ライフサイエンスコーパス: Pa

1 Pa contained a remarkably high density of axons and axon

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-MAP 1.9 was active against Gram-negative planktonic b

6 Pa-projecting neurons were localized in the same nuclei

7 ing horizontal and vertical saccades was 1.0 Pa (Pascal) and 2.5 Pa, respectively, and was dependent

8 rterial circulation (ie, on the order of 1.0 Pa).

9 entation, and material moduli from 10-10,000 Pa on adult neural stem-cell (aNSC) behavior.

10 eas harder gels ( approximately 1,000-10,000 Pa) promoted glial cultures.

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

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

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

14 ratory acidosis (arterial pH, 7.22 +/- 0.08; Pa(CO(2)), 86 +/- 21 mm Hg).

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

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

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

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

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

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

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

22 gut contents to organism (D(go)'; mol d(-1) Pa(-1)) and organism to gut contents (D(og); mol d(-1) P

23 d organism to gut contents (D(og); mol d(-1) Pa(-1)) were quantified to test the hypothesis that the

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

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

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

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

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

29 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

30 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

31 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(

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

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

34 ytoplasmic shear modulus to approximately 10 Pa.

35 on substrata with moduli of approximately 10 Pa.

36 ely 0-200 Pa with a control resolution of 10 Pa.

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

38 d)) of PLFE LUVs changes from 3.59 x 10(-10) Pa(-1) at 25 degrees C to 4.08 x 10(-10) Pa(-1) at 78 de

39 10) Pa(-1) at 25 degrees C to 4.08 x 10(-10) Pa(-1) at 78 degrees C.

40 90 Pa), and macrophages (MPHs, 900 +110/-100 Pa).

41 (800 +/- 100 Pa) and relaxation (600 +/- 100 Pa) in response to chemical treatments.

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

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

44 e maximum pressure is only approximately 100 Pa, much smaller than typically found in the microcircul

45 employed with H(2) pressure ranging from 100 Pa to 10 MPa.

46 eptide-modified vmIPNs with moduli of >/=100 Pa.

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

48 with a Young's modulus of approximately 1000 Pa, whereas hippocampal neurite outgrowth is independent

49 A7 cells on the softest gels examined (1000 Pa).

50 on substrates with a Young's modulus of 1000 Pa strengthen considerably after 18-30 h.

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

52 in dynamic viscosity from < 0.1 to > 10(13) Pa s.

53 tlands, a weak zone (shear strength 500-1450 Pa) was observed approximately 30 cm below the marsh sur

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

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

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

57 the head caused a maximum shear stress of 16 Pa, largely independent of GF.

58 of invasion is found to be approximately 165 Pa.

59 ts in mantle viscosities of 10(17) to 10(18) Pa s in regions of high strain rate (10(-12) s(-1)), and

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

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

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

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

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

65 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

66 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=

67 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

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

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

70 tunable over a range of approximately 0-200 Pa with a control resolution of 10 Pa.

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

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

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

74 ns can resist to pressures up to 540 +/- 220 Pa.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 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.

94 stant at shear stresses below a threshold (3 Pa), whereas above the threshold ATP release is increase

95 along the axon (9.6 x 10(3) +/- 7.5 x 10(3) Pa.s).

96 spiration studies of human neutrophils (5-30 Pa.s), our computational model predicts the velocities a

97 en compressed with pressures up to 65 +/- 30 Pa for 10 min, while dorsal root ganglia axons can resis

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

99 ina produced shear stresses between 425-3600 Pa, sufficient to cause widespread erosion of the low sa

100 han the gel composed of twisted fibrils (367 Pa at 6 rad/s).

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

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

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

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

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

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

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

108 ellular osmotic pressure (e.g., from 7 to 40 Pa for N2a cells) through unregulated ion influx.

109 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.

110 nds had no such zone (shear strengths > 4500 Pa) and contained deeper rooting.

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

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

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

114 ertical saccades was 1.0 Pa (Pascal) and 2.5 Pa, respectively, and was dependent on GF.

115 shear stress increases ( approximately 0-3.5 Pa).

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

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

118 with storage moduli G' of around 10(4)-10(5) Pa, similar to that of natural tissues.

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

120 0 microm height) capable of resolving sub-50 Pa changes in pressure with sub-100 Pa detection limits

121 ar moduli ranging from approximately 9 to 50 Pa.

122 h serum, softer gels ( approximately 100-500 Pa) greatly favored neurons, whereas harder gels ( appro

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

124 a-tubulin III, was observed on vmIPNs of 500 Pa, near the physiological stiffness of brain tissue.

125 sted fibrils is more mechanically rigid (517 Pa at 6 rad/s) than the gel composed of twisted fibrils

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

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

128 migration on gels with elasticity below 5500 Pa in comparison to individual cells, suggesting these c

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

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

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

132 ed into the chamber to maintain a 5 x 10(-6) Pa oxygen environment.

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

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

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

136 osity of the axon (3 x 10(6) +/- 2.4 x 10(6) Pa.s) and the friction coefficient for laminin/polyornit

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 A 1.8-Pa stress over a focal adhesion activated Src to the sam

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

155 fen from less than 20 Pascal (Pa) to over 80 Pa.

156 2.5, 5.0, and 7.5 wt % were 20, 380, and 850 Pa, respectively.

157 ximately 3.77 kPa and eta approximately -860 Pa.s; values of eta for live C. elegans are negative bec

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

159 /-80 Pa), dendritic cells (DCs, 440 +110/-90 Pa), and macrophages (MPHs, 900 +110/-100 Pa).

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

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

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

163 ived standardized therapy for newly acquired Pa.

164 lations of BfrB from Pseudomonas aeruginosa (Pa BfrB) in K(2)HPO(4) solutions at different ionic stre

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

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

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

168 biosynthetic pathway in Pantoea agglomerans (Pa) is reported.

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

170 with COPD) with AHRF (arterial pH < 7.35 and Pa(CO(2)) > 45 mm Hg) treated with a similar protocol of

171 rating that release of iron from Pa BfrB and Pa FtnA is likely subject to different regulation in P.

172 the specific recognition between Pa-BfrB and Pa-Bfd is of widespread significance to the understandin

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

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

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

176 cal DNA-binding proteins, Tgo polymerase and Pa-UDG.

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

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

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

180 bacterioferritin-associated ferredoxin (apo Pa Bfd).

181 1.92; 95% confidence interval, 1.80-2.21 at Pa(O)(2) of 23 mm Hg).

182 t Pseudomonas aeruginosa bacterioferritin B (Pa BfrB) has been determined from crystals grown from pr

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

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

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

186 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.

187 l ferritin (Pa FtnA) and a bacterioferritin (Pa BfrB) in P. aeruginosa.

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

189 the bfrB gene as a genuine bacterioferritin (Pa BfrB), indicate the coexistence of a bacterial ferrit

190 esting that the specific recognition between Pa-BfrB and Pa-Bfd is of widespread significance to the

191 a significant nonlinear relationship between Pa(O)(2) and PICU mortality.

192 BfrB requires not only electron delivery by Pa Fpr but also the presence of a "regulator", the apo f

193 minant entry route for the uptake of iron by Pa BfrB.

194 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

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

196 izing antipseudomonal therapies during early Pa infection.

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

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

199 ate the coexistence of a bacterial ferritin (Pa FtnA) and a bacterioferritin (Pa BfrB) in P. aerugino

200 For Pa-N64Q (Ht-Q64N) it is proposed that the favorable rele

201 ence demonstrating that release of iron from Pa BfrB and Pa FtnA is likely subject to different regul

202 erial gas, 207 patients (11%) had hyperoxia (Pa(O)(2) >/=300 mm Hg) and 448 (24%) had hypoxia (Pa(O)(

203 (2) >/=300 mm Hg) and 448 (24%) had hypoxia (Pa(O)(2) <60 mm Hg).

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

205 It previously has been shown that Asn64 in Pa cyt c551 and in Ht-Q64N interacts with the heme axial

206 I level and JNK activation are attenuated in Pa-4 cells by dominant negative PKCdeltaKD or in mouse e

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

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

209 o a rapid and transient activation of JNK in Pa-4 or mouse embryo fibroblast cells.

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

211 these areas labeled neurons specifically in Pa.

212 tase (Pa Fpr), the release of iron stored in Pa BfrB requires not only electron delivery by Pa Fpr bu

213 reas the efficient release of iron stored in Pa FtnA requires only the input of electrons from a ferr

214 A retrograde tracer injection into Pa combined with immunohistochemistry demonstrated that

215 Following a retrograde tracer injection into Pa, labeled neurons were found in the hypothalamus, dors

216 with moderate CB1 signals, including the LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic ne

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

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

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

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

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

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

223 ections of paraventricular thalamic nucleus (Pa) following small anterograde and retrograde tracer in

224 ferroxidase iron into the interior cavity of Pa FtnA.

225 terface that enables the [2Fe-2S] cluster of Pa-Bfd to promote heme-mediated electron transfer throug

226 The connections of Pa and its innervation by 5-HT, ORX, and CRH suggest tha

227 172 (69%) achieved sustained eradication of Pa during the trial (sustained eradicators).

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

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

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

231 tures also revealed a pore on the surface of Pa BfrB that likely serves as a port of entry for Fe(2+)

232 ((in)), and external, Fe((out)), surfaces of Pa BfrB.

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

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

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

236 alamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammillary (LM), and ve

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

238 al tissues stiffen from less than 20 Pascal (Pa) to over 80 Pa.

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

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

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

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

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

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

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

246 % with FFR threshold <0.75 when comparing Pd/Pa at peak and stable hyperemia.

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

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

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

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

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

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

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

254 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

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

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

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

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

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

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

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

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

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

264 phloroglucinol (Tp) with p-phenylenediamine (Pa-1) and 2,5-dimethyl-p-phenylenediamine (Pa-2), respec

265 (Pa-1) and 2,5-dimethyl-p-phenylenediamine (Pa-2), respectively, in 1:1 mesitylene/dioxane.

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

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

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

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

270 electrons from a ferredoxin NADP reductase (Pa Fpr), the release of iron stored in Pa BfrB requires

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

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

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

274 permeances as high as 2.0 x 10(-6) mol/m2.s.Pa at 295 K and a feed pressure of 224 kPa.

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

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

277 rliest modern humans in western Eurasia, Tam Pa Ling establishes a definitively modern population in

278 we report on a modern human cranium from Tam Pa Ling, Laos, which was recovered from a secure stratig

279 ferritin, which we propose should be termed Pa FtnA.

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

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

282 d lanthanides (Ce and Eu) and actinides (Th, Pa, U, and Np) from fresh and salt water systems.

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

284 The MD simulations also show that Pa BfrB ferroxidase centers are highly dynamic and perma

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

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

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

288 ndings suggest that Fe(2+) passes across the Pa BfrB shell via B-pores and that the ferroxidase pores

289 Residues at the Pa-BfrB-Bfd interface are highly conserved in Bfr and Bf

290 he antigenic homologs included in any of the Pa vaccines currently in use.

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

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

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

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

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

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

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

298 en proposed that current acellular vaccines (Pa) composed of only a few bacterial proteins may be les

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

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