ライフサイエンスコーパス: TRAP

1 TRAP is delivered using adenovirus- and vaccinia virus-b

2 TRAP proteins are thought to play an integral role in pa

3 TRAP staining showed that osteoclast numbers were reduce

4 TRAP+ osteoclast numbers were the highest in the STZ+L g

5 TRAPs, which remain hidden to prior flow diagnostics, th

6 , and tartrate-resistant acid phosphatase 5 (TRAP) with receptor activator of NF-kappaB ligand-evoked

7 and tartrate-resistant acid phosphatase 5b (TRAP-5b), and calcium and alveolar bone levels in rats w

8 of the malaria parasite Plasmodium express a TRAP family protein called merozoite-TRAP (MTRAP) that h

9 sition of VcSiaP, the SBP of the sialic acid TRAP transporter from V. cholerae.

10 rotein is the SBP of VcSiaPQM, a sialic acid TRAP transporter from Vibrio cholerae.

11 In addition, TRAP may help to keep translation at its peak efficiency

12 the chemokine ligand 5 (CCL5, RANTES); after TRAP activation, platelets release over 25 ng/mL CCL5.

13 The protective effects of ANP against TRAP/HTV-induced lung injury were linked to the increase

14 8, the animals were sacrificed, serum B-ALP, TRAP-5b, and calcium levels were measured, gingiva speci

15 1321N1 and C6 glioma cells without altering TRAP-6 and carbachol Ca(2+) responses.

16 l traversal and hepatocyte invasion [3]; and TRAP, which is necessary for gliding motility and invasi

17 gingival IL-1beta and IL-10, serum B-ALP and TRAP-5b levels, or alveolar bone compared with conventio

18 gingival IL-1beta and IL-10, serum B-ALP and TRAP-5b, and calcium and alveolar bone levels between th

19 AsA and TRAP levels were significantly lower (1.1 +/- 0.4 vs. 1.

20 obtained for antioxidant analysis of AsA and TRAP.

21 vity are associated with COPD and asthma and TRAP is involved in regulating macrophage migration.

22 odium berghei homologues of antigens CSP and TRAP are combined.

23 ific to sporozoite surface-expressed CSP and TRAP proteins, but not intracellular glideosome-associat

24 This suggests that a combination of CSP and TRAP subunit vaccines could enhance protection against m

25 ell-known pre-erythrocytic antigens, CSP and TRAP, yet thousands of genes are expressed in the liver-

26 brogates the expression of NFATc1, Cstk, and TRAP during OC differentiation.

27 acterial RNAs, activate PKR in TRAP-free and TRAP/l-Trp-bound forms.

28 and epicatechin showed the highest ORAC and TRAP antioxidant activity.

29 ALP activity in osteoblasts and TRAP activity in RAW264.7 cells co-cultured with MC3T3-E

30 eated wounds at day 1 (P = 0.03), and P2 and TRAP induced a similar effect at days 3 (P = 0.002 and P

31 in the lung, heart, spleen, and plasma, and TRAP deposits were quantified in the lungs of both male

32 1beta; immunostaining increase for RANKL and TRAP; reduction of OPG and leukocytosis, which were sign

33 tion of Runx2, and up-regulation of Spp1 and TRAP.

34 Both TEN and TRAP are absent in the putative Tribolium TERT that has

35 n all identified TERTs and find that TEN and TRAP have coevolved as telomerase-specific domains.

36 re, comparative analysis of whole-tissue and TRAP-selected mRNAs identified LPS-induced differences t

37 for trp operon attenuation beyond TrpL- and TRAP-mediated mechanisms described in other bacteria.

38 rp RNA-binding attenuation protein) and anti-TRAP (AT).

39 nsmembrane proteins in apicomplexans such as TRAP in Plasmodium and MIC2 in Toxoplasma.

40 Surface-associated TRAP (thrombospondin-related anonymous protein) family p

41 nannotated junctions with publicly available TRAP-seq data.

42 Only children with high average TRAP exposure from birth through age 7 years were at sig

43 We developed an axon-TRAP-RiboTag approach in mouse that allows deep-sequenci

44 Associations between TRAP exposure and allergic sensitization, lung function,

45 We examined the relationship between TRAP exposure and longitudinal wheezing phenotypes and a

46 The relationship between TRAP exposure and wheezing phenotypes and asthma was exa

47 This indicates that motor-binding TRAP family members function not just in parasite motili

48 excessive number of osteoclasts, detected by TRAP staining and histomorphometric quantification.

49 On the basis of the (68)Ga chelators TRAP (triazacyclononane-triphosphinate) and NODAGA, we s

50 ethods: On the basis of the (68)Ga chelators TRAP (triazacyclononane-triphosphinate) and NODAGA, we s

51 tand the association between early childhood TRAP exposure, and subsequent asthma, allergies and sens

52 ggest pathological consequences from chronic TRAP exposure, including sex differences indicating fema

53 We refer to this new method as PRV-Circuit-TRAP (PRV circuit-directed TRAP).

54 In contrast, TRAP exposure at participants' current homes significant

55 Osteoclastogenesis was assessed by counting TRAP-positive multinucleated cells in PB CD14+ monocytes

56 ess at 14 d, which correlated with decreased TRAP+ osteoclasts and F4/80+ macrophages.

57 rovide several examples of a droplet digital TRAP (ddTRAP) assay for telomerase activity, including q

58 od as PRV-Circuit-TRAP (PRV circuit-directed TRAP).

59 of a previously uncharacterized TERT domain (TRAP) with unanticipated interactions with the telomeras

60 We propose that during TRAP, assembled ribosomes associated with misfolded nasc

61 In addition, EC-TRAP limits changes in gene expression after EC isolatio

62 rates considerably greater sensitivity of EC-TRAP for the detection of low abundant transcripts.

63 Application of EC-TRAP to examine the in vivo host response to lipopolysac

64 Comparison of our EC-TRAP with published single-cell RNA sequencing data furt

65 anslating ribosome affinity purification (EC-TRAP) combined with high-throughput RNA sequencing analy

66 We then created a transgenic Pcp2-L10a-Egfp TRAP hPSC line to profile gene expression in differentia

67 As a first step, we used Tg(Pcp2-L10a-Egfp) TRAP mice to profile actively transcribed genes in devel

68 Using CX(3)CR1-EGFP/TRAP tdTomato mice, we found CX(3)CR1 expression in mono

69 Reduced RANKL immunolabeling and fewer TRAP-positive multinucleated cells were observed in the

70 There were fewer TRAP-positive cells in the SRP/SA group than in the NT g

71 stomorphometry, and immunohistochemistry for TRAP.

72 traffic exposure zones (TEZs) as a proxy for TRAP.

73 f several solute binding proteins (SBPs) for TRAP (tripartite ATP-independent permease) transporters

74 Typical substrates for TRAP transporters are organic acids including the sialic

75 icantly attenuated the cells ability to form TRAP positive, multinucleated giant cells.

76 eader RNA but cannot dissociate a pre-formed TRAP-RNA complex.

77 dentate granule cells using conditional Fos-TRAP mice.

78 Exercise-activated neurons (Fos-TRAPed) showed an input-selective increase in dendritic

79 We assign positions to the four TRAP subunits within the complex, providing insights int

80 ultiple fluorescent OC in cell cultures from TRAP tdTomato mice, but not from WT mice.

81 However, CX(3)CR1-expressing cells generated TRAP(+) OC on bone within 5 d in CX(3)CR1CreERT2/Ai14 td

82 ession levels of the osteoclast marker genes TRAP, Cathepsin K, dendritic cell-specific transmembrane

83 sus other groups were confirmed by a greater TRAP-positive cell number and reabsorption surface on bo

84 High TRAP exposure at birth was significantly associated with

85 ts of the population reside in zones of high TRAP exposure.

86 In conclusion, higher TRAP expression/activity are associated with COPD and as

87 We found higher TRAP activity/expression in lungs of patients with chron

88 However, higher TRAP(+) MNC numbers were observed in tibiae versus MB un

89 (TEN) and insertions in fingers domain (IFD)-TRAP regions of the human telomerase catalytic protein s

90 d or produced locally by leukocytes, impairs TRAP-mediated PGA formation to the same level as specifi

91 Osteoclasts were counted in TRAP-stained sections.

92 ly, expression of CathepsinK was detected in TRAP-negative cells of the inner periosteal layer also e

93 inflammatory macrophages were higher only in TRAP-exposed male spleens.

94 e typical of bacterial RNAs, activate PKR in TRAP-free and TRAP/l-Trp-bound forms.

95 stent with the open and closed forms seen in TRAP SBP crystal structures.

96 ter for carboxylate-containing substrates in TRAP transporters by engineering the SBP to recognize a

97 oscopy density in a published map, including TRAP in previously unassigned density as well as telomer

98 Although Phlpp1 deficiency increased TRAP(+) cell numbers, it suppressed actin-ring formation

99 on, increased cartilage thickness, increased TRAP activity, and mineralization.

100 Syngr4, and Plekhb1 mRNAs in an independent TRAP experiment.

101 identified is a tripartite ATP-independent (TRAP) transporter, not previously associated with sugar

102 nvestigate impacts of air-cleaning on indoor TRAP levels and indoor chemistry in a renovated school a

103 Air-cleaning reduced indoor TRAP to below or near urban background.

104 OPD were tested for their capacity to induce TRAP.

105 use macrophages, but only RANKL also induced TRAP activity in mouse lung slices.

106 RANKL) and Xanthine/Xanthine Oxidase induced TRAP mRNA expression in mouse macrophages, but only RANK

107 nds were tested for their ability to inhibit TRAP activity and [Au(4,4'-dimethoxy-2,2'-bipyridine)Cl2

108 AubipyOMe also inhibited TRAP activity in murine macrophage and human lung tissue

109 levels of immature platelet fraction (IPF), TRAP-stimulated platelet surface CD42b, unstimulated pla

110 Studies of isolated TRAP and AT showed that AT can prevent TRAP from binding

111 N-gamma exhibited low levels of Cathepsin K, TRAP, RANK, and tumor necrosis factor receptor-associate

112 arily divergent organisms and disease-linked TRAP mutant fibroblasts from human patients.

113 Even relatively low TRAP exposures confer an increased risk of adverse respi

114 -L10a upregulation in kidney, confirming Mac(TRAP) responsiveness in vivo.

115 d macrophage-specific polysomal RNA from Mac(TRAP) kidneys and conducted RNA sequencing followed by b

116 rization found no gross abnormalities in Mac(TRAP) mice and confirmed transgene expression across var

117 enerate c-fms-eGFP-L10a transgenic mice (Mac(TRAP)).

118 Immunohistological analyses of Mac(TRAP) kidneys identified eGFP-L10a expressing cells in t

119 CS and 2 of 15 (13%) receiving ChAd63-MVA ME-TRAP achieved sterile protection after CHMI.

120 CS and 5 of 15 (33%) receiving ChAd63-MVA ME-TRAP demonstrated a delay in time to treatment, compared

121 the liver parasite burden, but ChAd63-MVA ME-TRAP remains the most promising antigenic insert for a v

122 79%, compared with 79%-84% for ChAd63-MVA ME-TRAP.

123 efficacy of ChAd63-MVA CS with ChAd63-MVA ME-TRAP.

124 -thrombospondin-related adhesion protein (ME-TRAP).

125 adenovirus with a vaccine expressing the ME-TRAP malaria antigen had no significant effect on the im

126 o address this, we employed a viral-mediated TRAP (Targeted Recombination in Active Population) techn

127 press a TRAP family protein called merozoite-TRAP (MTRAP) that has been implicated in erythrocyte inv

128 Randomly microdissected TRAP(+) OCs from 16 MF patients harbored JAK2 or calreti

129 en cells both in vitro and in vivo Using miR-TRAP affinity purification technology, we identified the

130 PD) and asthma compared to controls and more TRAP activity in lungs of mice with experimental COPD or

131 g method's accuracy of 73-78% based on motif TRAP scores.

132 se in the formation of giant, multinucleated TRAP(+) cells capable of F-actin ring formation.

133 mononuclear cells, but not in multinucleated TRAP(+) OC.

134 sors that differentiated into multinucleated TRAP-positive cells in the presence of EPAC-selective st

135 d reduced the total number of multinucleated TRAP+ cells in mice that received ligature attachment.

136 PL neurons TRAPed during later memory retrievals are more likely to

137 projections throughout the brain, PL neurons TRAPed later have a stronger functional recruitment of c

138 Finally, while neurons TRAPed during earlier and later retrievals have similar

139 An essential component of TRAP transporters is a periplasmic substrate binding pro

140 To investigate the conservation of TRAP and TEN across species, we performed multiple seque

141 a development specifically in the context of TRAP exposure.

142 Here we show that the I domain of TRAP is essential for sporozoite gliding motility, mosqu

143 in D supplementation mitigates the effect of TRAP exposure on asthma development, asthma exacerbation

144 However, the effects of TRAP on the cardiopulmonary system in most animal studie

145 Different members of the DctP family of TRAP SBPs have binding sites that recognize a diverse ra

146 ere numerous tdTomato(+) OC in the femurs of TRAP tdTomato mice but almost none in WT mice.

147 s unclear and potent selective inhibitors of TRAP are required to assess functional aspects of the pr

148 e development of peptide-based inhibitors of TRAP transporters.

149 ut only long-term exposure to high levels of TRAP throughout childhood was associated with asthma dev

150 zones assumed to have the highest levels of TRAP, was positively associated with high-density lipopr

151 ty and traffic exposure zones, as markers of TRAP exposure, and metabolic biomarkers for cardiovascul

152 Proxy measures of TRAP exposure were associated with intermediate metaboli

153 s is consistent with the known mechanisms of TRAP transporters and consider how the role of sugar oxi

154 ysis showed a significantly higher number of TRAP and Osteocalcin positive cells at 4 weeks in the ce

155 5), as identified by the increased number of TRAP(+) osteoclasts (P < 0.01) in the Tregs/pre-osteocla

156 Increased number of TRAP-positive cells was observed in DBG/LV and DBG/HV (P

157 In PDCimG, the number of TRAP-positive osteoclasts and IL-6, MMP-1, and MMP-9-imm

158 The number of TRAP-stained cells was higher in the estrogen-deficient

159 Together, our findings support the power of TRAP-seq to identify cell type specific changes in gene

160 2)) is a major component and common proxy of TRAP.

161 in biogenesis and sheds light on the role of TRAP in human congenital disorders of glycosylation.

162 The substrate binding proteins (SBP) of TRAP transporters are the best studied component and are

163 ity, and that PKG regulates the secretion of TRAP, an adhesin that is essential for motility.

164 ng densely-packed DNA, comparable to that of TRAP.

165 Additionally, sex-dependent toxicity of TRAP exposure has rarely been evaluated.

166 Chemogenetic inhibition of TRAPed PL cortex ensembles reduced conditioned suppressi

167 some affinity purification (TRAP) from Olig2-TRAP transgenic mice.

168 and rowanberry via different methods (ORAC, TRAP, HORAC and inhibition of lipid peroxidation).

169 ereas higher-order complexes containing OST, TRAP, and TRAM were stabilized following substrate trans

170 in SSR4 and also reduces expression of other TRAP complex proteins.

171 stogenesis during homeostasis, we parabiosed TRAP tdTomato mice (CD45.2) on a C57BL/6 background with

172 otal radical trapping antioxidant parameter (TRAP) methods.

173 d with thrombin receptor-activating peptide (TRAP) using ex vivo flow cytometry assays.

174 els of thrombin receptor activating peptide (TRAP)-stimulated percent P-selectin- and activated glyco

175 ive (EMD), tyrosine-rich amelogenin peptide (TRAP), and a synthetic proline-rich peptide (P2) on acut

176 The tripartite ATP-independent periplasmic (TRAP) transporters are a widespread class of membrane tr

177 Tripartite ATP-independent periplasmic (TRAP) transporters are secondary transporters that have

178 FATc1), tartrate-resistant acid phosphatase (TRAP) and cathepsin K in vitro.

179 ned for tartrate-resistant acid phosphatase (TRAP) and immunohistochemical staining for five bone met

180 ated by tartrate-resistant acid phosphatase (TRAP) staining and pit formation.

181 Tartrate-resistant acid phosphatase (TRAP) staining, resorption pit assays, and real-time pol

182 ined by tartrate-resistant acid phosphatase (TRAP) staining.

183 tion of tartrate-resistant acid phosphatase (TRAP) were also performed.

184 G), and tartrate-resistant acid phosphatase (TRAP) were assessed.

185 (OPG), tartrate-resistant acid phosphatase (TRAP), and activated caspase-3 were performed at the fur

186 RANKL), tartrate-resistant acid phosphatase (TRAP), and osteoclast-associated receptor increased sign

187 13) and tartrate-resistant acid phosphatase (TRAP), leading to an acceleration in periodontal breakdo

188 nd less tartrate-resistant acid phosphatase (TRAP)-positive cell induction than M0 or M2 macrophage t

189 creased tartrate-resistant acid phosphatase (TRAP)-positive cell number, and enhanced osteoclast acti

190 h fewer tartrate-resistant acid phosphatase (TRAP)-positive cells in alveolar bone.

191 Tartrate-resistant acid phosphatase (TRAP)-positive osteoclasts in the alveolar process surfa

192 by tartrate-acid resistant acid phosphatase (TRAP)-positivity.

193 G), and tartrate-resistant acid phosphatase (TRAP).

194 cleated tartrate-resistant acid phosphatase (TRAP)/cathepsin K(+) OCs expressing phosphorylated Janus

195 enzyme tartrate resistant acid phosphatase (TRAP, two isoforms 5a and 5b) is highly expressed in alv

196 N], and tartrate-resistant acid phosphatase [TRAP]) analyses were performed.

197 stology (Tartrate-Resistant Acid Phosphatase-TRAP, Osteocalcin and human specific anti-mitochondria a

198 In a functional assay with physiological TRAP substrate osteopontin, AubipyOMe inhibited mouse ma

199 nship between traffic-related air pollution (TRAP) and risk factors for cardiovascular disease needs

200 Traffic-related air pollution (TRAP) exposure is associated with allergic airway diseas

201 rly childhood traffic-related air pollution (TRAP) exposure on development of asthma and allergies re

202 he effects of traffic-related air pollution (TRAP) exposure.

203 m exposure to traffic-related air pollution (TRAP) in relation to progression in physical disability.

204 Traffic-related air pollution (TRAP) is made up of complex mixtures of particulate matt

205 h exposure to traffic-related air pollution (TRAP), but the TRAP-attributable burden remains poorly q

206 th asthma and traffic-related air pollution (TRAP).

207 e students to traffic-related air pollution (TRAP).

208 artrate-resistant acid phosphatase-positive (TRAP+) OCs and alveolar bone loss.

209 artrate-resistant acid phosphatase-positive (TRAP+) osteoclast numbers were also evaluated.

210 A) and total reactive antioxidant potential (TRAP) with glaucoma and vitreous status.

211 lated TRAP and AT showed that AT can prevent TRAP from binding to the trp leader RNA but cannot disso

212 vering hidden TRansient Attracting Profiles (TRAPs) in ocean-surface velocity data.

213 5-, thrombospondin-related adhesion protein (TRAP) 130-138-, or circumsporozoite protein (CSP) 252-26

214 to thrombospondin-related adhesion protein (TRAP) by using a viral vector.

215 red thrombospondin-related adhesive protein (TRAP), provide only intermediate to low levels of protec

216 he thrombospondin-related anonymous protein (TRAP) family, is a secreted protein important for T. gon

217 The translocon-associated protein (TRAP) complex is an integral component of the translocon

218 erotetrameric translocon-associated protein (TRAP) complex.

219 called trp RNA binding Attenuation Protein (TRAP) controls attenuation of the tryptophan biosyntheti

220 tryptophan RNA-binding attenuation protein (TRAP), which binds its target RNA sequence close to the

221 dditionally, the trp 5'-UTR binds a protein, TRAP (tryptophan RNA-binding attenuation protein), which

222 l mechanism are the homo-oligomeric proteins TRAP (trp RNA-binding attenuation protein) and anti-TRAP

223 The telomere repeat amplification protocol (TRAP) for the human reverse transcriptase, telomerase, i

224 Translating Ribosome Affinity Purification (TRAP) and CREB-target gene repositories.

225 Translating ribosome affinity purification (TRAP) and in vitro luciferase reporter assay indicate th

226 translating ribosome affinity purification (TRAP) and RNA sequencing, TRAP-seq, in larval zebrafish

227 translating ribosome affinity purification (TRAP) and RNA-seq to identify mistranslating mRNAs in CA

228 translating ribosome affinity purification (TRAP) and RNAseq.

229 translating ribosome affinity purification (TRAP) from Olig2-TRAP transgenic mice.

230 Translating Ribosome Affinity Purification (TRAP) methodology to purify ribosome-associated mRNAs an

231 ranslational ribosome affinity purification (TRAP) mice (both sexes).

232 translating ribosome affinity purification (TRAP) of mRNA populations in CRE-expressing cells.

233 translating ribosome affinity purification (TRAP) to conduct transcriptomic analyses of caudate/puta

234 translating ribosome affinity purification (TRAP) with RNA sequencing to identify molecular changes

235 translating ribosome affinity purification (TRAP) with RNASeq to identify mRNAs in cortical axons pr

236 ranslational Ribosome Affinity Purification (TRAP)- approach and designed a transgene that expresses

237 translating ribosome affinity purification (TRAP).

238 translating ribosomal affinity purification (TRAP).

239 r Translating Ribosome Affinity Purification(TRAP).

240 We applied pY-TRAP to create highly specific binders to folded Ub-pY59

241 sine Targeting by Recombinant Ab Pair, or pY-TRAP, for in vitro engineering of binders for native pY

242 This pY-TRAP approach serves as a generalizable method for engin

243 The pY-TRAPs do not have detectable binding to wild-type protei

244 -gamma reduced the mRNAs encoding for RANKL, TRAP, and Cathepsin K.

245 tivated receptor 1 (PAR1) thrombin receptor (TRAP-stimulated P-selectin, activated GPIIb-IIIa, and CD

246 Retro-TRAP (translating ribosome affinity purification) techno

247 Retro-TRAP uses an anti-GFP ribosomal tag (expressed virally o

248 Using these viruses and Retro-TRAP (translating ribosome affinity purification), a pre

249 aser-capture microdissection and FACS, Retro-TRAP is a high-throughput methodology that requires mini

250 y purification coupled with deep-sequencing (TRAP-seq) in Caenorhabditis elegans, we have obtained hi

251 nity purification (TRAP) and RNA sequencing, TRAP-seq, in larval zebrafish to identify genes differen

252 mophilus influenzae virulence-related SiaPQM TRAP transporter.

253 table from a single velocity-field snapshot, TRAPs act as short-term attractors for all floating obje

254 pplied a new, responsive macrophage-specific TRAP mouse line, defining the translational profile of r

255 artrate-resistant acid phosphatase staining (TRAP).

256 nchronously developing granule neurons (Sync-TRAP) showed that conditional knockout of the core NuRD

257 w domains of TER and TERT, including the TEN-TRAP complex, can interact in a conserved manner to regu

258 This ribosome entrapment pathway, termed TRAP (Translational Relocalization with Aberrant Polypep

259 There was some evidence that TRAP was associated with eczema and hay fever.

260 n a growing body of evidence suggesting that TRAP exposures may accelerate aging-related declines in

261 vide biochemical and structural support that TRAP transporters function predominantly as high affinit

262 ferent ocean field experiments, we show that TRAPs computed from measured as well as modeled velociti

263 ed the ~17-kDa ameloblastin (Ambn-N) and the TRAP (tyrosine-rich amelogenin peptide) fragments.

264 raffic-related air pollution (TRAP), but the TRAP-attributable burden remains poorly quantified.

265 hain-breaking activity, as determined by the TRAP method.

266 collagen accumulation was found only in the TRAP-exposed female hearts.

267 dissecting the molecular organization of the TRAP complex.

268 f the marker and of the other members of the TRAP complex.

269 d SBPs as well as permease components of the TRAP transporters, members of the DUF1537 family, and a

270 ent tumor delineation-were obtained with the TRAP-based monomer (68)Ga-avebehexin.

271 ent tumor delineation-were obtained with the TRAP-based monomer (68)Ga-avebehexin.

272 to remote memory retrieval compared to those TRAPed during learning or early memory retrieval.

273 P and TRAcP 5b were decreased as were tibial TRAP+ osteoclasts.

274 ivity, increases PGA formation when added to TRAP-stimulated blood.

275 exhibited increased platelet aggregation to TRAP (thrombin receptor-activating peptide) (children wi

276 on of T(H)2/T(H)17 cells after coexposure to TRAP and allergen but not to allergen alone.

277 eek-old male and female rats were exposed to TRAP or filtered air for 14 months in a novel facility d

278 ion were higher in the rat hearts exposed to TRAP, with female rats being more susceptible than males

279 f asthma and allergic outcomes if exposed to TRAP.

280 We sought to determine whether exposure to TRAP in middle age is associated with allergic sensitiza

281 Exposure to TRAP in participants' early life and at current home add

282 Early-life exposure to TRAP is associated with increased risk for persistent wh

283 Also, early childhood exposure to TRAP was associated with development of asthma across ch

284 In summary, exposure to TRAP was related to asthma and allergic diseases.

285 Participants' time-weighted exposure to TRAP, from birth through age 7 years, was estimated usin

286 We measured participants' exposures to TRAP using two surrogates: residential proximity to majo

287 ne expressing a multiepitope string fused to TRAP and 3 doses of RTS,S/AS01B (group 1; n = 20) or 3 d

288 ibited the differentiation of macrophages to TRAP-positive osteoclasts, distinctive osteoclast specif

289 lation in asthmatic patients and response to TRAP.

290 ndicating females may be more susceptible to TRAP-induced cardiac fibrosis.

291 te ATP-independent periplasmic transporters (TRAPs) to scavenge sialic acid from host tissues.

292 ide on the triazacyclononane-triphosphinate (TRAP) chelator, followed by automated (68)Ga labeling.

293 mpared to no protection using virus-vectored TRAP alone and 40% protection using adenovirus-CSP prime

294 es is seen when combined with virus-vectored TRAP, and the combination is no more protective than eit

295 maintained when combined with virus-vectored TRAP.

296 rt of snoring was positively associated with TRAP aggregation (Kendall's tau-c = 0.23; P < 0.05).Conc

297 n conclusion, these data are consistent with TRAP SBPs undergoing a simple two-state transition from

298 SCs, their presence and co-localisation with TRAP-positive chondroclasts was noted in the vascular ch

299 nses was also achieved by combining R21 with TRAP-based viral vectors and protective efficacy was sig

300 f chronic exposure to unmodified, real-world TRAP in both female and male rats.