ライフサイエンスコーパス: ps

1 can be augmented by protein supplementation (PS).

2 the brain response to the food portion size (PS).

3 ve FS to achieve clear pathological section (PS).

4 from ultrasonic activation of persulfate (US-PS).

5 re of the membrane lipid phosphatidylserine (PS).

6 gm and exploiting phase sensitive detection (PSD).

7 under the P rofile of S hannon D ifference (PSD).

8 dioxythiophene) polystyrene sulfonate (PEDOT:PSS).

9 88; 95% CI: 0.42, 1.34) gains in response to PS.

10 er shows these structures interconvert in 30 ps.

11 cingulate cortex (ACA) are activated during PS.

12 having time separation in the range 10-3000 ps.

13 state show good agreement with data after 15 ps.

14 azacoronene (EH-TAC), gold, and also MoS2 on PS.

15 garine without (control) and with added 7.5% PS.

16 71.8) for Vi-TT and 52.0% (23.2-70.0) for Vi-PS.

17 uring dynamic relaxation is obtained as 0.13 ps.

18 repopulates the ground state with tau = 362 ps.

19 cation for including these covariates in the PS.

20 The MD and PSD.

21 rotein kinase II (CaMKII) to the hippocampal PSD.

22 epresent a potential strategy for preventing PSD.

23 interactions involving Agap2 outside of the PSD.

24 odes for IL-12p35, have been associated with pSS.

25 e IL-12/IL-35 balance in the pathogenesis of pSS.

26 and (iv) low-crystallinity conducting PEDOT:PSS.

27 end toward a lower level among patients with pSS.

28 MA can mysteriously "pass through" layers of PSS.

29 with CD, 12 subjects with moderate to severe PS, 10 subjects with both AD and CD, and 10 HC with no h

30 fied subset of doxorubicin-resistant tumors, PS-1001 resulted in enhanced antitumor activity, increas

31 oteins (viz., GluR1, GluR4, NR1, PSD-95, and PSD-93), that TH cell somata and tapering neurites are a

32 Here, we find that the postsynaptic proteins PSD-93, PSD-95, and SAP102 differentially regulate excit

33 We found that the postsynaptic scaffold PSD-95 (postsynaptic density protein 95) undergoes K63 p

34 rkers in vivo reveal that 20% of spines lack PSD-95 and are short lived.

35 differential participation in complexes with PSD-95 and gephyrin, which may underlie its role in main

36 mutation facilitates the interaction between PSD-95 and its binding partners.

37 Here we show that phosphorylation of PSD-95 at Ser-561 in its guanylate kinase (GK) domain, w

38 How MEF2 activation results in PSD-95 degradation and why this is defective in Fmr1 KO

39 NMDA receptors, drives rapid, CYLD-mediated PSD-95 deubiquitination, mobilizing and depleting PSD-95

40 5 deubiquitination, mobilizing and depleting PSD-95 from synapses.

41 l mechanistic insight into the regulation of PSD-95 in dendritic spine structural plasticity through

42 ordingly, increased binding of Ca(2+)/CaM to PSD-95 induced by a chronic increase in Ca(2+) influx is

43 At both stages, PSD-95 puncta are enriched in the most lateral neuropil

44 gephyrin puncta increasing to match that of PSD-95 puncta at the larval stage.

45 At the embryonic stage, we found that PSD-95 puncta outnumber gephyrin puncta, with the number

46 erlying structural and functional changes in PSD-95 that mediate its role in plasticity remain unclea

47 tivity decreases SH3-GK interaction, causing PSD-95 to adopt an open conformation.

48 polyubiquitination, which markedly modifies PSD-95's scaffolding potentials, enables its synaptic ta

49 increase in postsynaptic density protein 95 (PSD-95) by overexpression caused correlated increases in

50 Postsynaptic density protein-95 (PSD-95) localizes AMPA-type glutamate receptors (AMPARs)

51 Postsynaptic density protein 95 (PSD-95), a member of the MAGUK family, recruits Kv1.3 in

52 ld protein, postsynaptic density protein 95 (PSD-95), a process that is deficient in the mouse model

53 c density proteins (viz., GluR1, GluR4, NR1, PSD-95, and PSD-93), that TH cell somata and tapering ne

54 find that the postsynaptic proteins PSD-93, PSD-95, and SAP102 differentially regulate excitatory sy

55 AF6) is identified as a direct E3 ligase for PSD-95, which, together with the E2 complex Ubc13/Uev1a,

56 tsynaptic densities, cleaves K63-chains from PSD-95.

57 size and number of NR2B and cluster size of PSD-95.

58 complex Ubc13/Uev1a, assembles K63-chains on PSD-95.

59 ed reduced surface expression and binding to PSD-95.

60 e bubble-water interface as the location for PS activation by high temperature with (*)OH contributin

61 hese data may provide links into how loss of PS activity inhibits glutamatergic synaptic function in

62 The abrogation of Cho1 induction and PSS activity by a CHO1 UASINO mutation suppressed pah1De

63 the pah1Delta-mediated induction of Cho1 and PSS activity.

64 We observed that PEDOT-PSS adhered significantly better to GC than Pt, and allo

65 nular magnetic field profile was observed 5 ps after the interaction, indicating a relatively smooth

66 PubMed reports of observational studies with PS analysis that evaluated a surgical procedure and desc

67 f the use and reporting of propensity score (PS) analysis in observational studies assessing a surgic

68 directly that one molecule each of 18:0/18:1 PS and 18:0/20:4 PC can bind specifically to purified hu

69 id not detail the covariates included in the PS and 77% (n = 100) did not report a justification for

70 Specifically, BTZ and CFZ absorption in both PS and COP were all in the range of approximately 100-30

71 In the empirical example, PS and DRS matching gave similar results and showed good

72 We assessed the effect of PS and ES on mesocorticolimbic circuit activation, VTA g

73 We found that PS and ES similarly induced DeltaFosB in the hippocampus

74 Fos expression was similarly reduced by both PS and ES.

75 The objective is to better understand hMSC PS and HC effects on human cardiac contractility and arr

76 putational study helps unravel relative hMSC PS and HC effects on human cardiac contractility and arr

77 Thus, phenolics in PS and MDBP may serve as antioxidants and antimicrobial

78 Phenolic acids were present in PS and MDBP whereas proanthocyanidins and monomeric flav

79 h from the second end, suggesting a role for PS and membrane charge in polarized cell growth.

80 ase" occurred in solid-state materials: when PS and Mn2(CO)10 were embedded in electrospun nonwoven f

81 e the transcriptome after the application of PS and OS.

82 stal structures, the underlying mechanism of PS and PC/PE effects emerges.

83 ic mechanisms, specific interactions of both PS and PC/PE have been inferred.

84 For cancer therapy in mice, tumor PS and photothermal therapy of anti-CD11b Abs-linked gol

85 reater lean mass and leg strength gains when PS and RET were used than with RET alone, with the stand

86 Functional analysis of PSD and non-PSD interactomes illustrates both common and

87 lation between the nature of the hydrophilic PSs and that of the hydrophobic components, of linkers,

88 lial cells (ECs) through phosphatidylserine (PS) and examined the effect of platelet clearance on pro

89 Significant changes in polysaccharide (PS) and oligosaccharide (OS) base wine composition and c

90 ar-size of a mixture of various polystyrene (PS) and polyacrylate (PACR) nanoparticles has been obtai

91 charge-transfer lifetime of 100 picoseconds (ps) and room-temperature photoluminescence.

92 rous endpoints, including paradoxical sleep (PS) and slow-wave sleep (SWS), as well as the circadian

93 ace hydrophobicity (H0), protein solubility (PS)) and emulsifying (emulsion capacity (EC), droplet si

94 assisted delivery of an oxidant, persulfate (PS), and low temperature electrical resistivity heating

95 ylene (PE), polypropylene (PP), polystyrene (PS), and polyethylene terephthalate (PET) are extremely

96 deviation (MD), pattern standard deviation (PSD), and visual field index (VFI).

97 "semi-dark" trions and biexcitons to be 10 ps, and analyse how these complexes appear in the temper

98 c signatures in serum from subjects with AD, PS, and CD compared with healthy controls (HC).

99 in the case of the glycerophospholipids (PE, PS, and PC), via ester bond cleavage.

100 monium), PDADMA, and poly(styrenesulfonate), PSS, are at least 2 orders of magnitude faster than the

101 s occurs when the bilateral palatal shelves (PS), arising from maxillary prominences, fuse at the mid

102 n, inverse probability weighting, and use of PS as a covariate.

103 and monomeric flavonoids were found only in PS as identified by HPLC-DAD-ESI-MS(n).

104 porting the potential exploitation of PJ and PS as sources of bioactive compounds.

105 were prepared with poly(styrene sulphonate) (PSS) as an inert component, across a range of degrees of

106 duction of Alix also substantially decreased PS-ASO activities without affecting total PS-ASO uptake.

107 ed PS-ASO activities without affecting total PS-ASO uptake.

108 lar uptake and intracellular distribution of PS ASOs are mediated by protein interactions.

109 PS-ASOs are known to be internalized via a number of end

110 PS-ASOs can enter cells without additional modification

111 Chemically modified PS-ASOs can mediate efficient target reduction by site-s

112 tidic acid (LBPA) is required for release of PS-ASOs from LEs.

113 MICA-pSS association was studied in two independent (French a

114 PS asymmetry on the plasma membrane depends on the activ

115 Moreover, it was found that activating PS at approximately 36 degrees C eliminated more PCE tha

116 ery similar rotation rates ( approximately 8 ps) at room temperature, despite differences in other te

117 ofiling of structured polymers (polystyrene (PS)-b-polymethyl methacrylate (PMMA) block copolymers (B

118 thiophene):polystyrenesulfonate-based (PEDOT(PSS)-based) solid contact (SC) ion-selective electrodes

119 infiltration induced by photosensitization (PS) because the systemic depletion of neutrophils comple

120 rate was <15%, higher FN rate increased the PSD (beta = 0.51 dB; P < 0.001), and the effect was slig

121 Integrin alphaM(PS)beta2 BMDMs also exhibited higher levels of active Rh

122 els of IL-6 and TNF-alpha in integrin alphaM(PS)beta2 BMDMs were significantly higher than those of i

123 ased with repeated stress, and some changes (PS bouts, SWS time, body temperature, locomotor activity

124 r and induced structural rearrangements with PSS breakpoints.

125 stems, an unusually slow ( approximately 400 ps) but ultimately efficient charge generation mediated

126 Finally, externalization of PS by necroptotic cells drives recognition and phagocyto

127 Weight loss, performance status (PS), C-reactive protein (CRP), albumin, the nutritional

128 extinction-dependent changes in hippocampal PSD CaMKII expression and S831 GluA1 phosphorylation.

129 PS cDKO mice display classical features of neurodegenera

130 with long-term contextual memory deficits in PS cDKO mice.

131 ted by contact angle measurements over PEDOT(PSS)-coated Au, GC, and Pt electrode surfaces.

132 gly and specifically increased in RSC during PS compared with aWK.

133 RBC dendrites expand, they form fewer multi-PSD contacts with rods.

134 PS-containing liposomes blocked HCV cell attachment and

135 The postsynaptic density (PSD) contains a collection of scaffold proteins used for

136 sing three different materials (polystyrene (PS), cyclo-olefin polymer (COP), and PDMS).

137 In addition, we identified TbPSD as type I PS decarboxylase in the mitochondrion and found that it

138 740 nm, we observe a final approximately 150 ps decay assigned to trapping by charge separation, and

139 After a 4.5 ps delay, another distinct surface species forms with a

140 ces of epoxy-, 7-keto-, 7-hydroxy- and triol-PS derived from sitosterol and campesterol were 40.0, 34

141 activities of P4-ATPases, and disruption of PS distribution can lead to various disease conditions.

142 incorporated experimentally calibrated hMSC PS effects on cardiomyocyte L-type calcium channel/sarco

143 iologically specifically active during basal PS episodes.

144 clinical stage (CS), final pathologic stage (PS), estrogen receptor status (E), and nuclear grade (G)

145 receptor, NKG2D, both attributes relevant to pSS' etiology.

146 e observes an ultrafast ( approximately 0.06 ps) evolution that reflects relaxation from initial nonp

147 d), with conductances ranging from 28 to 689 pS, except for their ionic selectivity, which was slight

148 ing as an attachment receptor for binding to PS exposed on the HCV envelope.

149 Furthermore, inhibition of pMLKL after PS exposure can reverse the process of necroptosis and r

150 cium (Ca(2+)) influx and phosphatidylserine (PS) exposure on the outer leaflet of the plasma membrane

151 with a greater reduction of phyllosilicates(PS)-Fe(III) to PS-Fe(II), relative to the oxic near-surf

152 reduction of phyllosilicates(PS)-Fe(III) to PS-Fe(II), relative to the oxic near-surface and sandy g

153 rent with the greatest PS-Fe(III) reduction (PS-Fe(II)/Fe(III) ratio approximately 1.2 (Mossbauer) or

154 were detected, concurrent with the greatest PS-Fe(III) reduction (PS-Fe(II)/Fe(III) ratio approximat

155 mum thick galvanostatically deposited PEDOT(PSS) films.

156 ess of the electrochemically deposited PEDOT(PSS)-films on the hydrophilicity of these films has been

157 onic fibroblasts (MEFs) exhibited diminished PS flippase activity and increased exposure of PS on the

158 py)2](2+) to the largest known value at 17.4 ps for [Fe(dbtpy)2](2+).

159 tend the lifetime of the (5,7)MLCT from 14.0 ps for [Fe(dftpy)2](2+) to the largest known value at 17

160 tion with single-channel conductances of 20 pS for inward currents and 80 pS for outward currents.

161 er underlined the great significance of this PS for mitochondria targeted PDT applications in deep ti

162 tances of 20 pS for inward currents and 80 pS for outward currents.

163 o-valent iron combined with persulfate (NZVI/PS) for enhanced degradation of brilliant red X-3B in an

164 um and (iii) represents the unique route for PS formation in T. brucei.

165 accumulate at presynaptic terminals lacking PS function.

166 Shoot-/root-specific expression of PS-GFP in Arabidopsis, and grafting experiments, reveale

167 CaMKII site, along with an increase in total PSD GluA1.

168 15-year actuarial overall patient survival (PS), graft survival (GS), death-censored GS (DCGS), and

169 p, and 13 (35%) of 35 participants in the Vi-PS group to give vaccine efficacies of 54.6% (95% CI 26.

170 (one in the Vi-TT group and three in the Vi-PS group).

171 lenge (31 in the control group, 35 in the Vi-PS group, and 37 in the Vi-TT group) and were included i

172 igned; 34 to the control group, 37 to the Vi-PS group, and 41 to the Vi-TT group.

173 Cells depleted of PS have altered cell dimensions and fail to properly reg

174 er 6 months, grit-blasted acid-etched (GBAE) PS implants with and without a MACH neck were randomly i

175 We also found that ectopic expression of PS improves Arabidopsis resistance to the necrotrophic f

176 first demonstration of H2O2 production using PS in an MPPC, and the energy requirement for H2O2 produ

177 istics with tauS = 310 ps in toluene and 150 ps in benzonitrile.

178 ate approximations, the dissociation rate of PS in cavitating bubble systems was determined to be 3 o

179 am is probably an effective strategy to stop PS in children.

180 diagnosis are at risk for deficits in IQ and PS in the absence of cranial radiation, regardless of MT

181 %) and mannoproteins (38-55%) were the major PS in the base wines.

182 iate optical characteristics with tauS = 310 ps in toluene and 150 ps in benzonitrile.

183 o gain insight into the role of presenilins (PS) in excitatory synaptic function, we address the rele

184 Functional analysis of PSD and non-PSD interactomes illustrates both common and unique func

185 dicate that inhibition of Nrxn processing by PS is deleterious to glutamatergic function.SIGNIFICANCE

186 ed by the present findings, we conclude that PS is sufficient to account for the perceptual organizat

187 thetic 127-nt fragment encompassing improved PSs is swapped onto the RNA otherwise lacking CP recogni

188 Phosphatidylserine (PS) is an abundant charged lipid that may regulate charg

189 of the ISM and activity changes at the PEDOT(PSS)|ISM interface.

190 ived chemokine (MDC)), CD (10 proteins), and PS (kynureninase (KYNU)).

191 Discrepancy still exists at early time 0-15 ps, likely due to non-equilibrium conditions.

192 We report that Sp-configured PS linkages are stabilized relative to Rp, providing ste

193 n was highest in shallow-fried potatoes with PS liquid margarine (64.44mg per portion food plus resid

194 In conclusion, PS liquid margarine increased POP content in foods with

195 h control vs. 44.1, 23.8, 29.6 and 2.4% with PS liquid margarine.

196 PS liquid vs. control margarine resulted in a higher med

197 iation between %5 mC and LTL in females (all ps < 0.01), but not in males.

198 risk of death or heart transplantation (all Ps<0.001).

199 agnetoelectric coupling coefficient of 0.057 ps/m.

200 polydimethylsiloxane (PDMS), or polystyrene (PS) macromonomer.

201 ubjects with a clinical diagnosis of PS, non-PS (mainly essential tremor), probable DLB, and non-DLB

202 Among 164 PS-matched patients, support duration was longer for the

203 d performance in terms of covariate balance (PS matching) and controlling confounding in the dry-run

204 ventional covariate adjustment with 4 common PS matching, stratification, inverse probability weighti

205 Cues regarding food PS may be processed in the lateral prefrontal cortex, wh

206 ion time of neat BmimNTf2 liquid (870 +/- 20 ps) measured with optical heterodyne-detected optical Ke

207 These data confirm details of the PS-mediated assembly mechanism for STNV and identify an

208 Our results suggest that PS-mediated clearance of activated platelets by the endo

209 PS methods are not necessarily superior to conventional

210 2) of Bdnf promoter IV in the hippocampus of PSD mice.

211 ed using commercially available polystyrene (PS) microparticles with a size comparable to cancer cell

212 Here, we tested the PS model by recording neural responses to alternating (A

213 A crucial test of the PS model is whether it can account for the observation t

214 esent study, we successfully established the PSD model using male C57BL/6 J mice by photothrombosis o

215 MENT According to the population separation (PS) model of auditory stream segregation, sounds that ac

216 cent and pristine polystyrene microplastics (PS-MPs) particles with two diameters (5 mum and 20 mum)

217 However, whether PS mRNA is transferable and its role in systemic defense

218 and grafting experiments, revealed that the PS mRNA moves in a bi-directional manner.

219 pplication of paper spray mass spectrometry (PS-MS) combined with a chemometric supervised method (pa

220 conductance of the channels to be 244 +/- 11 pS (n = 17; symmetrical 150 mm K(+) ) with open probabil

221 Individuals on the psychosis spectrum (PS; n=19) and healthy young individuals (HC; n=17) under

222 The resulting AuNPs/PEDOT:PSS nanocomposites were subsequently characterized under

223 cluded subjects with a clinical diagnosis of PS, non-PS (mainly essential tremor), probable DLB, and

224 ignaling proteins through modulation of fast ps-ns sidechain dynamics.

225 s, with the inverse agonist suppressing fast ps-ns timescale motions at the G protein binding site.

226 or and junior radiologists was excellent for PS/NS distinction (ICC = 0.87; 95% CI: 0.83, 0.90) and f

227 n of soluble proteins (PN), polysaccharides (PS), nucleic acids (NA) and humic-like substances (HS) i

228 B) reactor, and examined the effects of NZVI/PS on anaerobic microbial communities during the treatme

229 flippase activity and increased exposure of PS on the cell surface.

230 re of negatively charged phosphatidylserine (PS) on adherent leukocytes, and clot burden after 48 hou

231 IFNgamma is captured by phosphatidylserine (PS) on the surface of viable cells both in vitro and in

232 -mediated effects were most pronounced under PS-only conditions, where developed force increased appr

233 transplant, RDP did not lead to decreased in PS or GS, or an increase in graft dysfunction but as ass

234 , who subjectively classified the nodules as PS or NS.

235 Blocking externalized PS or suppressing TMEM16F inhibited Env-mediated fusion.

236 Vi-conjugate (Vi-TT), Vi-polysaccharide (Vi-PS), or control meningococcal vaccine with a computer-ge

237 ticles created are incomplete, implying that PSs outside this region are required for correct assembl

238 13.20mg versus 0.23mg, 0.06-0.90mg), a lower PS oxidation rate (0.63 vs. 1.29%) and lower oxidation s

239 Plant sterol (PS) oxidation products (POP) derived from sitosterol and

240 eyes, vs 104 for VFI (P = .0013) and 107 for PSD (P = .029).

241 conversion was 100% in Vi-TT and 88.6% in Vi-PS participants, with significantly higher geometric mea

242 containing different number of polystyrene (PS) particles and by varying the applied voltages, flow

243 luble MICA proteins were detected in sera of pSS patients compared to healthy controls.

244 n peripheral blood mononuclear cells from 13 pSS patients, using comet assay.

245 This is particularly true for the areas of PS patterning and growth as well as medial epithelial se

246 as shown to be significantly associated with pSS (pcor=2.61 x 10-35).

247 s of electrode modification, ratio of PEDOT: PSS, pH of electrolyte, time required for AuNP depositio

248 atidylethanolamine (PE), phosphatidylserine (PS), phosphatidylcholine (PC), and sphingomyelin (SM) ca

249 ith a norbornene-functionalized polystyrene (PS), polylactide (PLA), or polydimethylsiloxane (PDMS) m

250 tions of fibrotic cardiac tissue, where hMSC PS protected from potential proarrhythmic effects of HC

251 In Arabidopsis, PS protein can be processed and SYS is secreted.

252 oteome complexity, the postsynaptic density (PSD) proteome of zebrafish has lower complexity than mam

253 fied by resection margin (group I: FS-R0 --> PS-R0; group II: FS-R1 --> PS-R0; group III: FS-R1 --> P

254 roup I: FS-R0 --> PS-R0; group II: FS-R1 --> PS-R0; group III: FS-R1 --> PS-R1).

255 up II: FS-R1 --> PS-R0; group III: FS-R1 --> PS-R1).

256 ving donor recipients, the actuarial 15-year PS rates were similar between groups.

257 nd autoimmune disorders caused by defects in PS receptors and signaling molecules.

258 HIV-1-induced PS redistribution depends on Ca(2+) signaling triggered

259 hypothesis that MTHFR variants contribute to pSS-related lymphomagenesis.

260 Based on these findings, we conclude that PS remains a plausible neurophysiological model of audit

261 target rear only at later time-scales of 10 ps, resulting in a commensurate large-scale filamentatio

262 layer graphene transferred onto polystyrene (PS), semiconducting thienoazacoronene (EH-TAC), gold, an

263 PGBD5 was physically associated with genomic PSS sequences that were also sufficient to mediate PGBD5

264 duced DeltaFosB in the hippocampus, but only PS significantly increased DeltaFosB expression in the p

265 randomization on a time scale of 900 +/- 20 ps, significantly slower than observed for SeCN(-) but i

266 usion of PDADMA sites is faster than that of PSS sites, accounting for the asymmetric nature of multi

267 ts that we attribute to improved accuracy of PSS standards and changes in the column packing.

268 CP-binding motif, the relative placement of PS stem-loops, their number, and their folding propensit

269 We demonstrate that phosphorothioate (PS) stereochemistry substantially affects the pharmacolo

270 Externalized PS strongly promotes Env-mediated membrane fusion and HI

271 By coating the PEDOT(PSS) surface with an ISM, the negative potential drift i

272 leading to PE synthesis in eukaryotes, while PS synthesis has not been studied experimentally.

273 nd ACA were significantly more active during PS than during aWK and SWS, respectively.

274 C and ACA contain neurons firing more during PS than in any other state.

275 eration of broken, PM "bubbles" with exposed PS that are released from the surface of the otherwise i

276 ls, such as externalized phosphatidylserine (PS), that are recognized in a specific context by recept

277 Mutation to remove all AXXA motifs in PSs throughout the genome yields an RNA that is unable t

278 -phenylenevinylene] (MDMO-PPV), polystyrene (PS), thus breaking a new ground on the controlled prepar

279 ing different polymers, i.e. F8BT, MDMO-PPV, PS, thus providing micrometric-sized taggants suitable f

280 nt transfer for charge separation on the 150 ps timescale.

281 *)OH contributing a minor role in activating PS to SO4(*-).

282 mice to the PS19 human tau transgenic line (PS) to investigate whether loss of TREM2 function affect

283 ference strains (RSs) and a parental strain (PS) to substantially improve the predicted flux distribu

284 ransfer occurs from triplet excited-state (3)PS* to a photolabile triplet state of Mn2(CO)10, which,

285 rical resistivity heating (ERH), to activate PS, to achieve remediation of contaminated, low permeabi

286 Dominance of hMSC PS was also revealed in simulations of fibrotic cardiac

287 (IQ), working memory, and processing speed (PS) was conducted 8 to 24 months after treatment complet

288 ioxythiophene)-poly(styrenesulfonate) (PEDOT-PSS) was selectively electrodeposited on both sets of de

289 actions of pomegranate juice (PJ) and seeds (PS) were evaluated.

290 viation (MD) and pattern standard deviation (PSD), were analyzed with multivariable regression models

291 metal chelation of the soluble fraction from PS, were higher than those for PJ.

292 of CHO1-encoded phosphatidylserine synthase (PSS), which catalyzes the committed step for the synthes

293 l as the oxidation state of structural Fe in PS, which could significantly affect nutrient cycling an

294 channel conductance of AMPARs in SCs is 8-11 pS, which is comparable to that in neurons.

295 nitial radical formation time of 1.3 +/- 0.2 ps, which is identical to the time to populate the surfa

296 cies forms with a time constant of 36 +/- 10 ps with a yet undetermined structure.

297 ixing in solution a triplet photosensitizer (PS) with the photoCORM and shining red light, energy tra

298 ngle channels had a conductance close to 250 pS, within the range of all known BKCa channels.

299 A PS x ED interaction was shown in the superior temporal g

300 y crystals, each collected with a single 100 ps X-ray pulse exposure per crystal using a setup optimi