ライフサイエンスコーパス: min

1 able of fatty acid hydroxylation at a >3,000 min(-1) turnover rate.

2 t, the mean decay constant was 0.29 +/- 0.09 min-1, equivalent to a half-life of approximately 2.4 mi

3 CBS device with analysis times as short as 1 min per sample when 96 extractions are simultaneously co

4 only 1 muL of sample in a fast (less than 1 min per sample) and high-throughput (up to 384 samples p

5 s) into passwords (responses) in less than 1 min.

6 responders (ie, Delta >=1.32 mL O(2).kg(-1).min(-1)).

7 All nine livebirths had a 1-min Apgar score of 8-9 and a 5-min Apgar score of 9-10.

8 HR achieved minus the HR at: 30-s (HRR30), 1-min (HRR1), 2-min (HRR2), 3-min (HRR3), 4-min (HRR4) or

9 First-phase insulin secretion (0-10 min) increased by 70%, while second-phase insulin secret

10 ction limits below 435 cells.mL(-1) after 10 min in aquaponic water samples.

11 every minute for 20 min during and after 10 min systemic hyperoxia; and on day 3, electroretinograph

12 W) powers of 180, 360 and 540 W for 5 and 10 min were evaluated for their influence on oil yield, che

13 ar concentration of about 65% as early as 10 min after incubation.

14 MW roasting at 540 W for 10 min significantly increased the oil yield, TPC, OSI, RSA

15 Bacteria were automatically mixed for 10 min with serially diluted antibiotics with a novel, memb

16 MW roasting (540 W for 10 min) is recommended for improving quality and stability

17 quipment failure; and treatment duration >10 min), a battery-operated thermal ablator that is lightwe

18 fects of analogous PEMF exposure (1.5 mT, 10 min/week), with and without exercise, on systemic metabo

19 A second 10 min "empty bladder" rs-fMRI scan was conducted immediate

20 E are performed simultaneously during the 10 min agitation.

21 All experiments detected mcr-9 in under 10 min, and both platforms showed no statistically signific

22 d 5-log reduction for both strains within 10 min in most scenarios, except for TLF thicker than 0.6 m

23 dependence of I(Na) inactivation (within 10 min) and subsequent superimposed positive activation and

24 ng detection of 10(-14) mol of ATP within 10 min.

25 A 10-min exposure of A549 human lung cancer cells to sequenti

26 nificantly reduced reaction times (10 to 100 min).

27 ion range from 50 to 10(7) CFU/mL within 100 min was achieved.

28 n), followed by the BS-Cat (123.81 +/- 30.11 min) and BT-Cat groups (186.00 +/- 42.34 min; P < .001),

29 was shortest in the US-Cat (91.62 +/- 26.12 min), followed by the BS-Cat (123.81 +/- 30.11 min) and

30 ere, high-throughput growth, completed in 12 min, of 6-inch wafer-scale monolayer MoS(2) and WS(2) is

31 of 13 patients (median: 9 min; IQR: 6 to 12 min).

32 ow metabolism in blood (69% of parent at 120 min), a high plasma free fraction of 38.5%, and a suitab

33 cans (median dose, 317 MBq; uptake time, 120 min) within a median of 4 d (range, 1-11 d).

34 g suitable for RT albumin removal within 120 min.

35 viduals underwent PET/CT scanning with a 120-min dynamic PET scan centered on the pancreas.

36 The median total procedure time was 125 min (IQR: 108 to 166 min) (including a median of 28 min

37 The separation was achieved in 13 min using the C18 column by gradient LC programme.

38 AA content decreased very quickly and at 14 min (203-205 degrees C) its concentration was lower than

39 nar Cu foil fails after 5110, 3012, and 1410 min, respectively.

40 low intrinsic clearance of 17d (T(1/2) > 145 min and CL(int(mic)) < 9.6 mL/min/kg).

41 s off the east coast of Costa Rica for 83.15 min (+/- 9.12 SD) to determine their movements and swimm

42 duration of time (which can be capped at 15 min) until the experimenter returns so that they can rec

43 eated with microwave at 125 degrees C for 15 min.

44 ore, the method is quick (analysis time <=15 min), requires low-cost instrumentation and sensor chips

45 ons (SFs) of the virus were then measured 15 min post nebulization.

46 al saline, both given as an infusion over 15 min.

47 89)Zr-DFO-azepin-onartuzumab in less than 15 min, with an isolated decay-corrected radiochemical yiel

48 ibiotic susceptibility of bacteria within 15 min, which is a significant advantage over existing tech

49 edian uptake time of 79.5 min (range, 60-153 min).

50 response was ~0.1 mg/L (detected in just 16 min), while changes in different metabolites suggest a c

51 n] for voltage mapping), with a median of 16 min (IQR: 12 to 23 min) fluoroscopy.

52 ing the first (10-80 min) and second (90-160 min) hyperglycemic clamp steps increased by 3.8-fold and

53 procedure time was 125 min (IQR: 108 to 166 min) (including a median of 28 min [IQR: 25 to 33 min] f

54 (95% CI): 266 (77, 455) nmol.min-1.kg-1.180 min; P = 0.01; eta2p = 0.44].

55 % CI): 4266 (261, 8270) mumol.min-1.kg-1.180 min; P = 0.04; eta2p = 0.31] and branched-chain amino ac

56 its equilibrium capacity within 0.64 +/- 0.2 min.

57 counting rate within 10-20 trials (under 1-2 min of testing), captured approximately 10% more varianc

58 e was the enhanced throughput, requiring 1.2 min of analysis per analyte.

59 (CPB) time (146.9 +/- 40.6 vs 189.6 +/- 41.2 min for DHCA; p < 0.05) and higher nasopharyngeal temper

60 cytometry; fast association/dissociation (~2 min)] revealed 26 as a useful molecular tool to determin

61 overtly (verbally) recalled memories for ~2 min periods.

62 trations were quantified accurately within 2 min in the full breath-relevant range (10-1000 ppm) in e

63 ate and during a two-step (10 and 20 mU/m(2)/min) hyperinsulinemic-euglycemic clamp with stable isoto

64 nus the HR at: 30-s (HRR30), 1-min (HRR1), 2-min (HRR2), 3-min (HRR3), 4-min (HRR4) or 5-min (HRR5) o

65 0 and 220 degrees C, during 9, 12, 15 and 20 min, and characterized in relation to color change, oxal

66 heat-induced oil isolation (90 degrees C/20 min), but pH-shift-produced oils had higher amounts of n

67 blood flow was measured every minute for 20 min during and after 10 min systemic hyperoxia; and on d

68 o 10 nm post-treatment with 0.8% NaOH for 20 min.

69 CS (sham, left DLPFC and right DLPFC) for 20 min.

70 nteraction experiments can be analyzed in 20 min per sample.

71 ing demonstrated high tumor uptake within 20 min.

72 chicken meat in raw meat mixtures within 20 min.

73 participants showing higher levels from 210 min postprandially.

74 The CHD samples were dried in 210 min; with higher drying rates, CHD samples showed no sig

75 drug to have diabetes, respiratory rate >22/min, abnormal chest imaging findings, O2 saturation lowe

76 ing), with a median of 16 min (IQR: 12 to 23 min) fluoroscopy.

77 d at 5, 10, 20, 30, 40, 50, 60, 120, and 240 min after (18)F-FDG administration (370 +/- 16 MBq).

78 and increased standing times of 120 and 240 min with accuracies ranging from 85.5 to 88.0%, because

79 tandardised digestion protocol from 0 to 240 min and subsequently analysed by SDS-PAGE, quantitative

80 uisitions at scheduled time points up to 248 min after the administration of (18)F-rhPSMA-7.3 (mean a

81 ame later by ~50 min during weekdays and ~25 min on weekends, and thus the difference between weekend

82 At longer exposures (25 min) the s-MNPs/SOD1 dispersion destabilizes.

83 In 25 min of operating time, density gradient centrifugation r

84 food matrices with a total assay time of 25 min.

85 e with a sensitivity of 100 copies within 25 min and generated stronger specific fluorescence signals

86 n be prepared at the point-of-care within 26 min using fresh blood, it can be easily delivered using

87 R: 108 to 166 min) (including a median of 28 min [IQR: 25 to 33 min] for voltage mapping), with a med

88 2 complexes have increased dwell time, 2 ~ 3 min, compared to less than 1 s for monomeric Dvl2.

89 d usage of short (median 7.4, range 4.1-20.3 min) and long (median 17.2, range 6.1-47.7 min) video fo

90 ssed every 20 s for 6 min during and after 3 min flicker light (12 Hz) stimulation; on day 2, retinal

91 lvent switches allowed for fast screening (3 min per polarity).

92 UHPLC runtime was 3 min with retention times of (min); 0.63 (GA), 0.97 (RT),

93 g the data with K(i) < 5.3 x 10(-3) mL/cm(3)/min.

94 30-s (HRR30), 1-min (HRR1), 2-min (HRR2), 3-min (HRR3), 4-min (HRR4) or 5-min (HRR5) of recovery.

95 ween the results of the nuc-aAST after 15-30 min of antibiotic exposure and the results of the gold-s

96 cantly correlate with pancreas SUVR-1 (20-30 min) (R (2) = 0.36, P = 0.16).

97 Pancreas SUV ratio minus 1 (SUVR-1) (20-30 min; spleen as reference region) demonstrated a statisti

98 tivities of lipase and lipoxygenase after 30 min steam autoclaving were 6.25% and 18.60%, respectivel

99 lved i.e. three soaking times (0, 15, and 30 min), three temperatures (20, 25, and 30 degrees C) and

100 ion units <100; measured by VerifyNow) at 30 min post-dose.

101 bacteria heat inactivation (99 degrees C/30 min), and enrichment for mycobacteria DNA were achieved

102 in extraction, rapid enzymatic digestion (30 min compared to overnight), and subsequent MS-analysis f

103 tients were in the fasted state and every 30 min for 4 h following meal ingestion.

104 oaked in 10 mg/L of carbaryl solution for 30 min and then washed for 30 min in one of the five washin

105 Furthermore, LFS for 30 min before a pro-convulsive stimulus successfully preven

106 od flow were simultaneously monitored for 30 min in 22 healthy males.

107 l solution for 30 min and then washed for 30 min in one of the five washing solutions and the results

108 ted enzyme caused 1 pH unit difference in 30 min, with an initial rate of 0.35 pH.min(-1) To understa

109 ngendorff preparation were exposed to IR (30 min ischaemia) after 4 treatments administered randomly,

110 After just 30 min of training, we found this "electro-haptic" stimulat

111 ective of this work was to enable rapid (<30 min), sensitive (>100-fold improvement), and high-throug

112 d >1 h to access motorised boreholes but <30 min, increasing to 30-60 mins, for hand-pumped boreholes

113 ith an optimal analytical performance of ~30 min, the resulting bacterial detection platform was demo

114 id bolus (10mL/kg of Ringers-Lactate over 30 min) for management of shock and/or hypoperfusion within

115 eep deprivation than after normal sleep: (30 min [interquartile range [IQR], 17-41] vs. 60 min [IQR,

116 pedance changes are recorded in less than 30 min, in comparison with >8 h in the best alternative rep

117 eved ~100 copies/muL sensitivity in under 30 min of measurement time and accurately detected pre-extr

118 y confirmed that delivery occurred within 30 min of administration, to 100% of cells.

119 s to building inlet concentrations within 30 min.

120 % inspired oxygen ( FI,O2 ) followed by a 30-min exposure to 100% FI,O2 .

121 ng administration protocols prescribing a 30-min infusion time.

122 nly K (1) was reproducible from truncated 30-min datasets (intraclass correlation coefficient, 0.96).

123 he CTX-OCT was completely released after 300 min in phosphate buffer pH 7.4.

124 37.56 +/- 15.69 min; BS-Cat: 32.33 +/- 17.31 min; BT-Cat: 37.50 +/- 18.67; P = .087).

125 (including a median of 28 min [IQR: 25 to 33 min] for voltage mapping), with a median of 16 min (IQR:

126 .11 min) and BT-Cat groups (186.00 +/- 42.34 min; P < .001), contrary to the duration of surgery (US-

127 FPH takes an average of 1.4 min longer to complete than does FBH+, but has the poten

128 created charge-dependent accumulation 2 to 4 min after the onset of flow.

129 elivers sensor response to raw fish within 4 min, reflecting its freshness status in comparison to th

130 , and one commercial enzyme (on average 0.4%/min), while all exogenous enzymes were able to hydrolyse

131 1-min (HRR1), 2-min (HRR2), 3-min (HRR3), 4-min (HRR4) or 5-min (HRR5) of recovery.

132 PET scans (20-40 min after injection) were evaluated visually for complet

133 ning protocol at baseline and following a 40 min infusion of ketamine (0.5 mg/kg).

134 At 40 min after the injection, well after the intraocular pres

135 single ketamine infusion (0.5 mg/kg) over 40 min.

136 ieving one-step multiplex analysis within 40 min.

137 ed cold pressor pain tolerance before and 40-min after double-blind injection of .08 mg/kg morphine o

138 lity (60%), and emulsion stability index (42 min) were registered for F1.

139 he run times for each assay are 3.5 h and 45 min, respectively.

140 not require RNA purification, and takes ~45 min from sample collection to results.

141 982 patients contributed 7,073,486 min during 1,263 monitoring sessions.

142 The toasting of bread for 2.5 min considerably enhanced the formation of acrylamide an

143 -410 MBq), with a median uptake time of 79.5 min (range, 60-153 min).

144 Increased antioxidant activities at 3 and 5 min of blanching varied with the type of fruit peelings.

145 However, shortly boiled blue cabbage (5 min) had the highest isothiocyanate levels (0.08 umol/g

146 bladder accumulation is low until at least 5 min post injection.

147 n protocol with a maximum infusion time of 5 min.

148 00 mg/m(2) administered intravenously over 5 min, followed by a 46 h infusion of fluorouracil 2400 mg

149 ion with saturation occurring in less than 5 min.

150 set of positive clinical samples in under 5 min.

151 R848-TSLs released 80% of R848 within 5 min at 42 degrees C.

152 for LMG detection can be completed within 5 min without any incubation, washing and blocking steps.

153 CFU reductions observed as early as within 5 min, and in vivo by causing structural damage due to sal

154 RIC consisted of 4 x 5 min cycles of left hind limb ischemia.

155 irths had a 1-min Apgar score of 8-9 and a 5-min Apgar score of 9-10.

156 -min (HRR2), 3-min (HRR3), 4-min (HRR4) or 5-min (HRR5) of recovery.

157 estigated the effect of roasting time (10-50 min) and temperature (110-160 degrees C) on the potentia

158 the slope of the time-activity curves (20-50 min after injection) were determined.

159 degrees C or 180 degrees C up to 119 and 50 min, respectively; commercial soybean oil (SO) was teste

160 ed sample obtained by using Anolyte_450mA-50 min.

161 Sleep timing became later by ~50 min during weekdays and ~25 min on weekends, and thus th

162 A) was higher than the control group by 8.54 min/day (95% CI 1.37, 15.71, p = 0.02).

163 infusion time for infection reduction (24.6 min before incision).

164 ion time, significantly predicted SSI (<24.6 min infusion, AUC = 0.762).

165 vels less than or equal to 2,000 (4.8 vs 5.6 min; p = 0.001).

166 ance (strength phenotype; 17 proteins) and 6 min walk performance (endurance phenotype; 17 proteins)

167 nal blood flow was assessed every 20 s for 6 min during and after 3 min flicker light (12 Hz) stimula

168 ung bases were acquired with a duration of 6 min.

169 allow complete iron replacement within 15-60 min in one visit.

170 As expected, the response time (15-60 min) primarily depends on the CRE diffusion across the A

171 Here, we exposed wild-type male mice to 5-60 min of 40 Hz or control flicker and assessed cytokine an

172 es, were lower in the MHD group at 30 and 60 min post meal ingestion compared to controls (P < 0.05).

173 g/mL) and oxidative haemolysis (IC(50) at 60 min = 46.0 +/- 0.8 ug/mL).

174 f 1.3 +/- 0.4 in AS solution in the first 60 min of reaction time.

175 e on inhibitory control are sustained for 60 min in children with ADHD.

176 imic DCD, pig kidneys underwent 0, 30, or 60 min of warm ischemia, before hypothermic machine perfusi

177 scanned by dynamic (18)F-FDG PET/CT over 60 min, and quantified images were compared with those acqu

178 During the past 60 min, oil companies have extracted 6 trillion liters of o

179 r radioactivity that plateaued from 40 to 60 min and was significantly reduced by pretreatment with k

180 nd PPA by EC was reached only after 45 to 60 min of incubation.

181 in [interquartile range [IQR], 17-41] vs. 60 min [IQR, 45-60], P = 0.002).

182 GA were as follows: an incubation time of 64 min, incubation temperature of 32 degrees C, and enzyme

183 duration of surgery (US-Cat: 37.56 +/- 15.69 min; BS-Cat: 32.33 +/- 17.31 min; BT-Cat: 37.50 +/- 18.6

184 CT ranged from 13.7 (BRS Embaixador) to 21.7 min (KID44).

185 3 min) and long (median 17.2, range 6.1-47.7 min) video formats for the same procedures.

186 ement times were 5(IQR: 4-6) and 6(IQR: 5-7) min, mild adverse events occurred in 4(9.4%) and 4(14.2%

187 ion condition in short reaction times (10-70 min).

188 ate 2 to 3 mice each for an approximately 75 min duration or 15 individually housed rats.

189 om patients diagnosed with RA and in just 75 min.

190 rtile range [IQR]: 38-71) and 60(IQR: 48-77) min, median LP placement times were 5(IQR: 4-6) and 6(IQ

191 in was greater (P < 0.05) by actinidin (0.8%/min) when compared to papain, bromelain, and one commerc

192 se insulin secretion during the first (10-80 min) and second (90-160 min) hyperglycemic clamp steps i

193 action time, which were 100 degrees C and 80 min, respectively.

194 An 80-min scan was sufficient to quantify V (T) and BP (ND) Th

195 was achieved in 13 of 13 patients (median: 9 min; IQR: 6 to 12 min).

196 provide a balance between scans at 60 and 90 min of uptake, parameters compliant and noncompliant wit

197 +/- 4.7% and 2.4% +/- 1.6% within 60 and 90 min, respectively.

198 e followed by nuclear medicine imaging at 90 min, 4 h, 24 h, and 48 h (if required).

199 juice in which browning was avoided, even 90 min in the presence of oxygen at room temperature.

200 kemia underwent whole-body PET/CT imaging 90 min after injection of (18)F-SKI (mean, 241.24 +/- 116.3

201 o be removed to below detection limits in 90 min of treatment time.

202 The SUVR-1 of (18)F-SynVesT-1 from 60 to 90 min matched best with 1TC BP (ND) Conclusion: The novel

203 layed extensive fathering behavior within 90 min.

204 80 male rats underwent 90-min middle cerebral artery occlusion.

205 nd a minimum absorption coefficient of alpha(min) = 1.67 x 10(-6) cm(-1).

206 eeks: sustained AFL; sustained AF (600 beats/min atrial tachypacing); AF superimposed on an AFL subst

207 Over a mean of 182.6 (88.6) follow-up days (min-max: 0-364 days), 22 TEAEs were reported by 7 (2.8%)

208 erfusion was elevated to 79.3 +/- 9 mL/100 g/min and T(2)* was decreased by 6 +/- 3%.

209 .47, 9.60 kcal), faster eating rates (0.40 g/min; 0.21, 0.59 g/min), and larger lunch intakes (7.05 k

210 aster eating rates (0.40 g/min; 0.21, 0.59 g/min), and larger lunch intakes (7.05 kcal; 3.37, 10.74 k

211 rain using (60)Co gamma irradiation (~0.6 Gy/min, 7.5-12.5 Gy).

212 since it takes place simultaneously at +/- k(min).

213 and placebo persisted (+0.71 +/- 0.13 mg/kg/min, P < 0.01).

214 flozin was 22% greater (+0.66 +/- 0.11 mg/kg/min, P < 0.05) than in subjects receiving placebo, and i

215 ak Vo(2) (13.1+/-3.4 versus 22.7+/-4.0 mL/kg/min; P<0.001) and heart rate (122+/-20 versus 155+/-14 b

216 wever, when infusion rates exceeded 20 ul/kg/min, signs of injury occurred at pressures from 0.39 to

217 0.69 +/- 0.07 l min(-1) , P < 0.05) and muscle diffusive O(2) conductanc

218 cending aorta and superior vena cava (0.14 L/min +/- 0.12).

219 igher than in the pulmonary arteries (0.15 L/min +/- 0.10) and descending aorta and superior vena cav

220 th in patients with supplemental oxygen >2 L/min at diagnosis was 6.18 ([1.33, 26.83], P = 0.02).

221 e of oxygen supplementation of more than 4 L/min flow; use of high-flow nasal cannula; use of non-inv

222 viation of cardiac output in the aAo (0.58 L/min +/- 0.45) was significantly (P < .001) higher than i

223 e to cardiac output with exercise >3 mm Hg/l/min.

224 usion was similar (Fontan = 2.50 +/- 1.02 ml min(-1) ml(-1) ; Fontan control = 3.09 +/- 0.58, PAH = 3

225 re not different (Fontan = -0.23 +/- 0.09 ml min(-1) ml(-1) cm(-1) ; Fontan control = -0.29 +/- 0.23,

226 ecreasing the flow rate from 0.50 to 0.25 mL min(-1).

227 aCl(2) : -1 +/- 17 vs. control: 30 +/- 28 ml min(-1) 100 mmHg(-1) ; n = 9; P = 0.004) and attenuated

228 ; 10 A m(-2), 50% water recovery, and 0.5 mL min(-1)).

229 capable of producing flow rates up to 1.6 mL min(-1).

230 egrees C), as well as flow rate (0.6-0.75 mL min(-1)), were optimized.

231 oth rest (mean difference: -0.034+/-0.035 mL.min(-1).cc(-1), limits of agreement: [-0.103 to 0.035] m

232 ), limits of agreement: [-0.103 to 0.035] mL.min(-1).cc(-1)) and stress (mean difference: 0.057+/-0.3

233 nd stress (mean difference: 0.057+/-0.361 mL.min(-1).cc(-1), limits of agreement: [-0.651 to 0.765] m

234 estimated glomerular filtration rate <60 mL.min(-1).1.73 m(-2), albuminuria, and diuretic use (each

235 ), limits of agreement: [-0.651 to 0.765] mL.min(-1).cc(-1)) MBF measurements.

236 earance calculated on POD3 (63.6 +/- 19.0 mL/min) compared with HAMP (13.5 +/- 10.3 mL/min, P = 0.001

237 rest MBF (1.08 mL/min/g +/- 0.23 vs 1.07 mL/min/g +/- 0.23, P = .83).

238 /- 0.59, P = .94) and mean rest MBF (1.08 mL/min/g +/- 0.23 vs 1.07 mL/min/g +/- 0.23, P = .83).

239 3 m(2) (interquartile range: 30.9 to 60.1 ml/min/1.73 m(2)), and was <60 ml/min/1.73 m(2) in 74.9% of

240 a3818+/-1222 vs. BQ-123: Delta4812+/-1469 ml/min; P = 0.001).

241 s (in 39 patients) with eGFR less than 15 mL/min/1.73 m(2), and 34 examinations in 27 patients underg

242 Median eGFR was 23 ml/min per 1.73 m(2).

243 flow (MBF; 2.25 mL/min/g +/- 0.59 vs 2.24 mL/min/g +/- 0.59, P = .94) and mean rest MBF (1.08 mL/min/

244 n stress myocardial blood flow (MBF; 2.25 mL/min/g +/- 0.59 vs 2.24 mL/min/g +/- 0.59, P = .94) and m

245 tions (in 94 patients) with eGFR of 15-29 mL/min/1.73 m(2), 40 examinations (in 39 patients) with eGF

246 mL/min) compared with HAMP (13.5 +/- 10.3 mL/min, P = 0.001) and SCS (4.0 +/- 2.6 mL/min, P = 0.001).

247 mated glomerular filtration rate was 42.3 ml/min/1.73 m2, and median urine albumin-to-creatinine rati

248 ng/(mL.h) for patients with CrCl 25 to 30 mL/min or >30 mL/min, respectively.

249 estimated glomerular filtration rate < 30 mL/min or graft loss at 1 y, n = 66) were analyzed by using

250 than 80%, or a creatinine clearance of 30 mL/min or more but less than 60 mL/min, or those who refuse

251 (estimated glomerular filtration rate <30 mL/min per 1.73 m(2)) from the Swedish Heart Failure Regist

252 ears, 36% female) with new-onset eGFR <30 ml/min per 1.73 m(2), 1553 (15%) stopped RAS inhibitor ther

253 estimated glomerular filtration rates <30 mL/min who received >=5 days of ceftaroline, 3 developed en

254 out severe renal (creatine clearance <=30 mL/min) or liver disease were included in this analysis (n=

255 patients with CrCl 25 to 30 mL/min or >30 mL/min, respectively.

256 ng/(mL.h) for patients with CrCl 25 to 30 mL/min.

257 lomerular filtration rate (eGFR) 59 to 30 mL/min/1.73 m2 on two consecutive previous blood tests were

258 nd 41% were black; the median eGFR was 43 ml/min per 1.73 m(2).

259 years; postnephrectomy baseline eGFR, 48 ml/min per 1.73 m(2)), 117 progressive CKD events, 183 nonc

260 he fluid at a high flow rate of up to 1.5 mL/min.

261 e not clinically important (56.6 vs. 57.5 mL/min/1.73m for ideal comparator kidneys; p < 0.001).

262 3 mL/min, P = 0.001) and SCS (4.0 +/- 2.6 mL/min, P = 0.001).

263 (T(1/2) > 145 min and CL(int(mic)) < 9.6 mL/min/kg).

264 cident CKD (stage 3 or higher) as eGFR<60 ml/min per 1.73 m(2) and >=25% decline from baseline, CKD-r

265 ant association between baseline eGFR <60 ml/min per 1.73 m(2) and risk for dementia or MCI.

266 come (>=40% decline in eGFR, with eGFR<60 ml/min per 1.73 m(2), or ESKD), and linear mixed models for

267 nce of 30 mL/min or more but less than 60 mL/min, or those who refused chemotherapy.

268 .9 to 60.1 ml/min/1.73 m(2)), and was <60 ml/min/1.73 m(2) in 74.9% of the patients.

269 ltration rate (eGFR) before imaging (>=60 mL/min/1.73 m(2) or <60 mL/min/1.73 m(2)).

270 AKI with eGFR greater than or equal to 60 mL/min/1.73 m(2) was 2.2% (20 of 889) for CT and US (odds r

271 usted P = .95) and with eGFR less than 60 mL/min/1.73 m(2) was 5.6% (two of 36) and 11.1% (four of 36

272 ore imaging (>=60 mL/min/1.73 m(2) or <60 mL/min/1.73 m(2)).

273 ive glomerular filtration rate (GFR) >=60 mL/min/1.73 m; GFR between 30 and 60; and GFR <30.

274 iabetes), and lower eGFR (<60 versus >=60 ml/min/1.73m2).

275 r than 6, a creatinine clearance of 30-69 mL/min, or both.

276 lomerular filtration rate (eGFR) was 43.7 ml/min/1.73 m(2) (interquartile range: 30.9 to 60.1 ml/min/

277 +/- SD 87.4 +/- 23.9 versus 80.1 +/- 20.7 mL/min/1.73 m(2); p < 0.0001), while CD had more severe May

278 normal kidney function (eGFR 84 +/- 11.7 ml/min/1.73m(2)) and norm-albuminuria at baseline, UPPod:CR

279 3 increased blood flow at rest (79 +/- 87 ml/min; P = 0.03) and augmented the exercise-induced hypera

280 h enrolled children with an eGFR of 30-90 ml/min per 1.73 m(2) and then assessed eGFR annually.

281 ted glomerular filtration rate [eGFR] <90 mL/min/1.73 m2 >=90 days apart).

282 d model, factors associated with eGFR <90 mL/min/1.73 m2 included white race, older age, higher body

283 58 years (IQR, 52-65), median eGFR was 95 ml/min per 1.73 m(2) (IQR, 74-100) using the CKD-EPI formul

284 Quantitative MBV [%] and perfusion [ml/min/g] maps were acquired during adenosine stress and at

285 stimated glomerular filtration rate >=15 mL/(min.1.73 m(2)) were identified between October 1, 2010 t

286 . mL-1; Control: 0.041 (0.035, 0.048) mug . min-1 . mL-1, P = 0.039] and infant cobalamin intake [Bo

287 n in milk [Bolus: 0.054 (0.047, 0.061) mug . min-1 . mL-1; Control: 0.041 (0.035, 0.048) mug . min-1

288 difference (95% CI): 4266 (261, 8270) mumol.min-1.kg-1.180 min; P = 0.04; eta2p = 0.31] and branched

289 tion of paraoxonase 1 (PON1) activity (mumol/min/mg) when compared with WT apoA-I and comparable PON1

290 roup difference (95% CI): 266 (77, 455) nmol.min-1.kg-1.180 min; P = 0.01; eta2p = 0.44].

291 C runtime was 3 min with retention times of (min); 0.63 (GA), 0.97 (RT), 2.00 (QT) and 2.41 (LT).

292 mpared to India, mean RR was 9.6 breaths per min higher in Guatemala, 12.1 breaths per min higher in

293 r min higher in Rwanda, and 16.1 breaths per min higher in Peru (likelihood ratio test p<0.0001).

294 er min higher in Guatemala, 12.1 breaths per min higher in Rwanda, and 16.1 breaths per min higher in

295 latin (area under the curve of 4.5 mg/mL per min administered intravenously) or cisplatin (70 mg/m(2)

296 lomerular filtration rate >=25 to <75 mL per min per 1.73 m(2), treated with optimized renin-angioten

297 e in 30 min, with an initial rate of 0.35 pH.min(-1) To understand the interplay in these composite s

298 ncentrations at ~2.5 nmol/g of heart protein/min, representing ~0.003-0.006% of glycolysis.

299 flux at ~2.3 and 2.5 nmol/g of heart protein/min, respectively.

300 volutionary correlations between P50 and psi(min) and between K(s) and Hv show signs of deeper evolut