ライフサイエンスコーパス: reactive

1 separation processes using reactive and non-reactive absorption and adsorption, membranes, and cryog

2 (2) Why is there so much variation in reactive aggression/violence between people living in th

3 nantioselectivities are higher with the less reactive allylphenyl carbonates as chemoselective copper

4 Immune-reactive alpha-lactalbumin and beta-lactoglobulin were f

5 The reactive and dissipative sensing methods, characterized

6 makes the nanoscale tunnel junctions highly reactive and facilitates strongly confined chemical reac

7 uffering from such viral infections, broadly reactive and highly sensitive influenza rapid diagnostic

8 Anti-Flavivirus antibodies are highly cross-reactive and may facilitate Zika virus (ZIKV) infection

9 H2S separation processes using reactive and non-reactive absorption and adsorption, mem

10 recent years due to the generation of highly reactive and selective sulfate radical (SO4(*-)).

11 ification of H-d-Pro-Pip-Glu-NH2 as a highly reactive and stereoselective amine-based catalyst that a

12 which is usually achieved by mixing NCs with reactive anion precursors.

13 form a homogeneous and dense LiF coating on reactive anode materials, with in situ generated fluorin

14 engue virus (DENV) endemic regions and cross-reactive antibodies (Abs) could potentially affect ZIKV

15 Self-reactive antibodies and parasite-specific IgG in female

16 Studies have demonstrated that broadly reactive antibodies require Fc-Fc gamma receptor interac

17 V3 were mainly neutralized by serotype cross-reactive antibodies.

18 pigs developed high titers of broadly cross-reactive antibodies; mice and ferrets exhibited narrower

19 Having a calculated panel-reactive antibody (cPRA) of 80% or greater was independe

20 nt of a numeric metric, the calculated panel-reactive antibody (CPRA) that predicts the likelihood of

21 1/2005 (clade 2.3.4) vaccine to elicit cross-reactive antibody responses to these emerging viruses.

22 oups, with the exception of calculated panel-reactive antibody which was lowest in the D+/R- group.

23 blotted HDM extract, and the presence of IgE-reactive antigens in HDM was demonstrated by qualitative

24 Two major types of aggression, proactive and reactive, are associated with contrasting expression, el

25 , few studies have examined the influence of reactive astrocytes in the tripartite synapse following

26 This suggests that reactive astrocytes may not be the main CSPG contributor

27 Reactive astrogliosis is a critical process in neuropath

28 mplexes of Pt(II) and their drastically more reactive Au(III) congeners.

29 centers (GCs) in lymphoid tissues where self-reactive B cells expand and differentiate.

30 We suggest that broadly reactive B cells may interact with a larger fraction of

31 ers, with FZD5/FZD8-specific and broadly FZD-reactive binding domains.

32 the cell attachment to the surface of immune-reactive biochips and during the SPR analysis.

33 50 and 100 Envs either to characterize cross-reactive breadth for sera identified as having potent ne

34 covalent chemistry enables self-assembly of reactive building blocks into structurally complex yet r

35 Recent strategies for installing reactive carbonyl groups and alpha-nucleophiles into bio

36 lines revealed that the elimination of toxic reactive carbonyl species during germination and seedlin

37 DNA damage induced by reactive carbonyls (mainly methylglyoxal and glyoxal), c

38 1-like response was also detected in Dau c 1-reactive CD3(+) CD4(+) CFSE(low) cells.

39 e deletion of high- or low-affinity InsB9-23-reactive CD4(+) T cells; however, we observe an increase

40 Similarly, reactive center loop insertion into sheet A decreased he

41 We demonstrate that a highly reactive CF3(-) adduct can be synthesized from alkali me

42 Many compounds with potentially reactive chemical motifs and poor physicochemical proper

43 eam point of application reduces the flux of reactive chemical species reaching the sample, potential

44 In conclusion, Nlrp3 is expressed in reactive cholangiocytes, in both murine models and patie

45 ng nitro and nitroso compounds, and the most reactive cis/syn isomer was transformed into ortho-nitro

46 oduct velocity distributions for a series of reactive collisions of the type X(-) + RY with X and Y d

47 Furthermore, HD myeloid cells are hyper-reactive compared to control.

48 a distinct TCR repertoire and are more self-reactive compared with conventional T cells.

49 We propose that the involvement of STN in reactive control is restricted to its ventromedial porti

50 Neurosyphilis was defined as (i) a reactive CSF Venereal Disease Research Laboratory test (

51 ), a chemical probe that specifically labels reactive cysteine sulfhydryls.

52 Although some cross-reactive dengue virus (DENV)-specific antibodies can enh

53 m a coproheme compound I intermediate to the reactive deprotonated tyrosine, forming Tyr(*).

54 ion, causes mass production and discharge of reactive dissolved organic matter (DOM).

55 al transmission lines by spatially arranging reactive DNA hairpins on a DNA origami.

56 by catalyzing DNA synthesis and removal of a reactive DNA repair intermediate during base excision re

57 fecting this process, as long as the bromine-reactive DOM sites are in excess and a sufficient chlori

58 Aqua Regia that under- and overestimate the reactive element contents, respectively.

59 We report reactive ensemble Monte Carlo simulations for the CO2 me

60 to the short length scales involved and the reactive environments of interest.

61 Cross-reactive epitopes bind with higher affinity to alpha/bet

62 emixed, or partially premixed nonequilibrium reactive flows.

63 robust EV staining strategy, with the amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein

64 Massively Parallel Simulator (LAMMPS) with a reactive force-field (ReaxFF).

65 Finally, transduction with a pan-cancer-reactive gammadelta TCR used in conjunction with CRISPR/

66 nding affinities were mapped for human cross-reactive GAS proteins, including M5 and M6.

67 Reactive gases can be adsorbed onto aerosol particles wh

68 Abeta) plaques, neurofibrillary tangles, and reactive gliosis.

69 Importantly, higher cross-reactive haemagglutination-inhibition antibody titres ag

70 Reactive halogens influence the oxidative capacity of th

71 playing nonadiabatic tunneling, the dominant reactive hydrogen donor-acceptor distance (DAD) is typic

72 anced oxidation process that produces highly reactive hydroxyl radicals (HO(*)) and chlorine radicals

73 ffect on endothelial function as measured by reactive hyperaemia index, or on retinopathy.

74 ntracellular Ca(2+) release in HUVEC and FXa reactive IgG from patients with APS and/or SLE potentiat

75 Factor (F) Xa reactive IgG isolated from patients with antiphospholipi

76 Analysis of EHV-1-reactive IgG subtypes demonstrated that vaccination with

77 L2(-/-)) mice produced significantly more PC-reactive IgM and IgA.

78 group) where Pasteurella pneumotropica ( Pp)-reactive immune response activated T cells to produce re

79 cial CIV H3N8 IIV but provided limited cross-reactive immunity and heterologous protection against H3

80 In the presence of the peptidase, the reactive intermediates are converted to a known genotoxi

81 Together, these reactive intermediates enable the reduction of multiple

82 s borylenes, RB, which have been inferred as reactive intermediates in a number of reactions.

83 ydrogen bonds in purine nucleosides produces reactive intermediates that are important in nucleic aci

84 These reactive intermediates, including metal-superoxo, -(hydr

85 as the main Maillard reaction pathway, other reactive intermediates, often of higher molecular weight

86 I review aspects of my research on reactive intermediates, specifically the physical organi

87 lithography, thin film vacuum deposition and reactive-ion etching processes eliminating complicated p

88 ive iron pools, showing that 25-62% of total reactive iron is directly associated to OC through inner

89 -complexed Fe to the total sediment iron and reactive iron pools, showing that 25-62% of total reacti

90 ctivator gave the structurally authenticated reactive iron(V)oxo units (Fe(V)O), wherein the iron ato

91 lytic CO extrusion and that, although highly reactive, is sufficiently long-lived to react intermolec

92 highly variable, numerous instances of cross-reactive killing were observed.

93 ent C and Si contents are synthesized by the reactive-magnetron-sputtering technique.

94 aracterized rare affinity-matured human NANP-reactive memory B cell antibodies elicited by natural Pf

95 In keeping with the role of reactive metabolite formation in APAP-induced chemical s

96 , which are known to bioactivate APAP to the reactive metabolite N-acetyl-p-benzoquinone imine (NAPQI

97 ione biosynthesis, which protects cells from reactive metabolites, increased the potency of curcumin

98 A by reaction with S-adenosylmethionine, the reactive methyl donor, and by reaction with alkylating a

99 we show that mitochondrial fission/fusion in reactive microglia is differentially regulated from that

100 ical MSCs triggered earlier astrocytosis and reactive microglia.

101 Reactive mineral-water interfaces exert control on the b

102 In this work, we report multiscale reactive molecular dynamics simulations that characteriz

103 situ observations, combined with large-scale reactive molecular dynamics simulations, reveal the deta

104 source of oxidizing agents for combustion of reactive nanomaterials.

105 The uniquely reactive nature of the selected zwitterions allows their

106 ts amine-based NDMA precursors to their more reactive, neutral forms.

107 racterized a panel of vaccine-elicited cross-reactive neutralizing MAbs targeting the Env V3 loop tha

108 of 2,5-diphenyltetrazoles, affording highly reactive nitrile imines, is probed via a monochromatic w

109 sensitivity approach and 0.5 ppbv by tagging reactive nitrogen oxides.

110 gamma-Tocopherol is effective scavengers of reactive nitrogen species and prevents DNA bases nitrati

111 etronome found their movements to be largely reactive, not predictive.

112 ylbenzaldehydes, leading to the formation of reactive o-quinodimethanes (photoenols), and the photoly

113 of Mn(II) from solution by reaction with the reactive oxidant species produced through Fe(II) oxidati

114 from 6.5 to 8.5, which implicates different reactive oxidants in acidic and alkaline solutions.

115 uding photodegradation, thermal degradation, reactive oxidative species (ROS) oxidation, extracellula

116 Plasma-derived reactive oxygen and nitrogen species (ROS/RNS) are assum

117 ne and catalase, suggesting that HDM-induced reactive oxygen and nitrogen species can be neutralized

118 s that may involve activation of an integrin/reactive oxygen axis.

119 oncentrations, total antioxidant capacity or reactive oxygen metabolites.

120 treatment induces significant mitochondrial reactive oxygen production, which contributes to NLRP3 a

121 ansient increases in mitochondrially-derived reactive oxygen species (ROS) activate an adaptive stres

122 d rapid responses, such as the production of reactive oxygen species (ROS) and mitogen-activated prot

123 estricting protein translation and levels of reactive oxygen species (ROS) and Myc.

124 ia coli, inhibited PMA-induced generation of reactive oxygen species (ROS) and neutrophil extracellul

125 Liver damage, reactive oxygen species (ROS) and paracrine tumor necros

126 so had significantly increased production of reactive oxygen species (ROS) and upregulated expression

127 There was significant generation of Reactive Oxygen Species (ROS) by MCs on co-culture with

128 y (hypoxia) leads to increased production of reactive oxygen species (ROS) by the electron transport

129 Reactive oxygen species (ROS) can damage DNA, proteins,

130 Reactive oxygen species (ROS) can induce oxidative stres

131 Inhibiting xanthine oxidase, a major reactive oxygen species (ROS) contributor during acute i

132 onally, an rpaA mutant accumulates excessive reactive oxygen species (ROS) during the day and is unab

133 optosis induction by YC-1 involved excessive reactive oxygen species (ROS) generation.

134 Reactive oxygen species (ROS) have been suggested as suc

135 ibrosis (CF), despite abundant production of reactive oxygen species (ROS) in lung tissue.

136 er found that PA increased the production of reactive oxygen species (ROS) in podocytes and that NAC

137 een shown that cryptochromes also synthesize reactive oxygen species (ROS) in response to light, sugg

138 The hypothesis that increased generation of reactive oxygen species (ROS) in vivo plays a key role i

139 tracellular ATP concentrations decreased and reactive oxygen species (ROS) increased.

140 e MM cell line, MM1.S, demonstrated enhanced reactive oxygen species (ROS) levels.

141 Reactive oxygen species (ROS) play a critical role in ce

142 Microbial pathogens are exposed to damaging reactive oxygen species (ROS) produced from a variety of

143 NADPH oxidases contribute to LPS-induced reactive oxygen species (ROS) production and modulate TL

144 Reactive oxygen species (ROS) production, degranulation,

145 titution, which is reported to cause reduced reactive oxygen species (ROS) production, predisposes to

146 causes eosinophil apoptosis associated with reactive oxygen species (ROS) production.

147 els have now demonstrated that mitochondrial reactive oxygen species (ROS) signal to support adipocyt

148 ells experience higher oxidative stress from reactive oxygen species (ROS) than do non-malignant cell

149 ofilm, neutrophils generate higher levels of reactive oxygen species (ROS) when presented with plankt

150 fects upon Caco-2 cells (MTT, cell cycle and reactive oxygen species (ROS)) were evaluated in Colombi

151 ial biogenesis, glycolysis and production of reactive oxygen species (ROS), in a manner mediated by t

152 eural tubes (nSR-BI(-/-)) had high levels of reactive oxygen species (ROS), intermediate ROS levels b

153 luded assessment of viability, mitochondrial reactive oxygen species (ROS), membrane damage, mitochon

154 TRX1 inhibition elevates reactive oxygen species (ROS), p53 levels and cell death

155 Oxidative DNA bases modified by reactive oxygen species (ROS), primarily as 7, 8-dihydro

156 inc1623 in mice, in the setting of hyperoxia/reactive oxygen species (ROS)-induced lung injury.

157 this infective form and more susceptible to reactive oxygen species (ROS)-induced stress.

158 ibuted to excess mitochondrial production of reactive oxygen species (ROS).

159 n, synthesis of hormones, and homeostasis of reactive oxygen species (ROS).

160 utant, suggesting an increased production of reactive oxygen species (ROS).

161 phyll precursor protochlorophyllide produces reactive oxygen species (ROS).

162 ht to be major targets of receptor-activated reactive oxygen species (ROS).

163 e the generation of intra- and extracellular reactive oxygen species (ROS).

164 ng protein (p66Shc) is a master regulator of reactive oxygen species (ROS).

165 te was found to: 1) induce the production of reactive oxygen species (ROS); 2) decrease succinate deh

166 ling nitroxide to mitochondria could prevent reactive oxygen species accumulation, limiting downstrea

167 t lipid overload and increased production of reactive oxygen species after reoxygenation.

168 al tissue overgrowth via the accumulation of reactive oxygen species and activation of the Jun kinase

169 activity and resulted in the accumulation of reactive oxygen species and cell death in the absence of

170 ay stimulate the production of mitochondrial reactive oxygen species and contribute to alcohol-induce

171 cardiac myocytes subjected to I/R increased reactive oxygen species and necrotic cell death, both of

172 on of mitochondrial DNA along with increased reactive oxygen species and reduced superoxide dismutase

173 this harsh acidic environment which contains reactive oxygen species due to the mycobacterial genomes

174 Furthermore, phalloidin staining and reactive oxygen species estimation of Wnt5a-treated macr

175 ited mitochondrial dysfunction, indicated by reactive oxygen species expression, reduced expression o

176 nanofactories protect human cells from toxic reactive oxygen species for up to a week.

177 diseases through their role in respiration, reactive oxygen species generation, and energy productio

178 aHS on high glucose-induced NOX4 expression, reactive oxygen species generation, and, matrix laminin

179 Phenformin induces production of reactive oxygen species in granulocytic myeloid-derived

180 Furthermore, increase in vascular reactive oxygen species induced by ER stress is mitigate

181 an early destructive phase, where a burst of reactive oxygen species induces loss of E-cadherin-media

182 Such glycolytic flux and elevated reactive oxygen species is supported by increased antiox

183 antly, Nrf2 activation significantly reduced reactive oxygen species levels and associated lipid pero

184 adducts that result from diverse chemicals, reactive oxygen species or UV light.

185 n, we assessed cytotoxicity, nitric oxide or reactive oxygen species production, and phagocytosis.

186 HDM stimulated cellular reactive oxygen species production, increased mitochondr

187 ucleotide phosphate/NADPH levels, phagocytic reactive oxygen species production, neutrophil extracell

188 , treatment of atherosclerotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine re

189 which was prevented by co-treatment with the reactive oxygen species scavenger Tempol.

190 miR-193b also stimulated reactive oxygen species signaling by targeting the antio

191 Mitochondria comprise the primary reactive oxygen species source and also their main effec

192 stigated the effects of H2O2, a prototypical reactive oxygen species that is also present at sites of

193 defective in endocytosis, scavenging of the reactive oxygen species, and in the response to endoplas

194 ing via second messengers-cytosolic calcium, reactive oxygen species, and nitric oxide.

195 eir role in ATP production and generation of reactive oxygen species, but little is known about the m

196 taxis, opsonophagocytosis, and production of reactive oxygen species, closely mimicking the defective

197 wed increased expression of genes related to reactive oxygen species, inflammation, and proliferation

198 Compound SA-2 scavenged reactive oxygen species, inhibited proliferation and mig

199 f cardiac troponin I and elevated amounts of reactive oxygen species, lower phosphorylated extracellu

200 od, we evaluate cell viability, formation of reactive oxygen species, mitochondrial health, as well a

201 ipid headgroups and allows 5-HT to intercept reactive oxygen species, preventing membrane oxidation.

202 phatase 2 phosphatase activity by scavenging reactive oxygen species, thus preventing spleen tyrosine

203 ted in attenuated cell invasion and elevated reactive oxygen species, whereas such phenotypes were re

204 cell damage, QD aggregation or the level of reactive oxygen species, which have to be taken into acc

205 ydia maintain mitochondrial integrity during reactive oxygen species-induced stress that occurs natur

206 l dynamics are achieved as a balance between reactive oxygen species-regulated effects on polymerizat

207 ex III activity, and increased production of reactive oxygen species.

208 y low membrane potential and a high level of reactive oxygen species.

209 mor necrosis factor, interleukin (IL)-6, and reactive oxygen species.

210 robust p53 activation, which is mediated by reactive oxygen species.

211 ence p16(INK4a) , p53, p21 and mitochondrial reactive oxygen species.

212 cer cells results in increased production of reactive oxygen species.

213 d DNA damage consistent with the exposure to reactive oxygen species.

214 5'-GG-3' sequence contexts after exposure to reactive oxygen species.

215 act the effects of relatively high levels of reactive oxygen species.

216 d changes in the concentration levels of the reactive oxygen-scavenging pigments were observed by Ram

217 obe shows high selectivity to HNO over other reactive oxygen/nitrogen and sulfur species.

218 The factors affecting the molybdate reactive P (MRP) in these waters were analyzed using the

219 Upon reactive pathway progression, as in Gilbert's Syndrome (

220 t is able to distinguish and select the most reactive pathways, generating a reaction selection index

221 able to search chemical space using the most reactive pathways.

222 SG) mice received intraperitoneally allergen-reactive PBMC from birch pollen-allergic patients togeth

223 vely thiazolylidene systems by combining the reactive peculiarities of both beta-amidothioamides (ATA

224 e simple solution-phase generation of highly reactive phosphaborenes, RP=BR, and demonstrate their us

225 ate the utility of the assay by isolating Ag-reactive plasmablasts from cryopreserved PBMC obtained f

226 s (OH(*)) is typically accomplished by using reactive probe molecules, but prior studies have not tho

227 r to detailed investigations of inelastic or reactive processes.

228 r electronic, structural, spectroscopic, and reactive properties of cluster-mediated ionic dissociati

229 H2O2-activating distal environment with the reactive propionic acids (2 and 4) on the opposite side

230 equalities in inflammation -assessed using C-reactive protein (CRP) and fibrinogen- varied across the

231 C-reactive protein (CRP) is a biomarker of the inflammator

232 Elevated levels of C-reactive protein (CRP), a sensitive marker of inflammati

233 Weight loss, performance status (PS), C-reactive protein (CRP), albumin, the nutritional risk in

234 d certain micronutrient biomarkers such as C-reactive protein (CRP), alpha-1-acid glycoprotein (AGP),

235 lipopolysaccharide binding protein (LBP), C-reactive protein (CRP), ILT-4, C-C motif ligand 18 (PARC

236 Genetically elevated circulating levels of C-reactive protein (CRP), interleukin-1 receptor antagonis

237 e responsiveness was associated with serum C-reactive protein (CRP), tumor necrosis factor, interleuk

238 s of triglycerides, total cholesterol, and C-reactive protein (CRP).

239 High-sensitivity C-reactive protein (hs-CRP) is independently associated wi

240 mmatory markers including high-sensitivity C-reactive protein (hsCRP) and lipoprotein-associated phos

241 sulted in lower levels of calprotectin and C-reactive protein (P < 0.0001), coinciding with recovery.

242 uric acid, serum albumin, albuminuria, and C reactive protein as non-GFR determinants of eGFRcys.

243 had significantly higher highly sensitive-C-reactive protein levels compared to Controls (2.1 +/- 0.

244 High-sensitivity C-reactive protein was elevated beyond the clinical cutoff

245 s significantly increased by 24 h, whereas C-reactive protein was unchanged.

246 in, N-terminal B-type natriuretic peptide, C-reactive protein, and leukocyte count.

247 ood glucose, LDL-to-HDL cholesterol ratio, C-reactive protein, angiotensin II, and albuminuria reduct

248 Proximal DVT alone, higher C-reactive protein, D-dimer, peak thrombin, lower Ks, shor

249 es, and its addition to a 3-BRS comprising C-reactive protein, fibrin degradation product, and heat s

250 lammatory signals, including cytokines and C-reactive protein, have been described in posttraumatic s

251 tein cholesterol, coronary artery disease, C-reactive protein, HbA1c, height, obesity, smoking status

252 (higher HDL cholesterol, lower BMI, lower C-reactive protein, lower waist circumference, and lower o

253 obtained: interleukin 6, high-sensitivity C-reactive protein, soluble receptors for tumor necrosis f

254 ood count, erythrocyte sedimentation rate, C-reactive protein, tuberculin skin test, syphilis serolog

255 biomarkers such as S100 beta proteins and C-reactive proteins (CRP).

256 category 1 had a higher proportion of poorly reactive pupils (P < 0.001) and abnormal ocular movement

257 unique versatility compared to other highly reactive radical-trapping antioxidants (e.g., phenols, d

258 with the unprecedented capability to harness reactive radicals through discrete, single-electron tran

259 The resulting localization of reactive regions, determined by hot-carrier transport fr

260 ry phenotype and impaired CD8(+) T cell allo-reactive responses, including their ability to induce ta

261 us infection induced detectable Dengue cross-reactive serum IgG responses that significantly amplifie

262 nical decision making when applying TDM in a reactive setting.

263 AgNPs within microglia and formation of non-reactive silver sulphide (Ag2S) on the surface of AgNPs.

264 range 100ng to 1microg due to the increased reactive sites and distance.

265 n of SO2 at the water surface can affect the reactive sites and electrophilicity of SO2.

266 When most reactive sites were consumed by chlorine, Cl-substituted

267 may thus alter metal uptake by blocking key reactive sites.

268 alytic reactivity and that the adsorption of reactive species can cause reconstruction of metal surfa

269 Intracellular reactive species content was assayed using 2',7'-dichlor

270 tensity of individual molecular formulas and reactive species production demonstrate the influence of

271 chnique facilitates the targeted delivery of reactive species to a downstream point without compromis

272 tion of NO and increases oxygen and nitrogen reactive species, and (ii) l-citrulline can reverse this

273 Fe-H intermediate is postulated to be a key reactive species.

274 ll development, promoting enrichment of self-reactive specificities into the follicular mature compar

275 ive probe that identifies the experimentally reactive spin state.

276 very that astrocytes have different types of reactive states has important implications for the devel

277 or the constant bearing angle (CBA) model, a reactive strategy that ensures interception since the be

278 % reduction (P<0.001) in thiobarbituric acid reactive substances, effective inhibition of protein oxi

279 l ester, which is composed of a pyrene and a reactive succinimide ester group, interacts with graphen

280 e decomposition due to enhanced formation of reactive surface hydroxo complexation.

281 o its enhanced surface area to volume ratio, reactive surface oxygen vacancy concentration and superi

282 ting to a reduction in the frequency of self-reactive T cells and resistance to autoimmunity.

283 ur reactivity assays, we predict that tumour reactive T cells are frequently present in NSCLC.

284 tively transferred polyclonal cancer antigen-reactive T cells deficient in the regulator diacylglycer

285 utoimmune diabetes-prone NOD mice, beta-cell-reactive T cells homed to these scaffolds and became enr

286 It has been proposed that gluten-reactive T cells in children recognize deamidated and na

287 concept that LAIVs boost preexisting, cross-reactive T cells in children to genetically diverse infl

288 Preexisting cross-reactive T cells to genetically diverse IAV strains were

289 of autologous dendritic cells and even tumor-reactive T lymphocytes.

290 We studied the long-term cross-reactive T-cell response in 14 trivalent LAIV-vaccinated

291 LAIV boosts durable, cross-reactive T-cell responses in children and may have a cli

292 eveloped and commercially available carbonyl-reactive tandem mass tags (aminoxyTMT) enable multiplexe

293 ific MAbs, nearly 20% (6/33) displayed cross-reactive tier 2 virus neutralization, which recapitulate

294 surfaces utilizing a reduced-dimension (1D) reactive transport model.

295 Additionally, the multispecies reactive transport models demonstrated no significant di

296 Reactive transport models were developed in CrunchTope b

297 nal strength cutoffs corresponding to >/=4/7 reactive treponemal tests.

298 found that the synbodies were broadly cross-reactive with affinities that ranged from 0.5 to 8 nM.

299 The 19 mammalian Wnt proteins are cross-reactive with the 10 FZD receptors, and this has complic

300 d a significantly higher level of antibodies reactive with these membrane antigens in patients who de