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 was added to two clarified grape juices with and wit

4 AGP-interacting residues were compared with Rosi-interac

5 AGPs were abundant in kanuka honey with lesser amounts i

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

7 [32P]AGP bound PPARgamma with an affinity (Kdapp 60 nm) simil

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

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

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

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

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

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

14 eraction demonstrated that the protein is an AGP.

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

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

17 sion models analyzed the kinetics of CRP and AGP by infection status, and nutritional biomarkers by i

18 tribution of SF after correction for CRP and AGP by the BRINDA method was comparable with the estimat

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

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

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

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

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

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

25 In WRA, the association of PZC with CRP and AGP was weak and inconsistent.

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

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

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

29 versely associated with sICAM-1, hs-CRP, and AGP, which were positively associated with BMI.

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 ntrations for CRP [16.0 (7.9-29.5) mg/L] and AGP [0.9 (0.8-1.2) g/L] on day 3 and day 4 postexposure,

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

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

35 abolished binding and activation by Rosi and AGP.

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

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

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

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

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

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

42 from -0.13 to 0.08, and correlations between AGP and serum folate between -0.21 and 0.02.

43 from -0.25 to 0.16, and correlations between AGP and vitamin B-12 ranged between -0.07 and 0.14.

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

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

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

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

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

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

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

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

52 cause they differentially fucosylate certain AGPs.

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

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

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 cover the plasma membrane and are highly glycosylat

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

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

60 linkage that caps the side chains of complex AGPs.

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

62 alyze the independent relations between CRP, AGP, and biomarkers for iron, vitamin A, vitamin D, vita

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

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

65 Women receiving SPAZ had lower delivery AGP and CRP levels (p < 0.001).

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

75 ged from -0.07 to 0.08 for CRP and -0.04 for AGP (1 country).

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

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

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

79 The K(a) measured by proxy ligand-ESI-MS for AGP, Hp1-1 and alpha2M (4 x 10(5) M(-1), 2 x 10(5) M(-1)

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

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

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

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

84 cidation of arabinogalactan biosynthesis for AGPs.

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

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

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

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

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

90 nogalactans connected to proteins which form AGP glycoprotein, a macro-molecule responsible for the e

91 4,5-unsaturated uronic acid, is removed from AGP by a glycoside hydrolase located in family GH105, pr

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

93 of inflammation (alpha-1-acid glycoprotein (AGP) and C-reactive protein (CRP)) were measured at 6 an

94 protein (CRP) and alpha1-acid glycoprotein (AGP) and serum vitamin B-12 and serum and RBC folate amo

95 alpha-1-Acid glycoprotein (AGP) and transferrin (Tf) are the main glycoproteins pre

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

97 protein (CRP) and alpha-1-acid glycoprotein (AGP) by infection status, model kinetics of micronutrien

98 bonuclease B, and alpha-1 acid glycoprotein (AGP) by PGC-LC-MS.

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

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

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

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

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

104 ation patterns of alpha-1 acid glycoprotein (AGP) could be used as a marker for early detection of he

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

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

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

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

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

110 protein (CRP) or alpha-1-acid glycoprotein (AGP) was observed: 1) exclude individuals with CRP > 5 m

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

112 human serum GPs, alpha-1-acid glycoprotein (AGP), haptoglobin phenotype 1-1 (Hp1-1) and alpha-2-macr

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

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

115 ve protein (CRP), alpha-1-acid glycoprotein (AGP), soluble endoglin (sEng), soluble fms-like tyrosine

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

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

118 tein (hs-CRP), and alpha1-acid glycoprotein (AGP)] for which observational associations were detected

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

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

121 otein (CRP) and/or alpha1-acid-glycoprotein (AGP).

122 ve protein [CRP], alpha-1-acid glycoprotein [AGP]) and biomarkers of MN status (pF, soluble transferr

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

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

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

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

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

128 At delivery, higher AGP levels were strongly associated with low birthweight

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

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

131 Glycosylation analysis of human AGP revealed the potential use of PGC-LC-MS for extensiv

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

133 olol and HPLC columns containing immobilized AGP.

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

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

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

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

138 Functionally important AGP glycans are synthesized in the Golgi apparatus, but

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

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

141 ined by the involvement of galactosidases in AGP glycan biosynthesis.

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

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

144 of a putative GLCAT gene family involved in AGP biosynthesis by examining its sequence diversity, ge

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

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

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

148 erases (GLCATs), is the only acidic sugar in AGPs with the ability to bind calcium.

149 les, and to a lesser extent, with increasing AGP deciles.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

167 onsible for the partial PPARgamma agonism of AGP.

168 ed binding of Rosi but maintained binding of AGP.

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

170 Determination of AGP and Tf was successfully demonstrated in the analysis

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

172 associated with an increase in the extent of AGP cell wall association, as demonstrated by Yariv phen

173 nregulation, and decreased the generation of AGP.

174 s showed that the trifucosylated N-glycan of AGP (triFc_AGP) could differentiate HCC from cirrhosis w

175 MALDI-MS profiling of N-glycans of AGP purified from 20 muL of patient serum in HCC (n = 72

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

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

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

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

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

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

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

183 Intranasal administration of AGPs induced intrapulmonary production of proinflammator

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

185 intranasal/intrapulmonary administration of AGPs.

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

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

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

189 s used here to elucidate functional roles of AGPs.

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

191 Several types of AGPs provided strong protection against influenza virus

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

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

194 s of within-individual changes in CRP and/or AGP, were estimated from general linear models, accounti

195 and inconsistent correlations between CRP or AGP and vitamin B-12 or folate biomarkers, there is no r

196 Spearman correlations between CRP or AGP and vitamin B-12 or folate concentrations were exami

197 the study population (10th percentile CRP or AGP concentration).

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

199 negative association between PZC and CRP or AGP, application of the RC approach is supported.

200 se from cell wall-extracted glycoproteins or AGP-rich gum arabic.

201 1) exclude individuals with CRP > 5 mg/L or AGP > 1 g/L; 2) apply arithmetic correction factors; and

202 , inflammation was defined as CRP >5 mg/L or AGP >1 g/L, or both.

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

204 up-regulated by arabinogalactan proteins or AGPs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

220 icipated in an aerosol generation procedure (AGP) at least once during the viral respiratory season w

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

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

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

224 1517 families from an Autism Genome Project (AGP).

225 Resource Exchange and Autism Genome Project (AGP).

226 8,000 samples from the American Gut Project (AGP) microbiome crowdsourcing effort.

227 projects to date, the American Gut Project (AGP), we obtain differential abundance vectors for micro

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

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

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

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

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

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

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

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

236 Plant arabinogalactan proteins (AGPs) are a diverse group of cell surface- and wall-asso

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

238 mercial product of arabinogalactan proteins (AGPs) from Acacia senegal.

239 0K) are two pistil arabinogalactan proteins (AGPs) that share a conserved C-terminal domain (CTD) and

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

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

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

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

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

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

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

247 e glycosylation of arabinogalactan proteins (AGPs).

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

249 Arabinogalactan-proteins (AGPs) are glycoproteins that interact with other cell wa

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

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

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

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

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

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

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

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

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

259 een for immobilized AGP and that for soluble AGP.

260 greement with previous studies using soluble AGP.

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

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

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

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

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

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

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

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

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

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

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

272 specification of the adrenal cortex from the AGP.

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

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

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

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

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

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

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

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

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

282 Glucuronic acid, which is transferred to the AGP glycan by beta-glucuronosyltransferases (GLCATs), is

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

284 ntal condition information provided with the AGP metadata, such as patient age, dietary habits, or he

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

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

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

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

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

290 ses approximately two-fold with exposures to AGP.

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

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

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

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

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

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

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

298 ot involving the formation of a complex with AGPs.

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

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

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