ライフサイエンスコーパス: sieve

1 pproaches: spectral count, spectra index and SIEVE.

2 prediction and show that the PCM acts like a sieve.

3 tity that acts as a size-dependent molecular sieve.

4 ample, as structural scaffolds and molecular sieves.

5 r boron in a suite of borosilicate molecular sieves.

6 ed and hence more easily retained on the top sieves.

7 resulting membranes can be used as molecular sieves.

8 ntred emission, ion exchangers and molecular sieves.

9 roved by adding polar additive and molecular sieves.

10 candidates for tunable atomic and molecular sieves.

11 ick silicates that can function as molecular sieves.

12 cations for catalysis, storage, or selective sieving.

13 inement and achieve accurate and tunable ion sieving.

14 l determinants of endothelial macromolecular sieving.

15 nce ion discrimination by altering molecular sieving.

16 thermodynamics and/or kinetics and molecular sieving.

17 n of sample preconcentration (onto Molecular Sieve 5A) at a flow rate of 200 mL min(-1).

18 g., of DNA), as the high viscosity of linear sieving additives, such as linear polyacrylamide or poly

19 ders the introduction and replacement of the sieving agent in microscale channels.

20 eavors are pursued to target ideal molecular sieves among diverse porous materials, over the past sev

21 suggest an important role for neutralization sieve analyses as an informative component of comprehens

22 emonstrates proof-of-concept that phenotypic sieve analyses can elucidate mechanistic correlates of i

23 ata access tool for exploring the results of sieve analyses performed on four major preventive HIV-1

24 development of novel methodology for future sieve analyses.

25 Sieve analysis also corroborated a genetic signature of

26 Neutralization sieve analysis compares the neutralization sensitivity o

27 We performed a T-cell-based sieve analysis of breakthrough viruses in the RV144 tria

28 immune responses can be investigated through sieve analysis of HIV-1 breakthrough infections (infecte

29 e of the vaccine itself, a technique called 'sieve analysis', one can identify functional specificiti

30 In a sieve analysis, high capture and low capture were distin

31 Here, we conducted a T-cell-based sieve analysis, which compared the genetic sequences of

32 ressed HLA A*02, an allele implicated in the sieve analysis.

33 tion stage, which employs a carbon molecular sieve and an adsorption/thermal desorption cycle, can in

34 he outer membrane as an unspecific molecular sieve and indicate a higher degree of selectivity and re

35 that the C-terminus functions as a molecular sieve and stabilizer of the oligomeric MscL structure as

36 tions of albuterol sulfate and budesonide in sieved and milled lactose, respectively, were dispersed

37 type photocatalysts, such as Ti-Si molecular sieves and carbon quantum dots (CQDs), are also briefly

38 Mesh size of sieves and filters used during sampling or sample proces

39 pect to pure micro- and mesoporous molecular sieves and other hierarchical zeolites are critically an

40 shape selectivity in the pores of molecular sieves and the polarisation effect at the metal-support

41 However, their use in ion sieving and desalination technologies is limited by a pe

42 Molecular sieving and differences in diffusivities were identified

43 ed boluses were measured by using mechanical sieving and laser diffraction (primary outcome).

44 r later values are consistent with molecular sieving and transient binding of dissociated proteins.

45 s given rise to the definition of "molecular sieves" and has been the basis for a variety of separati

46 s, alkali-exchanged stannosilicate molecular sieves, and amorphous TiO2-SiO2 coprecipitates.

47 lications like membranes, sensors, molecular sieves, and optoelectronics.

48 processing: density separation, filtration, sieving, and visual sorting of microplastics.

49 Crystalline molecular sieves are used in numerous applications, where the prop

50 ges of utilizing phospholipid pseudogels for sieving are the ease with which they are introduced into

51 re density and altered pore structure in the sieve areas associated with impaired phloem function.

52 rrelation with end wall types, the number of sieve areas per end wall was found to scale with SE leng

53 ular transport, harbours specific junctions, sieve areas, between the conducting cells.

54 with its function in the elaboration of the sieve areas, CHER1 has a sustained, polar localization i

55 framework related to the biogenesis of these sieve areas.

56 temperature in the presence of 4A molecular sieves as dehydrating agent.

57 This leads to fast DNA sieving as demonstrated here on the capillaries of 750 n

58 under vacuum or in the presence of molecular sieves, B(C(6)Cl(5))(3) (6) is completely stable to refl

59 zite zeolites, what appears to be "molecular sieving" based on dimension is actually separation based

60 described here provides a new innovation to sieving-based capillary separations.

61 This characteristic is useful for sieving-based electrophoretic separations (e.g., of DNA)

62 loss of ultrafiltration capacity and sodium sieving before the onset of overt EPS.

63 but, if immersed in water, act as molecular sieves, blocking all solutes with hydrated radii larger

64 of all time, mysticetes depend on keratinous sieves called baleen to capture enough small prey to sus

65 be exposed, to achieve competitive molecular sieving capabilities.

66 portant industrial applications as molecular sieves, catalysts and in gas separation and storage.

67 Without modification of sieving characteristics, these membranes can be made exc

68 ects of manganese oxide octahedral molecular sieve chitosan microspheres (Fe3O4@OMS-2@CTS) on anaerob

69 ed the factors that influence the glomerular sieving coefficient for albumin (GSC(A)) in an effort to

70 s albumin overload, we quantified glomerular sieving coefficients (GSC) and PT uptake of Texas Red-la

71 Analysis of sieving coefficients revealed 80% reduction in cytokines

72 s a typical silicoaluminophosphate molecular sieve, constitutes instead a new family of inorganic-org

73 essure ethylene over a pure-silica molecular sieve containing framework tin (Sn-Beta) to produce the

74 r in the presence of a pure-silica molecular sieve containing framework zirconium (Zr-Beta) for 6 h t

75 examples of hydrothermally stable molecular sieves containing extra-large pores.

76 The CD is apparently a molecular sieve covering the channel that optimizes loss of osmoly

77 he surface of dealuminated zeolite molecular sieves (DAZMS) for CO oxidation under actual automobile

78 tected in high molecular weight fractions of sieved dermal extracts and visualized by electron micros

79 parylene-MWCNT nanochannels was used as size sieving devices for nano-scale biomolecules.

80 rks (COFs) are good candidates for molecular sieves due to the chemical diversity of their building b

81 rabinoxylan (AX) and starch retention on the sieves, due to physical incorporation of AX and starch i

82 e findings suggest the presence of an innate sieve effect and may inform HIV-1 vaccine development.

83 Here, we report a robust neutralization sieve effect in a nonhuman primate simian immunodeficien

84 Though we hypothesized that the observed sieve effect indicated postacquisition T-cell selection,

85 The quantum sieving effect between D2 and H2 is examined for a serie

86 as a platform for rapid reinterpretation of sieve effects and as a portal for organizing and sharing

87 69 and 181, which were implicated in vaccine sieve effects in RV144.

88 velopment, and vaccine protection, including sieving effects on breakthrough virus strains.

89 ate (SDS)-protein complexes are separated by sieving electrophoresis in a microfluidic device or chip

90 lity using free solution CE or by size using sieving electrophoresis of SDS complexes.

91 is study dealt with the visualization of the sieve element (SE) cytoskeleton and its involvement in e

92 ethod allows high-resolution measurements of sieve element and sieve plate geometries.

93 tomic force microscopy indicates that phloem sieve element cell walls have a lower indentation modulu

94 a glycan epitope that is specific to phloem sieve element cell walls in several systems.

95 uch as sugars are transported through phloem sieve element cells in plants.

96 ffuse through plasmodesmata up to the phloem sieve element companion cell complex (SECCC).

97 s spectrometry-based proteomics of exudates, sieve element contents and microdissected stem tissues e

98 proteins (about 10%) were shared between the sieve element contents of FP and EFP, and enriched Gene

99 We show that sieve element differentiation involves enucleation, in w

100 iant, interferes not only with commitment to sieve element fate but also with the formative sieve ele

101 etermines cellular commitment to protophloem sieve element fate, with OPS acting as a positive, quant

102 rs to be a secondary effect of discontinuous sieve element files and subsequent systemically reduced

103 d three-dimensional reconstruction to follow sieve element morphogenesis in Arabidopsis.

104 The sieve element occlusion (SEO) gene family originally was

105 Both types are encoded by members of the sieve element occlusion (SEO) gene family, which compris

106 eve element fate but also with the formative sieve element precursor cell division that creates proto

107 In the absence of the formative sieve element precursor cell division, metaphloem identi

108 tophloem in Arabidopsis roots by locking the sieve element precursor cell in its preceding developmen

109 sely with plant height because of a shift in sieve element structure along the length of individual t

110 a cells feeding H(+)-coupled import into the sieve element-companion cell complex.

111 AVP1 localized at the plasma membrane of the sieve element-companion cell complexes functions as a sy

112 ssion of the transporter was targeted to the sieve element-companion cell complexes of the leaf phloe

113 ons, we identified the small heat shock-like SIEVE ELEMENT-LINING CHAPERONE1 (SLI1).

114 r subsequent active uptake into cells of the sieve element/companion cell complex.

115 n of wall ingrowths adjacent to cells of the sieve element/companion cell complex.

116 sgenic lines expressing Arabidopsis thaliana Sieve-Element-Occlusion-Related1 (SEOR1)-yellow fluoresc

117 In the sieve elements (SEs) of the phloem, carbohydrates are tr

118 the vRNA-dependent RNA polymerase in phloem sieve elements and in xylem vessels.

119 e phloem; it moved from companion cells into sieve elements and into a previously undiscovered sympla

120 GPAs had difficulty feeding from sieve elements and tapping into the xylem of lipoxygenas

121 Phloem sieve elements and xylem vessels from Potato virus X-inf

122 lls, guard cells, phloem companion cells and sieve elements are clearly described, this is not the ca

123 Given that phloem sieve elements are enucleate and lack translation machin

124 o be able to travel between plant organs via sieve elements as a putative long-distance signaling mol

125 teins formed parietal agglomerates in intact sieve elements as well as sieve plate plugs after woundi

126 Small amounts of dilute, mobile sap from sieve elements can be obtained, although there is eviden

127 Adapted for effective transport, sieve elements develop as enucleated living cells.

128 Thus, sieve elements differentiate through a specialized autol

129 ehavior indicates that the GPA stylets found sieve elements faster when feeding on the adf3 mutant co

130 Suc unloading from de-energized protophloem sieve elements in meristematic zones may be mediated by

131 , we were able to locate the same FP-labeled sieve elements in semithin and ultrathin sections.

132 nated LM26, binds to the cell wall of phloem sieve elements in stems of Arabidopsis (Arabidopsis thal

133 fic loss of proteins from companion cells to sieve elements may explain the plethora of macromolecule

134 the GPA fed for a more prolonged period from sieve elements of adf3 compared to the wild-type plant.

135 lutionary origin for P-proteins found in the sieve elements of all dicotyledonous plants and demonstr

136 morphine detected corresponding antigens in sieve elements of the phloem, as described previously fo

137 ly function in Suc retrieval into metaphloem sieve elements to maintain a high turgor to drive sympla

138 owed that SLI1 is confined to the margins of sieve elements where it lines the parietal layer and col

139 ters were expressed specifically in immature sieve elements, and GFP-SEO fusion proteins formed parie

140 In addition, once they found the sieve elements, the GPA fed for a more prolonged period

141 deposition in the phloem, especially in the sieve elements, was greatly reduced in cs7 mutants.

142 ridine biosynthesis appears to occur only in sieve elements, whereas conversion of thebaine to morphi

143 , other than SbSUT4, were immunolocalized to sieve elements, while for elongating and recently elonga

144 plasmodesmata from mesophyll cells into the sieve elements.

145 be involved in the rapid sealing of injured sieve elements.

146 cell border interfaces between mesophyll and sieve elements.

147 movement between phloem companion cells and sieve elements.

148 c movement of mRNA from companion cells into sieve elements.

149 semble measurements and electrophysiological sieving experiments show that the open-diameter of the c

150 This process produces selective molecular sieve films that are as thin as 100 nm and exhibit recor

151 es with the optimal size and geometry act as sieves for blocking the biomolecules from inhibiting the

152 ls of graphene are shown to act as efficient sieves for hydrogen isotopes pumped through graphene ele

153 er the past several decades, ideal molecular sieves for the separation and purification of light hydr

154 xposure, the hydrogel toggles from molecular sieving for size-based separation to a covalent immobili

155 to a further size fractionation to isolate "sieved fragmented products" (SFP) that are representativ

156 paradigm shift in conceptualizing molecular sieves from conventional ordered frameworks to disordere

157 omerular capillary hypertension and impaired sieving function with consequent protein overload play a

158 nctional materials such as tunable molecular sieves, gated membranes and controlled-release nanoconta

159 ion of antibody into and along the molecular sieving gel requires that the probe must traverse throug

160 technique for fabrication of PAGE molecular sieving gels in PDMS microchannel networks.

161 V2 would have a selective effect against, or sieve, HIV-1 breakthrough viruses.

162 demonstrated the essential role of molecular sieves in this complex amidation process.

163 Realization of ideal molecular sieves, in which the larger gas molecules are completely

164 discovered a family of mesoporous molecular sieves including discrete structures - MCM-41 (hexagonal

165 The sediment was sieved into 7 grain size fractions that each exhibited d

166 Under isothermal conditions, Ogston sieving is achieved for DNA fragments smaller than 500 b

167 A new molecular sieve, ITQ-38, containing interconnected large and mediu

168 This technique is used to create sieving layers of Al(2)O(3) (thickness, 0.4-0.7 nm) with

169 ilter for transport of large molecules and a sieve-like filter for diffusion of small molecules (<9 n

170 x from surface-attached biofilms generates a sieve-like network that captures cells and other biomass

171 where tethering loses its effect, features a sieve-like structure of bundles and frequent cross-links

172 Molecular sieving materials are widely regarded as the next-genera

173 s for these processes are based on molecular sieving materials to simultaneously achieve high through

174 er than complex high voltage power supplies, sieving matrices, and wall coatings.

175 A high concentration of sieving matrix (1.8% w/v HEC) was introduced at one end

176 sotachophoresis method in combination with a sieving matrix and ionic spacer was used to perform in-l

177 A electrophoresis through a novel artificial sieving matrix based on the highly regular submicrometer

178 The gel layer functions as both a molecular sieving matrix during PAGE and a blotting scaffold durin

179 on chemical functionalization of either the sieving matrix or the antibody, making assay customizati

180 ine mistranslation and reveal a novel triple-sieve mechanism of editing that relies exclusively on tr

181 Both the sieving mechanism of the membrane and chelation of lead

182 r impact on the design of advanced molecular sieving membrane materials for gas separation, adjusting

183 However, most polymeric molecular sieve membranes are based on a few solution-processable

184 We created free-standing carbon molecular sieve membranes that translate the advantages of reverse

185 y for the preparation of polymeric molecular sieve membranes with hierarchical and tailorable porosit

186 e range of applications, including molecular sieve membranes, catalytic membrane reactors, permeation

187 s, facilitating the fabrication of molecular sieve membranes.

188 rove the separation performance of molecular-sieve membranes.

189 er membranes and traditional rigid molecular-sieve membranes.

190 lms are formed and demonstrated as molecular-sieving membranes for selective gas separation.

191 Ultrathin, molecular-sieving membranes have great potential to realize high-f

192 are fabricated into thin films and molecular-sieving membranes.

193 Molecular sieving metal-organic framework (MOF) membranes have gre

194 methods than with a prior analysis using the SIEVE method with the same data.

195 e well with a recent estimate for the Ogston sieving mobility in a colloidal crystal.

196 dary amines in the presence of 4 A molecular sieves (MS) afforded products with up to 99% ee in isola

197 Molecular sieves (MS) significantly accelerated the reaction rates

198 entrating device based on nano-electrostatic sieving (NES) mechanism that is facilitated by multi-nan

199 00 mum-5 mm, which are retained by a 500 mum sieve/net, and (ii) 1-500 mum, or fractions thereof that

200 can exact mass measurements determined using SIEVE nondifferential LC-MS analysis software.

201 Size-exclusive sieving of CO2 over CH4 and N2 has rarely been achieved.

202 ultrafast water transport, precise molecular sieving of gas and solvated molecules shows great promis

203 n kinetics based separation and/or molecular sieving of gases and vapors.

204 indows, it allows in principle for molecular sieving of gases such as H(2) and CH(4).

205 cy, may allow ultrafast and highly selective sieving of gases, liquids, dissolved ions and other spec

206 hat particle encounter is dictated by simple sieving of particles larger than the mesh spacing, a low

207 able size that segregated due to diffusional sieving of small, mobile M1-AQP4-enriched arrays into la

208 40 mM, rt, CH2Cl2, piperidine/AcOH/molecular sieves) of a dihydrodipyrrin-carboxaldehyde (AD half) an

209 talline manganese based octahedral molecular sieve (OMS) nanowires on silicon substrates, and (iii) t

210 , a dynamic and highly selective filter that sieves on the basis of molecular size and electrical cha

211 The development of novel molecular sieves opens opportunities in the development of more se

212 encapsulation, the introduction of molecular sieving or stimuli-responsive "auxiliary" functionalitie

213 The nanoporous PAG molecular sieve physically induces a mobility shift that acts to e

214 as not enriched in the phloem, including the sieve plate area.

215 resolution measurements of sieve element and sieve plate geometries.

216 r by analysing sieve tube anatomy, including sieve plate geometry, using recently developed preparati

217 into SEs, leading to forisome dispersion and sieve plate occlusion in fava bean (Vicia faba).

218 omerates in intact sieve elements as well as sieve plate plugs after wounding.

219 We suggest that the callose lining of sieve plate pores is essential for normal phloem transpo

220 sl7 mutants of Arabidopsis revealed that the sieve plate pores of stems and roots lack the callose li

221 er the conductance of sieve tubes, including sieve plate pores, is sufficient to allow pressure flow.

222 ommon phloem proteins (P-proteins) that plug sieve plates after wounding.

223 has been known for more than a century that sieve plates in the phloem in plants contain callose, a

224 sustained, polar localization in the forming sieve plates.

225 he phloem, especially in the vicinity of the sieve plates.

226 canning electron microscopy for fenestrae in sieve plates.

227 nitially establish three contiguous zones of sieving polymer, electrolyte, and denaturant concentrati

228 a are attributed to the in-parallel molecule sieving process as conducted by the many nanochannels fo

229 n unintentionally mix other foods during the sieving process.

230 tense interest due to their unique molecular sieving properties combined with fast permeation.

231 We attribute organic solvent permeation and sieving properties to randomly distributed pinholes inte

232 failure of the glomerular filtration barrier sieving properties, or different collagen fragments, sug

233 hin microporous polymers and their molecular sieving properties.

234 it very interesting and unexpected molecular sieving properties.

235 ure ( approximately 8%)] and milled (70 mesh sieve) pumpkin flesh matrix increased SC-CO(2) extractio

236 otocols and the ability of NaA micropores to sieve reactants based on molecular size.

237 al crystals for DNA separation in the Ogston sieving regime do not require exquisite control over the

238 n of starch and AX on the smaller and larger sieves, respectively.

239 d announce the availability of our tool, the SIEVE server.

240 rates decrease exponentially with decreasing sieve size but water transport is weakly affected (by a

241 9.8 A to 6.4 A are demonstrated, providing a sieve size smaller than the diameters of hydrated ions.

242 flour with attrition milling machine (0.5mm sieve size).

243 challenging, since the gel must effectively sieve small proteins while permitting effective probing

244 same approach to investigate the function of sieves/strainer vessels, providing direct chemical evide

245 ed nanofilter arrays served as the molecular sieve structures to conduct a continuous size-based anal

246 cts the active site opening, or "pore", that sieves substrates on the basis of their geometries.

247 Membranes made from polymeric molecular sieves such as polymers of intrinsic microporosity (pore

248 tome data with a machine learning algorithm (SIEVE, SVM-based identification and evaluation of virule

249 er of Bacillus anthracis acts as a molecular sieve that is chiefly size-dependent, favoring catalytic

250 model reveals a negatively charged molecular sieve that presents both a charge and size barrier to re

251 They also act as molecular sieves that isolate the virus genome from host defense m

252 In the presence of molecular sieves, the ester production increased to 62.9% in tert-

253 The molecular basis of endothelial protein sieving, the critical vascular barrier function that res

254 uccessful synthesis of a specified molecular sieve through the use of an OSDA that was predicted from

255 flour for 60 seconds every 10 seconds after sieving through three types of flour sifter, constructed

256 pplication of alpha-hemolysin as a molecular sieve to differentiate nanostructures as well as the pot

257 veloped a rare variant-detection algorithm V-Sieve to screen for rare alleles in pooled DNA samples w

258 l, previously homogenized, freeze-dried, and sieved to 250 mum, with 50 mL of 40% (v/v) acetonitrile

259 e transport as they grow taller by analysing sieve tube anatomy, including sieve plate geometry, usin

260 jor to minor veins; the volume of individual sieve tube and vessel members increases from minor to ma

261 increasing distance between source and sink, sieve tube conductivity and turgor increases dramaticall

262 ing tissue dissection and direct sampling of sieve tube contents, we show that FP in fact does contai

263 ecrease in exudation probably due to partial sieve tube occlusion by callose.

264 In sum, wounding triggered transient sieve tube occlusion, enhanced energy metabolism, and ac

265 s, thus confirming the role of P-proteins in sieve tube sealing.

266 Because sieve tube structure defines frictional interactions in

267 rding the nature of other metabolites in the sieve tube system (STS) at specific sites along the path

268 The angiosperm sieve tube system contains a unique population of transc

269 The anucleate sieve tube system of the angiosperm phloem delivers suga

270 with respect to functioning of the enucleate sieve tube system, as eIF5A was recently detected in Cuc

271 paration protocol has been generated showing sieve tube ultrastructure of unprecedented quality.

272 A reconstruction of sieve tube ultrastructure served as basis for tube resis

273 Sieve tube-specific conductivity and its reduction by ca

274 e to the conclusion that obstructions in the sieve-tube path were due to preparation artifacts.

275 n higher plants takes place in the enucleate sieve-tube system of the phloem.

276 Sap is driven through phloem sieve tubes by an osmotically generated pressure gradien

277 n electron microscopic images suggested that sieve tubes contain obstructions that would prevent pass

278 the first ultrastructural investigations of sieve tubes in the early 1960s, their structure has been

279 ration artifacts due to injury, the lumen of sieve tubes is free of obstructions, and phloem flow is

280 Moreover, major phloem proteins in sieve tubes of FP differ from those that predominate in

281 In cucurbits, phloem latex exudes from cut sieve tubes of the extrafascicular phloem (EFP), serving

282 Long distance transport in plants occurs in sieve tubes of the phloem.

283 The key issue is whether the conductance of sieve tubes, including sieve plate pores, is sufficient

284 in the lumen are a general feature of living sieve tubes.

285 This molecular sieving type separation is attributed to the pore size o

286 arger than 0.2 mm, being the diameter of the sieve used, were considered for the data analyses, resul

287 room air collected by passive sampler and in sieved vacuum dust (<150 mum).

288 The stability of the modified molecular sieves was monitored by (29)Si-MAS NMR, transmission ele

289 ariate analysis revealed that loss of sodium sieving was the most powerful predictor of EPS.

290 imetic ion transport manipulation, molecular sieving, water treatment, and nanofluidic energy convers

291 ylboronic acids in the presence of molecular sieves were developed.

292 Molecular sieves were found to have a considerable effect when use

293 be used, at least in principle, as molecular sieves where molecules smaller than the window size are

294 other cage-containing microporous molecular sieves, where some of the most industrially relevant zeo

295 dimensional microporous octahedral molecular sieve with manganese oxide framework.

296 ite-type zeolite, the archetype of molecular sieves with cages and the most widely used as a catalyst

297 on are shape-selective microporous molecular sieves with hierarchical pore morphologies of reduced di

298 nstrate exceptional performance as molecular sieves with high gas permeabilities and good selectiviti

299 nstrate exceptional performance as molecular sieves with high gas permeabilities and selectivities fo

300 We fabricated continuous molecular sieving ZIF-8 membranes in single and multiple poly(amid