oment

250 For example, DAS has enabled small experimental groups to integrate their data into the Ens

251 hange in a control group with weight loss in experimental groups told to eat breakfast or to skip bre

252 ssion of CKD, we used two groups of rats: an experimental group undergoing 5/6 nephrectomy only and a

253 The experimental group underwent localized accelerations at

254 nts were enrolled and divided into 2 groups: experimental group (using genioplasty templates) and con

255 We included 4 experimental groups: vehicle-treated animals with extrac

256 verse events were diarrhoea (41 [10%] in the experimental group vs five [1%] in the control group), n

257 Lower mortality in the experimental group was also found among the least educat

258 One experimental group was conditioned about the effects of

259 stment for confounders, participation in the experimental group was found to be protective against jo

260 baseline activity was recorded and then the experimental group was injected with amphetamine (0.6mg/

261 The experimental group was injected with MSCs (0.3x10(6)) in

262 The experimental group was injected with PTH (80 mug/kg) dai

263 strating a higher stable disease rate in the experimental group was less than 9% even under the most

264 Between-groups analyses showed that the experimental group was matched with the control group in

265 e of secondary interventional therapy in the experimental group was significantly lower than that in

266 Enrollment in the experimental group was stopped when the 85% Bayesian pre

267 The experimental group was subdivided into CsA or saline con

268 e we observed behavioral idiosyncrasy in all experimental groups, we suspect it is present in most be

269 At 6 mo, serum ucOC concentrations in the experimental group were 0.96 +/- 0.08 ng/mL compared wit

270 The rats in the experimental group were fed 30 mg/kg CsA daily for 4 wee

271 Those in the experimental group were found to have significantly grea

272 patients in the placebo group and 140 in the experimental group were included in the final analysis.

273 operative time for the control group and the experimental group were nearly identical, the turnover t

274 Those in the experimental group were rewarded for responding to subst

275 x/ascites (6.9% vs. 16.5%, P = 0.019) in the experimental group were significantly lower than those i

276 All three experimental groups were able to utilize the embedded pr

277 Experimental groups were as follows: unchallenged contro

278 ted ED(50) values for each fibre type within experimental groups were calculated, a significant (P<0.

279 Experimental groups were compared at baseline, day 2, 1

280 Four experimental groups were evaluated: control (nontreated)

281 All experimental groups were exposed to 3 lighting condition

282 Two experimental groups were instructed that treatment with

283 In total, 401 experimental groups were manually annotated from 74 peer

284 erent commercial meat starter cultures, five experimental groups were prepared: no further addition;

285 Five experimental groups were prepared: unstimulated T cells,

286 The experimental groups were stimulated three times per minu

287 In addition, teeth with PCCR (experimental group) were matched with contralateral teet

288 No MMNm responses were recorded in either experimental group when stimuli were presented at SOAs f

289 p (n=6; 18 individual zones of ablation) and experimental groups where antennas were spaced 2.5 cm (n

290 4 years) were randomly assigned to either an experimental group which received a weekly subcutaneous

291 s were detected between samples derived from experimental groups which experienced fearful or neutral

292 Patients in the experimental group who entered the trial with higher sym

293 f 10 mg/kg rifampin, followed by consecutive experimental groups with 15 patients each receiving rifa

294 An experiment containing three experimental groups with eight subjects each can take as

295 rol group with uninjured lungs (n = 4) and 2 experimental groups with surfactant deactivation induced

296 e 120 min whisker stimulation period in four experimental groups with treatment initiated 0, 1, 2 (pr

297 37 cytokines increased significantly in all experimental groups, with 21 cytokines showing the highe

298 ional level, we found lower mortality in the experimental group within the strata that settled for co

299 Adaptive assignment to experimental groups within each disease subtype was base

300 We hypothesized that the experimental group would gain weight at a slower rate th