ライフサイエンスコーパス: hour

1 of 31 mm per hour (normal range, 0-29 mm per hour).

2 enced <=24 hours postoperatively (range 2-72 hours).

3 median 94 hours; interquartile range, 49-150 hours).

4 rs, 8 mg/4 hours, 12 mg/6 hours, and 24 mg/6 hours).

5 very short interval of each other (sometimes hours).

6 of -0.04 (95% CI,-0.18 to 0.11) minutes per hour.

7 id turnover with a t(1/2) of approximately 1 hour.

8 concentration within a reasonable time of an hour.

9 ours and an initial rate of 28 turnovers per hour.

10 Y, Norman OK) improves time-to-result to one hour.

11 reactions can be easily quantified in a few hours.

12 patients underwent an intervention within 24 hours.

13 reatment-resistant depressed patients within hours.

14 engagement were evaluated at 24, 96 and 144 hours.

15 able muscle activity, and was induced within hours.

16 he emergency department, and 85.9% within 48 hours.

17 ch were subjected to temperature abuse for 6 hours.

18 c signal enhancement of up to 649 % after 10 hours.

19 % O2) for 24 hours, with reoxygenation for 6 hours.

20 ng artemether-lumefantrine treatment was 6.7 hours.

21 xperienced improved renal function within 48 hours.

22 th acceptable in-hospital delays of up to 24 hours.

23 for all meropenem and imipenem courses > 72 hours.

24 , where it circulated the globe within a few hours.

25 ated using a real-time cell analyzer for 142 hours.

26 rses and health care assistants from 8 to 12 hours.

27 % of drugs were rapidly deactivated within 8 hours.

28 exposure to catechins but increased after 24 hours.

29 isk Pulmonary Embolism; 8 mg/2 hours, 8 mg/4 hours, 12 mg/6 hours, and 24 mg/6 hours).

30 n duration of cardiopulmonary bypass was 4.6 hours (2-16.5 hr) compared with 170.4 hours (70-1,008 hr

31 ent in 14% (17/119) of patients at 24 and 48 hours (24% at either time) compared with routine blood c

32 pleen and kidneys, particularly in the first hour (33.25 %ID/g and 207.6 %ID/g, respectively, at 1 h

33 nts initially treated with bevacizumab at 24 hours (40% vs. 74%; P = 0.0115), 48 hours (53% vs. 79%;

34 the goal of beta-lactam antibiotics within 1 hour (44.6% vs 57.3%; odds ratio, 2.27; 95% CI, 1.34-3.8

35 %), 21% (70%), and 34% (74%) for a single 24-hour, 48-hour, 72-hour, 7-day, or 30-day continuous moni

36 Cytokine production was assessed after 24 hours, 48 hours, and 7 days using ELISA.

37 ab at 24 hours (40% vs. 74%; P = 0.0115), 48 hours (53% vs. 79%; P = 0.0453), and 7 days (79% vs. 100

38 rker at baseline that were still positive at hour 6, risk was reduced for patients who became negativ

39 ; odds ratio, 2.27; 95% CI, 1.34-3.86) and 3 hours (7.6% vs 24.5%; odds ratio, 4.31; 95% CI, 2.01-10.

40 34% (74%) for a single 24-hour, 48-hour, 72-hour, 7-day, or 30-day continuous monitoring, respective

41 as 4.6 hours (2-16.5 hr) compared with 170.4 hours (70-1,008 hr) on extracorporeal membrane oxygenati

42 70%), and 34% (74%) for a single 24-hour, 48-hour, 72-hour, 7-day, or 30-day continuous monitoring, r

43 Intermediate-Risk Pulmonary Embolism; 8 mg/2 hours, 8 mg/4 hours, 12 mg/6 hours, and 24 mg/6 hours).

44 ociated with an increase in HbA1c (0.02% per hour [95% CI 0.00 to 0.05]; P = 0.045).

45 fidence interval {CI}, 5.2-6.0 hours] vs 6.4 hours [95% CI, 6.0-6.9 hours]; P = .005).

46 administered 40 mg (clearance half-life 5.5 hours [95% confidence interval {CI}, 5.2-6.0 hours] vs 6

47 112), respectively (absolute difference, 22 hours; 95% CI, 14 to 30).

48 o 17), respectively (absolute difference, 28 hours; 95% CI, 22 to 34); the conservative-oxygen group

49 ver 100 hundred experiments (~8 experimental hours) - a factor of 5x faster than our previously repor

50 were expected not to be extubated within 24 hours, a lower PEEP strategy was noninferior to a higher

51 tes on short timescales (five minutes to one hour) across multiple (more than ten) nucleophile classe

52 sing discharge delay and was lowest at 48-72 hours (adjusted odds ratio, 0.87; 95% confidence interva

53 d in some units, increased further) up to an hour after conditioning.

54 Renal resistive index was measured within 12 hours after admission, and urinary tissue inhibitor of m

55 adverse events, and major bleeding within 72 hours after BEC directed therapy.

56 ty than endoscopy performed between 6 and 24 hours after consultation.

57 after drug administration, or blood levels 2 hours after drug administration levels between 7 and 10,

58 a median of Tac, CsA blood trough levels 12 hours after drug administration, or blood levels 2 hours

59 erved minor alterations in protein levels, 2 hours after drug administration, which relates to the C(

60 o 3 groups based on SBP goal in the first 24 hours after EVT.

61 he release of cTns and copeptin in the first hours after experimental balloon-induced ischemia in hum

62 Twenty-four hours after exposure, participants underwent bronchoscop

63 choalveolar wash and lavage were obtained 24 hours after exposure.

64 all of fear extinction memory when tested 24 hours after extinction training.

65 evofloxacin was initiated from 0 to up to 30 hours after fever onset.

66 yed: if the weaning trial took place over 24 hours after fulfilling criteria.

67 e: if the weaning trial took place within 24 hours after fulfilling the criteria, and 3) delayed: if

68 eding or death, endoscopy performed within 6 hours after gastroenterologic consultation was not assoc

69 analysis identified an optimal window of 44 hours after hospitalization for transfusing COVID-19 pat

70 embolism, or both, diagnosed greater than 24 hours after ICU admission and confirmed by ultrasound, C

71 pHLIP ICG is non-toxic, marks blood flow for hours after injection, and effectively delineates tumors

72 ows that Lbs are expressed as early as a few hours after inoculation and that their mRNAs are also de

73 skin biopsies were taken at 0, 2, 48, and 96 hours after nickel patch test in six nickel-allergic pat

74 were recorded on admission and 2-4 to 12-24 hours after NIV start and were tested for correlation wi

75 Pes/DeltaPl ratio were significantly lower 2 hours after NIV start in patients who successfully compl

76 ere intubated, died, or discharged within 24 hours after presentation to the emergency department (st

77 45.8% of the patients were treated within 24 hours after presentation to the emergency department, an

78 me B and IFN-gamma occurred within the early hours after reactivation and correlated with local viral

79 Within 38 +/- 4 hours after returning from the ISS, mice were euthanized

80 ARDS expected not to be extubated within 24 hours after start of ventilation.

81 Twenty-four hours after stroke, significantly more circulating plate

82 irements compared to placebo in the first 72 hours after surgery.

83 Nasal biopsies were taken 24 hours after the 1st and 5th challenges with diluent and

84 Hours after the first intake, she felt a "strange prurit

85 m of Brazil, endovascular treatment within 8 hours after the onset of stroke symptoms in conjunction

86 ted of its stabilizing subunit calstabin-1 6 hours after the onset of the mechanical ventilation, 1 a

87 At 6 hours after the procedure, NSAIDs provide a clinically m

88 model showed around 15-20% ITCH silencing 48 hours after transfection.

89 primary monocytes to (nor)adrenaline for 24 hours, after which cells were rested and differentiated

90 rved no effect of fluid balance on either 48-hour AKI, 7-day AKI, or on the need for postoperative re

91 ncrease in total ischemic time from 3 to 3.4 hours (all P < .001).

92 e time point groups: 1 hour or less, 1 to 24 hours (although data were available only at 6 hours), an

93 erquartile range [IQR], 0.1-5.1) minutes per hour among patients in the acetaminophen group and 1.1 (

94 hen group and 1.1 (IQR, 0.1-6.6) minutes per hour among patients in the placebo group (P = .29), with

95 aggregation commences after approximately an hour and continues to develop over a period of weeks.

96 OEF was increased after 3 hours and 3 days of BCCAO, but was not different from th

97 n of hydrogen with 170 +/- 5 turnovers in 24 hours and an initial rate of 28 turnovers per hour.

98 or TARE with US-triggered MB destruction 1-4 hours and approximately 1 and 2 weeks after TARE.

99 l recruitment is delayed in early wounds (12 hours and day 1), whereas late wounds (day 7) show eleva

100 tion criteria for greater than or equal to 6 hours and determined whether patients met complete pedia

101 s, who were on a ventilator for more than 24 hours and less than 14 days.

102 anging from shorter than ten minutes to five hours and longer.

103 reported, but it used more than 150,000 CPU hours and weeks of wall-clock time.

104 in alive and ventilated for an additional 48 hours and who were receiving enteral nutrition or expect

105 f 100 mm per hour (normal range, 0-30 mm per hour), and a C-reactive protein level of 203.8 mg/L (194

106 f 100 mm per hour (normal range, 0-30 mm per hour), and a C-reactive protein level of 203.8 mg/L (194

107 ours (although data were available only at 6 hours), and 24 hours or more.

108 mbolism; 8 mg/2 hours, 8 mg/4 hours, 12 mg/6 hours, and 24 mg/6 hours).

109 quests resulted in an intervention within 96 hours, and 36% of these patients underwent an interventi

110 e production was assessed after 24 hours, 48 hours, and 7 days using ELISA.

111 ntibody assay is accurate, requires only 2.5 hours, and uses 5 ng of antigen per test.

112 ymptomatic intracranial hemorrhage within 36 hours; and all-cause death.

113 tice retinal specialty clinics, 41% of after-hours appointment requests resulted in an intervention w

114 remains relatively quiescent during the next hour as it is patterned by maternal inductive signals an

115 years as a smoker, packs smoked per day, and hours as a passive smoker per week.

116 gas values were significantly improved at 24 hours, as were peak airway pressures, intrinsic positive

117 Its steep rise up to 72 hours before clinically overt deterioration has the pote

118 el movements in any 24-hour period in the 48 hours before stool collection) and a positive stool C. d

119 III-deficient mice received IV emicizumab 24 hours before tail-clip bleeding was performed.

120 exposure to noninvasive ventilation within 6 hours before tracheal intubation.

121 Masked uncontrolled hypertension and mean 24-hour BP associated with high risk of cardiovascular dise

122 Twenty-four-hour BP phenotypes conferred a small incremental advanta

123 aptation process (1 in 1,000 cells adapt per hour) by simultaneously measuring metabolism and divisio

124 nse to a 4-hour mixed-meal tolerance test (4-hour C-peptide AUC) at week 52.

125 rved in the hearts perfused in WM (median 11-hour cardiac index/1-hour cardiac index: WM=27% versus n

126 rfused in WM (median 11-hour cardiac index/1-hour cardiac index: WM=27% versus non-WM=9.5%, P=0.022).

127 t 12-hour clock exists in addition to the 24-hour circadian clock to coordinate metabolic and stress

128 ing protein 1 (XBP1) disrupts the hepatic 12-hour clock and promotes spontaneous non-alcoholic fatty

129 A distinct 12-hour clock exists in addition to the 24-hour circadian c

130 Circadian (~24 hour) clocks have a fundamental role in regulating daily

131 ation after carbon monoxide treatment at 0.5 hours compared with extracorporeal resuscitation alone (

132 ntain their 3D tissue state during the multi-hour CRRC procedure.

133 otericin) had 1.32-fold increased odds of 24-hour culture positivity, although this was not statistic

134 Grafts with all cells cultured >=96 hours did not contain more beta cells but a higher endoc

135 all acute and chronic time points and, at 24 hours, discriminated between focal and diffuse injuries.

136 effect is temporary and confined to daylight hours during the growing season.

137 point-of-care test quantifying HCV RNA in <1 hour, enabling same-visit diagnosis and treatment.

138 strongly consolidating the waking state for hours, even during a period of elevated sleep drive.

139 otein expression levels were reduced after 2 hours exposure to catechins but increased after 24 hours

140 Leukocytes were collected every 4 hours for 24 hours from 10 patients with moderate, persi

141 s were no longer expected to survive as 19.7 hours for ciprofloxacin and 26.5 hours for levofloxacin.

142 ive as 19.7 hours for ciprofloxacin and 26.5 hours for levofloxacin.

143 ian time to alleviation of symptoms was 79.0 hours for the oseltamivir arm and 84.0 hours for the pla

144 79.0 hours for the oseltamivir arm and 84.0 hours for the placebo arm (P =; .34) in those with confi

145 93.6% and a false positive rate of 0.16 per hour (FP/h); furthermore, our method observes potential

146 ukocytes were collected every 4 hours for 24 hours from 10 patients with moderate, persistent asthma

147 sought treatment emergently and after clinic hours from 3 academic nonhospital-associated retina-only

148 Patients were randomized within the first 24 hours from intubation to either nonsedation with suffici

149 pecies that can be performed in four to five hours from start to end.

150 t identifying patients with lesion age < 4.5 hours from symptom onset.

151 eir temperature measurements in the first 72 hours from the onset of infection.

152 hemic stroke with intravenous tPA within 4.5 hours from the time they were last known to be well at G

153 kness hours over the total scheduled working hours (full time equivalents) in a given week.

154 One hour hydrolysis of WPC-80 reduced the protein antigenici

155 e analysis performed colony counts on the 24-hour images, and results were compared with the VLP.

156 ] surfaces operating at 200 degrees C for an hour in a vacuum oven.

157 gical disability for one newborn child every hour in the United States.

158 Surgery was performed within 24 hours in 18% (n = 180), within 48 hours in 20.6% (n = 20

159 within 24 hours in 18% (n = 180), within 48 hours in 20.6% (n = 203), within 72 hours in 21.7% (n =

160 ithin 48 hours in 20.6% (n = 203), within 72 hours in 21.7% (n = 214), and within 96 hours in 22.6% (

161 n 72 hours in 21.7% (n = 214), and within 96 hours in 22.6% (n = 223) of the appointment.

162 exposed to H(2) flow at 150-250 sccm for 2-4 hours in a sealed reaction cell.

163 hibited a plastic response on a timescale of hours in nonsteady-state.

164 of inclusion and after 6, 24, 48, 72, and 96 hours in patients with shock.

165 H)-dione), has a long plasma half-life (~ 24 hours) in mice, suggesting possible binding to serum com

166 olus and in-hospital tranexamic acid (1 g) 8-hour infusion (bolus maintenance group; n = 312), out-of

167 c acid (2 g) bolus and in-hospital placebo 8-hour infusion (bolus only group; n = 345), and out-of-ho

168 ital placebo bolus and in-hospital placebo 8-hour infusion (placebo group; n = 309).

169 9 hours (interquartile range, 5 to 78) and 1 hour (interquartile range, 0 to 17), respectively (absol

170 Spo(2) exceeding 96%, with a duration of 27 hours (interquartile range, 11 to 63.5) and 49 hours (in

171 urs (interquartile range, 11 to 63.5) and 49 hours (interquartile range, 22 to 112), respectively (ab

172 of targeted temperature management was 32.9 hours (interquartile range, 23.7-37.8).

173 eal membrane oxygenation support time was 96 hours (interquartile range, 26-181 hr).

174 l-oxygen group, with a median duration of 29 hours (interquartile range, 5 to 78) and 1 hour (interqu

175 d early (duration of combined MCS: median 94 hours; interquartile range, 49-150 hours).

176 ay 1 and 4 times on day 2 through day 4 at 2-hour intervals, and 34 blood samples were collected over

177 early morning IOP than the maximum in-office hours IOP.

178 Median time to surgery was 11 hours (IQR 4-40).

179 94 %, and continuous operation for over 100 hours is demonstrated.

180 HSCs were isolated 24 hours later, and fibrogenic/inflammatory parameters were

181 Hours later, cells inactivate APC/C(CDH1) and cross the

182 duce significant delayed vector mortality 72 hours later.

183 of vascular smooth muscle cells can drive an hour-long disruption.

184 ial cardiomyocytes tachypaced at 3 Hz for 24 hours mimicked AF-type [Ca(2+)](Nuc) changes and L-type

185 curve for C-peptide level in response to a 4-hour mixed-meal tolerance test (4-hour C-peptide AUC) at

186 For contacts with <250 exposure hours, no difference in prevalence was observed per 50 e

187 erythrocyte sedimentation rate of 31 mm per hour (normal range, 0-29 mm per hour).

188 an elevated sedimentation rate of 100 mm per hour (normal range, 0-30 mm per hour), and a C-reactive

189 an elevated sedimentation rate of 100 mm per hour (normal range, 0-30 mm per hour), and a C-reactive

190 A 12-hour observational period was used to evaluate the follo

191 study 1, the change in EGP (baseline to last hour of EGP measurement) in subjects receiving dapaglifl

192 nce (6 m) and near (0.3 m) fixation after >1 hour of monocular occlusion at preoperative and postoper

193 with a 90% removal capacity after the first hour of testing.

194 005) and mean increase in IOP outside office hours of 2.7 mmHg (95% CI, 0.61-4.7; P = 0.013) than the

195 nts confirm that responses occur within five hours of a pulse disturbance, demonstrating rapid adapta

196 plete echocardiographic evaluation within 24 hours of admission and were compared with reference valu

197 and resistance data were obtained within 48 hours of admission as part of routine care.

198 lity of greater than 30% within the first 24 hours of admission.

199 Mice euthanatized immediately after 6 hours of anesthesia (n = 15) or after 6 hours of anesthe

200 er 6 hours of anesthesia (n = 15) or after 6 hours of anesthesia and 10 days of recovery (n = 5) serv

201 Gdf15 is rapidly upregulated within a few hours of bilateral ischemia-reperfusion injury at these

202 right ventricle (RV, n=4) after 0, 4, and 8 hours of cold storage in histidine-tryptophan-ketoglutar

203 iral clearance always predominated within 24 hours of detection even when viral load exceeded 1 x 107

204 mia and then reimplanted following either 16 hours of either SCS, HAMP (LifePort 1.0), or NEVKP befor

205 sually naive ferrets were exposed to several hours of experience with unusual spatiotemporal patterns

206 Within 72 hours of extubation, all patients received a flexible en

207 lational plague when administered within 2-6 hours of fever onset in African green monkeys (AGM).

208 To address this question, we collected hours of functional magnetic resonance imaging data from

209 s were sampled using miniature BAL within 24 hours of ICU admission.

210 nd levels of circulating alphaviruses within hours of infection through a bile acid-pDC-IFN signaling

211 all newborns were tested within the first 60 hours of life, with a positive screening result defined

212 nm (BrC Abs(405)) measured in the first few hours of plume evolution, despite accounting for just 4

213 ng genes (EcSAM, EcPAL and EcLOX) at 72 hpi (hours of post infestation) in both stem and roots compar

214 BC markers nor periodontitis were related to hours of sleep.

215 evaluated, with treatment initiated within 2 hours of TBI: out-of-hospital tranexamic acid (1 g) bolu

216 th zero-calorie beverages) for the remaining hours of the day.

217 transmitted to a human host, that is, within hours of tick attachment, which is distinctive when comp

218 susceptible to TOL-TAZ and treated with >=72 hours of TOL-TAZ between January 2018 and December 2019

219 teroids; in 4 cases, this occurred within 72 hours of vaccination.

220 d by bed census on the calendar day (daytime hours) of admission was associated with decreased risk-a

221 tion of patients with zero/near-zero last-24-hour OME and limiting prescriptions to a conservative mu

222 to a conservative multiplier of the last-24-hour OME.

223 e independently associated with zero last-24-hours OME (all P <= 0.040).

224 d strains of mice, SibeliaZ runs in under 16 hours on a single machine, while other tools did not run

225 at 2 mg/cm2 to 75% of body surface area at 0 hours on day 1 and 4 times on day 2 through day 4 at 2-h

226 following postprocedure time point groups: 1 hour or less, 1 to 24 hours (although data were availabl

227 abitated with an opposite-sex partner for 24 hours or 3 weeks, and transcriptomic regulations in the

228 wheat, are detectable in breastmilk for many hours or days after ingestion.

229 hysicians through day and night shifts of 16 hours or less (intervention schedules).

230 on work schedules that included shifts of 24 hours or more (control schedules) and schedules that eli

231 data were available only at 6 hours), and 24 hours or more.

232 = 0.003), duration of surgery of more than 3 hours (OR 1.86, P = 0.010), administration of vasopresso

233 Superior early and 24-hour outcomes were observed with PEG-20k LVR compared to

234 le is defined as the ratio of total sickness hours over the total scheduled working hours (full time

235 prevalence increase of 8.2% per 250 exposure hours (P < .0001).

236 e in prevalence was observed per 50 exposure hours (P = .63).

237 7.8% at 24 hours (p = 0.022) and 15.0% at 48 hours (p = 0.0001) for patients receiving bilateral stim

238 ckness increased from baseline by 7.8% at 24 hours (p = 0.022) and 15.0% at 48 hours (p = 0.0001) for

239 07-1.64 for a delay of >24 hours versus <=24 hours; p = 0.009).

240 5.2-6.0 hours] vs 6.4 hours [95% CI, 6.0-6.9 hours]; P = .005).

241 g the eating window to a specified number of hours per day (usually 4-10 h), and fasting (with zero-c

242 ows a high capacity of about 164 milliampere hours per gram of LiFePO(4), and almost no degradation f

243 , the differential change in rate of nursing hours per patient day following implementation of the Di

244 d pigs averaged $50 per wild pig (6.8 effort hours per wild pig) for removing the first 99% of the an

245 The 24-hour period constellation reduces the overall required v

246 nset diarrhea (>=3 bowel movements in any 24-hour period in the 48 hours before stool collection) and

247 on [quartile 1-quartile 3]: 78.3 [66.3-83.0] hours/person).

248 were randomized to flexible or standard duty-hour policy.

249 n relation to BB use: prior to admission, 24-hour post-admission and on discharge in patients with a

250 d was collected at baseline, 2, 4, 6, and 24 hours post administration of placebo or one of 3 doses o

251 tions compared with a control VNAR-hFc at 18 hours post-injection in wt mice.

252 e consistently higher and then stabilized 48 hours postcannulation for patients successfully weaned-o

253 (Copan), and plates were imaged at 0 and 24 hours postinoculation.

254 efined early feeding as feeds commenced <=24 hours postoperatively (range 2-72 hours).

255 ry 2) first dose of analgesic at home, 3) 24 hours postoperatively, and 4) 72 hours postoperatively.

256 ty were measured preoperatively and up to 48 hours postoperatively, and cognitive function was assess

257 home, 3) 24 hours postoperatively, and 4) 72 hours postoperatively.

258 igration than monocultures at 24, 48, and 72 hours postseeding.

259 gression model showed that changes within 96-hour poststroke in APOF, APOL1, APMAP, APOC4 (apolipopro

260 rigerated storage, autologous 51-chromium 24-hour posttransfusion RBC recovery (PTR) studies were per

261 syngeneic cardiac transplant recipients at 1-hour posttransplant with Anakinra, a US Food and Drug Ad

262 an arm (removal of the tip with a scalpel) 6 hours prior led to increased targeting by black sea bass

263 hours), providing a pragmatic strategy to redisperse deg

264 7 906 participants with up to 5 web-based 24-hour-recall food frequency questionnaires (2009-2012), w

265 Duty hour reform showed no significant effect on 30-day morta

266 Night shift (p<0.001) and 12-hour shift workers (p<0.001) had higher chronic fatigue.

267 s and family/social life, whereas working 12-hour shifts predicted higher satisfaction with daily tas

268 lso leads to an increase in the frequency of hours spent at higher wind speeds, which has implication

269 Outcomes included 24-hour survival rates, mean arterial pressure, lactate, he

270 l tolerated and rapidly absorbed with a 14.5-hour terminal half-life.

271 en attributed in part to women working fewer hours than men, but evidence to date is limited by self-

272 emoval ratio of NOF reached 95% within three hours; the adsorption and degradation ratios reached 46%

273 In only 4 hours, this compound killed the juvenile form of F. hepa

274 to the TVB-N and TVC method which takes many hours to complete involving many sophisticated steps.

275 The protocol takes only a few hours to complete, excluding the time spent culturing C.

276 ensed information for durations ranging from hours to days.

277 antage over existing techniques that consume hours to days.

278 for the target area under the curve over 24 hours to minimum inhibitory concentration (AUC/MIC).

279 We used the apnea-hypopnea index (events per hour) to define obstructive sleep apnea severity (normal

280 l frequency, approximately 96 injections per hour, together with adequate detection limit of 4.7 mumo

281 e increase in mortality associated with each hour until antibiotics, and failure to control for large

282 We measured plasma and 24-hour urine concentrations of endogenous candidate secret

283 Twenty-four hour urine oxalate excretion is an inaccurate measure fo

284 ction under constant, 3-hour variable, and 6-hour variable exposures to sublethal hypoxia, and compar

285 tion, and gonad production under constant, 3-hour variable, and 6-hour variable exposures to subletha

286 or (AMPAR) antagonist, during a follow-on 24-hour vEEG to investigate the role of AMPARs in Syngap1 h

287 = 1.33, 95% CI: 1.07-1.64 for a delay of >24 hours versus <=24 hours; p = 0.009).

288 hours [95% confidence interval {CI}, 5.2-6.0 hours] vs 6.4 hours [95% CI, 6.0-6.9 hours]; P = .005).

289 that compared 7.5, 15.0, 22.5, and 30.0 MET hours/week to no leisure-time physical activity, and sta

290 ity (MD = -1.41 metabolic equivalent of task-hours/week, 95% CI: -2.07, -0.71), and worse A-MeDi scor

291 Time scales ranging from milliseconds to one hour were simulated.

292 st CT and at least one RT-PCR test within 48 hours were included.

293 elet treatment and follow-up CT at 24 +/- 12 hours were included.

294 Only 39% had fever in the first 24 hours, whereas 41% had hypoxia at admission.

295 d or older, with an ICU stay greater than 24 hours, who were on a ventilator for more than 24 hours a

296 SHE) for 20 hours with a turnover number (TON) of 266 300, and photo

297 GPRX2 expression in both, stimulation for 24 hours with anti-IgE, C5a, fMLP, and IL-3 in basophils an

298 pHAECs were infected for 48 hours with Pg in vitro using the Human oxygen-Bacteria a

299 ells into a hypoxic incubator (1% O2) for 24 hours, with reoxygenation for 6 hours.

300 lood culture(s) if they were afebrile for 24 hours without evidence for complicated infection (eg, ab