ライフサイエンスコーパス: PS

1 PS and SiO(2) beads affected the food availability of C.

2 PS has been associated with transgenerational passage of

3 PS oleogel was the firmest sample followed by RW and MG

4 PS was treated with acetic acid and sodium bicarbonate t

5 PS-modified nucleic acid therapeutics show improved meta

6 PS-MS was used in the identification and quantification

7 PS-NPs were mainly detected in the intestine and brood c

8 PS-OCT imaging enables the visualization of significant

9 PS/TAC pre-treatment caused greater TAC internalization

10 of the c(8)-ring module to the complete F(1)-PS complex.

11 The Li(3) N-LiF layer coating on Li(3) PS(4) SSE achieves a record-high critical current of >6

12 The Li(3) N-LiF/Li(3) PS(4) SSE enables LiCoO(2) cathodes to achieve 101.6 mAh

13 in an archetypical sodium-ion conductor Na(3)PS(4) are not fully understood.

14 ctivation volume for Na(+) migration in Na(3)PS(4), which is ~30% higher for the ball-milled samples.

15 the synthesis-property relationships in Na(3)PS(4).

16 cy was obtained with a pH of 7 and a ZnSO(4)/PS ratio of 1:1, and the removal ratio of NOF reached 95

17 The pH, the ZnSO(4)/PS ratio, and ions and quenchers, were investigated.

18 PET-2 was classified according to both 5-PS and percentage DeltaSUV.

19 , all had FDG-avid disease at baseline; by 5-PS, 55 (35%) remained positive on i-PET and 28 (18%) on

20 ation: the Deauville visual 5-point scale (5-PS) and a change in SUV (DeltaSUV) by semiquantitative e

21 using the visual Deauville 5-point scale (5-PS), and by calculating percent change in FDG uptake (ch

22 Visual 5-PS on i-PET did not predict outcome.

23 Results: Both with 5-PS and with DeltaSUV-based evaluations, significant diff

24 toff was 48.9% and that when combined with 5-PS assessment, a positive PET-2 result was highly predic

25 PA (n = 56), PS (n = 42) and nonsensitized nonallergic (NA, n = 10) p

26 n supported lipid bilayers (SLBs), forming a PS-Zn(2+) complex with an equilibrium dissociation const

27 ICAM-1 and neutrophil adhesion levels, in a PS-dependent manner, compared with MPs collected at stea

28 pre-photosensitizer as it is converted to a PS by the mutual presence of glutathione (GSH) and hydro

29 ively charged (amine-modified polystyrene; a-PS) or negatively charged (polystyrene; PS) particles th

30 tality was lower with warfarin versus no AC (PS matched: hazard ratio [HR], 0.65; 95% confidence inte

31 ; 95% CI, 0.40-0.73) and DOACs versus no AC (PS matched: HR, 0.68; 95% CI, 0.50-0.93; MSM models: HR,

32 t, to our knowledge, AFM imaging of adsorbed PS films under physiologically relevant conditions using

33 ous studies have suggested that the adsorbed PS film is composed of an interfacial monolayer, plus a

34 After PS training, increases of 30%, 25% and 8% (P < 0.05) in

35 = 704 in the warfarin and DOAC cohorts after PS matching, respectively) with a median of 4.6 years of

36 holipids (PE (P-16:0/22:6, m/z 746.5099, and PS (38:3), m/z 812.5440)].

37 0.66-0.71) and 0.64 (0.59-0.68) for DCGS and PS.

38 C was also involved in both Ca(2+) entry and PS exposure.

39 Yoda1 caused an increase in [Ca(2+)](i) and PS exposure, which was inhibited by its antagonist Dooku

40 Maternal Pb and PS exposures were carried out in F0 mice.

41 to be altered by Pb, PS, or combined Pb and PS in F1 offspring: behavioral performance [fixed-interv

42 rone levels, whereas F3 males showed Pb- and PS-related alterations in behavior and total percent DNA

43 Liposomes containing both PE and PS bound to GAS6 and were engulfed by AXL-expressing cel

44 rate that simultaneous recognition of PE and PS maximizes PS receptor-mediated virus entry and effero

45 Nanodiscs with unique compositions of PE and PS were determined.

46 peri-implant mucosa as a response to PM and PS appear negligible.

47 a strong correlation between anemia and anti-PS antibodies.

48 amyloid precursor protein/presenilin-1 (APP/PS-1) human transgenic double-knock-in mouse model of AD

49 The presence of PE on the same surface as PS dramatically enhances recognition of PS by PS-binding

50 Baseline models were CARES and ASA-PS.

51 Batch (PS: Pot Still) or continuous (CS: Coffey Still) distilla

52 has tended to explore relationships between PS deficits and specific diagnoses in isolation of one a

53 measurements differed significantly between PS and SPECT/CT in right lung lobes, with a mean differe

54 on parameters differed significantly between PS and SPECT/CT, no significant differences were found b

55 s manuscript, we investigate synergy between PS and phosphatidylethanolamine (PE)-a lipid of much hig

56 icipants were randomly assigned to bilateral PS (n = 14), monolateral PS (n = 13) or no PS training (

57 mediated by GRAMD1/Aster proteins that bind PS and cholesterol.

58 te the entry of enveloped viruses by binding PS in the virion membrane.

59 Our data indicate that M6PR binds PS-ASOs and facilitates their vesicular escape.

60 lacked Sting or gap junctions were blocked, PS-GAMP-mediated adjuvanticity was substantially abrogat

61 artery FMD%, respectively, occurred in both PS training groups.

62 ure, and modification of any such effects by PS, is unknown.

63 S dramatically enhances recognition of PS by PS-binding proteins such as GAS6, PROS, and TIM1.

64 aflet where they are recognized by so-called PS receptors on surveilling phagocytes.

65 both produce structurally identical capsular PS, and their genetic backgrounds influence the amount o

66 , both produce chemically identical capsular PS.

67 istics showed that flavonoids characterizing PS were the most discriminant compounds during the in vi

68 nsitivity to positive and negatively charged PS nanoparticles, illustrating their potential value as

69 much more efficiently than those containing PS alone.

70 d regarding their potential as pH-controlled PS for PDT.

71 tematic analysis to determine if controlling PS chirality in the DNA gap region can enhance the poten

72 We also found that controlling PS chirality of only two PS linkages in the DNA gap was

73 erall, our work shows that while controlling PS chirality can modulate RNase H1 cleavage patterns, AS

74 nts when compared to WS, and, after cooking, PS flours had greater resistant starch (from 4.2 to 21.4

75 halpy required (~44%) to gelatinize cornmeal-PS blend and the tendency for retrogradation (from 2188

76 Reduction of M6PR levels also decreased PS-ASO activity in mouse cells and in livers of mice tre

77 PS-ASO release from endosomes and decreased PS-ASO activity in human cells.

78 , Child-Pugh class A liver disease, and ECOG PS 0-1.

79 e analysis identified baseline TMTV and ECOG PS as independently associated with PFS and OS.

80 tive Oncology Group Performance Status (ECOG PS) 0-1, and following management of esophageal varices,

81 Moreover, TMTV combined with ECOG PS may identify an ultra-risk DLBCL population.

82 significant association between SMI and ECOG-PS (p = 0.0324), while no correlations were found regard

83 First, we tested an ED/PS cell in series with pertraction and achieved a maximu

84 Second, we evaluated our ED/PS as a stand-alone unit when integrated with the anaero

85 anolamine (PE) synergizes with PS to enhance PS receptor-mediated efferocytosis and virus entry.

86 evented by blocking accessibility of exposed PS using Annexin V or through microglial loss of TREM2.

87 Externalised PS is prothrombotic and attractive to phagocytes and act

88 t machinery between LE and Golgi facilitates PS-ASO release.

89 In mealworms fed PS containing high HBCD levels, only 0.27 +/- 0.10%, of

90 In the ocean, foamed PS is subject to wind-assisted transport and fracturing

91 tro-intestinal blockage, ingestion of foamed PS exposes animals to harmful chemicals, and of greatest

92 This review focuses on foamed PS in the marine setting, including its sources, transpo

93 GCTs) is 10%-20% but increases to >= 50% for PS IIB disease.

94 To adjust for PS, principal component analysis (PCA)-based ancestry pr

95 ith midpoint survival analyses, adjusted for PS-quintile.

96 h negative binomial regression, adjusted for PS-quintile.

97 Adjuvant EPx2 for PS II NSGCT is highly effective, has acceptable toxicity

98 rrelation coefficient (ICC) between the four PS measures, as well as PC1, were calculated to assess r

99 chirality into the backbone such that a full PS 16-mer oligonucleotide is comprised of 215 distinct s

100 -binding protein PC4, in complex with a full PS 2'-OMe DNA gapmer ASO.

101 ility of different doses of the HB-CS and HB-PS to flocculate 2 and 10 wt % MFT, prepared by diluting

102 B) corn starch (HB-CS) and potato starch (HB-PS), with lower critical solution temperatures (LCSTs) r

103 In terms of ISRs, the HB-PS was a considerably better flocculant than the HB-CS,

104 Hence, PS-SGCLs provide a platform to systematically elucidate

105 However, PS exposure did not necessitate an increase in [Ca(2+)](

106 lexes that regulate clot formation; however, PS is of limited abundance physiologically.

107 polymer type (hydrophilic PAN or hydrophobic PS), CNT loading (i.e., values increased with weight per

108 Photosystem II (PS II) captures solar energy and directs charge separati

109 in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activ

110 In PS-quintile-adjusted analysis, those on newer DMTs had a

111 ifically M6PR shuttling mediated by GCC2, in PS-ASO trafficking and activity.

112 nding to one Ara h 9 peptide were greater in PS than in PA patients.

113 t deposition location and spray stability in PS-MS and the ionization region humidity and analyte eva

114 sis decreased as oleogel strength increased (PS < RW < MG).

115 In contrast, increasing PS content enhanced accumulation of asymmetric compounds

116 t Daphnia (F0) were exposed to 1 and 50 mg/L PS-NPs until the production of the neonates (F1) followe

117 l theory (TDDFT) calculations on the largest PS II RC model reported to date.

118 ynthetic glycopeptide combinatorial library (PS-SGCL) that vary in number and location of cancer-asso

119 These studies reveal that one lipid-PS-controls the movement of another lipid-cholesterol-be

120 We assessed pre-LT PS using the 5-point modified Eastern Cooperative Oncolo

121 ultaneous recognition of PE and PS maximizes PS receptor-mediated virus entry and efferocytosis and u

122 In binomial regression models, PSs indexing 6 risk factors (major depressive disorder [

123 Modified PS ASOs display better binding affinity to the target RN

124 r container is a strategy to directly modify PSs, enlightening the precise regulation on Li-S batteri

125 Here, monodisperse PS nanoparticles (MPNPs) are synthesized via emulsion po

126 signed to bilateral PS (n = 14), monolateral PS (n = 13) or no PS training (n = 12).

127 Moreover, PS ASO protein interactions can affect many aspects of t

128 m platelets, and that it was abolished by MP PS capping using annexin V.

129 nd sensitivity to polystyrene nanoparticles (PS) were evaluated.

130 ry NPs, fluorescent polystyrene nanospheres (PS-NPs; 20 nm), and water leachate of weathered single-u

131 ure and topography of animal-derived natural PS films at physiologically relevant low surface tension

132 l PS (n = 14), monolateral PS (n = 13) or no PS training (n = 12).

133 Despite the vast O-PS chemical diversity, most are produced in bacterial ce

134 The activity of PS-ASOs is strongly influenced by association with both

135 The addition of PS restores cholesterol transport to the ER.

136 nto the origins for the enhanced affinity of PS for proteins.

137 d new avenues for the medicinal chemistry of PS-ASOs and research on all elements of the molecular ph

138 rved when amphiphilic triblock copolymers of PS-block-poly(2-vinylpyridine)-block-poly(ethylene oxide

139 ng a synergistic anti-inflammatory effect of PS/drug formulations.

140 e conclude that the environmental effects of PS ingestion need further evaluation as the generation o

141 We investigated the effects of PS training on vascular function and stiffness of the in

142 The efficacy of PS-assisted TAC vehiculization was also evaluated in viv

143 a result of reduced microglial engulfment of PS(+) presynaptic inputs.

144 retinogeniculate synapses and engulfment of PS-labeled material by microglia occurs during establish

145 Our examination of PS in a large, transdiagnostic sample suggested more spe

146 ccordingly, we got a positive fingerprint of PS when just 10 ng of the polymer was present within the

147 ited Kingdom and Ireland to assess impact of PS on mortality separately for HCC and non-HCC recipient

148 ith which PS ASOs interact, the influence of PS ASO protein interactions on ASO performance, and the

149 ve profound influences on the interaction of PS-ASOs with specific proteins.

150 known about the chemistry of interaction of PS-ASOs with this protein.

151 cular forces that govern the interactions of PS ASOs with cellular proteins and provide a potential m

152 the structural basis of the interactions of PS nucleic acids with proteins.

153 The mechanism of PS exposure remains uncertain but it can follow increase

154 D) are caused by inheritance of mutations of PS.

155 pecific for PSD and in which the presence of PS causes only negligible background.

156 -HCC recipients and across the full range of PS.

157 e as PS dramatically enhances recognition of PS by PS-binding proteins such as GAS6, PROS, and TIM1.

158 and the structure activity relationships of PS ASO modification and protein interactions.

159 ith large, quasi-permanent reorientations of PS(4)(3-) anions.

160 As a result, the role of PS chirality on the performance of antisense oligonucleo

161 Elucidating the multifunctional roles of PS receptors in virus-host interaction is important for

162 rd (<10% RSD) and compare the sensitivity of PS-MS and TDGD-MS.

163 o results establish the potential utility of PS to open novel effective delivery strategies for inhal

164 gical studies have emphasized the overlap of PSs and other psychiatric illnesses.

165 phosphorothioate antisense oligonucleotides (PS-ASOs) from late endosomes (LEs) is a rate-limiting st

166 e one interface binds the 5'-terminal 2'-OMe PS flank of the ASO, while the other interface binds the

167 Spectroscopic studies on PS II RCs are difficult to interpret due to large spectr

168 For each individual, one PS and one platform-matching (PM) implants were placed u

169 t exposures of previous generations to Pb or PS may influence the brain and behavior of future genera

170 nally, the PS/TAC combination but not TAC or PS alone attenuated the LPS-induced pro-inflammatory eff

171 ian cohort enrolled 542 patients with TOF or PS and mild to severe TR who underwent isolated PVR (66.

172 xture of beta-sitosterol and gamma-oryzanol (PS).

173 een NIH Toolbox Pattern Comparison and other PS scales (0.14-0.27).

174 g the MRI parameters, the median v(p), F(p), PS, and K(trans) values of the metastatic lymph nodes we

175 In particular, PSs during adolescence appear to be a nonspecific precur

176 tcomes previously found to be altered by Pb, PS, or combined Pb and PS in F1 offspring: behavioral pe

177 ple of a DFT guided search for efficient PDT PSs with a substantial spectral red shift toward the bio

178 Activated persulfate (PS) is a common method used to generate sulfate radicals

179 daptive Pattern Generator Pattern Shaper (PG/PS) architecture that autonomously generates a desired v

180 Phosphatidylserine (PS) exposure is increased in red cells from sickle cell

181 Phosphatidylserine (PS) on presynaptic elements binds GPR56 in a domain-spec

182 membrane components in a phosphatidylserine (PS) dependent manner to assemble multi-protein complexes

183 between immune cells and phosphatidylserine (PS) molecules exposed on the surface of apoptotic-tumor

184 re, we show that exposed phosphatidylserine (PS) represents a neuronal "eat-me" signal involved in mi

185 llular vesicles exposing phosphatidylserine (PS), detected at high concentration in the circulation o

186 cal processes.IMPORTANCE Phosphatidylserine (PS) and phosphatidylethanolamine (PE) are usually seques

187 ainst the membrane lipid phosphatidylserine (PS).

188 talyze the conversion of phosphatidylserine (PS) to phosphatidylethanolamine (PE), a critical step in

189 a significant number of phosphatidylserine (PS)+ platelets in PNAs in CypDplt+/+ mice.

190 Specifically, phosphatidylserine (PS) receptors - including members of the human T cell im

191 enzyme that synthesizes phosphatidylserine (PS), a phospholipid constituent of the inner layer of th

192 how that Zn(2+) binds to phosphatidylserine (PS) lipids in supported lipid bilayers (SLBs), forming a

193 annexin-V (A5) binds to phosphatidylserine (PS)-rich membranes leading to high Ca(2+)-concentrations

194 cally modified and include phosphorothioate (PS) backbone modifications and different ribose and base

195 e often modified using the phosphorothioate (PS) backbone modification which enhances stability from

196 by the distribution of the photosensitizer (PS) and the illuminated area.

197 inical success of approved photosensitizers (PSs), their application is sometimes limited due to poor

198 Currently, photosensitizers (PSs) that are microenvironment responsive and hypoxia ac

199 ene, which encodes a subunit of photosystem (PS) I.

200 S (PS) that has been derived from platelets (PS(plt)) by showing that PS(plt) limits thrombin formati

201 gically relevant zwitterionic polysaccharide PS A1 via an oxime link.

202 Polystyrene (PS) particle models with controlled surface functionaliz

203 nto polyacrylonitrile (PAN) and polystyrene (PS) ENMs.

204 ered MPs (polyethylene (PE) and polystyrene (PS) microspheres, and polyester (PEST) fibers).

205 Foamed polystyrene (PS) that may be either expanded (EPS) or extruded (XPS)

206 The detection limit for polystyrene (PS) obtained is <1 ng of the compound present in a sampl

207 exabromocyclododecane (HBCD) in polystyrene (PS)-degrading mealworms and in mealworm-fed shrimp.

208 The latex monodisperse polystyrene (PS) colloids are important for different advanced applic

209 vestigated the toxic effects of polystyrene (PS) beads (0.1-10.0 mum) and the underlying mechanisms t

210 In this study, polystyrene (PS), Parylene C, and SU-8 thin films of varying thicknes

211 e; a-PS) or negatively charged (polystyrene; PS) particles that flowed into a polydimethylsiloxane (P

212 ulate connections, have elevated presynaptic PS exposure and reduced PS engulfment by microglia.

213 n mortality of the recipient's pretransplant PS is principally limited to the first 3 months after LT

214 ed, namely, PE synergizes with PS to promote PS receptor-mediated virus infection and clearance of ap

215 Psoriasis (PS) is a chronic skin inflammation.

216 Raw PS flours were characterized by greater tannin and kafir

217 elevated presynaptic PS exposure and reduced PS engulfment by microglia.

218 Both reduced PS exposure whilst chelerytherine chloride also reduced

219 while the other interface binds the regular PS DNA central part in the opposite polarity.

220 terol moves to the ER in a process requiring PS.

221 tainer is highly efficient in the reversible PS transformation to multiply affect electrochemical beh

222 tanding puzzle of the function of protein S (PS) that has been derived from platelets (PS(plt)) by sh

223 perative FEV1 and DLCO were derived from SC, PS, and SPECT/CT.

224 ensional planar lung perfusion scintigraphy (PS).

225 AC on outcomes, we applied propensity score (PS) matching and marginal structural models (MSMs) to ac

226 the HerQLes and SF-12 MS and 4/5 (80%) SF12-PS.

227 ing to the proposed genome packaging signal (PS), mutagenesis experiments show that PS is not require

228 laterals terminating in the posterior slope (PS) (T6I), the ventral complex (T6II), and the ventrolat

229 ecies, the container molecule converts small PSs into large organosulfur species.

230 Polyphenols from five pigmented sorghum (PS) flours were in vitro evaluated as possible modulator

231 the relationships between processing speed (PS), mental health disorders, and learning disorders.

232 (RPLND) for patients with pathologic stage (PS) IIA nonseminomatous germ cell tumors (NSGCTs) is 10%

233 nized into F(1)-catalytic, peripheral stalk (PS), and c(8)-rotor ring modules.

234 ed genome editing in human pluripotent stem (PS) cells mainly employ plasmids or ribonucleoprotein co

235 alogy of Fallot (TOF) or pulmonary stenosis (PS) referred for pulmonary valve replacement (PVR).

236 Population stratification (PS) is a major confounder in genome-wide association stu

237 Acute passive stretching (PS) effects on blood flow ( Q ), shear rate ( Y ), and v

238 ilable and also reacts with PSD's substrate, PS, producing an adduct with lower fluorescence yield th

239 ons in individuals experiencing subthreshold PSs and individuals with overt psychotic disorders suppo

240 ndogenous neurosteroid pregnenolone sulfate (PS) and heat, and altered response to ligand modulation.

241 ntial for strategizing pulmonary surfactant (PS) for drug delivery over the respiratory air-liquid in

242 Pulmonary surfactant (PS) is a lipid-protein complex that adsorbs to the air-w

243 We synthesized pulmonary surfactant (PS)-biomimetic liposomes encapsulating 2',3'-cyclic guan

244 predicting 5- and 10-year patient survival (PS) and death-censored graft survival (DCGS) based on 66

245 individuals experiencing psychotic symptoms (PSs) in the general population.

246 on vascular adjustments induced by long-term PS training.

247 Therefore, our findings indicate that PS can contribute to improved phytochemical and function

248 These findings indicated that PS-mediated increase in TAC uptake blunted the pro-injur

249 HPLC analysis revealed that PS flour added compounds which were absent from cornmeal

250 gnal (PS), mutagenesis experiments show that PS is not required for production of infectious SFV or C

251 ved from platelets (PS(plt)) by showing that PS(plt) limits thrombin formation in large veins.

252 Our hypothesis was that PS-induced changes in Q and Y would improve central and

253 Additionally, the PS/TAC combination but not TAC or PS alone attenuated th

254 y of C. elegans, with greater effects by the PS beads.

255 R and of GCC2 with ASOs is influenced by the PS modifications, which have been shown to enhance the a

256 ropic expansion played a bigger role for the PS effects.

257 e ocelli converge in tight apposition in the PS.

258 lternative pathways operate to introduce the PS module (including associated membrane subunits e, f,

259 The observed effect of the PS beads on the nematodes correlated well with the total

260 or the adsorption-induced squeeze-out of the PS film, which likely results in an interfacial monolaye

261 rticle size and structural properties of the PS MPNPs is established by different thermomechanical an

262 The size of the PS MPNPs is tailored by controlling the reaction time, t

263 its OSCP and F(6) The final component of the PS, subunit d, is added subsequently to form a key inter

264 spray, a microhole array patterned onto the PS thin film by laser dewetting was sprayed with dyed PV

265 In one pathway, the PS is built up by addition to the core subunit b of memb

266 understanding of the mechanisms by which the PS film attains low surface tensions and stabilizes the

267 The protein interacts with the PS nucleic acid through a network of electrostatic and h

268 proposed for the direct modification on the PSs species.

269 Therefore, PS flours might be good candidates for the formulation o

270 t viral release reveals a new role for these PS receptors.

271 -0.55), but this did not differ according to PS score (P = 0.39 and 0.61, respectively).

272 nexin A5 (AnxA5) binds with high affinity to PS externalized by apoptotic cells, thereby hindering th

273 of uninfected erythrocytes after binding to PS exposed in their membrane.

274 h 3 were bound more by IgE of PA compared to PS patients on the microarray.

275 via the voltage sensor domain in response to PS stimulation.

276 tion-sensitive optical coherence tomography (PS-OCT) is a high-speed volumetric imaging modality that

277 tion-sensitive optical coherence tomography (PS-OCT) with a conical scanning optics design.

278 er and more robustly compared to traditional PS-OCT metrics.

279 Superior to traditional PSs, the activated aPS contributed to efficient generati

280 nd that controlling PS chirality of only two PS linkages in the DNA gap was sufficient to modulate RN

281 e summarize recent progress in understanding PS ASO protein interactions, highlighting the proteins w

282 GCC2 relocated to LEs upon PS-ASO treatment, and M6PR also co-localized with PS-ASO

283 nstrate a novel computational approach using PS-OCT for the assessment of fibrosis.

284 ory, and various disease comorbidities using PS matching.

285 of ca. < 10% in the positive ion mode using PS-MS/MS.

286 In vivo, PS exposure at both hippocampal and retinogeniculate syn

287 , significantly fewer platelets in PNAs were PS+ in CypDplt-/- counterparts.

288 ctions, highlighting the proteins with which PS ASOs interact, the influence of PS ASO protein intera

289 interactions of divalent metal cations with PS lipids were further investigated by a combination of

290 In anesthetized mice, TAC combined with PS was intra-nasally (i.n) instilled prior administering

291 ial homing of AnxA5 to the TME enriched with PS+ tumor cells, we demonstrate in vivo that fusing tumo

292 shrimp) were fed mealworm biomass grown with PS containing HBCD.

293 O treatment, and M6PR also co-localized with PS-ASOs in LEs or on LE membranes.

294 Up to 30% of the patients with PS develop psoriatic arthritis (PsA), a condition charac

295 All patients with PS II NSGCT seen at Memorial Sloan Kettering Cancer Cent

296 n livers of mice treated subcutaneously with PS-ASO, indicating a conserved mechanism.

297 hosphatidylethanolamine (PE) synergizes with PS to enhance PS receptor-mediated efferocytosis and vir

298 sses is enhanced, namely, PE synergizes with PS to promote PS receptor-mediated virus infection and c

299 in the arteries involved and uninvolved with PS training, suggesting modifications in both central an

300 One-year survival decreased with worsening PS in non-HCC recipients where 1-year survival was 91.9%