ライフサイエンスコーパス: protection

1 ellular immune responses that correlate with protection.

2 that together provide immediate and durable protection.

3 nity in latent TB and potential correlate of protection.

4 a novel mechanism for WRN's role in telomere protection.

5 e, respectively, indicating incomplete cross-protection.

6 on-neutralizing antibodies can contribute to protection.

7 ained and these may continue to provide some protection.

8 a better understanding of its mechanisms of protection.

9 th services is a poor indicator of financial protection.

10 n oxide emission abatement for environmental protection.

11 NS1 protein and are potential correlates of protection.

12 al to decipher its critical role in neuronal protection.

13 replication fork reversal, and stalled fork protection.

14 on of vitamin D play roles in cardiovascular protection.

15 vaccine for HCV with potential for universal protection.

16 res negatively correlated with and predicted protection.

17 ction provided stronger effects than partial protection.

18 ional CD4 memory T cells was associated with protection.

19 Revaccination may renew protection.

20 d effector memory T cells that contribute to protection.

21 GUM clinics will partially benefit from herd protection.

22 nce among unvaccinated females suggests herd protection.

23 le for CD8(+) T-cells in mediating rVSV-EBOV protection.

24 ithelial cell loss mediated by microvascular protection.

25 operationalise the concept of centrality of protection; (2) integrate affected persons into national

26 The protection afforded by CpoS is limited to the inclusion

27 We observed that the protection afforded by the particulate vaccine was compa

28 izing antibodies (VNAs), resulting in better protection against a lethal challenge than that seen wit

29 alum adjuvant, and they resulted in enhanced protection against a low-dose intravaginal challenge wit

30 known as Rv21, able to provide 100% sterile protection against a stringent sporozoite challenge in r

31 ay of a prokaryotic cell which maximizes its protection against a viral attack.

32 the Solanaceae family and are implicated in protection against abiotic and biotic stress.

33 ce of endogenous Treg, IVIg failed to confer protection against AHR and airway inflammation.

34 The improved protection against amalgam saturation allows Hg disc-wel

35 tionable CRPC therapeutic target through its protection against AR-induced redox stress.

36 At 4.5 years, protection against asthma by farm-milk exposure was part

37 he contribution of different IgG isotypes to protection against bacteria such as S.

38 aryotic adaptive immune systems that provide protection against bacteriophage (phage) and other paras

39 ent with known anticarcinogenic effects, but protection against breast cancer has not been establishe

40 distinct bacterial taxa was correlated with protection against CDI: Bacteroidetes, Lachnospiraceae,

41 her infection with TC-PC177 can induce cross-protection against challenge with a highly virulent PEDV

42 ific virulence-associated genes induce solid protection against challenge with parental viruses.

43 4788863 in SLC16A5, that was associated with protection against cisplatin-induced ototoxic effects in

44 nfants and that its presence correlates with protection against clinical malaria during infancy.

45 Mucosal immunity is considered important for protection against Clostridium difficile infection (CDI)

46 lues >-0.5 (RR: 0.579; 95% CI: 0.463, 0.724).Protection against delivering an SGA neonate offered by

47 of a neutralizing antibody to correlate with protection against dengue virus have highlighted the nee

48 accine approaches that can provide long-term protection against dengue virus infection is needed.

49 o the identification of robust correlates of protection against dengue virus.

50 not appear to have a role in explaining the protection against depression.

51 production, and insulin secretion as well as protection against diabetes.

52 Where symbionts provided protection against different natural enemies, no alterat

53 e-PEG copolymer, enabling up to a 1,000-fold protection against digestion by serum nucleases.

54 bodies alone are sufficient to provide broad protection against divergent virus strains in vivo.

55 ls vaccinated with the cVLP showed 20% cross-protection against drifted (Philippines) and 60% protect

56 ssessment that rVSV-ZEBOV offers substantial protection against Ebola virus disease, with no cases am

57 presented demonstrate that EBOTAb conferred protection against EBOV when given post-exposure and sho

58 and B cell-mediated immunity, especially for protection against EBV and humoral immunity.

59 influenza virus vaccine efficacy and provide protection against emerging influenza viruses.

60 ted erythrocytes without conferring enhanced protection against febrile malaria.

61 ide genetic evidence for a role for IFI16 in protection against genital herpes.

62 D treatment or Cav-3 knockdown abolished the protection against H/R-induced myocytes injury by AS-1.

63 ning high anthocyanins provided the greatest protection against H2O2.

64 ted cross-reactive immunity and heterologous protection against H3N2 CIV.

65 onses, involved in providing long-term cross-protection against H3N2 influenza virus when compared to

66 gher levels of IGF-1 appeared to confer some protection against hearing impairment in some older adul

67 Protection against herpes zoster (HZ) induced by the liv

68 more conserved fusion protein contribute to protection against heterologous CDV strains.IMPORTANCE R

69 iC MNP-boosted group also possessed enhanced protection against high lethal dose challenges against h

70 the RV144 vaccine trial elicited significant protection against HIV-1 acquisition, but the efficacy a

71 ection against drifted (Philippines) and 60% protection against homologous (Aichi) H3N2 viruses.

72 Collectively, these data suggest durable protection against homologous and heterologous Pf parasi

73 d induced immune memory, suggesting possible protection against HPV vaccine types after a single dose

74 designing effective and enduring therapeutic protection against human or avian influenza viruses.

75 ceed in raising safe, effective, and durable protection against human Zika virus infections or syndro

76 s play an important role in vaccine-mediated protection against infection but the underlying mechanis

77 Protection against infection increased with the order of

78 in SPH2015 from Brazil resulted in continued protection against infection, no viral shedding, and boo

79 Protection against infections can be achieved through va

80 these viral vectors can mediate more potent protection against influenza virus infection in animal m

81 have been used successfully to induce broad protection against influenza viruses in humans, and our

82 ti-cancer capacity, it can offer significant protection against inhibitors of PLK1, but the events un

83 bacterial killing in macrophages and boosted protection against intravenous bacterial challenge.

84 st group B Streptococcus (GBS) might provide protection against invasive GBS disease in infants.

85 eed for a booster dose to sustain individual protection against invasive meningococcal disease.

86 ntion due to its varied applications such as protection against loss of bone mass, chronic diseases,

87 the liver expresses IFN-gamma and can confer protection against M. avium infection in immunocompromis

88 found OP of merozoites to be associated with protection against malaria and further shows IgG3 and GL

89 suggest that vaccination may provide better protection against meningococcal disease in patients tre

90 for purposes of simplicity, cost, and broad protection against multiple National Institute of Allerg

91 pulation of peripheral CD4 T cells conferred protection against new tumors and was significantly expa

92 at Cu is a host effector that is involved in protection against pathogen colonization of the urinary

93 ia vaccine candidate and confers significant protection against Plasmodium falciparum infection in hu

94 nase (G6PD) deficiency is believed to confer protection against Plasmodium falciparum malaria, but th

95 We suggest that protection against predators conferred by their high tox

96 , HVEM-deficient recipients failed to afford protection against respiratory reinfection with influenz

97 ng RSV fusion (F) protein to confer bivalent protection against RSV and HPIV3.

98 wo gene variants provide different levels of protection against sleeping sickness, but this comes wit

99 Helicobacter pylori confers protection against the anaphylaxis associated with ovalb

100 er, CD8(+) T cell-depleted mice displayed no protection against the heterosubtypic virus challenge af

101 Where symbionts provided protection against the same natural enemy, the level of

102 There is also evidence of herd protection against the vaccine-specific and cross-protec

103 und in amphibians, commensal bacteria confer protection against this pathogen.

104 2 expression was required and sufficient for protection against V8 protease-mediated integrity damage

105 haemolymph of infected flies, confer passive protection against virus challenge in naive animals.

106 ty epitope provided strong, T cell-dependent protection against viruses or tumors.

107 an blood cells are likely to be important in protection against zoonotic infection with FeLV.IMPORTAN

108 values that exceeded the U.S. Environmental Protection Agency (USEPA) health-based acceptable risk l

109 nt concentrations exceeded the Environmental Protection Agency limits for discharging to publicly own

110 w transplantation and local muscle radiation protection allows for the identification of a myeloid ce

111 ressed within the early M45 gene provided no protection, although MCMV vectors expressing the high-av

112 dies has been reported to be associated with protection and a measure of vaccine potential.

113 ), BA and stenting (n=52), or DA with distal protection and bailout stenting (n=55).

114 feguarding natural habitats for biodiversity protection and carbon storage alongside promoting areas

115 In addition, they showed superior protection and lung viral reduction against lethal viral

116 atment was associated with significant organ protection and markedly reduced mortality compared with

117 lored the relationships between the level of protection and MPA size, age, and enforcement.

118 toward a holistic approach that incentivizes protection and promotes sustainable human-wildlife coexi

119 ew variants, it is essential to induce broad protection and restrict pneumococcal colonization.

120 TRF2(TRFH) domain orchestrates telomere end protection and reveals how the phosphorylation status of

121 Homeostatic programs balance immune protection and self-tolerance.

122 d avoidance, it is critical to emphasize sun protection and skin cancer screening in individuals who

123 .IMPORTANCE The lack of a known correlate of protection and the failure of a neutralizing antibody to

124 pecies in particular need of new or stricter protections and 514 species in need of improvements to f

125 reases chromosomal breakage, uncoupling fork protection, and chromosome stability.

126 on of resulting products, removal of benzoyl protection, and conversion of hydroxymethyl group into m

127 art failure (HF), the mechanisms behind this protection are not fully understood, and not all patient

128 gous recombination (HR) and replication fork protection are sequentially bypassed during the acquisit

129 te H2A at T121, are not perturbed in cohesin protection as long as Mps1 is functional.

130 ls by Abs can effectively participate in HIV protection, as suggested by the RV144 immune correlate a

131 However, immune correlates of protection, as well as the safety of prophylactic and th

132 To provide a first line of protection at these entry ports, vaccines are being deve

133 There was no interference in protection between the different vaccines.

134 g such therapy beyond 5 years offers further protection but has additional side effects.

135 ittle significance with regards to predation protection but has consequences in terms of energy alloc

136 increase nutrient storage and improve storm protection, but cause declines in habitat availability f

137 partial vaccine series provided considerable protection, but not to the same level as a full series.

138 reciprocal components for signal routing and protection, but their chip-scale integration is not yet

139 V1/V2 antibody responses, whereas potential protection by gp120, but not MVAgp140 boosts, may be fur

140 T progressively disabled a host mechanism of protection by inducing endogenous neuraminidase activity

141 , neutrophils can contribute to optimal host protection by limiting the extent of endotoxin-induced i

142 ired bacterial clearance and eliminated host protection conferred by Gal-1 deficiency.

143 new immunomodulatory role could explain the protection conferred by THP during AKI.

144 against the same natural enemy, the level of protection corresponded to the higher of the two symbion

145 ted to water splitting, catalysis, corrosion protection, degradation of pollutants, disinfection of b

146 o-2-alkenones with guanidine avoiding its NH-protection/derivatization prerequisite for electronic mo

147 e a class I recommendation to use of embolic protection devices (EPD) for saphenous vein graft (SVG)

148 cacy and adverse effects of cerebral embolic protection devices in reducing ischemic central nervous

149 patients, that had exclusive use of embolic-protection devices, and that compared CAS against CEA fo

150 g the inflammatory milieu that supports host protection during infection by fine-tuning NF-kappaB act

151 tial adverse effects of FA overdoses, and FA protection during processing and storage could lead to m

152 Those polysaccharides had also a protection effect against hydroxyl radical-induced DNA d

153 reported statistically significant indirect protection effectiveness (IPE) with point estimates rang

154 Immunogenicity and protection efficacy were better than that observed with

155 ic immune responses responsible for pathogen protection enables vaccine development and provides insi

156 nd the other using only sunscreen with a sun protection factor of 100.

157 T(TM), enhanced vaccine efficacy and sterile protection following malaria challenge.

158 people, most prominently by providing storm protection, food and fodder.

159 ogous A/PR/8/34 and A/Aichi/2/68 viruses and protection for a majority of immunized mice against a he

160 fections in humans, the immune correlates of protection for avian influenza vaccines cannot be determ

161 ropriate for the derivation of correlates of protection for DENV vaccines on the basis of cellular im

162 ch umbrella alone may not provide sufficient protection for extended UV exposure.

163 hese red blood cells into naive mice affords protection for up to 28 days.

164 l response in immunized mice does not impair protection from a homologous challenge; however, it does

165 Subsequent infants obtained limited protection from a single antenatal dose, but revaccinati

166 and IL-33 to enhance Treg- and ILC2-mediated protection from AKI, bears strong therapeutic potential.

167 By contrast, we observe protection from all symptomatic dengue disease at high a

168 D88 signaling is required for proliferation, protection from apoptosis and expression of activation/m

169 This newly defined mechanism confers protection from autoimmunity during pregnancy and repres

170 ces and hijack their regulatory function for protection from complement activation.

171 However, neutrophil depletion abrogated protection from death in Nlrp3(-/-) mice in response to

172 Our results showed protection from death in NLRP3-deficient (Nlrp3(-/-)) an

173 one to delirium should validate their use in protection from delirium.

174 INTERPRETATION: Economic opportunities and protection from deportation for undocumented immigrants,

175 al family Lachnospiraceae as a correlate for protection from disease.

176 nd essential turmeric oils provides superior protection from DSS-induced colitis than curcumin alone,

177 easing GVHD through two opposing mechanisms: protection from fatal immunity by amphiregulin expressio

178 selective stabilization of host proteins and protection from host defense.

179 mechanism by which BSJYD provides myocardial protection from hypertension.

180 ved in evasion of antitumor immune response, protection from hypoxia, angiogenesis, DNA repair, cell

181 Further, protection from injury is achieved by pharmacologic bloc

182 pleted C57BL/6 mice demonstrated significant protection from injury, which was not seen in CD4(-/-) m

183 by cells at the injury site is critical for protection from IRI through bone marrow-derived adenosin

184 rp3 suppression is required for aPC-mediated protection from IRI.

185 f STIM2 results in lower cytokine levels and protection from mortality in a mouse model of systemic i

186 these studies are truly the genes conferring protection from or risk of disease but also to define th

187 als during previous infection correlate with protection from reinfection, suggesting that an effectiv

188 did not alter IgA responses associated with protection from rotavirus disease.

189 tory cytokine production was associated with protection from subsequent Pf infection, but also with a

190 Not accounting for protection from the use of ITNs during pregnancy, expand

191 arasitic exploitation, thermoregulation, and protection from ultraviolet light, microbes, and abrasio

192 ematically the literature on "herd"/indirect protection from vaccinating children aged 6 months to 17

193 We conclude that environmental protection goals relying on measures of richness could u

194 c-Fc gamma receptor interactions for optimal protection; however, the innate effector cells responsib

195 munization experiments in mice and conferred protection in a murine model of Mycobacterium tuberculos

196 where IgG2a antibodies were associated with protection in absence of detectable PvCSP-specific T cel

197 PfSPZ Vaccine showed significant protection in African adults against P falciparum infect

198 strates the lack of the skyrmion topological protection in finite-sized magnetic systems.

199 pathogens, and we hypothesized that reduced protection in infancy could be due to impaired establish

200 wth of MRSA was inhibited, and a significant protection in mice against the bacterial challenge was o

201 week post-I/R provided little to no further protection in mice with ablation of GRK2 in activated fi

202 Compared with 100% protection in piglets initially inoculated with PC21A, 8

203 al carriage and are unlikely to provide herd protection in the context of an outbreak response.

204 dings establish a novel mechanism of humoral protection in the eye involving FcRn and may facilitate

205 (Cerebral Protection in Transcatheter Aortic Valve Replacement [SE

206 anisms by which alveolar macrophages mediate protection in vivo, namely antibody-induced inflammation

207 that Sgo2 at the centromere is required for protection.In meiosis I centromeric cohesin is protected

208 ar pathogens, such as Plasmodium spp., where protection is likely mediated by cellular immune respons

209 emonstrate by an in vitro approach that this protection is mediated by the anti-sigma domain of CrsR.

210 cGAMP-PC7A NP-induced protection is mediated through type I IFN signaling and

211 This protection is sustained by heme-hemopexin complexes in b

212 In addition, we review protection layer approaches and their stabilities for a

213 ture, in which an insulator film serves as a protection layer, can prevent corrosion but must also al

214 se the charge transfer mechanism through the protection layers for both photoanodes and photocathodes

215 evation of PI3,5P2 Our study reveals a rapid protection mechanism regulated by Pho85/CDK5 via signali

216 fork remodeling as a global fork slowing and protection mechanism.

217 nologies, emissions reduction, environmental protection, mining accident prevention, chemical and pro

218 e and comprehensive approach to biodiversity protection, most insights are still focused on a single

219 Protection mutualisms were historically considered rare

220 ors constitute a dynamic version of the edge-protection negative design strategy used in protein evol

221 formally protected and only 8.9% have strict protection, new large-scale conservation efforts to prot

222 oth gp120 and MVAgp140 can augment potential protection of a DNA/MVA vaccine by enhancing gp120 and V

223 eactions, therefore providing a satisfactory protection of amino compounds.

224 phagy as a novel mechanism for IL-6-mediated protection of beta cells from stress-induced apoptosis.

225 f MSPs as support for controlled release and protection of bioactive molecules in food matrices in di

226 y, high LLL12 encapsulation efficiency, well protection of bioactivity, and steadily long shelf time.

227 on rates in soil of 11 biocides used for the protection of building materials were determined in labo

228 This resulted in the protection of cells from the toxicity of l-Abeta42 at co

229 for EAF2 as a key factor mediating androgen protection of DNA damage via Ku70/Ku80 in prostate cance

230 e in relation to scientific research and the protection of human subjects, and its impacts are antici

231 and secretory IgA Ab-mediated system in the protection of intestinal mucosal surface.

232 rolonged state ownership was associated with protection of life chances during the post-socialist tra

233 oritization of particular configurations for protection of maximal cross-scale habitat structural com

234 ugments long-term potentiation, resulting in protection of memory.

235 have evolved an adaptive mechanism involving protection of meristems within specialized structures na

236 , induction of strong adaptive immunity, and protection of mice from wild-type (WT) WNV infection.

237 ent (98-99%) indicating a good potential for protection of microencapsulated carotenoids during the s

238 The protection of nanoencapsulated quercetin was at least 3

239 he assembly of mature nad5 mRNA precedes the protection of PPR78.

240 l export rule are unlikely to compromise the protection of resident adults.

241 sion, our results suggest that CsrR-mediated protection of sigma(S) during exponential growth enables

242 netic field, which anisotropically lifts the protection of surface Dirac fermions from backscattering

243 owever, its complete removal resulted in the protection of the adjacent 26-32 region, suggesting that

244 able delivery strategy demands not only good protection of the cargo but also reversibility in conjug

245 aintenance of cellular integrity and for the protection of the cell from external aggressors - such a

246 he Hck SH3 or tandem SH3-SH2 domains induces protection of the Nef alphaB-helix from deuterium uptake

247 ed that the mother's immediate and expansive protection of the newborn decreases the limbic-hypothala

248 e critically involved in the maintenance and protection of the renal microvascular endothelium.

249 Protection of the stalled replication fork is crucial fo

250 ife, also provides the potential to leverage protection of the young against infection and disease th

251 Insight into the mechanisms of protection of these variants may facilitate the developm

252 levels of government to meaningfully enhance protection of these vulnerable waters.

253 Bis-o-nitrobenzyl protection of tyrosine phosphate enabled its incorporati

254 rally low connectivity are that the loss (or protection) of any non-breeding site will have a diffuse

255 lf-epitope specific Treg cells that leads to protection or causation of autoimmunity.

256 ge of livestock yield increases with habitat protection or restoration, as well as a deeper understan

257 h no pharmaceutical intervention for hearing protection or restoration.

258 sm is distinct from the BRCA2-dependent fork protection pathway, in which stable RAD51 filament forma

259 unlike other POPs thought to diminish innate protection, POP2 reduces detrimental inflammation while

260 The other objectives included financial protection (potentially better provided upstream by keep

261 policies, despite strict regulation of plant protection product and biocide use.

262 Following the application of two plant protection products (containing the above-mentioned acti

263 The personal protection provided by a bednet decreased over the study

264 Full protection provided stronger effects than partial protec

265 ffector cells responsible for mediating this protection remain largely unknown.

266 segments of proximal tubules, and full renal protection required both macrophages and renal tubular c

267 the most cost-effective action; and (4) land protection should be prioritised if the catchment is rel

268 nd expansion are similar and low; (2) marine protection should take precedence if the rate of marine

269 Any IRS protection significantly reduced malaria incidence durin

270 Public protected areas with low and medium protection status are more prevalent on the non-breeding

271 Lower protection status areas experienced higher forest losses

272 menable to any of the previously developed N-protection strategies known to enable remote aliphatic C

273 ditions under which the economically optimal protection strategy is to protect all species, no specie

274 vitro growth inhibition of MRSA, and in vivo protection studies in mice against the lethal MRSA chall

275 after hypoperfusion possibly via endothelial protection supporting its potential use in the treatment

276 reduced with transcatheter cerebral embolic protection (TCEP).

277 inuous combo therapy afforded no greater T1D protection than did BAFFR-Fc alone.

278 ng antibody (nAb) titers are associated with protection, the Ab repertoire induced by LATVs remain un

279 ion with disease is through promotion versus protection, thereby linking statistical association to b

280 masking of cysteine residues with orthogonal protection to enable site-specific conjugation of each d

281 itro, and are sufficient to provide enhanced protection to infection with C. rodentium.

282 ut cell line models showed that Pak1 confers protection to keratinocytes from UV-B-induced apoptosis

283 nsidered as the wedge that balances clinical protection to malaria.

284 aundry formulations, whereby enzymes require protection to prevent their deactivation by bleach.

285 sident memory T cells (TRMs) mediate optimal protection to respiratory pathogens, and we hypothesized

286 induce both IgG1 and IgG2a in mice, provide protection to S.

287 obust antibody response, conferring complete protection upon challenge.

288 goal was to unravel the mode of Idd22-based protection using in vivo and in vitro models.

289 Protection via heat-killed DK128 was correlated with an

290 The mechanism of protection was found to be a novel pathway of direct TGF

291 Of note, this protection was lost when GOT was knocked down.

292 This protection was mediated by neonatal crystallizable fragm

293 When Notch1 was inhibited, this E2-mediated protection was not observed, whereas ectopic overexpress

294 different natural enemies, no alteration in protection was observed in the presence of co-infections

295 the International Commission on Radiological Protection, was used to develop the dose estimates, and

296 oocytes are defective in centromeric cohesin protection, whereas oocytes devoid of Bub1 kinase activi

297 se and a selective loss of pregnancy-induced protection, whereas reproductive success was unaffected.

298 munity and identifying correlates of malaria protection, which could, for instance, inform the choice

299 We observed decreasing influenza vaccine protection with increasing time since vaccination across

300 roqueRag1(-/-) mice actually led to enhanced protection with reduced bacterial load, decreased chemok