ライフサイエンスコーパス: Pa

1 Pa biofilm formation and viability were elevated in cond

2 Pa ESP associated with kinetochore microtubules in metap

3 Pa ESP deficiency perturbed anisotropic expansion and re

4 Pa ESP was expressed in the proliferating embryonal mass

5 Pa(O(2))/Fi(O(2)) and Crs were dissociated.

6 Pa-MAP 1.9 was active against Gram-negative planktonic b

7 ed in a stepwise manner (between 0.3 and 5.0 Pa), with each step being maintained for 15 s.

8 kin, with high levels of sensitivity (~0.005 Pa) and fast response times (~0.1 ms).

9 viously thought, in the range of 0.006-0.010 Pa s, which are ~2 to 3 orders of magnitude lower than t

10 hear-stress impulses of J less, similar0.035 Pa s leaves the cells unaffected.

11 kPa(-1)) over a broad pressure regime (0.08 Pa-360 kPa), and an ultrahigh pressure resolution (18 Pa

12 ielded Young's modulus values of 0.5 +/- 0.1 Pa and 1.6 +/- 0.3 Pa, respectively, suggesting both hig

13 astic network, with a modulus of roughly 0.1 Pa.

14 deformability at any given shear stress >=1 Pa.

15 S [>/=1 Pascal (Pa)], those with low ESS (<1 Pa) showed higher prevalence of lipid-rich plaques (37.5

16 ement uncertainty for vapor pressures near 1 Pa.

17 duces low average traction on the order of 1 Pa.

18 a shear-stress impulse J greater, similar0.1 Pa s ensures cell lysis or necrosis, whereas exposures i

19 nge of 0.035 less, similarJ less, similar0.1 Pa s preserve cell viability while also enabling molecul

20 above 10 MPa and melt viscosity lower than 1 Pa.s.

21 tane permeance of 3.5x10(-7) mol m(-2) s(-1) Pa(-1) (ca. 1000 GPU).

22 C ranged from 2.90 to 7.85 mumol m(-2) s(-1) Pa(-1) .

23 tection limit of 1 x 10(-17) mol m(-1) s(-1) Pa(-1) = 0.03 barrer).

24 ermeability = 1.65 x 10(-14) mol m(-1) s(-1) Pa(-1) = 49 barrer) but impermeable for nitrogen (permea

25 permeability = 2.4 x 10(-14) mol m(-1) s(-1) Pa(-1) = 72 barrer).

26 ity stabilized at 2.0x10(-8) mol m(-2) s(-1) Pa(-1) and 67, respectively, during long-term operation

27 high as (2.87+/-0.15)x10(-7) mol m(-2) s(-1) Pa(-1) at 22 degrees C while maintaining a decent N2 /CH

28 te 4A permeance = 8 x 10(-9) mol m(-2) s(-1) Pa(-1), permeability = 1.65 x 10(-14) mol m(-1) s(-1) Pa

29 ged, permeance = 12 x 10(-9) mol m(-2) s(-1) Pa(-1), permeability = 2.4 x 10(-14) mol m(-1) s(-1) Pa(

30 tection limit of 5 x 10(-12) mol m(-2) s(-1) Pa(-1), permeability below detection limit of 1 x 10(-17

31 to reversibly form soft (G' approximately 10 Pa) free-standing physical gels after 10 min at 55 degre

32 ytoplasmic shear modulus to approximately 10 Pa.

33 s range from soft (10(8) Pa) to hard (10(10) Pa) depending on the method used.

34 90 Pa), and macrophages (MPHs, 900 +110/-100 Pa).

35 (800 +/- 100 Pa) and relaxation (600 +/- 100 Pa) in response to chemical treatments.

36 ses upon actomyosin contraction (800 +/- 100 Pa) and relaxation (600 +/- 100 Pa) in response to chemi

37 mbination of low modulus ( approximately 100 Pa), high strain at break ( approximately 1,000%), and e

38 As little as 100 Pa causes a rapid (<10 s), sustained shift to movement w

39 eceiver had a noise equivalent pressure <100 Pa over a 20 MHz bandwidth.

40 g sub-50 Pa changes in pressure with sub-100 Pa detection limits and a response time of 90 ms is demo

41 ity (i.e., prior shear exposure (PSE) to 100 Pa x 300 s).

42 rengths varied significantly (in the 60-1000 Pa range) between sediments, with coarser-grained and hi

43 hanical compression model to apply CSS (<115 Pa) to well-characterized LN229 and U251 GBM cell lines

44 ascular endothelial cells, G was 20.4 +/- 12 Pa and decreased by 20% and 22% with increasing shear st

45 h storage moduli ranging from 190 Pa to 1450 Pa.

46 ation, namely, ER (mug m(-1) h(-1)) = 1464P (Pa) x M (g mol(-1)).

47 indoor-outdoor differentials of about 10-15 Pa, and the tests should last for at least nine indoor a

48 normal liver matrix stiffness was around 150 Pa and increased to 1-6 kPa in areas near fibrillar coll

49 of invasion is found to be approximately 165 Pa.

50 a), and an ultrahigh pressure resolution (18 Pa or 0.0056%) over the full pressure range, together wi

51 erties, with storage moduli ranging from 190 Pa to 1450 Pa.

52 imum contents were observed when tau was 0.2 Pa or 0.

53 M7 is mechanosensitive to shear force of 1.2 Pa, which is much lower than 98 Pa pressure loading repo

54 low ice adhesion strength ( approximately 2 Pa) and stability in shear flows up to Reynolds number o

55 vity (14.4 kPa(-1) ), low detection limit (2 Pa), fast response ( approximately 24 ms), low power con

56 microgreens in bags of 29.5 pmol s(-1) m(-2) Pa(-1) oxygen transmission rate (OTR) maintained better

57 OSI=7.75.10(-6) m(2), t(r)=6.16.10(-4) m(2)/Pa) gave the most favorable results compared with T-sten

58 OSI=10.40.10(-6) m(2), t(r)=6.87.10(-4) m(2)/Pa) or the culotte technique (TAWSS=1.30. 10(-4) N, OSI=

59 OSI=7.52.10(-6) m(2), t(r)=5.57.10(-4) m(2)/Pa) with bifurcational area subjected to OSI values >0.2

60 OSI=9.87.10(-6) m(2), t(r)=8.78.10(-4) m(2)/Pa).

61 uations at a sensitivity of 20 pN/mum(2) (20 Pa).

62 Moreover, at reduced pressures (10-200 Pa), the increased speed of thermal transpiration throug

63 ogical range of substrate stiffness (50-2000 Pa).

64 ma caused by the slight overpressure of 2000 Pa within the interface.

65 to a threshold shear stress between 8 and 21 Pa; the propagation of this calcium response is a result

66 layed similar viscosities ( approximately 21 Pa s) to lower mass-loaded flow electrodes (20% carbon c

67 ll lines displayed a peak in migration at 23 Pa, cells displayed differential response to CSS with ei

68 ium-230 ((230)Th) and protactinium-231 ((231)Pa), which are produced in sea water and removed by part

69 ange through the Fram strait may export (231)Pa.

70 Because no enhanced sink for (231)Pa has yet been found in the Arctic, our records suggest

71 In highly resolved cores, Heinrich (231)Pa/(230)Th ratios exceed glacial ratios at nearly all de

72 all time intervals reveal a deficit in (231)Pa burial that can be balanced only by lateral export in

73 The data reveal a net (231)Pa deficit during each period, consistent with persisten

74 rds provide a comprehensive overview of (231)Pa and (230)Th burial in Arctic sediments during glacial

75 d consistent evidence for the export of (231)Pa from the deep Arctic and may indicate continuous deep

76 al water tracers (the isotope ratios of (231)Pa/(230)Th and (143)Nd/(144)Nd), which are not directly

77 phytoplankton productivity (using opal, (231)Pa/(230)Th and excess Ba), and the degree of nitrate con

78 each period, consistent with persistent (231)Pa export.

79 ere we present new Atlantic sedimentary (231)Pa/(230)Th data from the Holocene, the last glacial maxi

80 ate a spatially distributed sedimentary (231)Pa/(230)Th database.

81 The marine sedimentary (231)Pa/(230)Th ratio is a promising paleocirculation proxy,

82 Sedimentary (231)Pa/(230)Th ratios decrease nearly linearly with increasi

83 s of metals suspended at stresses below 0.24 Pa were greater than in the underlying sediment.

84 n internal force (associated with a -80+/-25 Pa stress) within the biofilms, similar to the forces th

85 lus values of 0.5 +/- 0.1 Pa and 1.6 +/- 0.3 Pa, respectively, suggesting both high porosity and a la

86 oxia with a P50 of 15 mm Hg (1 mm Hg = 133.3 Pa) in normal Tyrode or 46 mm Hg in Ca(2+)-free Tyrode.

87 RCD at shear stresses of 1.7 Pa and 30 Pa was reduced significantly in patients who died, compa

88 ithelial barriers is on the order of 100~300 Pa, and is modulated by ion channel activity.

89 n temperature with static pressure of 93,325 Pa and for 1.5 s residence time.

90 tivity (0.6 mS cm(-1) ), low viscosity (0.35 Pa s), and wide range of potential window (0-4.85 V) at

91 ations of cells, with a mean of 300 and 3500 Pa, whereas the standard DI output was unable to disting

92 f fibrin viscosity increases from 150 to 376 Pa whereas the storage modulus of the gel increases from

93 c devices, with a pressure resolution of 2.4 Pa, achieving high levels of noise immunity and signal s

94 ic CO2 was below 300 ppm (approximately 30.4 Pa).

95 rom 20 Hz to 3 kHz at amplitudes as low as 4 Pa.

96 our orders of magnitude (G' 6 Pa-3.6 x 10(4) Pa) independently of polymer concentration and molecular

97 wer, a vapor pressure of greater than 10(-4) Pa is required to achieve a sufficiently good quality sp

98 erials with vapor pressures less than 10(-4) Pa, in thin film form, by between 4 and 7 orders of magn

99 The isolated soft tumor cells (< 400 Pa) but not the stiff ones (> 700 Pa) can form a tumor i

100 9 to 17.9, 1.34 to 31.28 mg/kg, 2.48 to 8.42 Pa s, 18.2 to 47.5 meq/kg, 51.31% to 68.30%, 0.60% to 0.

101 identical (p > 0.08) over a large range (47 Pa - 36 kPa).

102 anch caused a WSS increase of 0.7 Pa and 0.5 Pa, respectively.

103 grees C and a pressure scanning rate of -0.5 Pa/s and then further separated via SDS-PAGE in a 25 mm

104 lowest reported (Young's modulus of 85 +/- 5 Pa).

105 he low-modulus (G' approximately 1.0 x 10(5) Pa at 90 degrees C) cross-linked SPEs reported herein ex

106 VOCs of vapor pressure (VP) exceeding 10(-5) Pa and corresponding calculated log K(dust-air) (m(3) g(

107 of ammonium adipate was 2.5 +/- 0.8 x 10(-5) Pa at 298 K, similar to that of adipic acid.

108 greater vorticity and thus instability in 5-Pa flow compared with unsheared control.

109 0 microm height) capable of resolving sub-50 Pa changes in pressure with sub-100 Pa detection limits

110 serve that a compression of the order of 500 Pa flattens the cells under gel by up to 50%.

111 vels now exceed 400 ppm (approximately 40.53 Pa) and contrast with the low-pCO2 conditions under whic

112 To study 3D migration in a soft (550 Pa) environment, we use self-assembled collagen networks

113 The complex modulus of 176.6 Pa and lower allowed cardiac fibroblast to maintain its

114 and an interstitial pressure of 3.9 +/- 3.6 Pa, relative to the central blastocoel cavity of the emb

115 be tuned over four orders of magnitude (G' 6 Pa-3.6 x 10(4) Pa) independently of polymer concentratio

116 mated vapor pressure of 1.7 +/- 0.8 x 10(-6) Pa at 298 K.

117 piezoresistance coefficient of -5.1 x 10(-6) Pa(-1) .

118 piezoresistance coefficient of -4.4 x 10(-6) Pa(-1), and conductance and capacitance tunable by exter

119 because of the oxygen flooding at 5 x 10(-6) Pa) was much higher with C(60)(+) than with Ar(+).

120 ound that MKs grown in a medium of 30- to 60-Pa stiffness more closely resembled those in the BM in t

121 osis and branch caused a WSS increase of 0.7 Pa and 0.5 Pa, respectively.

122 RCD at shear stresses of 1.7 Pa and 30 Pa was reduced significantly in patients who d

123 a cell hydrostatic pressure of 16.8 +/- 1.7 Pa and an interstitial pressure of 3.9 +/- 3.6 Pa, relat

124 ubin level, and RCD at a shear stress of 1.7 Pa were each independently correlated with plasma lactat

125 lue at a stenosis at the bifurcation was 2.7 Pa.

126 lapping range of applicability (~10(3)-10(7) Pa s); fitted curves from DCIC data show variable agreem

127 ment was under ultrahigh vacuum (<5 x 10(-7) Pa).

128 pressures ranged from about 10(-2) to 10(-7) Pa.

129 fferent shear forces with a range of [0, 0.7]Pa on the inner surface of pipelines in drip irrigation

130 imately 130 P(a) vs. K(w) = approximately 70 Pa); both matters stiffened with increasing strain.

131 seconds forming a mechanically rigid (~1,700 Pa) gel offering a maximum adhesive stress of ~2.8 kPa.

132 lls (< 400 Pa) but not the stiff ones (> 700 Pa) can form a tumor in immunocompetent mice with 100 ce

133 erestingly, however, an ECM stiffness of 700 Pa maximizes expression of pan-neuronal markers.

134 w desorption temperature and low vacuum (730 Pa).

135 Sound levels ranged from 0.02 to 12,738 Pa(2), with larger measurements observed on outgoing tid

136 essure sensitivity of up to approximately 8%/Pa for the whiskers, which is >10x higher than all previ

137 ch protein aggregates range from soft (10(8) Pa) to hard (10(10) Pa) depending on the method used.

138 For T > 237 K and P approximately 10(-8) Pa, G(T) and D(T) have super-Arrhenius ("fragile") tempe

139 onocytes (Ms, storage modulus of 520 +90/-80 Pa), dendritic cells (DCs, 440 +110/-90 Pa), and macroph

140 2.5, 5.0, and 7.5 wt % were 20, 380, and 850 Pa, respectively.

141 t internal hydrostatic pressure (37 +/- 10.9 Pa).

142 that amyloid materials are very stiff (10(9) Pa).

143 /-80 Pa), dendritic cells (DCs, 440 +110/-90 Pa), and macrophages (MPHs, 900 +110/-100 Pa).

144 force of 1.2 Pa, which is much lower than 98 Pa pressure loading reported recently, and mediates dist

145 Hg) and WSS (mean absolute error within 0.99 Pa) for patients with this disease.

146 36 patients with phenotype L, 58 (43%) had a Pa(O(2))/Fi(O(2)) < 150.

147 f the gymnosperm Norway spruce (Picea abies, Pa) ESP.

148 harge without the occurrence of ICU-acquired Pa infection (the primary outcome), as competing events.

149 m does not significantly reduce ICU-acquired Pa infections in non-outbreak situations.

150 dence and the incidence rate of ICU-acquired Pa infections were 3.38% (55/1625) vs 3.44% (57/1658) an

151 ve patients on the incidence of ICU-acquired Pa infections.

152 tion is whether children with newly acquired Pa infection who are able to achieve sustained eradicati

153 ived standardized therapy for newly acquired Pa.

154 enes and metallacyclocumulenes of actinides (Pa-Pu) that makes them distinct from their corresponding

155 ributory factors for reducing P. aeruginosa (Pa) infections in intensive care units (ICUs) remains qu

156 istic human pathogen Pseudomonas aeruginosa (Pa) causes several infections acquired in a healthcare s

157 riophage produced by Pseudomonas aeruginosa (Pa) in suppression of immunity against bacterial infecti

158 Pseudomonas aeruginosa (Pa) is the most important pathogen infecting the airways

159 ) (a model for Mtb), Pseudomonas aeruginosa (Pa), Legionella pneumophila (Lp), and Enterococcus faeca

160 e common CF pathogen Pseudomonas aeruginosa (Pa).

161 istic human pathogen Pseudomonas aeruginosa (Pa).

162 i (Ec, m/z 1797) and Pseudomonas aeruginosa (Pa, m/z 1446) using on-tissue acid hydrolysis to cleave

163 Pseudomonas aeruginosa(Pa) was present in CF sputum in 11 patients, 4 had ident

164 ] vs. 8 [6-9]; P = 0.002), without affecting Pa(CO(2)) (P = 0.80) and comfort (P = 0.50).

165 Aging Pa-3 Li2B12H12 under 450 degrees C/125 bar H2 pressure f

166 ombinations of B with Z-C, Pa-Z, Pa-Z-C, and Pa-C, or C or Z alone, or standard combination treatment

167 s, the ion corresponding to the major Ec and Pa lipid A species (m/z 1797 and 1446, respectively) wer

168 ogen interactions between CF macrophages and Pa.

169 osphorus (P) per unit leaf area (Ma , Na and Pa , respectively), and chlorophyll from 210 species at

170 At any given Na and Pa , the fraction of N allocated to photosynthesis was h

171 lear, however, and may be confounded by anti-Pa antibiotic usage.

172 ined eradicators had significantly less anti-Pa antibiotic usage during follow-up compared with nonsu

173 analysis was performed to calculate aortic (Pa), distal intracoronary (Pd), and reservoir (Pr) press

174 1.92; 95% confidence interval, 1.80-2.21 at Pa(O)(2) of 23 mm Hg).

175 B-Pa-Z, including two novel agents without resistance in p

176 a-Z-C, and 0.076 (95% CI, 0.005-0.145) for B-Pa-C.

177 confidence interval [CI], 0.075-0.257) for B-Pa-Z, 0.151 (95% CI, 0.071-0.232) for standard treatment

178 for B-Z-C, 0.115 (95% CI, 0.039-0.189) for B-Pa-Z-C, and 0.076 (95% CI, 0.005-0.145) for B-Pa-C.

179 of Pseudomonas aeruginosa bacterioferritin (Pa-BfrB) in complex with bacterioferritin-associated fer

180 A near complete dissociation between Pa(O(2))/Fi(O(2)) and Crs was observed.

181 mized to receive combinations of B with Z-C, Pa-Z, Pa-Z-C, and Pa-C, or C or Z alone, or standard com

182 had a 74% reduced risk of developing chronic Pa (hazard ratio [HR], 0.26; 95% confidence interval [CI

183 izing antipseudomonal therapies during early Pa infection.

184 t 24 hours was calculated as (24-h post-ECMO Pa(CO(2)) - pre-ECMO Pa(CO(2)))/pre-ECMO Pa(CO(2)).

185 ated as (24-h post-ECMO Pa(CO(2)) - pre-ECMO Pa(CO(2)))/pre-ECMO Pa(CO(2)).

186 CMO Pa(CO(2)) - pre-ECMO Pa(CO(2)))/pre-ECMO Pa(CO(2)).

187 ice for parallel-electromembrane extraction (Pa-EME) was developed to enable simultaneous and high-th

188 with bacterioferritin-associated ferredoxin (Pa-Bfd) at 2.0 A resolution.

189 reased risk of mortality after adjusting for Pa(O(2))/Fi(O(2)), and positive end-expiratory pressure

190 tact precautions to standard precautions for Pa-positive patients on the incidence of ICU-acquired Pa

191 tact precautions to standard precautions for Pa-positive patients with a surveillance screening progr

192 A surveillance screening program for Pa was implemented.

193 ontraction, the An-C distance increases from Pa to Pu.

194 n mice and are associated with chronic human Pa wound infections.

195 Dl(CO) (30% [12-79%]) and severe hypoxemia (Pa(O(2)) 56 [38-99] mm Hg).

196 in CF sputum in 11 patients, 4 had identical Pa strains in the stomach.

197 The relative change in Pa(CO(2)) in the first 24 hours was calculated as (24-h

198 The median relative change in Pa(CO(2)) was -31% (interquartile range, -46% to -12%).

199 Patients with a large relative decrease in Pa(CO(2)) (>50%) had an increased incidence of neurologi

200 ratory failure, a large relative decrease in Pa(CO(2)) in the first 24 hours after ECMO initiation is

201 A large relative decrease in Pa(CO(2)) was independently associated with neurological

202 Rationale: Large decreases in Pa(CO(2)) that occur when initiating extracorporeal memb

203 Herein, we investigate differences in Pa phenazine production and dynamics in polymicrobial co

204 The fall in Pa closely correlated with the reduction in peripheral P

205 f the reduction in Pd was because of fall in Pa.

206 d liquid vapor pressure (log PL) > -5 (PL in Pa), as well as the total suspended particle concentrati

207 As compared with HFNC, helmet NIV increased Pa(O(2))/Fi(O(2)) (median [interquartile range]: 255 mm

208 During initial stages of infection, Pa produces redox-active phenazine metabolites, includin

209 was obtained as [0, 0.20] [0.35, +infinity] Pa.

210 her bacterial pathogens noticeably influence Pa phenazine production and dynamics.

211 Soil [P] and leaf Pa were key explanatory factors for models of area-based

212 ingle phase crystalline anhydrous Li2B12H12 (Pa-3 structure type) and studied its sensitivity to wate

213 could not be matched were younger, had lower Pa(o(2))/Fi(o(2)) ratio, had higher plateau pressure, bu

214 icators were defined as those who maintained Pa-negative cultures for 12 months after initial antipse

215 utophagy lies downstream of metacaspase mcII-Pa, a key protease essential for suspensor cell death.

216 With a high-pressure sensitivity of 10.79 mV/Pa, a wide working frequency bandwidth from 0 Hz to 40 H

217 ponses with a very high sensitivity (89.3 nm Pa(-1) ), which is three orders of magnitude higher than

218 tions, and their importance for complexes of Pa and U in particular.

219 lexes, our calculations include complexes of Pa, Np, and Pu.

220 172 (69%) achieved sustained eradication of Pa during the trial (sustained eradicators).

221 a wide range of stiffness, from hundreds of Pa to hundreds of kPa, T cell metabolic properties and c

222 Objectives: To determine if the magnitude of Pa(CO(2)) correction upon ECMO initiation is associated

223 e suggest NIV with targeted normalization of Pa(CO(2)) in patients with hypercapnic COPD on long-term

224 ovides important evidence about the onset of Pa infections.

225 etics and microscopy to explore the roles of Pa ESP during embryogenesis.

226 Here we focused on the study of Pa-MAP 1.9, a rationally designed AMP derived from the p

227 few pascal and viscosities as low as tens of Pa.s.

228 dex (SDI) and the transmission index (TI) of Pa isolates were derived from pulsed-field gel electroph

229 ore, we show that the essential function of (Pa) AmiB can be bypassed in mutants activated for a Cpx-

230 agreement with studies in other organisms, (Pa) AmiB and three LytM proteins were found to play cruc

231 luble thrombomodulin), impaired oxygenation (Pa(O(2))/Fi(O(2)) [P/F] ratio, oxygenation index), morbi

232 ration of hMSCs did not improve oxygenation (Pa(O(2))/Fi(O(2)) mean difference = -146 mm Hg; P = 0.07

233 informative ways from the E. coli paradigm; (Pa) AmiB was found to be essential for viability and the

234 with segments with higher ESS [>/=1 Pascal (Pa)], those with low ESS (<1 Pa) showed higher prevalenc

235 n stress produced by CE is 5.0+/-1.6 Pascal (Pa).

236 more, the cation/anion permeability ratio Pc/Pa is decreased in the W136R mutant and increased in the

237 (Pd/Pa vs iFR in an Unselected Population Referred for Invas

238 enosine zones for iFR of 0.86 to 0.93 and Pd/Pa of 0.87 to 0.94 in the hybrid strategy.

239 n either binary cutoff values for iFR and Pd/Pa or hybrid strategies incorporating iFR or Pd/Pa will

240 Baseline flow and Pd/Pa remained stable over time but FFR reduced significant

241 Binary cutoff values for iFR and Pd/Pa result in misclassification of 1 in 5 lesions.

242 % with FFR threshold <0.75 when comparing Pd/Pa at peak and stable hyperemia.

243 lower misclassification than whole-cycle Pd/Pa (P<0.001).

244 FFR, iFR, and whole-cycle Pd/Pa indices were recalculated and stenosis misclassificat

245 Whole-cycle Pd/Pa is more vulnerable to such reclassification than FFR

246 ion) values for FFR, iFR, and whole-cycle Pd/Pa were 0.81 (+/-0.11), 0.90 (+/-0.07), and 0.93 (+/-0.0

247 he cut point of FFR, iFR, and whole-cycle Pd/Pa, 34.6% (155), 50.1% (224), and 62.2% (278) of values,

248 classified with FFR, iFR, and whole-cycle Pd/Pa, respectively.

249 e assessed with FFR, iFR, and whole-cycle Pd/Pa.

250 values of </=0.90 for iFR and </=0.92 for Pd/Pa, and adenosine zones for iFR of 0.86 to 0.93 and Pd/P

251 We measured Pd/Pa, iFR, FFR, and hyperemic iFR.

252 rid analysis, 54% of iFR cases and 53% of Pd/Pa cases were outside the adenosine zone and rates of mi

253 or hybrid strategies incorporating iFR or Pd/Pa will result in similar levels of disagreement.

254 -cycle distal pressure/proximal pressure (Pd/Pa) indices.

255 Distal coronary to aortic pressure ratio (Pd/Pa) and instantaneous wave-free ratio (iFR) are indices

256 ic accuracy of iFR was similar to resting Pd/Pa and trans-stenotic pressure gradient and significantl

257 accuracy was similar for iFR and resting Pd/Pa with misclassification rates of 21% versus 20.2% (P=0

258 t iFR has superior diagnostic accuracy to Pd/Pa when compared with fractional flow reserve (FFR).We h

259 In the population of the VERIFY2 (Pd/Pa vs iFR in an Unselected Population Referred for Invas

260 e-trimethoprim; AR Scientific, Philadelphia, Pa) and a regimen of chlorhexidine washes were prescribe

261 onary pressure (Pd) to mean aortic pressure (Pa), and fractional flow reserve (FFR) in patients under

262 he new drugs bedaquiline (B) and pretomanid (Pa), combined with an existing drug, pyrazinamide (Z), a

263 ly, immunization of mice against Pf prevents Pa wound infection.

264 Pf promote Pa wound infection in mice and are associated with chron

265 halamic nuclei including: anterior pulvinar (Pa), ventroposterior inferior (VPI), ventroposterior sup

266 ting protection.Clinical trial registration: Pa n African Clinical Trials Registry (PACTR201103000280

267 l features that favor antibiotic-resistance, Pa-MAP 1.9 could be a promising candidate in the develop

268 rmeances as high as 1.2 x 10 (-7) mol/m(2) s Pa and separation selectivities of 35 for molar composit

269 rmeances as high as 1.2 x 10 (-7) mol/m(2) s Pa and separation selectivities up to 45 for molar compo

270 n average slope of 0.30 (mug PAH g(-1) soil) Pa(-1) and r(2)'s of 0.61-0.73.

271 Specifically, Pa was co-cultured with two pathogens of clinical releva

272 harm related to exposure to supraphysiologic Pa(O(2)) (hyperoxemia) in critically ill patients.Object

273 nical impact of failure to achieve sustained Pa eradication remains unclear, however, and may be conf

274 with similar transpulmonary pressure swings, Pa(CO(2)), and comfort.

275 e way the prevailing carbon dioxide tension (Pa(CO(2))) blunts the brain's response to hypoxia, effec

276 fficient was found to be [Formula: see text] Pa.s, which is on the same order of magnitude as the dyn

277 es and high viscosities ([Formula: see text] Pa[Formula: see text]s).

278 ctroscopy and in silico tools, we found that Pa-MAP 1.9 may be acting both on intracellular targets a

279 The Pa-3 Li2B12H12 phase is not observed during LiBH4 decomp

280 The Pa-BfrB-Bfd complex also revealed the first structure of

281 The Pa-EME device showed excellent extraction yields from 84

282 mia dose was defined as the area between the Pa(O(2)) time curve and a boundary of 13.3 kPa (100 mm H

283 g the kinematic tracer protactinium/thorium (Pa/Th) with the deep water-mass tracer, epibenthic delta

284 odynamic patterns were observed according to Pa and Pd change at peak and stable hyperemia.

285 We demonstrate that ToxI(Pa) can inhibit ToxN(Pa) in vitro both in its processed

286 embly are both mediated entirely by the ToxI(Pa) RNA, with no requirement for cellular factors or exo

287 tems from Pectobacterium atrosepticum (ToxIN(Pa)) and Bacillus thuringiensis (ToxIN(Bt)) that ToxI RN

288 e demonstrate that ToxI(Pa) can inhibit ToxN(Pa) in vitro both in its processed form and as a repetit

289 Moreover, we report that UbiU(Pa) and UbiT(Pa) can bind UQ and that the isoprenoid tail of UQ is th

290 inosa These three genes here are called ubiT(Pa) , ubiV(Pa) , and ubiU(Pa) We show that UbiV(Pa) acco

291 re are called ubiT(Pa) , ubiV(Pa) , and ubiU(Pa) We show that UbiV(Pa) accommodates an iron-sulfur [4

292 Moreover, we report that UbiU(Pa) and UbiT(Pa) can bind UQ and that the isoprenoid tai

293 three genes here are called ubiT(Pa) , ubiV(Pa) , and ubiU(Pa) We show that UbiV(Pa) accommodates an

294 , ubiV(Pa) , and ubiU(Pa) We show that UbiV(Pa) accommodates an iron-sulfur [4Fe-4S] cluster.

295 s (1.69 kHz) an output voltage of about 25 V/Pa was measured.

296 on of Escherichia coli derived gyrase versus Pa gyrase, and overexpression in the absence of antitoxi

297 Furthermore, whilst Pa ESP can rescue the chromatid nondisjunction phenotype

298 ethods: Fifteen patients with hypoxemia with Pa(O(2))/Fi(O(2)) < 200 mm Hg received helmet NIV (posit

299 hich typically populate infection sites with Pa.

300 is defined as [minute ventilation (ml/min) x Pa(CO(2)) (mm Hg)]/(predicted body weight x 100 x 37.5).

301 to receive combinations of B with Z-C, Pa-Z, Pa-Z-C, and Pa-C, or C or Z alone, or standard combinati