ライフサイエンスコーパス: return(ing|ed) to baseline

1 al, and every 30 min until LS and CAP values returned to baseline.

2 y lasted 1 to 4 hours before the participant returned to baseline.

3 ith the other dose levels, where mean values returned to baseline.

4 ght feedback, immune responses are tuned and returned to baseline.

5 elevated and persisting long after they had returned to baseline.

6 At 12 months, INR and albumin returned to baseline.

7 When the perturbation was removed, pitch returned to baseline.

8 xpression of LPL, plasma triglyceride levels returned to baseline.

9 factor, by which time surface Kit levels had returned to baseline.

10 essively poorer outcome as CTLA-4 expression returned to baseline.

11 e of 1,25(OH)2 D3 to rats and then gradually returned to baseline.

12 y revascularized, and the pericyte phenotype returned to baseline.

13 corrective actions, the rate of peritonitis returned to baseline.

14 beginning of vertebral movement but quickly returned to baseline.

15 removal of ghrelin, calcium currents slowly returned to baseline.

16 ROS challenge, whereas by 12 hours most had returned to baseline.

17 injection, and serum calcium values quickly returned to baseline.

18 nhanced proteasome inhibition that no longer returned to baseline.

19 and in anterior segments after facility had returned to baseline.

20 Other data returned to baseline.

21 HDMTX treatment, their plasma concentration returned to baseline.

22 ormal by insulin treatments, the AQP9 levels returned to baseline.

23 eived no treatment, and their liver function returned to baseline.

24 % of B, P = 0.046], and thereafter gradually returned to baseline.

25 er, all song measures that were affected had returned to baseline.

26 -fold expansions of NK cells that ultimately returned to baseline.

27 ecreased (P < .001), whereas Feno values had returned to baseline.

28 t until food- and drug-maintained responding returned to baseline.

29 s until food- and drug-maintained responding returned to baseline.

30 maximal regional cerebral oxygenation before returning to baseline.

31 reased from baseline to 48 hours, eventually returning to baseline.

32 sting 8 and 8.6 months, respectively, before returning to baseline.

33 dimer levels peaked 3 d postexposure, before returning to baseline.

34 bsequent reduction was noted, before finally returning to baseline.

35 nd peak was noted at days 9-11, before again returning to baseline.

36 1(WAF1/Cip) was increased transiently before returning to baseline.

37 infection, at which time AMP expression was returning to baseline.

38 ut had little or no effect on day 14 and had returned to baseline 1 week after ending treatment.

39 Regional blood flows returned to baseline 10 mins after discontinuation of pG

40 inally, in wild-type mice, CTLA-4 expression returned to baseline 17 days after receiving anti-CD45RB

41 min, flux increased by 300% and consistently returned to baseline 24 to 48 h after switching to norma

42 WT mice, responses to mechanical stimulation returned to baseline 3 weeks after CFA.

43 tients with incident status epilepticus, 238 returned to baseline (51.1%), 162 had new disability (34

44 p (53.5+/-7.6 vs. 45.3+/-10.1; P=0.0084) but returned to baseline 6 weeks after LDN (53.8+/-6.5 vs. 5

45 een found to initially decrease after LASIK, returning to baseline 6 to 12 months postoperatively.

46 and 41% on days 7, 14 and 28, respectively, returning to baseline (9%) on day 35.

47 ccurred and all donors had full recovery and returned to baseline activity.

48 ms to reach a peak from the initial rise and returned to baseline after 170 +/- 50 ms (n = 78 transie

49 tion of therapy, although HAZ scores had not returned to baseline after 2 years of observation in man

50 gh the increase of paracellular permeability returned to baseline after 24 h of recovery sleep.

51 ower than mean preflight values, but results returned to baseline after 48 hours.

52 to 98 au +/- 5, respectively; P = .023) and returned to baseline after 5 months (116 au +/- 10), as

53 95% confidence interval [CI], 1.04-3.62) and returned to baseline after 6 months of ART (adjusted PRR

54 me spent immobile in the modified FST, which returned to baseline after 72 h.

55 eased significantly at 4 hours (P=0.003) and returned to baseline after 8 hours' reperfusion (P=NS co

56 Though weight-for-age and BMI z scores returned to baseline after cessation of therapy, mean HA

57 persisters, became predominant in colistin, returned to baseline after colistin removal and was depe

58 transiently rose, then fell, and ultimately returned to baseline after external beam irradiation.

59 ly increased in the presence of a female and returned to baseline after removal of the female.

60 ined high during Hep II domain perfusion and returned to baseline after removal of the protein.

61 All these effects returned to baseline after stimulation was withdrawn.

62 median of 16 days before hospitalization and returned to baseline after treatment.

63 genes exhibited a reciprocal regulation and returned to baseline after weight loss (2163 genes) and

64 effect was reversible, with outflow facility returning to baseline after drug removal.

65 initiation of immunosuppression therapy; all returned to baseline allograft function.

66 lay process once neurocognitive function has returned to baseline and all symptoms have resolved.

67 e direction of shear stress as RhoA activity returned to baseline and Rac1 and Cdc42 reached peak act

68 At 30 mins of normocapnia, CBF had returned to baseline and remained at baseline until the

69 year after treatment, the CD4+ T-cell count returned to baseline and the clinical improvement waned,

70 Postoperatively, the patient's behavior returned to baseline, and he resumed development of new

71 in concentrations in male fathead minnow had returned to baseline, and testicular abnormalities were

72 at LT, [Ca(2+)](i) transiently increased but returned to baseline ( approximately 63 nm) in < 8 min.

73 nutes (87.9 U/mL, CI 78 to 99; P<0.0001) and returned to baseline at 12 hours (70.3 U/mL, CI 65 to 87

74 n stressed rats during the stress period but returned to baseline at 15 days post-stress.

75 els, which peaked at 1 hour of treatment and returned to baseline at 2 hours.

76 While patient-reported outcomes returned to baseline at 2 weeks, the number of daily ste

77 Although FMD returned to baseline at 2.5 h, EMPs and vascular endothe

78 Zif268 DNA methylation levels returned to baseline at 24 h.

79 crease in astrocytes was 30% after 1hour but returned to baseline at 8hours.

80 nd Snail at day 5 after heat exposure, which returned to baseline at day 12.

81 +/-325 versus 2911+/-165 pg/mL; P=0.046) but returned to baseline at POD4 (2838+/-224 pg/mL; P=0.90).

82 /-41.7 versus 11.1+/-1.1 pg/mL; P<0.001) and returned to baseline at POD4 (P=0.84 versus pre-CP/CPB).

83 .0 Meq/mL; 12 months: 38 Meq/mL; P <.05) and returned to baseline at the end of follow-up (11.0 +/- 2

84 in the ischemic zone increased initially but returned to baseline at the later times.

85 ramide (160% over control), with sphinganine returning to baseline at 4 h, and ceramide continuing to

86 ysis, increasing at low actin:Drp1 ratio but returning to baseline at high ratio.

87 d intestinal cytokines, such cytokine levels returned to baseline before administration of DSS.

88 s was similar to controls, and cytokines had returned to baseline, but aromatase mRNA and activity we

89 was transiently elevated 5 hr after SNL and returned to baseline by 1 d after SNL.

90 nd to be associated with object exploration, returned to baseline by 1 h in the same environment, but

91 These values returned to baseline by 1 week after drug treatment.

92 naptoneurosomes initially increased but then returned to baseline by 10 min after stimulation.

93 s with negative or uninformative results but returned to baseline by 12 months.

94 and lactate dehydrogenase peaked at 6 hr and returned to baseline by 120 hr after injury in all group

95 The post-meal CAP and LS values returned to baseline by 150 min.

96 th-muscle cell markers peaked at 4 weeks and returned to baseline by 16 weeks.

97 gulation of type I interferon responses that returned to baseline by 2 weeks postinfection, no detect

98 h after seizure onset, peaked at 3-6 h, and returned to baseline by 24 h in both hippocampus and neo

99 creased by 25% 3 h after preconditioning but returned to baseline by 24 h.

100 ted for at least 1 h after the last dose and returned to baseline by 24 h.

101 y PG levels increased by 6 h (P < 0.05), but returned to baseline by 24 h.

102 loid were also up-regulated >10-fold and all returned to baseline by 28 days after infection.

103 okines were induced at 1 to 14 dpi, but most returned to baseline by 28 dpi except interleukin 12 (IL

104 baseline, P = .012) noted at 1 month, but it returned to baseline by 3 months.

105 nd remained increased for at least 24 h, and returned to baseline by 30 h.

106 ng (75+/-5 to 109+/-11 microm2, P=0.007) but returned to baseline by 30 minutes (66+/-5 microm2).

107 After glucose ingestion, ghrelin returned to baseline by 4 h and increased to 1094 +/- 13

108 ne-1-phosphate levels at 10 min that rapidly returned to baseline by 40 min.

109 the kappa-opioid receptor; increased pJNK-ir returned to baseline by 48 h after treatment; and a seco

110 oximately 72% total cells was observed) that returned to baseline by 48 h.

111 24 hr after injection with FSGS factor, and returned to baseline by 48 hr after injection.

112 nificant 3 h increase in heat threshold that returned to baseline by 5 h after injection.

113 e alveolar spaces during the first 3 dpi and returned to baseline by 6 dpi.

114 .0001) and 64% (P<0.0001), respectively, and returned to baseline by 6 hours.

115 apoB-IC levels increased after PCI, but both returned to baseline by 6 hours.

116 Intraretinal signal intensity returned to baseline by 7 days after MnCl(2) injection.

117 tion, neutrophil numbers and cytokine levels returned to baseline by 72 h.

118 mpal neuropil at 1 week, all of which values returned to baseline by 8 weeks.

119 ity in lungs was reached by 72 hours, and it returned to baseline by 9 days.

120 and DC function recovered when IL-10 levels returned to baseline by convalescence.

121 matic elevation in viral p24 production that returned to baseline by day 15 and failed to rebound at

122 unction decreased on postoperative day 3 but returned to baseline by day 7.

123 significantly elevated on day 1 and rapidly returned to baseline by days 2-3.

124 maintained their QOL, and controls gradually returned to baseline by the end of the 6-month follow-up

125 T-cell responses peaked at week 4 and returned to baseline by week 12 after exposure.

126 = .0406 and P = .0325, respectively), which returned to baseline by week 26 (P = .0611).

127 cemia (2.7 mg/dl at week 2), but then levels returned to baseline by week 6 (1.4 mg/dl).

128 Levels of antibody to serotype 3 returned to baseline by year 2.

129 to 5 min after the final tecadenoson bolus, returning to baseline by 10 min.

130 g in SR, SL and hilum by 8-27% at 1 week and returning to baseline by 2 weeks.

131 sponse, levels peaking within 30 minutes and returning to baseline by 24 hours.

132 NCA is transient, peaking at 5 to 10 min and returning to baseline by 30 min.

133 teria by 24 and 48 hours, with all but IL-13 returning to baseline by seven days.

134 Plasma carotenoids returned to baseline concentrations by the middle of pha

135 Sleep and wakefulness returned to baseline conditions 2 to 5 days after antise

136 These diameters returned to baseline dimensions about 20 min after stopp

137 modified MSCs, fVIII activity levels rapidly returned to baseline due to the formation of anti-porcin

138 FVR returned to baseline during recovery, whereas MSNA signi

139 DE1S, JADE1L, and HBO1 protein levels, which returned to baseline during renal recovery.

140 week after immunization, with concentrations returning to baseline during convalescence.

141 regulated, increasing after wakefulness and returning to baseline during sleep.

142 At resolution, these phyla returned to baseline, except for synergistetes.

143 All 5 living patients returned to baseline exercise tolerance after 6 to 16 we

144 s measured when postchallenge DA levels have returned to baseline, following the initial competition

145 8+/-7.2 cm/s at 5 minutes (P=0.015) and then returned to baseline for the remainder of the infusion.

146 Patients who have not returned to baseline health should be considered for ext

147 In the post-apnoea recovery period, CFV returned to baseline in 45 +/- 4 s.

148 Platelet levels returned to baseline in all 26 surviving patients after

149 Immunoreactivity for pERK and c-fos returned to baseline in all retinal cells at 6 or 24 hou

150 20 min recovery period at 33 degrees C, V(I) returned to baseline in control pups but remained depres

151 d transient (<5 min) manner, as every neuron returned to baseline in less than 5-min post-application

152 nd a temporally precise phasic response that returned to baseline in tens of milliseconds.

153 he vehicle group (-32.2+/-11.8%, P<0.05) but returned to baseline in the AT1RB group (2.3+/-12.5%).

154 core of physical components score at 6 weeks returned to baseline in the laparoscopic group (86.4+/-1

155 n the year preceding the move (P = .031) but returned to baseline in the postmove years.

156 r zone during post-amputation weeks 2-3 that returned to baseline in the subsequent weeks.

157 ines and tumor necrosis factor alpha quickly returned to baseline in tlr3(-/-) mice, and these mice w

158 he Hep II domain administered after facility returned to baseline increased facility in two of three

159 Neuronal activity returned to baseline level after 30.0 +/- 3.1 minutes in

160 ventricular diastolic and systolic function returned to baseline level at 72 hrs postresuscitation.

161 id, significant decline in viral load, which returned to baseline level at day 30-45, coincident with

162 (P<0.01), but decreased from 5 h onward and returned to baseline level by 10 h.

163 inflammatory measures rapidly decreased and returned to baseline level.

164 %-80%); in six of these patients, AUC values returned to baseline levels (or greater) by 6 months.

165 Fluorescence returned to baseline levels 6 hours after NaF injection,

166 Rolling returned to baseline levels 7 hours after infusion.

167 ppaB was seen early after CD40 ligation, but returned to baseline levels after 4 h.

168 nterleukin-6 increased from 12 to 24 hrs and returned to baseline levels after 48 hrs.

169 ld decrease in mean arterial pressure, which returned to baseline levels after K201 discontinuation.

170 ction after onset of clinical gingivitis and returned to baseline levels after resolution of disease,

171 ed residual populations of immune cells that returned to baseline levels after several months.

172 IOP returned to baseline levels and possibly lower with prol

173 30% below baseline in patients with IAH but returned to baseline levels and remained there in the ot

174 y flooding, even after relative humidity has returned to baseline levels and remediation has removed

175 Postoperative symptoms returned to baseline levels at 12 months, but 32.1% of p

176 Trimethylated H3K4 levels returned to baseline levels at 24 h.

177 the procedure (354.1 mumol/L +/- 132.8) and returned to baseline levels at 24 hours (129.5 mumol/L +

178 at baseline, induced at 3 and 12 hours, and returned to baseline levels at 48 hours of reperfusion.

179 VA and CS returned to baseline levels at 6 months.

180 Renal perfusion had returned to baseline levels at day 21 after moderate (96

181 k of C57BL/6 of mice decreased at day 10 and returned to baseline levels at days 14 and 21.

182 In the obstructive model, these variables returned to baseline levels at T2 and remained in this r

183 o hours post-inoculation; however, cytokines returned to baseline levels by 18 hours.

184 significantly from baseline by 16 weeks and returned to baseline levels by 36 weeks.

185 rel compared with baseline (p < 0.0001), but returned to baseline levels by 7 days after discontinuat

186 r the start of methylphenidate treatment and returned to baseline levels during continuation of methy

187 After [Ca2+](i) had returned to baseline levels during continued AngII stimu

188 se of acquisition training and then activity returned to baseline levels during subsequent extinction

189 e, decreased immediately after allergen, and returned to baseline levels during the late asthmatic re

190 the control experiments, cerebral blood flow returned to baseline levels during the recovery period,

191 This returned to baseline levels during the second 2 h interv

192 In fact, body temperature returned to baseline levels faster in the beta-endorphin

193 on was elevated in active celiac disease but returned to baseline levels following implementation of

194 At the 6-month follow-up, most outcomes returned to baseline levels for all three groups.

195 rn in the 6 months after the suspension, but returned to baseline levels for those born 7 to 12 month

196 6% at baseline to 7.5% in digital year 1 and returned to baseline levels in digital year 3.

197 increased on d 2 and 4 postinjury but later returned to baseline levels on d 8 and 15 in wild-type (

198 hough circulating Vgamma2Vdelta2 T cells had returned to baseline levels weeks prior.

199 ed in B6 MC exposed to 25 mmol/l glucose but returned to baseline levels when the glucose concentrati

200 ts vs 15% of Sed rats; p < 0.01) and rapidly returned to baseline levels with detraining.

201 lation of OPN and CLU and expression of both returned to baseline levels with ensuing regeneration.

202 ignificantly decreased after vaccination but returned to baseline levels within 1 month.

203 Feno and FEV(0.5) values returned to baseline levels within 10 days.

204 ral blood cells were noted; however, numbers returned to baseline levels within 17 days.

205 ally decreased 1-2 orders of magnitude, they returned to baseline levels within 3 months of the first

206 ucose increased (P<0.05) in control pigs and returned to baseline levels within 60 min.

207 for more than 1 month, whereas inflammation returned to baseline levels within 7 days in wild-type m

208 IL-6 mRNA levels were maximal at 6 hours and returned to baseline levels within 72 hours.

209 or current at the onset of stimulation which returned to baseline levels within a few seconds, accomp

210 umber of nicotine infusions earned gradually returned to baseline levels, indicating tolerance to the

211 er triptan exposure, when sensory thresholds returned to baseline levels, rats showed enhanced cutane

212 ery period, after the heart rate had largely returned to baseline levels, with an expansion of activa

213 (up to day 17 after MI), after which time it returned to baseline levels.

214 hresholds measured 1 year following exposure returned to baseline levels.

215 because, upon removal, transgene expression returned to baseline levels.

216 Rather, dopamine returned to baseline levels.

217 ltered expression after 1 h of treatment had returned to baseline levels.

218 ls, and when MFP dosing was withdrawn, IGF-I returned to baseline levels.

219 contrast, OLC excretion peaked at week 1 and returned to baseline levels.

220 opril or candesartan, retinal KDR expression returned to baseline levels.

221 he 4-h post-SWL period, both GFR and RPF had returned to baseline levels.

222 t until drug- and food-maintained responding returned to baseline levels.

223 poststimulation with CD40 ligand, gradually returning to baseline levels after 6 days.

224 -1/KC in the blood at 3 hours post-exposure, returning to baseline levels by 18 hours.

225 atment (IRR, 3.91; 95% CI, 1.62-9.42) before returning to baseline levels during ongoing treatment (I

226 hroughout a 6 h period of sleep deprivation, returning to baseline levels immediately afterward.

227 sed significantly at day 2 </=1 month before returning to baseline levels of 1-year post-CMR.

228 ammation and epithelial proliferation levels returning to baseline levels of uninfected controls.

229 eased during 12 h of refeeding nearly 3-fold returning to baseline levels only after 24 h of refeedin

230 was observed by 1 week postinfection before returning to baseline levels.

231 onth (95% confidence interval, 2.01%-4.57%), returning to baseline levels.

232 y, thrombin and fibrin generation rates were returning to baseline levels.

233 SCr in reversible AKI returned to baseline </=48 h after CPB.

234 surgery (P = 0.0093) and then spontaneously returned to baseline, measuring 212.5 mu m at 3 months p

235 Pore currents fluctuated, transiently returned to baseline multiple times, and disappeared ~6

236 All patients with EMB ocular disease returned to baseline ocular status after discontinuation

237 te mRNAs increased during active disease but returned to baseline on disease remission.

238 Patients whose creatinine clearance returned to baseline (or nearly) were classified as tran

239 37.0 +/- 4.6 min in trials in which activity returned to baseline, or >68 min in trials in which acti

240 protocol, GG EMG burst amplitude transiently returned to baseline; over the next 60 min, burst amplit

241 After this point, Ba levels in enamel returned to baseline prenatal levels, indicating an abru

242 The sensor can be regenerated and returned to baseline quenching levels by washing away an

243 ; thereafter, myofibrillar protein synthesis returned to baseline rates even though plasma essential

244 ) and peaked at approximately 120 min before returning to baseline rates, despite elevated plasma AA

245 After prasugrel, >/=75% of patients returned to baseline reactivity by washout day 7 compare

246 nt was the cumulative proportion of patients returning to baseline reactivity after study drug discon

247 nuously monitor analyte concentrations or be returned to baseline readout values by removal of analyt

248 d thermal hypersensitivity than controls and returned to baseline sensory thresholds faster.

249 the mRNAs altered at 12 hr after injury had returned to baseline (sham-injured) levels except for in

250 In addition, error correction responses returned to baseline tap-tone asynchrony levels faster f

251 ions in the protein composition occurred but returned to baseline values after 6 to 12 h.

252 cy (-19.5+/-2% to -17.6+/-1.6%, P<0.001) and returned to baseline values after delivery (-19.5+/-2%).

253 uced antiplatelet effects with 150 mg, which returned to baseline values after resumption of standard

254 out the entire period of deafferentation and returned to baseline values afterward.

255 utes after lens insertion, all variables had returned to baseline values and remained that way for at

256 DHEA levels were maximum at 2 hrs and returned to baseline values by 6 hrs.

257 e in circulating CD4(+) T-cell counts, which returned to baseline values by day 30 in 26 of 30 evalua

258 All parameters returned to baseline values by month 12 and remained so

259 MFI values increased at the time of AAD and returned to baseline values during follow-up for these p

260 to 100 +/- 3 mmHg; P < 0.05) and heart rate returned to baseline values during PEMI (83 +/- 3 to 67

261 Elevated GABA+ concentrations returned to baseline values following drug clearance.

262 : n = 3, grade 3: n = 1) but creatinine/eGFR returned to baseline values in all patients.

263 hemodynamic and myocardial function quickly returned to baseline values in both experimental groups,

264 Serum cytokine concentrations returned to baseline values in both groups by 24 hrs.

265 Whereas the number of NK cells returned to baseline values in the blood, the GI tissues

266 lation stopped, NADH fluorescence and Psi(m) returned to baseline values much faster than mitochondri

267 Platelet counts generally returned to baseline values within 2 weeks after the end

268 0 minutes after beginning of KB infusion and returned to baseline values within 30 minutes thereafter

269 of underfeeding, lower-body fat had not yet returned to baseline values.

270 elength scans were performed until perfusion returned to baseline values.

271 ree months after the extraction, all markers returned to baseline values.

272 the majority of the subjects studied before returning to baseline values.

273 baseline GVF retinal area and ten (71%) had returned to baseline visual acuity letter values.

274 Both V(m) and [Ca2+]i returned to baseline well before ELH secretion, such tha

275 gnificantly during the abstinence phases and returned to baseline when marijuana smoking resumed.

276 The proliferation of Mz-ChA-1 cells returned to baseline when NTPDase2 expression in portal

277 ies increased and peaked at 1 month and then returned to baseline, whereas IgG autoantibodies increas

278 forelimb in rats with injury and stimulation returned to baseline, while the errors remained elevated

279 All MR parameters returned to baseline with 7 days of recovery.

280 eased and upon rapid restoration of RAP, RVR returned to baseline with a characteristic time course:

281 3 and plasma virus levels spiked but rapidly returned to baseline with reinitiation of ART.

282 parallel to dietary-induced weight gain and returned to baseline with weight loss.

283 line after acute exposure to altitude before returning to baseline with time.

284 At 24 hours, FEV1 had returned to baseline, with Feno values increased by 38.7

285 duction (>80 days [>35 days]), sCD200 levels returned to baseline, with no loss of grafts, but sera w

286 By 4 weeks, most marker levels had returned to baseline, with no significant differences be

287 This increase returned to baseline within 1 to 3 months.

288 he hypoxia-induced brain blood flow increase returned to baseline within 1 week as blood hemoglobin i

289 Post-meal CAP and LS values returned to baseline within 150 min following meals.

290 n VCAM-1 expression 4 h after treatment that returned to baseline within 16-24 h.

291 ocardial uptake of (99m)Tc-sestamibi, and CF returned to baseline within 20 minutes.

292 ween 7.5 and 10 ms following stimulation and returned to baseline within 40 ms.

293 activated between 5 hr and 3 d after SNL and returned to baseline within 5 d.

294 These hemodynamic, and metabolic changes returned to baseline within 5min of mannitol injection.

295 s, reached a peak in approximately 2 s, and returned to baseline within 7 s.

296 between 15 and 30 mins after reperfusion and returned to baseline within 90 mins (p < .0006).

297 binding potency of 1 peaked within 5 min and returned to baseline within 90-120 min; however, analges

298 Response returned to baseline within a 2-min washout period.

299 in mice, reaching a peak at 7 to 9 hours and returning to baseline within 24 hours; withdrawal severi

300 ry produces a transient increase in latency, returning to baseline within three weeks, while subseque