ライフサイエンスコーパス: AGP

1 AGP galactosyltransferase (GalT) activities in tobacco (

2 AGP showed some activity at fermentation temperatures (

3 AGP transcription was assessed with transcription elonga

4 AGP transcription was increased equivalently in both mod

5 AGP was added to two clarified grape juices with and wit

6 AGP-interacting residues were compared with Rosi-interac

7 AGPs were abundant in kanuka honey with lesser amounts i

8 increased ferritin by 49.6% (CRP) or 38.2% (AGP; both P lt 0.001).

9 [32P]AGP bound PPARgamma with an affinity (Kdapp 60 nm) simil

10 gamma ligand binding domain showed that [32P]AGP and [3H]rosiglitazone (Rosi) both specifically bind

11 dopsis (Arabidopsis thaliana) as follows: 85 AGPs (including classical AGPs, lysine-rich AGPs, arabin

12 ol mice died within 4 days of infection, all AGP-treated mice showed prolonged time-to-death, and 30-

13 en2 gene (Sh2r6hs), which encodes an altered AGP large subunit.

14 Although AGP transcription was similar in mild and fulminant seps

15 Although AGPs are ubiquitous in plants, there is a paucity of inf

16 gnal sequence, a phytocyanin-like domain, an AGP-like domain, and a hydrophobic carboxyl-terminal dom

17 Additional support that AtGALT2 encodes an AGP GALT was provided by two allelic AtGALT2 knock-out m

18 eraction demonstrated that the protein is an AGP.

19 A1]) that encoded the protein backbone of an AGP in the active fraction.

20 e that glycosylphosphatidylinositol-anchored AGPs function to link the plasma membrane to the cytoske

21 estimates incrementally increased as CRP and AGP deciles decreased (4% compared with 30%, and 6% comp

22 ntrations incrementally decreased as CRP and AGP deciles decreased for PSC and WRA, but the effect wa

23 e relation between estimated VAD and CRP and AGP deciles followed a linear pattern in PSC.

24 djustment for malaria in addition to CRP and AGP did not substantially change the estimated prevalenc

25 ty was associated with both elevated CRP and AGP in WRA.Recent morbidity and abnormal anthropometric

26 Effects of the concentrations of CRP and AGP on SF, sTfR, and TBI were generally linear, especial

27 Regression analyses suggested that CRP and AGP were significant predictors of SF (P < 0.001); howev

28 en, the correlations between RBP and CRP and AGP were too weak to justify adjustments for inflammatio

29 he estimated VAD after adjusting for CRP and AGP.The use of regression correction (derived from inter

30 igate abilities of the PCs of only ITIH4 and AGP to modulate the interaction of NPs with the host imm

31 unique anti-inflammatory proteins (ITIH4 and AGP), which were absent from the PC of both controls.

32 C-terminal PAC (for proline-rich protein and AGP, containing cysteine) domain.

33 PRPs (including PRPs and chimeric PRPs), and AGP/EXT hybrid HRGPs.

34 abolished binding and activation by Rosi and AGP.

35 idin, fetuin, asialofetuin, transferrin, and AGP) as well as a clade C HIV envelope glycoprotein, C.9

36 d assays, here we show that andrographolide (AGP)--a bicyclic diterpenoid lactone isolated from Andro

37 scribed in this work could be used to attach AGP to other materials, such as those used for surface p

38 s method was evaluated by using it to attach AGP to silica for use in high-performance affinity chrom

39 was done only for CRP concentrations because AGP concentrations were not measured; regression correct

40 A complex between AGP and PPARgamma was generated using molecular modeling

41 Correlations between AGP, CRP, urinary hepcidin, and SF were statistically si

42 LR4, and that structural differences between AGPs can have dramatic effects on agonist activity in vi

43 d for inhibitors of exchange factor binding, AGP derivatives reduced GTP loading of wild-type K-Ras i

44 therefore recommend the measurement of both AGP and CRP in population surveys that include an assess

45 associated with reduced levels of JIM8-bound AGP and JIM11-bound extensin epitopes, while silencing o

46 ion of PPARgamma reporter gene expression by AGP and Rosi showed similar potency, yet AGP-mediated ac

47 the activation of innate immune effectors by AGPs depends primarily on the lengths of the secondary a

48 rmone activity in plants can be modulated by AGPs.

49 lasmic arabinogalactan glycoprotein-calcium (AGP-Ca(2+) ) capacitor with tip-localized AGPs as the so

50 cause they differentially fucosylate certain AGPs.

51 ed AGP and to demonstrate that this chimeric AGP promotes cotton SE.

52 AGPs, plastocyanin AGPs, and other chimeric AGPs), 59 EXTs (including SP(5) EXTs, SP(5)/SP(4) EXTs,

53 cation and immunolocalization of a classical AGP (PtaAGP6, accession number AF101785) in loblolly pin

54 AtAGP30 is a non-classical AGP core protein from Arabidopsis that is expressed only

55 The lysine-rich classical AGP subfamily in Arabidopsis consists of three members,

56 the Hechtian Hypothesis translates classical AGP function as a Ca(2+) capacitor, pollen tube guide an

57 Classical AGPs and some nonclassical AGPs are predicted to have a

58 Classical AGPs cover the plasma membrane and are highly glycosylat

59 na) as follows: 85 AGPs (including classical AGPs, lysine-rich AGPs, arabinogalactan peptides, fascic

60 cAGP1, encodes a new class of non-classical' AGP with strong similarity to a family of basic proline-

61 was developed that identifies and classifies AGPs, EXTs, PRPs, hybrid HRGPs, and chimeric HRGPs from

62 linkage that caps the side chains of complex AGPs.

63 pproach used to adjust for inflammation (CRP+AGP), the estimated prevalence of VAD decreased by a med

64 Furthermore, dearabinosylated AGPs were not substrate acceptors for these enzymes, ind

65 ples were collected when no WHO 2009 defined AGP was being performed of which 8 (10.5%) contained vir

66 38) explained more of SF's variance than did AGP (R(2) = 0.17).

67 Elevated AGP was more common than CRP in young persons than in ad

68 elevated), and late convalescence (elevated AGP only).

69 ean were poorly predicted by either elevated AGP or CRP.

70 Zambian children, whereas 97.7% had elevated AGP, categorizing them as having no infection (2.3%) or

71 esidence, and socioeconomic status, elevated AGP was positively associated with stunting (height-for-

72 laria, stunting was associated with elevated AGP but not CRP in PSC, and obesity was associated with

73 -64.3% in PSC and 7.1-26.7% in WRA (elevated AGP).

74 tures of the maize (Zea mays) genes encoding AGP small subunits of leaf and endosperm.

75 cation from other closely related endogenous AGPs.

76 tional significance because cereal endosperm AGPs are cytosolic, whereas all other forms appear to be

77 d classical tomato (Lycopersicon esculentum) AGP containing a glycosylphosphatidylinositol plasma mem

78 f the major tomato (Lycopersicon esculentum) AGP, LeAGP-1, as an enhanced green fluorescent protein f

79 gnificant activity in the presence of excess AGP, although replacement of the piperidino groups at th

80 histosoma haematobium infection (n = 224 for AGP, CRP, SF, sTfR, and hemoglobin; n = 61 for urinary h

81 re the first enzymes to be characterized for AGP glycosylation and further our understanding of cell

82 d apoptosis suggests possible mechanisms for AGP activation and regulation of apoptosis-signaling pat

83 WRA, but the effect was more pronounced for AGP than for CRP.

84 proteins (AGPs), the enzymes responsible for AGP glycosylation are largely unknown.

85 WRA, respectively, with similar results for AGP).

86 owever, the specific mechanism of action for AGPs has not yet been determined.

87 cidation of arabinogalactan biosynthesis for AGPs.

88 ode alpha(1,2)fucosyltransferases (FUTs) for AGPs.

89 icker actin filaments, indicating a role for AGPs in actin polymerization.

90 ization of MTs, indicating a likely role for AGPs in cortical MT organization.

91 AtGALT2 is specific for AGPs because substrates lacking AGP peptide sequences di

92 icated that the two enzymes are specific for AGPs but are not functionally redundant because they dif

93 4,5-unsaturated uronic acid, is removed from AGP by a glycoside hydrolase located in family GH105, pr

94 Susceptibility of [(14)C]fucosylated AGPs to alpha(1,2)fucosidase, and not to alpha(1,3/4)fuc

95 G (IgG), and human alpha1-acid glycoprotein (AGP) as well as of sialylated oligosaccharide reference

96 ion between serum alpha-1 acid glycoprotein (AGP) concentration and plasma imatinib, and an inverse c

97 ations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L, 2) the application of arithm

98 ations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L, 2) the application of arithm

99 ations >5 mg/L or alpha-1-acid glycoprotein (AGP) concentrations >1 g/L; 3) apply arithmetic correcti

100 protein (CRP) and alpha1-acid glycoprotein (AGP) concentrations on estimates of ID according to seru

101 paring immobilized alpha1-acid glycoprotein (AGP) for use in drug-protein binding studies was develop

102 ificant augment in alpha1-acid glycoprotein (AGP) hepatic mRNA expression and serum protein levels.

103 mmobilization of alpha(1)-acid glycoprotein (AGP) in high-performance liquid chromatography (HPLC) co

104 ell as endogenous alpha-1-acid glycoprotein (AGP) in human plasma.

105 protein (CRP) and alpha1-acid glycoprotein (AGP) to identify the influence of inflammation on the di

106 ve protein (CRP), alpha-1-acid glycoprotein (AGP), ferritin, and retinol.

107 rotein (CRP) and alpha(1)-acid glycoprotein (AGP), individually and in combination, and to calculate

108 ns between serum alpha(1)-acid glycoprotein (AGP), serum C-reactive protein (CRP), and urinary hepcid

109 ute phase reactant alpha1-acid glycoprotein (AGP), would correlate with recovery from sepsis.

110 e serum protein, alpha(1)-acid glycoprotein (AGP).

111 protein (CRP) and alpha1-acid glycoprotein (AGP).

112 rug binding, the alpha(1)-acid-glycoprotein (AGP) and human serum albumin (HSA).

113 interface, using alpha(1)-acid-glycoprotein (AGP) as a chiral acute phase plasma protein.

114 Arabinogalactan glycoproteins (AGPs) are implicated in virtually all aspects of plant g

115 to purify and analyze a single glycosylated AGP and to demonstrate that this chimeric AGP promotes c

116 romoted SE, indicating that the glycosylated AGP domain was unnecessary for in vitro activity.

117 P1 and glutathione S-transferase (GST), GST::AGP CTD fusions.

118 l to Hyp of model substrate acceptors having AGP peptide sequences, consisting of non-contiguous Hyp

119 We report that apisimin shares with honey AGPs the ability to stimulate the release of TNF-alpha f

120 However, AGP displaced approximately 40% of bound [3H]Rosi even w

121 on equilibrium constants between immobilized AGP and R- or S-propranolol.

122 olol and HPLC columns containing immobilized AGP.

123 nt between the behavior seen for immobilized AGP and that for soluble AGP.

124 brium constants measured for the immobilized AGP with R- and S-propranolol at pH 7.4 and 37 degrees C

125 rved for both enantiomers on the immobilized AGP, in agreement with previous studies using soluble AG

126 ons of the Hechtian oscillator may implicate AGPs in osmosensing or gravisensing and other tropisms,

127 ds and indicate roles for MTs and F-actin in AGP organization at the cell surface and in Hechtian str

128 itions to oxidize the carbohydrate chains in AGP for attachment to a hydrazide-activated support.

129 is activity was specific for peptidyl Hyp in AGP sequences.

130 g galactose (Gal) to hydroxyproline (Hyp) in AGP protein backbones.

131 ork demonstrates that Arabidopsis mutants in AGP structure can be identified and characterized.

132 trometry indicated the presence of fucose in AGPs from transgenic cell lines but not in AGPs from wil

133 n AGPs from transgenic cell lines but not in AGPs from wild type cells.

134 an l-fucose containing epitope is present in AGPs in the cell wall of differentiating root cells.

135 Sh2r6hs transgenic wheat exhibited increased AGP activity in the presence of a range of orthophosphat

136 en the conventional markers of inflammation, AGP and CRP, was positive (r = 0.40, P < 0.01), and the

137 scavenger N-acetyl-l-cysteine also inhibits AGP-induced activation of ASK1, as well as apoptosis.

138 -neutralizing antibody specifically inhibits AGP-induced apoptosis signal, regulating apoptosis signa

139 A promising candidate is AGP, a mixture of Aspergillopepsins I and II.; a food gr

140 sis starting from the DNA sequences of known AGPs remained untested due to difficulties in purifying

141 specific for AGPs because substrates lacking AGP peptide sequences did not act as acceptors.

142 Ps, arabinogalactan peptides, fasciclin-like AGPs, plastocyanin AGPs, and other chimeric AGPs), 59 EX

143 m (AGP-Ca(2+) ) capacitor with tip-localized AGPs as the source of tip-focussed cytosolic Ca(2+) osci

144 The log AGP and CRP values were significantly correlated (r = 0.

145 altered large subunit gives rise to a maize AGP heterotetramer with decreased sensitivity to its neg

146 indicate that the endogenous lipid mediator AGP is a high affinity ligand of PPARgamma but that it b

147 oxidation involved the reaction of 5.0 mg/mL AGP at 4 degrees C and pH 7.0 with 5-20 mM periodic acid

148 cells in the presence and absence of 5 mg/mL AGP.

149 4)-beta-D-galactan and glucuronosyl-modified AGP biosynthesis is exacerbated.

150 l-fucose, which was reduced in level in mur1 AGPs.

151 In the fucose-deficient murus1 mutant, AGPs lack these fucose modifications.

152 with several known and putative nonclassical AGPs from other species: a putative signal peptide, a hi

153 Classical AGPs and some nonclassical AGPs are predicted to have a glycosylphosphatidylinosito

154 o BY2 cells, known to contain nonfucosylated AGPs, resulted in a staining of transgenic cells with ee

155 howed prolonged time-to-death, and 30-60% of AGP-treated mice survived.

156 Finally, administration of AGP abolished the effect of insulin treatment in diabeti

157 Administration of AGP in nondiabetic mice subjected to mild sepsis inhibit

158 Thus, preventive administration of AGP successfully modulated innate immune responses to ae

159 onsible for the partial PPARgamma agonism of AGP.

160 ed binding of Rosi but maintained binding of AGP.

161 utions containing constant concentrations of AGP (50 muM).

162 eta-d-galactan may be an event downstream of AGP function during cell expansion in the Arabidopsis se

163 The protective effect of AGP was lost in mice lacking IFN-gamma.

164 nregulation, and decreased the generation of AGP.

165 itions helped maximize the immobilization of AGP without significantly affecting its activity.

166 n of intracellular ASK1 reduces the level of AGP-induced oxidative stress and apoptosis.

167 lencing of SlP4H1 reduced only the levels of AGP proteins.

168 However, the mechanism of AGP-induced cancer cell death is unknown.

169 f propranolol enantiomers in the presence of AGP was found to be greater for (S)-propranolol than (R)

170 l for the identification and verification of AGP-specific GalT proteins/genes and an entry point for

171 ve the baseline rate (i.e. in the absence of AGPs) did not reach significance, there was a trend towa

172 Intranasal administration of AGPs induced intrapulmonary production of proinflammator

173 isteria model, intravenous administration of AGPs was followed by intravenous bacterial challenge 24

174 intranasal/intrapulmonary administration of AGPs.

175 Although precise functions of AGPs remain elusive, they are widely implicated in plant

176 ance, there was a trend towards hierarchy of AGPs, placing bronchoscopy and respiratory and airway su

177 ablished a baseline upon which mechanisms of AGPs in regulation of health and growth of animals can b

178 s demonstrate a route to the purification of AGPs and the use of the Hyp contiguity hypothesis for pr

179 s used here to elucidate functional roles of AGPs.

180 Testing of AGPs separated by reverse-phase high-performance liquid

181 Several types of AGPs provided strong protection against influenza virus

182 The withdrawal of AGPs and other restrictions have reduced total antimicro

183 considered in the light of current views on AGP structure and function.

184 cterize the microbiome of pigs receiving one AGP, tylosin, compared with untreated pigs.

185 In 2-group analyses (either CRP or AGP), we compared the ratios of log ferritin with or wit

186 n inflammation (CRP concentration >5 mg/L or AGP concentration >1 g/L) and covariates, such as demogr

187 up-regulated by arabinogalactan proteins or AGPs.

188 gical function been assigned to a particular AGP.

189 Two-step RT-PCR with the AgPath ID RT-PCR (AGP) kit performed best for both pan-HPeV and EV assays.

190 ton pump efflux that dissociates periplasmic AGP-Ca(2+) resulting in a Ca(2+) influx that activates e

191 beta-Yariv reagent (which binds and perturbs AGPs) were used to examine the role of LeAGP-1 as a cand

192 ctadecenyl-2-hydroxy-sn-glycero-3-phosphate (AGP), is a high affinity partial agonist of the peroxiso

193 agonist, aminoalkyl glucosaminide phosphate (AGP), would boost the innate immune system and compensat

194 med the aminoalkyl glucosaminide phosphates [AGPs]) was evaluated in murine infectious disease models

195 ing between NaPCCP and NaSBP1 and the pistil AGPs may contribute to signaling and trafficking inside

196 mparison of the maize genes with other plant AGP small subunit genes leads to a number of noteworthy

197 Plant AGPs are heterotetrameric, consisting of two large and t

198 hetic probe that specifically binds to plant AGPs and has been used to study AGP functions.

199 b, and an inverse correlation between plasma AGP concentration and imatinib clearance.

200 Atmospheric gas plasmas (AGPs) are able to selectively induce apoptosis in cancer

201 peptides, fasciclin-like AGPs, plastocyanin AGPs, and other chimeric AGPs), 59 EXTs (including SP(5)

202 ch used to adjust for inflammation (CRP plus AGP), the estimated prevalence of depleted iron stores i

203 e air samples were collected while potential AGPs were being performed of which 6 (26.1%) contained v

204 es and reductions in beta-Yariv-precipitated AGPs compared with wild type plants.

205 al cortex from the adrenogonadal primordium (AGP) have yet to be determined.

206 HO)-defined 'aerosol generating procedures' (AGPs) are thought to increase the risk of aerosol transm

207 hed CNV data from the Autism Genome Project (AGP) and exome sequencing data from the SSC and the Auti

208 ean ancestry from the Autism Genome Project (AGP) with a diagnosis of an ASD and at least one rare CN

209 Resource Exchange and Autism Genome Project (AGP).

210 1517 families from an Autism Genome Project (AGP).

211 e been used extensively as growth promoters (AGPs) in agricultural animal production.

212 use of antimicrobials for growth promotion (AGPs) in animal production through an on-going series of

213 rabidopsis thaliana arabinogalactan protein (AGP) encoded by hydroxyproline-rich glycoprotein family

214 fied a nonclassical arabinogalactan protein (AGP) gene, AGP31, and show that its mRNA decreased to ab

215 nsisting of a short arabinogalactan protein (AGP) motif, a His stretch, a Pro-rich domain, and a C-te

216 noaffinity-purified arabinogalactan protein (AGP) secreted aucus carota (carrot) cells in liquid cult

217 application of the arabinogalactan-protein (AGP) binding beta-glucosyl Yariv reagent (betaGlcY) that

218 itol (GPI)-anchored arabinogalactan-protein (AGP) in tomato (Lycopersicon esculentum).

219 his gene encodes an arabinogalactan-protein (AGP) that is known to play a role in root regeneration a

220 eight component in arabinogalactan-proteins (AGP/GP), and more "branched" carbohydrates present in gu

221 HRGPs such as arabinogalactan proteins (AGPs) and extensios play significant roles on cell wall

222 tory plant-derived arabinogalactan proteins (AGPs) and the honeybee-derived protein apisimin are pres

223 Arabinogalactan proteins (AGPs) are a family of extracellular plant proteoglycans

224 Arabinogalactan proteins (AGPs) are abundant plant proteoglycans implicated in pla

225 0K) are two pistil arabinogalactan proteins (AGPs) that share a conserved C-terminal domain (CTD) and

226 water-extractable arabinogalactan proteins (AGPs) were isolated from the leaves of Arabidopsis (Arab

227 Arabinogalactan proteins (AGPs), a family of hydroxyproline-rich glycoproteins, oc

228 nantly composed of arabinogalactan proteins (AGPs), a superfamily of hydroxyproline-rich glycoprotein

229 Arabinogalactan proteins (AGPs), a superfamily of plant hydroxyproline-rich glycop

230 res found in plant arabinogalactan proteins (AGPs), is described.

231 hyperglycosylated arabinogalactan proteins (AGPs), moderately glycosylated extensins (EXTs), and lig

232 tantial amounts of arabinogalactan proteins (AGPs), the enzymes responsible for AGP glycosylation are

233 e glycosylation of arabinogalactan proteins (AGPs).

234 Arabinogalactan-proteins (AGPs) are cell wall proteoglycans and are widely distrib

235 Arabinogalactan-proteins (AGPs) are extracellular proteoglycans that are implicate

236 Arabinogalactan-proteins (AGPs) are highly glycosylated hydroxyproline (Hyp)-rich

237 Since arabinogalactan-proteins (AGPs) are known to play a role in plant cell expansion w

238 hyperglycosylated arabinogalactan-proteins (AGPs) attempts to relate biological roles to the molecul

239 a Pro-rich domain, and a C-terminal PAC (PRP-AGP containing Cys) domain.

240 posite was developed by integrating purified AGP-rich ivy nanoparticles with pectic polysaccharides a

241 were able to fucosylate, in vitro, purified AGPs from BY2 wild type cells.

242 Plant ADP-glucose pyrophosphorylase (AGP) is a heterotetrameric enzyme composed of two large

243 steric enzyme ADP-glucose pyrophosphorylase (AGP) plays a key role in regulating starch biosynthesis

244 two monoclonal antibodies known to recognize AGPs: JIM16 and JIM133.

245 In contrast, the R288A showed reduced AGP binding but maintained Rosi binding.

246 ified AGP31 indicated it is a galactose-rich AGP.

247 AGPs (including classical AGPs, lysine-rich AGPs, arabinogalactan peptides, fasciclin-like AGPs, pla

248 Arabidopsis root AGPs were shown to contain l-fucose, which was reduced i

249 the contention that l-fucose containing root AGPs are required for the full elongation of root cells.

250 sion we studied the composition of mur1 root AGPs.

251 In addition, the N-terminal short AGP motif was assumed to be substituted by arabinogalact

252 ed due to difficulties in purifying a single AGP for analysis.

253 een for immobilized AGP and that for soluble AGP.

254 greement with previous studies using soluble AGP.

255 AGPs induces these genes through a specific AGP-based signaling mechanism or through a general mecha

256 We found that specific AGPs were produced by cotton (Gossypium hirsutum) calli

257 nds to plant AGPs and has been used to study AGP functions.

258 In this study, AGP is shown to up-regulate intracellular reactive oxyge

259 henylglycoside cross-linking of cell surface AGPs induces these genes through a specific AGP-based si

260 the effect of Yariv binding to plant surface AGPs and to further understand AGP functions, an Arabido

261 othesize that Yariv binding of plant surface AGPs triggers wound-like responses.

262 Bioinformatics indicated that AGP galactosyltransferases (GALTs) are members of the ca

263 utational and cell biology results show that AGP derivatives directly bind Ras, block GDP-GTP exchang

264 Together, these data suggest that AGP may be involved in reduction of neutrophil migration

265 n summary, this study provides evidence that AGPs and apisimin are commonly present in different flor

266 With our small sample size we found that AGPs do not significantly increase the probability of sa

267 Given that AGPs and pectic polysaccharides are also observed in bio

268 We hypothesized that AGPs exerted their growth promoting effect by altering g

269 says and mass spectrometry, we verified that AGPs bind Ca(2+) tightly (K(d) ~ 6.5 muM) and stoichiome

270 specification of the adrenal cortex from the AGP.

271 e essential transcription factor Sf-1 in the AGP above the threshold required to determine adrenal de

272 between the expression levels of Sf-1 in the AGP and the defects in adrenal development found in mice

273 nuclear hormone receptor Sf-1 (Nr5a1) in the AGP prior to the separation between gonad and adrenal co

274 ance threshold (P<7.1 x 10(-9)), GWAS in the AGP revealed an association between 'the degree of the r

275 The adaptation of the AGP and HSA FP assays to a 1,536-well format should allo

276 l residue in the arabinogalactan (AG) of the AGP and with arabinoxylan attached to either a rhamnosyl

277 The spheroidal shape of the AGP-rich ivy nanoparticles results in a low viscosity of

278 nd a putative cysteine protease bound to the AGP baits.

279 NaSBP1 binds to the AGP CTDs through its helical and RING domains.

280 the suspension-culture cells from which the AGP was obtained; in carrot seedlings the gene is only e

281 -HPeV-specific assay performed best with the AGP kit in a one-step RT-PCR.

282 ic interactions among carboxyl groups of the AGPs and the pectic acids give rise to the cross-linking

283 J mouse, demonstrating the dependence of the AGPs on toll-like receptor 4 (TLR4) signaling for the pr

284 When the AGPs were partly or fully deglycosylated, SE-promoting a

285 tum) calli undergoing SE and that when these AGPs were isolated and incorporated into tissue culture

286 ostly, adjustment for malaria in addition to AGP did not significantly change the estimated prevalenc

287 id, in some cases, restore susceptibility to AGP.

288 As typical AGPs contain c. 30 Ca(2+)-binding subunits and are bulk

289 icinity of H1N1 positive patients undergoing AGPs to help quantify the potential risk of transmission

290 plant surface AGPs and to further understand AGP functions, an Arabidopsis whole genome array was use

291 differentially expressed cellular genes upon AGP treatment of melanoma cells.

292 eported here to detect GalT activities using AGP peptide and glycopeptide acceptor substrates provide

293 9) positive aerosols when performing various AGPs on intensive care patients above the baseline rate

294 Whereas AGP completely ablated the activity of DP, the majority

295 orial characteristics of wines produced with AGP were not different from controls.

296 emarkably, however, prolonged treatment with AGP derivatives also reduced GTP loading of, and signal

297 ot involving the formation of a complex with AGPs.

298 Further, it synergizes with AGPs to enhance the release of TNF-alpha, via a mechanis

299 Mice treated with AGPs before and after inhalation of Francisella novicida

300 by AGP and Rosi showed similar potency, yet AGP-mediated activation was approximately 40% that of Ro