ライフサイエンスコーパス: latex

1 al five pathway enzymes were detected in the latex.

2 cent laticifers, which contain morphine-rich latex.

3 sPL) and carboxyl-modified (cPL) polystyrene latex.

4 crude enzyme extract from Calotropis procera latex.

5 iologic transverse EOM loading and isotropic latex.

6 pies or the collection and handling of their latex.

7 ployed transversely loaded EOM and isotropic latex.

8 ectric point of 3.5 was purified from papaya latex.

9 y the addition of sterically stabilized P2VP latex.

10 in extracts obtained from Hevea brasiliensis latex.

11 ynthesis were expressed at low levels in the latex.

12 d plant cells that synthesize and accumulate latex.

13 rotein levels and less TbCPT activity in the latex.

14 ansferase 3 (CPT3), exclusively expressed in latex.

15 ed cells phagocytose nonopsonized silica and latex.

16 B receptor and is predominantly expressed in latex.

17 fabrication of armored nanocomposite polymer latexes.

18 n all cases for chlorhexidine 19/44 (43%) or latex 21/44 (48%)], staffing [only 26/44 (59%) had speci

19 compared paired enzyme immunoassay (EIA) and latex agglutination (LA) assay results with 185 blood an

20 measured using lateral flow assays (LFA) and latex agglutination (LA) tests in 645 HIV-positive, ART-

21 edly more rapid and convenient than standard latex agglutination (LA), but has not yet been evaluated

22 ay can replace conventional testing based on latex agglutination (LA).

23 f performing a penicillin binding protein 2a latex agglutination (PBP-LA) assay directly on Bactec bl

24 h S. aureus were presumptively identified by latex agglutination (Staphaurex Plus; Remel, Lenexa, KS)

25 oli heat-labile enterotoxin reversed passive latex agglutination (VET-RPLA) assay.

26 Serotyping results were consistent between latex agglutination and mPCR/RLB for 331/387 (85.5%) iso

27 Isolates were serotyped by latex agglutination and multiplex PCR-reverse line blott

28 i, isolates (n = 1,135) were serotyped using latex agglutination and Quellung tests (LA/Q) as well as

29 Antigen titers were also reduced in a latex agglutination assay (CALAS) after 4 weeks at 37 an

30 in reaction assay (PCR) and reversed passive latex agglutination assay (RPLA), were selected for dete

31 raditional methods (culture, Gram stain, and latex agglutination for bacterial antigen) and qPCR for

32 r typing of GBS strains based on the Strep-B-Latex agglutination method and a novel multiplex PCR ass

33 The Strep-B-Latex agglutination method was the most widely used meth

34 nally negative with the Cryptococcal Antigen Latex Agglutination System (CALAS), were shown to become

35 We compared a rapid slide latex agglutination test (LAT; Oxoid, Basingstoke, Unite

36 ere compared to the reference standard PBP2a latex agglutination test for detection of mecA-mediated

37 The penicillin binding protein 2a (PBP2a) latex agglutination test using a blood culture pellet wa

38 The sensitivities of the Oxoid PBP2' latex agglutination test were 85.7% with uninduced growt

39 thods using Gram staining and a GAS-specific latex agglutination test.

40 Penicillin-binding protein (PBP) 2a latex agglutination was compared with conventional susce

41 had enhanced sensitivity over both ELISA and latex agglutination with values of 95%, 75%, and 25%, re

42 nzyme-linked immunosorbent assay [ELISA] and latex agglutination) with a molecular method for the det

43 xacillin screen agar, 94.3% and 96.7%; PBP2' latex agglutination, 93.7% and 98.5%; cefoxitin disk dif

44 C. difficile latex agglutination, an enzyme immunoassay for toxins A

45 owever, serotyping generally requires either latex agglutination, multiplex PCR with analysis of band

46 rmined by multiplex PCR, multibead assay, or latex agglutination.

47 s isolates identified by coagulase/protein A latex agglutination.

48 ordance between real-time PCR serotyping and latex agglutination.

49 ound between mecA PCR or Vitek II and PBP 2a latex agglutination.

50 ed centrifugation-decantation step to remove latex aggregates before absorbance measurements, elimina

51 hy was used to enrich the caricain in papaya latex and an enzyme-linked immunosorbent assay test kit

52 ated: antibiotics (49.6%), muscle relaxants, latex and anesthetics (15%), nonsteroidal anti-inflammat

53 A mixture of latex and black ink was injected into the arterial syste

54 derwent a proportionately greater decline in latex and cardenolides relative to species-poor lineages

55 ion to medications, foods, insect stings, or latex and idiopathic reactions in the previous 10 years.

56 imply cross-reactivity with tobacco, natural latex and plant-food-derived alcoholic beverages.

57 ermore, coalescence is promoted by repulsive latex and silica particles but inhibited by attractive c

58 nanoscale polymeric materials (polyurethane, latex and silicone), through entrapment, and subsequentl

59 n manufacturing high-value products, such as latex and superabsorbent polymers.

60 are beta-lactam antibiotics, natural rubber latex, and other agents used in medical and perioperativ

61 d that introduces copper into cotton fibers, latex, and other polymeric materials.

62 most potent resistance traits (cardenolides, latex, and trichomes) and an escalation of regrowth abil

63 ical traits to defense traits (cardenolides, latex, and trichomes) previously shown to impact herbivo

64 Chlorhexidine and latex are not part of routine testing in many centres.

65 Hymenoptera stings and natural rubber latex are the commonest triggers of OcAn.

66 y(methyl methacrylate) (-COOH) surfaces, AEX latex attachment is not stable over long periods in sign

67 Latex attachment on sulfonated COP surfaces are much str

68 ia a catheter with an air-filled thin-walled latex balloon inserted nasally or orally.

69 20 s) were produced by water inflation of a latex balloon placed into the duodenum.

70 Hg, 20 s) were induced by air inflation of a latex balloon surgically placed in the stomach.

71 , 20 s) was produced by water inflation of a latex balloon surgically placed into the duodenum.

72 A latex balloon was advanced into the right atrium.

73 , CED) were produced by water inflation of a latex balloon.

74 labeled with a fluorescent antibody [2] or a latex bead [5], are seen to move longitudinally down the

75 urified SOF N-terminal peptide could promote latex bead adherence to HEp-2 cells and inhibit GAS inva

76 an immunochromatographic assay (ICGA), and a latex bead agglutination assay (LBAA).

77 These latex bead compartments (LBCs) are encased in membrane a

78 Latex bead labeling of peripheral blood Gr1(lo) monocyte

79 of translocation of SK1G82D and SK1S225A to latex bead phagosomes were indistinguishable from those

80 Latex bead treatment did not affect adherence of trophoz

81 Latex bead treatment induced a significant infiltration

82 In vitro experiments examined the effect of latex bead treatment on the capacity of A. castellanii t

83 eomic analysis of the membrane fraction from latex bead-containing (LBC) phagosomes isolated from mac

84 taken to examine the mechanisms that mediate latex bead-induced resistance to Acanthamoeba keratitis.

85 In contrast, IgG-coated latex bead-induced ROS production in human polymorphonuc

86 used to evaluate the role of neutrophils in latex-bead-induced protection against Acanthamoeba kerat

87 and determine the role of macrophages in the latex-bead-induced resistance.

88 o the same degree that phagosomes containing latex beads acquired these markers after 1.5 h of infect

89 or bR did not occur around neutrally charged latex beads acting as cell surrogates, demonstrating tha

90 e, with the microcantilever technique, where latex beads affixed on silicon cantilevers were used as

91 osable dichlorodihydrofluorescein-conjugated latex beads and cyclic hydroxylamines with differing mem

92 nthesized alpha-1,2-trimannose cap sugars on latex beads and demonstrated that C57BL/6 mice coinocula

93 We illustrate this by using two sizes of latex beads and demonstrating the simultaneous detection

94 agocytic uptake of serum-coated or -uncoated latex beads and E. coli However, consistent with previou

95 een fibrinogen molecules covalently bound to latex beads and either wild-type alphaIIbbeta3 molecules

96 slowed the motility of phagosomes containing latex beads and endogenous pigment granules.

97 uction; and in vitro capacity to phagocytose latex beads and to migrate toward the chemokine (C-C mot

98 the ingestion process, cells were exposed to latex beads at 15-20 degrees C, which allows engulfment

99 Latex beads bound to the cell surface move in a myosin I

100 uMC generate ROS upon exposure to IgG-coated latex beads by 5-LO and COX; and ROS appear to have no s

101 Preferential uptake of latex beads by follicle-associated epithelium indicates

102 uptake of nonpathogenic Escherichia coli and latex beads by nonphagocytic mammalian cells.

103 hly scattering metal-coated polystyrene (PS) latex beads by using solvent-controlled heterocoagulatio

104 tent with a direct role of the minor pilins, latex beads coated with SpaB or SpaC protein bind specif

105 After 120 minutes of in vivo exposure, latex beads could be found in cervical lymph nodes.

106 IgG-coated latex beads did stimulate ROS production in huMC, and in

107 es of the murine eye that ingest fluorescent latex beads do not migrate to regional lymph nodes.

108 endocytic pathway do not permit endocytosed latex beads from reaching terminal lysosomes in an anter

109 n not expressed by Pn, but not with 1-microm latex beads in adjuvant.

110 phoP(+) or phoP mutant Y. pestis strains or latex beads in J774A.1 macrophages.

111 ults indicate that intracorneal injection of latex beads induces a remarkable resistance to Acanthamo

112 Instillation of sterile 1.0 microM latex beads into the central corneal epithelium renders

113 somes with phagosomes containing scintillant latex beads led to light emission in a reaction requirin

114 o microscopy by tracking 10 mum, polystyrene latex beads mixed into the solution.

115 s between micrometer sized particles, either latex beads or red blood cells (RBCs), create aggregates

116 CD103(+) DCs were able to ingest and traffic latex beads or soluble antigen.

117 during intracellular transport, we examined latex beads phagocytosed into living mammalian macrophag

118 Latex beads preferentially bound to a subpopulation of c

119 The uptake of latex beads showed that M-cell function was similar in a

120 osomes were specifically labeled with 800-nm latex beads that were conjugated with streptavidin and A

121 In fibroblasts plated on collagen-coated latex beads there are large increases of [Ca(2+)]i, time

122 Model phagosomes harboring latex beads undergo a coordinated Rab5-Rab7 exchange, wh

123 killed M.tb, live Staphylococcus aureus, or latex beads was associated with translocation of cytosol

124 ated epithelium, transcytosis of fluorescent latex beads was evaluated with confocal microscopy.

125 ocytosis of opsonized bacteria particles and latex beads was observed upon incubation of murine macro

126 Fluorescent 0.2-microm polystyrene latex beads were either instilled into the conjunctival

127 Within 20 minutes of an in vivo exposure, latex beads were internalized by the follicle-associated

128 athogen mimics (namely glycodendrimer-coated latex beads with acid-labile linkers) were synthesized.

129 Neutrophil depletion did not abrogate the latex beads' protective effect.

130 crophagicidal drug clodronate eliminated the latex beads' protective effect.

131 in vitro and opsonized particles (IgG-coated latex beads) in vitro and in vivo in intact mice.

132 bortus 2308, live Escherichia coli HB101, or latex beads).

133 polymerized from the surface of mDia1-coated latex beads, and deformed by manipulating both ends thro

134 th increased uptake of Ig-opsonized targets, latex beads, and fluid phase markers, and it was accompa

135 ts, up-converting phosphor technologies, and latex beads, between others) in LFBs.

136 re stably attached to 1 mum (bacteria-sized) latex beads, but not directly linked to each other, in c

137 MSU crystals, but not latex beads, directly bound recombinant soluble (s) CD14

138 during uptake of diverse targets, including latex beads, Escherichia coli, Salmonella typhimurium, a

139 In response to phagocytosis of latex beads, human embryonic kidney 293 cells synthesize

140 and LRG-47 localized to vacuoles containing latex beads, neither protein localized to vacuoles conta

141 albumin or ovalbumin), amino-functionalized latex beads, or dextran polymer and arrayed at the surfa

142 e optical labels such as gold nanoparticles, latex beads, or fluorescent nanoparticles to visualize t

143 Also analyzed were phagocytized black latex beads, phagocytized melanosomes pretreated to simu

144 ILC3s can take up latex beads, process protein antigen, and consequently p

145 e the opsonophagocytic uptake of ClfA-coated latex beads, protect against an intravenous challenge in

146 is factor alpha/fibrinogen, immunoglobulin G latex beads, Staphylococcus aureus, formyl-methionyl-leu

147 , having been tethered to glass or marked by latex beads, the rotation of the internal components has

148 tics and the ability to bind and translocate latex beads, which make it indistinguishable from antige

149 served following ingestion of oxidized OS or latex beads.

150 agocytosis of apoptotic neutrophils, but not latex beads.

151 ch as viruses, pathogenic bacteria, and even latex beads.

152 hagocytosis of M. tuberculosis or TDM-coated latex beads.

153 cules with monoclonal antibodies adsorbed to latex beads.

154 dvanced glycation end product-BSA-conjugated latex beads.

155 y their internalisation of 1 mum fluorescent latex beads.

156 reatment did not affect uptake of IgG-coated latex beads.

157 ed by motors driving tethered cells or 1-mum latex beads.

158 inding of unopsonized particles (e.g., TiO2, latex beads; 63 +/- 5 and 67 +/- 4% inhibition, respecti

159 developmental role of laticifer cells in the latex-bearing plant Euphorbia lathyris.

160 for specific ecophysiological adaptations of latex-bearing plants in natural environments.

161 To address these challenges, polymer latex binders with diverse particle morphologies have be

162 ted latex (n = 9) catheters with silicone or latex catheters.

163 four full-length cDNAs by screening the same latex cDNA library used in the EST analysis and confirme

164 e channels support a processive mechanism of latex cleavage.

165 hromatograph (OTIC) that uses anion exchange latex coated 5 mum radius silica and 9.8 mum radius poly

166 The chromatographic behavior of the AEX latex-coated COP capillaries are greatly dependent on th

167 With such a suppressor coupled to an AS18 latex-coated surface-sulfonated cyclo-olefin polymer (CO

168 After AS18 latex coating, the strong base anion exchange capacity w

169 The spatial deposition of polystyrene latex colloids (d = 1 mum) at rough mineral and rock sur

170 thors compared the effectiveness of the male latex condom and the female polyurethane condom by asses

171 nfected partners in epidemiologic studies of latex condom effectiveness for prevention of sexually tr

172 reover, the identification of laticifer- and latex-deficient mutants (pil mutants) allowed for the id

173 ion appears to be largely driven by enhanced latex delivery to leaves following damage.

174 ticles that account for 93% of rubber in the latex (despite constituting only 6% of total rubber part

175 We assessed the effect of provision of latex diaphragm, lubricant gel, and condoms (interventio

176 the Newick format to be drawn directly into LATEX documents.

177 Serum hs-CRP was measured by latex-enhanced immunoturbidimetric assay.

178 ) and serum amyloid A (SAA) were measured by latex-enhanced nephelometry.

179 om blacktip shark skin prepared using papaya latex enzyme with different degrees of hydrolysis (DHs:

180 is the major enzyme used in cheesemaking but latex enzymes are also used.

181 es of laticifer metabolism in the context of latex exploitation.

182 Stem cDNA libraries and latex extracts of eight opium poppy cultivars displaying

183 In cucurbits, phloem latex exudes from cut sieve tubes of the extrafascicular

184 track in vivo changes or modified to reduce latex flow to damaged areas.

185 s able to catalyze the oxidative cleavage of latex for biodegradation.

186 From the results, it is determined that latex from Calotropis procera can be used as an alternat

187 The stable latex from the ab initio emulsion ATRP had a particle si

188 The risk associated with latex glove use was not apparent after 2000.

189 was not noticed, except for sporadic use of latex gloves and surgical masks.This is believed to be t

190 R, 2.02; 95% CI, 1.20-3.40), use of powdered latex gloves between 1992 and 2000 (OR, 2.17; 95% CI, 1.

191 eactive protein levels were assessed using a latex immunoassay from archived maternal serum specimens

192 ally stabilized poly(2-vinylpyridine) (P2VP) latex in dilute aqueous solution) and also the spontaneo

193 he analysis of aroma component of mango sap (latex) in nine Pakistani varieties that are Anmol, Began

194 Latex injections and high frequency ultrasound (50 MHz)

195 normally refined out of the opioids that the latex is typically collected for, hence its presence in

196 st, the repertoire of the genes expressed in latex is unique.

197 ent a novel assay scheme that uses two-color latex labels for rapid multiplex detection of IgG/IgM.

198 e selectively targeted by model hybrid lipid-latex (LiLa) nanoparticles bearing phagocytic signals.

199 We investigated the fate of latex (LX) particles that were introduced into mice intr

200 rogel by disintegrating an assembled polymer latex made from poly(ethyl acrylate-co-methacrylic acid)

201 FG) or green (GFB) and red (RFB) fluorescent latex microbeads were injected iontophoretically or by p

202 retrograde tracer, red (RFB) or green (GFB) latex microbeads, was injected into the gustatory PBN un

203 Latex micrometric beads are manipulated by optical tweez

204 OCT latex microsphere concentration measurements were highly

205 nterior segment OCT system was used to image latex microsphere suspensions in vitro and the AC of uve

206 ducted with bromide and carboxylate-modified latex microspheres (20, 200, and 500 nm diameter).

207 Latex microspheres and ac cells were visualized as refle

208 rogradely labeled with rhodamine fluorescent latex microspheres and subsequently intracellularly fill

209 ripping analysis of gold nanoparticle-loaded latex microspheres as a signal-amplified hybridization t

210 eased phagocytic activity toward fluorescent latex microspheres as well as apoptotic cells, thus unco

211 ptake of colloidal gold particles as well as latex microspheres by HeLa cells.

212 apacity of iron-oxide coated sands to remove latex microspheres from water revealed that microsphere

213 s migration, we labeled SVZ cells with inert latex microspheres immediately post-injury.

214 e tracing with rhodamine-labeled fluorescent latex microspheres was used to determine whether the hyp

215 c targets, distinct green or red fluorescent latex microspheres were injected into the PGi and the CN

216 Iron oxide surface patches on latex microspheres were selectively wetted with liquid l

217 oxin B subunit, Fluoro-Gold, and fluorescent latex microspheres) into the thalamus to estimate the nu

218 colloidal gold nanoparticles and fluorescent latex microspheres.

219 ctive Fab domains of an antibody attached to latex microspheres.

220 gradient chromatography, using ion-exchange, latex-modified, open tubular and packed monolithic colum

221 one-coated silicone (n = 3) or silver-coated latex (n = 9) catheters with silicone or latex catheters

222 The latex nanoparticle was electrostatically attached to car

223 s to decreased retention of the carboxylated latex nanoparticle.

224 The RPS provided diameters of monodisperse latex nanoparticles agreed within the experimental error

225 c nanoparticles, carbon-based nanomaterials, latex nanoparticles and liposome nanoparticles) for dete

226 The utility of novel latex nanoparticles as pseudostationary phases for elect

227 Measured densities for latex nanoparticles of 160-300 nm in diameter were in th

228 ed with 65-nm-diameter anion exchanger (AEX) latex nanoparticles that attach electrostatically.

229 agnitude lower than those of the polystyrene latex nanoparticles, likely as a result of steric stabil

230 C-MWNT filtration experiments using carboxyl latex nanoparticles.

231 ure the density of monodispersed polystyrene latex nanoparticles.

232 (CdTe and CdSe) and carboxylated polystyrene latex (nPL) as a model nanoparticle using saturated labo

233 t Hevea brasiliensis (rHev b) natural rubber latex (NRL) allergen components have been developed to a

234 rs and 33 subjects exposed to natural rubber latex (NRL), all with work-related allergic symptoms.

235 thocyanidin oligomer extracted from the bark latex of Croton lechleri, is in clinical trials for secr

236 clotting activity has been purified from the latex of Euphorbia neriifolia by anion exchange and size

237 Latex of Hevea brasiliensis (Willd. ex A, Juss.) Mull. A

238 tionate glycyl endopeptidase from the papaya latex of Red Lady and Khack Dum cultivars.

239 kaloid found endemically and uniquely in the latex of the opium poppy.

240 to modify graphics parameters and produces a LaTeX output.

241 newicktree is a PSTricks-based LATEX package which enables phylogenetic trees described

242 , Eya1 and Six1 compound mutants at E17.5 by latex paintfilling.

243 The magnetic label consists of a latex particle of mean diameter 441+/-6 nm, bearing magn

244 croscopy was used to prepare digital maps of latex particle trapping patterns (eight per lung).

245 After 24 hrs, 4-microm-diameter fluorescent latex particles (2 x 10(8)) were infused into the pulmon

246 ted with nanosized (20 nm) carboxyl-modified latex particles (20nCL) and carboxyl-modified CdSe/ZnS q

247 d (1 mum) sulfate-functionalized polystyrene latex particles (designated as 20 nSL and 1 mSL, respect

248 to internalize LPS-coated, but not uncoated, latex particles and because MD2/TLR4-transfected human e

249 of monodisperse, highly charged polystyrene latex particles are polymerized within lightly cross-lin

250 Spherical latex particles are uniformly deposited on glass slides

251 abilized polystyrene latex; remarkably, such latex particles can be readily prepared by aqueous emuls

252 assay requires a flow cytometer, two sets of latex particles coated with pneumococcal polysaccharides

253 ynamic volume from calibrations with polymer latex particles in flow-FFF are compared to calibrations

254 ified through film-formation of soft polymer latex particles on the surface of the polymersome, hereb

255 In the second method, latex particles were codeposited with the silica by spin

256 C-albumin, Lsr-F, or fluorescent polystyrene latex particles were electrosprayed from aqueous buffer

257 lector interface; namely, on bare Al2O3, the latex particles were rigidly attached as compared to the

258 onstrated for a mixture of three polystyrene latex particles with different sizes as well as for the

259 Using latex particles, silica particles and carbon nanotubes a

260 structures are controlled by the size of the latex particles.

261 ingest both fibronectin and collagen-coated latex particles.

262 as not detected in phagolysosomes containing latex particles.

263 ntaining either silica particles or nontoxic latex particles.

264 olayer coverage of the surface by individual latex particles.

265 at of the non-articulated laticifer cells in latex plants, suggesting a common evolutionary origin.

266 organic solvent-based coatings by waterborne latex polymer coatings has substantially renovated the c

267 ional pattern is significantly correlated to latex production level.

268 of new proteins (m-type thioredoxins, major latex protein-like protein, ULTRAVIOLET-B RESISTANCE8 ph

269 A Ficus carica L. latex proteinase preparation was investigated for its ab

270 morphine were among the most abundant active latex proteins despite a limited occurrence in laticifer

271 Plant modification for latex reduction inhibited an induced cardenolide respons

272 ared using sterically stabilized polystyrene latex; remarkably, such latex particles can be readily p

273 omposite of a pliable rubber tube and a soft latex sheet is consistent with this mechanism and produc

274 CO2-responsive materials including polymers, latexes, solvents, solutes, gels, surfactants, and catal

275 this is the first in planta demonstration of latex-specific CPT activity in rubber biosynthesis.

276 od lengths from hydrodynamic models based on latex sphere calibrations.

277 M(w)= 65000 Daltons, diameter = 8 nm) and to Latex spheres (diameter = 900 nm).

278 Polystyrene latex spheres (PSL) with aerodynamic diameters ranging f

279 f PEG surface packing on monodisperse 200 nm latex spheres indicates that the size of the hydrophobic

280 We use latex spheres with diameters ranging from 190 to 780 nm

281 s detected in the whole stem, but not in the latex subproteome.

282 issues tested (leaves, stem, bark, xylem and latex), suggesting that HbXIP2;1 could take part in a wi

283 oducing stable PFS-poly(methyl methacrylate) latex suspensions.

284 olymerisation at the forefront of industrial latex synthesis.

285 positive rapid penicillin binding protein 2a latex test in conjunction with the phenotypic properties

286 ficantly outperformed commercially available latex tests (sensitivity for both latex tests, <15%) whe

287 available latex tests (sensitivity for both latex tests, <15%) when it was used directly with broth

288 unts of high-quality natural rubber in their latex, the milky cytoplasm of specialized cells known as

289 ability of the enzyme caricain (from papaya latex) to detoxify gliadin in whole wheat flour and deve

290 otgun proteomics performed on whole-stem and latex total protein extracts generated 2031 and 830 dist

291 This apparatus consisted of an 8-mm-diameter latex tube placed in a tissue-mimicking fluid.

292 The latex used contained a significant, additional amount of

293 ydimethylsiloxane Sylgard 184, polyurethane, latex, VHB and Ecoflex.

294 oup bacteriuria rate, control catheter type (latex vs. silicone), and patient sample (urology vs. oth

295 foods, 12 respiratory allergen sources, and latex was tested by using skin prick test and ImmunoCAP.

296 ights into the molecular events occurring in latex, we analyzed more than 20,000 cDNA-AFLP-based TDFs

297 ge isoforms of two key O-demethylases in the latex were revealed by two-dimensional immunoblot analys

298 Food, drugs, stinging insects, and latex were the most commonly identified triggers.

299 ivity (90 U g(-1) polymer) was observed with latex, while highest entrapment efficiency (93%) was obs

300 A library of 32 polystyrene copolymer latexes, with diameters ranging between 53 and 387 nm, w