ライフサイエンスコーパス: PE

1 PE can be a cause of decompensation in patients testing

2 PE caused robust vasoconstriction in resting skeletal mu

3 PE detection with this method is very sensitive and comp

4 PE is predicted to be an anchored membrane protein, but

5 PE microplastics and macroplastics from identifiable PE

6 PE plasmalogens were positively correlated with saturate

7 PE, PET, and PP were the most common polymers quantified

8 PE-mediated vasoconstriction was not attenuated by mild

9 Postoperative mortality occurred in 1 (PE on POD#8) and postoperative morbidity in 7 (12%).

10 Furthermore, PC(18:0/18:1), PE(18:1/18:2), SM(d18:0/22:0) and several other molecula

11 A total of 375 patients (181 PE patients and 194 controls) were analyzed.

12 ologists or optometrists were acquired by 29 PE-backed platform companies.

13 uble bonds, 36:6, 36:5, and 34:3 PC and 34:3 PE (all contain 18:3 fatty acid and decreased under HT)

14 er was not observed in either T(4)NDI or T(4)PE(2)NDI due to an insufficient PE(n) bridge length.

15 uring zero and two PE units (T(4)NDI and T(4)PE(2)NDI).

16 Therefore, T(4)PE(4)NDI can be selectively excited to form a charge-sep

17 th a naphthalene diimide (NDI) acceptor (T(4)PE(4)NDI) is demonstrated.

18 the T(4) and NDI components (T(4)NDI to T(4)PE(4)NDI).

19 , and call 911 immediately" (threshold, 85%; PE, 81.1%; 95% CI, 78.0 to 83.9).

20 ) and "Give the first dose" (threshold, 85%; PE, 98.2%; 95% CI, 96.9 to 99.0).

21 tion closely approximated the target of 90% (PE, 90.3%; 95% CI, 87.9 to 92.4).

22 ied to remove T-cell epitopes and contains a PE domain II truncation.

23 piezoelectric (PE) layer, which generates a PE potential that can be used to readout the magnetic st

24 otal lipid content validated the impact of a PE diet on FAM; in contrast to lipid-depleted starved an

25 erties are electrically controlled in such a PE/FM heterostructure and how a back-voltage is generate

26 and efficacy of surgical management of acute PE.

27 aging modalities used in patients with acute PE.

28 f imaging modalities for patients with acute PE.

29 After PE, patients should have clinical surveillance for chron

30 ture at the molecular scale is that although PE becomes more crystalline with environmental exposure,

31 ed for their capability to distinguish among PE, sodium dodecyl sulfate, and stearates.

32 The HE and PE estimates in the 1995 birth cohort for HPV18/31/33 we

33 pids bearing n-3 fatty acids (most in PC and PE) was also recorded.

34 fat/soup odors, all of them found in PP and PE samples.

35 ency by the liposomes containing both PS and PE compared to a mixture of liposomes separately compose

36 e of liposomes separately composed of PS and PE.

37 Although the TDS and PE both significantly affected the sensory profile of th

38 e as necessary to achieve the target TDS and PE.

39 iTrEnDi-modified PC ([PC(Tr)](+)) and PE ([PE(Tr)](+)) showed similar sensitivity enhancements

40 contrast to lipid-depleted starved animals, PE-fed caterpillars maintain lipid reserves similar to h

41 atty acids, which were falsely identified as PE by the applied analytical methods.

42 Male sex, presentation as PE (particularly if concomitant proximal DVT), a positiv

43 uring moderate intensity exercise attenuated PE-mediated vasoconstriction (DeltaFVC: -13 +/- 1 and -1

44 These data provide novel insights into beta-PE biosynthesis and advance our understanding of the mec

45 the similarity in chemical structure between PE and its natural honeycomb diet has endowed larvae of

46 asminogen activator) was 14 mgs in bilateral PE and 12 mgs in unilateral PE over 8 hours delivered vi

47 r, exogenous NBD-phosphatidylcholine, Bodipy-PE, and TopFluor-cholesterol were rapidly trafficked to

48 Liposomes containing both PE and PS bound to GAS6 and were engulfed by AXL-express

49 ilms show no significant oxidation caused by PE-ALD of Al(2)O(3).

50 mechanism by which virulence is regulated by PE synthesis is only partially understood.

51 An acyltransferase, called PE, subsequently catalyzes the transfer of phleic acids

52 Using the combined PE-MYH7-ACMG framework, the VUS decreased significantly

53 Among 38 025 patients with confirmed PE (53.1% female, age: 67.3+/-17 years), computed tomogr

54 we evaluated nanosafety of Gd-lip containing PE-DTPA chelating Gd(+3) prepared by lipid film hydratio

55 to phosphate-buffered saline (PBS) controls (PE = 84.1%; P < 0.02).

56 the addition of phenotype-enhanced criteria (PE-ACMG) using the HCM Genotype Predictor Score can furt

57 -energy CT (DECT) as part of the standard CT-PE protocol at a subset of the hospitals.

58 rmed COVID-19 infection who had undergone CT-PE between March 23 and April 6, 2020, in a large urban

59 rease virulence, and mutations that decrease PE synthesis decrease virulence.

60 Decreased PE synthesis from loss of EPT1 or PSD1 and PSD2 leads to

61 In contrast to mutants with decreased PE synthesis, there were no transcriptional differences

62 irulence observed for mutants with deficient PE synthesis.

63 for plasma enhanced atomic layer deposition (PE-ALD) of Al(2)O(3) on graphene for top gated field eff

64 GA], 16-24 weeks) who subsequently developed PE and 66 GA-matched controls with normal outcomes (mid-

65 lmonary angiographic examinations diagnosing PE.

66 ility of this biomarker panel to distinguish PE from non-PE, with comparable discrimination power to

67 catalyse the transfer of PEA from the donor PE lipid substrate to the recipient lipid A molecule by

68 ted girls, and the protective effectiveness (PE) for all girls were estimated.

69 the immunogenicity and protective efficacy (PE) of a refined and more stable chimera comprised of a

70 Asthma and pulmonary embolism (PE) can present with overlapping symptoms, and distingui

71 o automatically classify Pulmonary Embolism (PE) cases.

72 odality for diagnosis of pulmonary embolism (PE) could be influenced by provider, patient or hospital

73 f diagnostic testing for pulmonary embolism (PE) in US emergency departments (EDs), and no data have

74 Pulmonary embolism (PE) is a leading cause of maternal mortality, and deep v

75 Acute pulmonary embolism (PE) is associated with high morbidity and mortality beca

76 ein thrombosis (DVT) and pulmonary embolism (PE), is the third most common cause of vascular death af

77 acute intermediate-risk pulmonary embolism (PE).

78 ted endemism (WE) and phylogenetic endemism (PE) separately for all birds and amphibians across the g

79 s the agent-specificity of prediction error (PE) circuits for at least 24 h, modulating the extent to

80 ratings was reduced when prediction errors (PEs) increased, but pain perception was only partially u

81 chical precision-weighted prediction errors (PEs), and disturbances of this putative process play a k

82 ESBL-PE isolates underwent polymerase chain reaction-based de

83 ntention-to-treat analysis compared 209 ESBL-PE carriers in the baseline phase to 269 in the interven

84 Among the 90 ESBL-PE carriers, manifestations of Enterobacteriaceae infect

85 sh travelers, 90 (21%) of whom acquired ESBL-PE abroad.

86 as ExPEC/UPEC than DEC, travel-acquired ESBL-PE are more often associated with TD than UTI.

87 % to -.8%]), and rates of SSI caused by ESBL-PE were 6.5% and 0.9%, respectively (ARD, -5.6% [95% CI,

88 urvey identified 4 laboratory-confirmed ESBL-PE infections among the 430 travelers, all in subjects w

89 Laboratory-confirmed ESBL-PE infections were surveyed 5 years before and after tra

90 lactamase-producing Enterobacteriaceae (ESBL-PE) who receive cephalosporin-based prophylaxis have twi

91 se (ESBL)-producing Enterobacteriaceae (ESBL-PE), with undefined clinical consequences.

92 Screening for ESBL-PE carriage before colorectal surgery and personalizing

93 Patients were screened for ESBL-PE carriage before elective colorectal surgery.

94 tion phase, guidelines were changed for ESBL-PE carriers to receive ertapenem.

95 Despite more ESBL-PE strains qualifying as ExPEC/UPEC than DEC, travel-acq

96 Of ESBL-PE, 3 (3%) were ExPEC/UPEC-EAEC hybrids (2 associated wi

97 Potential ESBL-PE infections were detected in 15 of 90 subjects (17%).

98 travelers, all in subjects who screened ESBL-PE negative after returning home from their index journe

99 We tested whether ESBL-PE screening and personalized prophylaxis with ertapenem

100 d overdose" (threshold, 85%; point estimate [PE], 95.8%; 95% confidence interval [CI], 94.0 to 97.1)

101 nd have four substrate classes, namely, Esx, PE, PPE, and Esp proteins.

102 ates the secretion of a specific set of Esx, PE, and PPE proteins, raising the question of how these

103 hene (T(4)) and tetra(phenylene ethynylene) (PE(4)) donor blocks capped with a naphthalene diimide (N

104 ormed on strains with deficient or excessive PE biosynthesis to elucidate the mechanism.

105 SFs contain ultraconserved poison exon (PE) sequences that exhibit greater identity across speci

106 in various deimmunized Pseudomonas exotoxin (PE) domains.

107 n yields, as measured by percent extraction (PE), spanning the range of the classic Coffee Brewing Co

108 psis thaliana) for deconjugation of folates (PE-LC-MS/MS), or animal-origin deconjugase (rat serum an

109 sensitivity (95%) and specificity (71%) for PE diagnosis at 1394 ng/mL d-dimer units.

110 Methods: We identified adults evaluated for PE with VQ or CTPA from 2012 to 2016.

111 nges and PM are independent risk factors for PE particularly in primigravida.

112 Asthma may limit imaging for PE because of either worsened ventilation defects on ven

113 sample preparation, may also be mistaken for PE.

114 The yield rate for PE from CTPA scans was 1.3% (1.1%-1.5%) in Indiana and 4

115 the total volume) had a diagnostic test for PE, including 25 870 patients who had CTPA order without

116 Over-testing for PE in American EDs remains a major public health problem

117 We hypothesized that over-testing for PE remains a problem.

118 order without D-dimer (59% of all tests for PE).

119 traordinary capability to derive energy from PE as an exclusive food source through pre-existing meta

120 , and publicly available press releases from PE firms or platform companies.

121 A conserved motif (A[S/T]GGG[N/G]PE(946)) immediately upstream of E946 was identified in

122 Mutants in other proline-glutamate (PE)/PPE clusters, responsive to magnesium and phosphate,

123 and 382.3736 m/z) and glycerophospholipids (PE (P-16:0/22:6, m/z 746.5099, and PS (38:3), m/z 812.54

124 nts testing positive for COVID-19, 37.1% had PE, higher than 14.5% of pre-COVID-19 patients (P = .007

125 (PNPLA9, iPLA2beta), known to metabolize Hp-PE to lyso-PE and oxidized fatty acid, in mitigating fer

126 renoyl (C22:4)- phosphatidylethanolamine (Hp-PE).

127 Production of 15-HpETE-PE depends on activation of 15-lipoxygenase-1 (15LO1) in

128 generated ferroptotic phospholipid, 15-HpETE-PE, promoted LC3-I lipidation to stimulate autophagy.

129 rachidonoyl-phosphatidylethanolamines (HpETE-PEs) as proximate death signals.

130 plastics and macroplastics from identifiable PE packaging were collected in the Atlantic Ocean and co

131 In PE, systemic complement levels are further increased, an

132 the physical mechanisms of embrittlement in PE exposed to the marine environment.

133 tive pathway 50 (AP50) values were higher in PE pregnancies.

134 ol dehydrogenase) are considerably higher in PE-fed larvae, indicating that on a functional level, th

135 fetal CD46 SNPs were significantly higher in PE.

136 ce fibrinolysis and decrease inflammation in PE and DVT patients, respectively, and offers insights i

137 inhibitor activity is under investigation in PE patients to enhance endogenous fibrinolysis, whereas

138 t influenced aldehyde composition, mainly in PE and in total PL.

139 nal CFH/C3 variants were highly prevalent in PE patients compared to normotensive pregnancies.

140 evels of soluble CORIN have been reported in PE and are supposed to be cardiac in origin.

141 ncrease in CORIN production and secretion in PE cases compared with controls.

142 ly enhanced placental adenosine signaling in PE remains unclear.

143 d when measured against stepped increases in PEs.

144 rete a distinct set of substrates, including PE and PPE families of proteins, named for conserved Pro

145 Thus, mutations that increase PE synthesis increase virulence, and mutations that decr

146 d D-dimer ordering correlated with increased PE yield rate (Pearson's R(2)=0.43; P<0.001).

147 4)NDI or T(4)PE(2)NDI due to an insufficient PE(n) bridge length.

148 ntly diminished the expression of high-level PE responses, implying that NMDAR antagonism disrupts th

149 (102-207 ms poststimulus), while high-level PEs (about transition probability) are reflected by late

150 l-by-trial analysis indicated that low-level PEs (about stimulus transitions) are expressed early (10

151 PLA2beta), known to metabolize Hp-PE to lyso-PE and oxidized fatty acid, in mitigating ferroptosis in

152 compared, between 2005 and 2019, for massive PE (MPE) versus high-risk submassive PE (SMPE).

153 inducing pathways to effectively metabolize PE.

154 efficient extraction method yielding 3.6 mg PE/g biomass under the optimal conditions (t1 = t2 = 10

155 Furthermore, the combination of MTP-PE and IFN-gamma on AML blasts generated an inflammatory

156 myl tripeptide phosphatidylethanolamine (MTP-PE), a synthetic ligand for NOD2.

157 murine model of AML, dual treatment with MTP-PE and IFN-gamma led to a significant increase in mature

158 Multidisciplinary PE response teams can aid in selection of appropriate ma

159 In a large multinational PE registry, variations were observed in the use of imag

160 ency of these processes is enhanced, namely, PE synergizes with PS to promote PS receptor-mediated vi

161 ed in the Atlantic Ocean and compared to new PE boxes.

162 re subsequently sold or recapitalized to new PE investors by the end of this study period with a medi

163 effects of these tests on PE-related and non-PE-related outcomes warrant further investigation.

164 s biomarker panel to distinguish PE from non-PE, with comparable discrimination power to that of the

165 They comprised of 69 women without PE (non-PE group) and 65 women diagnosed with PE (PE group).

166 y higher in the PE group compared to the non-PE group.

167 s each EspG to discriminate among noncognate PE-PPE pairs.

168 only current structural characterization of PE-PPE-EspG heterotrimers is from the ESX-5 system.

169 ing to Nanodiscs with unique compositions of PE and PS were determined.

170 and underscore the important contribution of PE in these major biological processes.IMPORTANCE Phosph

171 ma can accurately predict the development of PE and showed good discriminatory power in patients with

172 Future research should assess the impact of PE investment on patient, provider, and practice metrics

173 n malaria-endemic regions, high incidence of PE is reported, with debilitating foeto-maternal effects

174 a complementary measurement of the length of PE polymer chains extending through the crystalline lame

175 ese findings might improve the management of PE in malaria-endemic regions.

176 oantibody (AT(1) -AA)-induced mouse model of PE.

177 The reactive nature of PE-ALD enables deposition of thin (2 nm) dielectrics dir

178 ere the 2 states with the greatest number of PE acquisitions with 22 and 19, respectively.

179 ates can cause substantial overestimation of PE.

180 gle X-ray scattering examines the packing of PE chains into semicrystalline lamellae.

181 Global patterns of PE can provide insights into complex evolutionary proces

182 ated with impaired diagnostic performance of PE imaging for either VQ or CTPA.

183 A(2B) receptor (ADORA2B) in the placentas of PE mouse models induced by AT(1) -AA or LIGHT, a TNF sup

184 can readily detect formation of 100 pmol of PE produced from Escherichia coli membranes, Candida alb

185 mester biomarker panel for the prediction of PE with five metabolites (SM C28:1, SM C30:1, LysoPC C19

186 as yet been proven useful for prediction of PE.

187 The presence of PE on the same surface as PS dramatically enhances recog

188 demonstrate that simultaneous recognition of PE and PS maximizes PS receptor-mediated virus entry and

189 ), and caused a dose-dependent relaxation of PE-induced contraction of aortic vascular rings.

190 can be used to stratify patients in terms of PE risk and severity.Supplemental material is available

191 t with lower fluorescence yield than that of PE.

192 ly functionally relevant in the unloading of PE-PPE heterodimers at the secretion machinery.

193 higher D-dimer ordering had higher yield of PE on CTPA.

194 signaling may elicit therapeutic effects on PE.

195 ts, and downstream effects of these tests on PE-related and non-PE-related outcomes warrant further i

196 theter-directed fibrinolysis in the OPTALYSE-PE trial (Optimum Duration and Dose of r-tPA With the Ac

197 First unprovoked proximal DVT or PE may be treated for 3 to 6 months or indefinitely.

198 cer), or a second unprovoked proximal DVT or PE, is generally treated indefinitely.

199 ngiography, a combination of these tests, or PE signs and symptoms plus imaging-confirmed proximal de

200 omographic pulmonary angiography to rule out PE unnecessary in 39%.

201 Total PL and PC, PE, phosphatidylinositol + phosphatidylserine and CL con

202 The ratio of PC/PE was clearly lower in HH group indicating a shift from

203 on-PE group) and 65 women diagnosed with PE (PE group).

204 iTrEnDi-modified PC ([PC(Tr)](+)) and PE ([PE(Tr)](+)) showed similar sensitivity enhancements and

205 evaluates the potential circularity of PET, PE, and PP flows in Europe based on dynamic material flo

206 ular contractility induced by phenylephrine (PE), and caused a dose-dependent relaxation of PE-induce

207 al intra-arterial infusion of phenylephrine (PE; alpha(1) -agonist) during (i) infusion of an endothe

208 Functional responsiveness to phenylephrine (PE) and sodium nitroprusside (SNP) decreased over time f

209 richment analyses, phosphatidylethanolamine (PE) plasmalogens were positively enriched for associatio

210 dylserine (PS) and phosphatidylethanolamine (PE) are usually sequestered to the inner leaflet of the

211 rgy between PS and phosphatidylethanolamine (PE)-a lipid of much higher abundance naturally.

212 rdiolipin (CL) and phosphatidylethanolamine (PE).

213 ncodes enzymes for phosphatidylethanolamine (PE) biosynthesis; however, exogenous NBD-phosphatidylcho

214 ally, elevation in phosphatidylethanolamine (PE), sphingomyelin (SM), phosphatidylcholine (PC) and th

215 tidylcholine (PC), phosphatidylethanolamine (PE), and triacylglycerol (TAG) species (> 50% of total l

216 tidylcholine (PC), phosphatidylethanolamine (PE), cardiolipin (CL) and sphingomyelin contents were hi

217 tidylcholine (PC), phosphatidylethanolamine (PE), phosphatidic acid (PA), and sphingomyelin (SM) in a

218 f the phospholipid phosphatidylethanolamine (PE) is required for virulence.

219 Here, we show that phosphatidylethanolamine (PE) synergizes with PS to enhance PS receptor-mediated e

220 idylserine (PS) to phosphatidylethanolamine (PE), a critical step in membrane biogenesis and a potent

221 ex lipids such as phosphatidylethanolamines (PE), lactosylceramides (LCER) and phosphatidylinositols

222 phosphocholine (PC) or phosphoethanolamine (PE) substituents.

223 The yield of phycoerythrin (PE) extracted, determined spectroscopically, was used as

224 uces an elastic stress in the piezoelectric (PE) layer, which generates a PE potential that can be us

225 ROP), generated their respective polyesters (PE) or poly(ester amides) (PEA).

226 There appeared to be polyethylene (PE) in almost all investigated glove leachates and with

227 Blanks revealed consistent polyethylene (PE), poly(ethylene terephthalate) (PET), and polypropyle

228 aterpillars fed honeycomb, fed polyethylene (PE), or starved for up to 72 h.

229 ng pristine and weathered MPs (polyethylene (PE) and polystyrene (PS) microspheres, and polyester (PE

230 rrangements of semicrystalline polyethylene (PE) packaging waste with the aim of understanding the ph

231 s responsible for off-odors in different PP, PE, multilayer cardboard and paper materials used for fo

232 in mid-trimester maternal plasma to predict PE.

233 This metabolomic model predicted PE better than PlGF (AUC [95% CI]: 0.868 [0.844-0.891] v

234 Preeclampsia (PE) is a hypertensive disease of pregnancy associated wi

235 Preeclampsia (PE) is a placental disorder with different phenotypic pr

236 Preeclampsia (PE) is a pregnancy specific hypertensive disorder.

237 patients at risk of developing preeclampsia (PE) would allow providers to tailor their prenatal manag

238 status with increased risk of Preeclampsia (PE) development.

239 osine signaling contributes to preeclampsia (PE).

240 Larger pristine PE MPs were the most resistant to coagulation and floccu

241 ept1Delta/Delta mutant, which cannot produce PE by the Kennedy pathway, exhibits decreased kidney fun

242 e, 63 years; range, 18-95 years) with proven PE.

243 We define sequences that regulate PE inclusion and protein expression of the oncogenic SF

244 xistence of multiple, hierarchically related PEs in a "roving MMN" paradigm.

245 Sequencing of gut transcripts revealed PE-fed larvae retain an expression profile consistent wi

246 ite anticoagulation and those with high-risk PE require additional advanced therapies, typically focu

247 therapy for both intermediate- and high-risk PE.

248 Patients with intermediate-risk PE who subsequently deteriorate despite anticoagulation

249 ility study of the BEC for intermediate-risk PE, there were no deaths or device-related adverse event

250 dulating the extent to which another agent's PE is experienced as one's own and influencing perspecti

251 ther factors did not demonstrate significant PE association.

252 massive PE (MPE) versus high-risk submassive PE (SMPE).

253 In women with suspected PE, the pregnancy-adapted YEARS algorithm is safe and ef

254 Patients with symptomatic PE and right ventricular to left ventricular diameter ra

255 2Delta/Delta mutant, which cannot synthesize PE by the cytidine diphosphate diacylglycerol (CDP-DAG)

256 nd proteomic approaches, we established that PE of Mycobacterium smegmatis is exported to the cell en

257 duction Trial (VDAART), we hypothesized that PE, maternal asthma, vitamin D insufficiency, and excess

258 We show that PEs in serine-arginine-rich (SR) proteins, a family of 1

259 The PE-LC-MS/MS provides fast quantification of various fola

260 of the mycobacterial outer membrane, and the PE/PPE proteins apparently act as solute-specific channe

261 tophagy inhibition, six of which encoded the PE/PPE protein family.

262 For the PE/PPE heterodimers, it has been shown that they interac

263 fast photoinduced electron transfer from the PE(4) segment to NDI when excited at 370 nm, but it does

264 charge separation (~4 ps) occurring from the PE(4) segment to NDI when excited at 370 nm, followed by

265 e previously solved ESX-5 heterotrimers, the PE-PPE heterodimer of our ESX-3 heterotrimer is interact

266 proportions were significantly higher in the PE group compared to the non-PE group.

267 on was investigated versus the length of the PE bridge unit in oligomers featuring zero and two PE un

268 nes the molecular weight distribution of the PE polymer chains and differential scanning calorimetry

269 clinically challenging manifestations of the PE spectrum.

270 ngths that offer selective excitation of the PE(4) and T(4) blocks.

271 Proper secretion of the PE-PPE proteins requires the presence of EspG, with each

272 s to changes in predicted threat despite the PEs (p < 0.05, corrected).

273 Differential expression of these PE/PPE proteins was observed in response to various stre

274 Mycobacterium smegmatis confirmed that these PE/PPE proteins inhibit autophagy and increase intracell

275 er in HH group indicating a shift from PC to PE.

276 layers on top of graphene channels prior to PE-ALD, the graphene is protected from oxidation enablin

277 specific complotypes and predispose women to PE.

278 o reverse the increased skipping of TRA2beta-PE detected in breast tumors, altering breast cancer cel

279 RS domain activity on regulation of TRA2beta-PE using CRISPR artificial SFs.

280 dge unit in oligomers featuring zero and two PE units (T(4)NDI and T(4)PE(2)NDI).

281 ur original HN3-immunotoxin with a wild-type PE domain (HN3-PE38).

282 mgs in bilateral PE and 12 mgs in unilateral PE over 8 hours delivered via the expanded BEC.

283 If untreated PE leads to life threatening condition, eclampsia.

284 and 99% were measured for PEST and weathered PE, respectively.

285 lower and 25% higher results was found when PE-LC-MS/MS was compared to MA and AE-LC-MS/MS, respecti

286 ous thrombosis, thus resulting in 38.7% with PE or deep venous thrombosis, despite 40% receiving prop

287 Factors associated with PE and arterial obstruction severity were evaluated by u

288 6.6, 95% CI 2.4-18.2) to be associated with PE.

289 of 15-lipoxygenase-1 (15LO1) in complex with PE-binding protein-1 (PEBP1).

290 E (non-PE group) and 65 women diagnosed with PE (PE group).

291 g mycobacteria, these findings obtained with PE from M. smegmatis may offer clues to glycolipid forma

292 One hundred thirty-six patients with PE (92 with SMPE and 44 with MPE) were identified.

293 cted outcome in this cohort of patients with PE and no cardiopulmonary disease, and it may provide a

294 d good discriminatory power in patients with PE at delivery.

295 otic syndrome, and up to 4% of patients with PE develop chronic thromboembolic pulmonary hypertension

296 metabolomic panel to identify patients with PE was compared also to a commonly used standard, the pl

297 um falciparum infection in the placenta with PE is underexplored.

298 ne-bis-aldehyde (DSB-3), whose reaction with PE produces a fluorescence signal.

299 a subset of conserved "core epitopes" within PE/PGRS domains are elicited during early TB.

300 They comprised of 69 women without PE (non-PE group) and 65 women diagnosed with PE (PE gro