ライフサイエンスコーパス: inactivated

1 c stress was markedly reduced when lon-1 was inactivated.

2 loses its grip on the RNA:DNA hybrid and is inactivated.

3 ion rates, transposons are then more rapidly inactivated.

4 s-proline-dependent Ssu72 CTD phosphatase is inactivated.

5 rature, conditions where trypsin is normally inactivated.

6 ranscriptional regulator oxyR is genetically inactivated.

7 d when p97's ATPase activity is inhibited or inactivated.

8 hough some underlying conductances should be inactivated.

9 This effect is reversed when RAP1 is inactivated.

10 that mediate fusion, become proteolytically inactivated.

11 Autoantibodies against leucine-rich glioma inactivated 1 (LGI1) are found in patients with limbic e

12 common in patients with leucine-rich, glioma-inactivated 1 (LGI1)-IgG associated and contactin-associ

13 (pCSF(NMDAR), n = 7) or Leucine-rich-glioma-inactivated-1-Ab (pCSF(LGI1), n = 6) associated AE suppr

14 human eosinophils and were internalized and inactivated (95% in <= 2 hours) as reflected by a reduce

15 Low doses of 1.7 and 1.2 mJ/cm(2) inactivated 99.9% of aerosolized coronavirus 229E and OC

16 plication and sister chromatid cohesion, and inactivated a third, the DNA damage checkpoint.

17 ination with either MF59- or AS03-adjuvanted inactivated A(H7N9) vaccines elicited robust, cross-reac

18 e a set of affinity optimized, enzymatically inactivated ACE2 variants that potently block SARS-CoV-2

19 Co-administration of a UV inactivated Ad4 vector with the Ad5-prM-E vaccine led to

20 four subjects suggest that vaccination with inactivated adjuvanted vaccine induce NA-reactive respon

21 ility complex (MHC) class I and II genes are inactivated and CD47 is over-expressed.

22 polarized, T-type VGCCs and A-type VGKCs are inactivated and CF-EPSPs activate P/Q-type VGCCs, high-v

23 he DNA-binding species with the binding site inactivated and eGFP as a calibration standard among lab

24 e et al., 2013, in which the hippocampus was inactivated and grid cells were recorded in the rat MEC.

25 These DCs are inactivated and removed upon Wnt signal transduction.

26 in the attention network when one of them is inactivated and reveals whether they might have a causal

27 Inactivated and subunit vaccines overcome some of the li

28 al strains have different methyltransferases inactivated and thus different methylation patterns.

29 li) bacterial pathogens as well as with heat-inactivated and viable fungi (Candida albicans).

30 n the vaccine without the need for purified, inactivated, and calibrated virus reference antigens.

31 ng chromosomal fusion, the neocentromere was inactivated, and the native centromere of the fused chro

32 recombinant antigens (RCA) and a whole-cell inactivated antigen vaccine (WCA), in conferring protect

33 Additionally, inactivated antioxidative pathways, increased reactive o

34 ar Ca(2+), but the mechanisms by which it is inactivated are less clear.

35 he 10 degrees C adapted strains were rapidly inactivated at higher temperatures.

36 athological sites when mobilized by distinct inactivated bacterial-based stimuli administered subcuta

37 WCV), but not avirulent (PII-WCV) whole-cell inactivated bacterium.

38 zed L. braziliensis transfectants were photo-inactivated before (Strategy #1) or after (Strategy #2)

39 Inactivated beta(2)-AR (Nb60) molecules are also largely

40 ify genes which are up or down regulated, or inactivated, between multiple conditions, producing a fi

41 e develop mice in which we have specifically inactivated both insulin receptors (IRs) and IGF-1 recep

42 iled to induce IFN-gamma production, whereas inactivated Bp induced IFN-gamma production.

43 Inactivated Bp, but not antigens, induced potent IFN-gam

44 ro1), and protein disulfide-isomerase can be inactivated by a feedback inhibition mechanism involving

45 ant plants, in which OsSBEIIb was completely inactivated by abolishing the catalytic center and C-ter

46 oading with L. braziliensis photodynamically inactivated by both strategies, including CD86 expressio

47 r of cytokine production that is cleaved and inactivated by caspase-8.

48 rahydrocannabinol (THC), are metabolized and inactivated by cytochrome P450 enzymes primarily within

49 Viruses can be inactivated by exposure to heat or bleach, but polioviru

50 ere randomly assigned to receive VZV vaccine inactivated by gamma irradiation (n=2637) or placebo (n=

51 d (1:1) to receive four doses of VZV vaccine inactivated by gamma irradiation or placebo approximatel

52 Either site can be inactivated by mutation resulting in enzyme variants tha

53 alphaviruses, CHIKV replicase was completely inactivated by mutations preventing palmitoylation of ns

54 tion-mediating memory, which subsequently is inactivated by Nep1 degradation.

55 atic, but not terminally expressed, KORs are inactivated by norBNI.

56 vates IRF3 and that this pathway is normally inactivated by NS3-NS4A during HCV infection.

57 ammonia by the nitrogenase enzyme, which is inactivated by oxygen.

58 synthase (GSa) - respectively activated and inactivated by phosphorylation - and their Ca(2+)-depend

59 nd active at 25 degrees C, but is completely inactivated by protein unfolding at higher temperatures.

60 overexpression of constitutively active Rabs inactivated by RN-tre failed to alter NMII RLC localizat

61 These molecules are rapidly inactivated by the action of dipeptidyl peptidase IV (DP

62 ransgenic DNA is recognized and then quickly inactivated by the assembly of a repressive chromatin st

63 Host antimicrobial peptides are inactivated by the capsule as it impedes their penetrati

64 mutation (p53HRmut) and wildtype p53 (p53WT) inactivated by the human papillomavirus 16 (HPV16) E6 on

65 ir potential to be rapidly hydrolyzed (i.e., inactivated) by extracellular peptidases during biologic

66 mpared the protective efficacies of formalin-inactivated C. burnetii Nine Mile phase I (PIV) and phas

67 luated the protective efficacy of a formalin-inactivated C. burnetii Nine Mile phase I vaccine (PIV)

68 Here we show that repair of the inactivated C16L/B22R gene of MVA enhances replication i

69 Inhibiting the alpha5-GABA(A)R in mice with inactivated CA1 VIP input could still improve spatial le

70 chnologies, we show that pigs with all PERVs inactivated can also be genetically engineered to elimin

71 Here, we repurpose a catalytically inactivated Cas9 (dCas9) construct as a generic, novel,

72 rx/TrxR restored the activity of polysulfide-inactivated caspase-3 in vitro, and TrxR inhibition pote

73 At the site of inactivated catalase, cell-generated H(2)O(2) enters the

74 he 2017-2018 influenza season, quadrivalent, inactivated cell-derived influenza vaccine (ccIIV4) vacc

75 minated by s.c. injection of active, but not inactivated, CG during sensitization.

76 several structures, including multiple open-inactivated conformations, further indication of a highl

77 of the Bay K8644 enantiomers exhibit similar inactivated conformations, suggesting that (S)-(-)-Bay K

78 These partially inactivated CRISPR-Cas variants might mediate guide RNA-

79 Finally, the acyclic amines inactivated CYP3A4 and this liability was addressed by m

80 In contrast, protease-inactivated D pteronyssinus had no effect on offspring g

81 mothers exposed to D pteronyssinus, protease-inactivated D pteronyssinus, or to PBS during lactation.

82 with PRSS1WT mice, as well as enzymatically inactivated Dead-PRSS1R122H mice, we unraveled that incr

83 gly, however, we found that vaccination with inactivated DENV enhanced ZIKV infection, mainly in the

84 ch in ISCs; its de-repression, when Notch is inactivated, drives progenitor cells to differentiate al

85 e chitin-active variants became more rapidly inactivated during catalysis than a natural chitin-activ

86 nally, we show that this circuit is normally inactivated during consumption and food-seeking.

87 Here, we report that glycolysis, which is inactivated during RLR activation, serves as a barrier t

88 as, which are active during wakeful rest and inactivated during task-based stimulation.

89 repressor, like the lambda CI repressor, is inactivated during the SOS response to DNA damage, and t

90 In contrast, T-type channels are inactivated during tonic mode and do not contribute to s

91 levels are decreased in cells where TP53 is inactivated, either by HPV16 E6, by expression of a domi

92 Because baculoviral vectors are inactivated elsewhere, gene delivery and in vivo genome

93 eal-time mobility behaviors of activated and inactivated endogenous conformers during agonist treatme

94 ctivity (DUBmut) and the other containing an inactivated endoribonuclease (EndoUmut).

95 This trial tested an oral, inactivated, enterotoxigenic E coli vaccine (ETVAX), whi

96 , also called MLL4) is among the most highly inactivated epigenetic modifiers in lung cancer.

97 to efficiently hydrolyze both activated and inactivated esters.

98 Ninety percent of infectious virus was inactivated every 6.8 minutes in simulated saliva and ev

99 ment midpoint are likely to be activated and inactivated first in each contraction.

100 itrogen from histidine in vitro, and strains inactivated for hutH are severely attenuated in a murine

101 JQ1 directly interacted with FOXA1 and inactivated FOXA1 binding to its interacting repressors

102 Centrioles must be eliminated or inactivated from the oocyte to ensure that only the two

103 RK pathway and is one of the most frequently inactivated genes in human cancers.

104 LTF is inactivated genetically or epigenetically in various can

105 Unexpectedly, when the Mgat4d gene was inactivated globally or conditionally in spermatogonia,

106 ted in an in vitro infection model with heat-inactivated Gram-positive (Staphylococcus aureus) and Gr

107 EBOV/Mak was inactivated (> 6 log(10)) by 70% ethanol after contact t

108 low-dose IL-15, alone or in combination with inactivated H3N2 virus; the associated NK cell response

109 tiple HCAs, hepatocyte nuclear factor 1alpha-inactivated HCAs showed a higher rate of progression com

110 disease, with hepatic nuclear factor 1alpha-inactivated hepatocellular adenomas being the most commo

111 eroxide and hydrogen peroxide production and inactivated HIF (hypoxia-inducible factor)-1alpha, which

112 Strains with inactivated hsmR or hsmA have increased sensitivity to r

113 in inoculation of mice with infectious or UV-inactivated HSV type 1.

114 t-limited media (saliva with 5%, 10%, or 20% inactivated human serum).

115 y, in cancer patients, Aalpha is found to be inactivated in a haploinsufficient manner.

116 Finally, we show that SLX4IP is inactivated in a subset of ALT-positive osteosarcomas.

117 JNK1/2 is inactivated in a substantial proportion of human LSCC an

118 ch orthopoxvirus species, numerous genes are inactivated in all other members of the genus.

119 ession of ATRX, a protein that is frequently inactivated in ALT tumors.

120 ntroducing ester functionalities that can be inactivated in blood as well as by the liver (dual-soft)

121 SNF chromatin remodeling gene, is frequently inactivated in cancers and is not directly druggable.

122 uppressor of cytokine signaling-1 (SOCS1) is inactivated in hematopoietic and solid cancers by promot

123 ymes can suppress tumors, but they are often inactivated in human cancers overexpressing inhibitory p

124 ndent tumour suppressors that are frequently inactivated in human cancers, and FOXO3 is the second mo

125 he MC903 model, whereas these cells remained inactivated in OVA sensitization model.

126 n of an actionable target downstream of RB1, inactivated in SCLC and other advanced tumors, could hav

127 f area 25, but not area 32, areas which when inactivated independently reduced and had no effect on a

128 Furthermore, immunization of Tc caprine with inactivated influenza A (H7N9) viruses followed by H7N9

129 ion rates are not well understood for 2-dose inactivated influenza vaccination (IIV) schedules in aut

130 ticipants received a standard-dose trivalent inactivated influenza vaccination (IIV3) at enrollment,

131 Available evidence indicates that seasonal inactivated influenza vaccination during pregnancy prote

132 Inactivated influenza vaccine (IIV) and pertussis vaccin

133 ecombinant HA vaccine (rHA) and cell-derived inactivated influenza vaccine (IIV) to egg-derived IIVs

134 uter-based system to intramuscular trivalent inactivated influenza vaccine (IIV3) or a control of ina

135 e) and indirect effectiveness of a trivalent inactivated influenza vaccine (IIV3).

136 posed to different combinations of trivalent inactivated influenza vaccine (TIV with or without adjuv

137 , comparator-controlled (trivalent high-dose inactivated influenza vaccine [IIV3-HD], or quadrivalent

138 ter-generated randomisation list, to receive inactivated influenza vaccine containing 15 mug of each

139 identified persons who were vaccinated with inactivated influenza vaccine from 1 September 2010 to 3

140 A regimen of double-dose inactivated influenza vaccine gave slightly greater immu

141 and safety of different dosing schedules of inactivated influenza vaccine in pregnant women living w

142 Standard-dose, seasonal, trivalent, inactivated influenza vaccine induces moderate-to-low ha

143 Our results suggest that effectiveness of inactivated influenza vaccine wanes during the course of

144 etected in patients on ICIs who received the inactivated influenza vaccine within ~ approximately 2 m

145 4 weeks after immunization with the seasonal inactivated influenza vaccine, but numbers returned to n

146 ost-administration of the seasonal trivalent inactivated influenza vaccine.

147 neutralizing antibody responses elicited by inactivated influenza vaccines (IIV), but neutralizing a

148 016 through 2017-2018, injectable, trivalent inactivated influenza vaccines (IIV3) and a nasal spray,

149 ter IV A(H3N2)v vaccine and several seasonal inactivated influenza vaccines (IIVs) in adults, elderly

150 cent influenza seasons, the effectiveness of inactivated influenza vaccines against circulating A(H3N

151 cells, which are not induced by traditional inactivated influenza vaccines and may provide protectio

152 recommends LAIV4 and injectable, tetravalent inactivated influenza vaccines replacing IIV3.

153 HD-MAPs were coated with a monovalent, split inactivated influenza virus vaccine containing A/Singapo

154 regarding the utility of currently licensed inactivated influenza virus vaccines and novel protein-b

155 Furthermore, inactivated influenza virus vaccines focus on the induct

156 lls were stimulated with soluble antigens or inactivated intact Bp and the presence or absence of blo

157 ry dermal endothelial cells with live and UV-inactivated KSHV demonstrated that viral gene expression

158 Cytosolic Par-1 bound, phosphorylated, and inactivated KSR scaffolding proteins ultimately inhibite

159 sults provide evidence that photodynamically inactivated L. braziliensis are susceptible to the degra

160 Here we use cortactin gene-inactivated male and female mice to study the role of th

161 ions (VAH), similar to those in humans given inactivated measles or respiratory syncytial virus vacci

162 in the context of full-length MGAT4D-L, also inactivated MGAT1 inhibitory activity.

163 s (43 degrees C for 25 min), germ cells with inactivated Mgat4d were markedly more sensitive to the e

164 n of 25 amino acids (aa) from the C terminus inactivated MGAT4D-L, but deletion of 20 aa did not.

165 We generated mice with an inactivated mIgE-ITT motif and analyzed serum IgE levels

166 okines; however, apoptotic and metabolically inactivated MSCs have more recently been shown to posses

167 les in synaptic transmission, we genetically inactivated mTORC1 or mTORC2 in cultured mouse glutamate

168 Inactivated myosin motors are folded against the filamen

169 r findings indicated that aBL preferentially inactivated N. gonorrhoeae, including antibiotic-resista

170 plasma potassium by oral gavage of potassium inactivated NCC within 1 hour in wild-type mice, but had

171 he selectivity of the Hsp70:CHIP complex for inactivated nNOS.

172 ly B (NOMV-FHbp), NOMV with FHbp genetically inactivated (NOMV-KO), and/or a control rFHbp vaccine ag

173 cells to lose their identity, we genetically inactivated Notch1 and Notch2, inactivated the Notch sig

174 the channels, it has more preference for the inactivated one.

175 mouse, in which the insulin receptor (IR) is inactivated only in skin, with no other metabolic conseq

176 in record time, allowing the development of inactivated or attenuated viral vaccines along with subu

177 pathological processes that were activated, inactivated, or unchanged vs. RVD with no intervention.

178 acids in mice in which Otop1 was genetically inactivated (Otop1-KO mice).

179 i-PD-L1 immune checkpoint blockade in ARID1A-inactivated ovarian cancer.

180 y a source of visual salience, we reversibly inactivated parietal cortex and simultaneously recorded

181 e in this system, here, we pharmacologically inactivated parts of vlPFC and simultaneously measured I

182 ealth include both modified live vaccine and inactivated pathogens.

183 owed the production of pigs with genomically inactivated PERVs.

184 To this end, we inactivated PI3K by genetic means in the fly fat body an

185 ity in competition studies using homologous (inactivated Pitman Moore rabies virus) and heterologous

186 l coverage through routine immunization with inactivated polio vaccine (IPV), to ensure type 2 immuni

187 r the 2008-09 northern hemisphere IIV3 or an inactivated polio vaccine (IPV).

188 booster dose of tetanus-diphtheria-pertussis inactivated polio vaccine (Tdap) 3 months later; BCG and

189 dministering daily intradermal injections of inactivated polio vaccine according to six different del

190 vaccinate children-who had only received the inactivated polio vaccine-with the oral polio vaccine (O

191 phtheria-tetanus toxoids-acellular pertussis-inactivated poliomyelitis-Haemophilus influenza type b-h

192 Intradermal (id) fractional inactivated poliovirus vaccine ([fIPV] one fifth of norm

193 Intradermal administration of fractional inactivated poliovirus vaccine (fIPV) is a dose-sparing

194 ted influenza vaccine (IIV3) or a control of inactivated poliovirus vaccine (IPV) in the beginning of

195 g OPV in the phase 4 study and either OPV or inactivated poliovirus vaccine (IPV) in the novel OPV2 p

196 Due to global shortage of inactivated poliovirus vaccine and withdrawal of oral va

197 causes defects in apical structures, even if inactivated post-mitotically.

198 een in CA1 via increased levels of oxidized, inactivated potassium channel Kv2.1, which undergoes dis

199 , we observed that immunization of mice with inactivated poxvirus primes a virtually undetectable CD4

200 Heat-inactivated PPE was used to generate a sham operative co

201 This study assessed inactivated prepandemic vaccine strains in a One Health

202 that additional distraction reactions, where inactivated proteases become competitive inhibitors to r

203 ed their potency in vivo in BALB/c mice with inactivated quadrivalent influenza vaccine (QIV) and tes

204 investigated cT(FH) responses to the 2017-18 inactivated quadrivalent influenza vaccine (QIV) in men

205 The VE of inactivated quadrivalent influenza vaccine for preventin

206 ssing technology to heat-stabilize FiloRab1 (inactivated rabies-based Ebola vaccine), a candidate Ebo

207 Vaccination with formalin-inactivated "rewired" viruses significantly enhances the

208 A formalin-inactivated RSV vaccine developed in the 1960s not only

209 ages of lager-brewing yeasts, have inherited inactivated S. cerevisiae alleles of critical phenolic o

210 hen simultaneously exposed to an inoculum of inactivated Salmonella Enteritidis and a chronic heat st

211 Analyzing heat-inactivated samples with a luciferase immunoprecipitatio

212 he present study, simulated sunlight rapidly inactivated SARS-CoV-2 suspended in either simulated sal

213 evaluated using mock test samples containing inactivated SARS-CoV-2 virions, added to in vitro derive

214 adjustment for age and prior LAIV (n = 436), inactivated seasonal vaccine (n = 100), or (H1N1)pdm09 v

215 y skin disease virus (LSDV), as well as, the inactivated serotype O.

216 expression of Snail, Twist, and Notch1; and inactivated several profibrotic signaling molecules in t

217 current study, we produced monoglycosylated inactivated split H1N1 virus vaccine from chicken eggs b

218 3-3 adaptor proteins that hold CaMKK2 in the inactivated state by preventing dephosphorylation of pho

219 Transition to the inactivated state involves a secondary structure change

220 of a drug for binding to the open versus the inactivated state of K(v)11.1 can also be inferred from

221 ide Nav1.7 channel blocker that binds to the inactivated state of Nav1.7 channels with high affinity

222 7 inhibitors that preferentially inhibit the inactivated state of the channel, ST-2262 is equipotent

223 which also bind with higher affinity to the inactivated state than the resting state but bind at a s

224 where a small fraction of channels are in an inactivated state under drug-free conditions, inhibition

225 N642H) can adopt a hyper-activated and hyper-inactivated state with resistance to dephosphorylation.

226 e of the channel, a protocol that favors the inactivated state, and a high frequency protocol.

227 nterface drive the channel into an hERG-like inactivated state, thereby obscuring its opening upon de

228 d the output is the occupancy of a long-term inactivated state.

229 states (with D4S4 in the inner position) and inactivated states (with D4S4 in the outer position).

230 SUMOylation of PTEN and then correspondingly inactivated the AKT/mTOR signaling pathway.

231 act of sensory evidence, we chemogenetically inactivated the excitatory projections from auditory cor

232 emia cells increased ceramide levels 2-fold, inactivated the key signaling protein extracellular sign

233 We selectively inactivated the Mmp14 gene in Mphis using a genetic stra

234 e genetically inactivated Notch1 and Notch2, inactivated the Notch signaling target Hes1, or induced

235 We inactivated the Sry (sex-determining region Y)-box 2 (So

236 Using CRISPR, we inactivated the TET1 gene in H9 human embryonic stem cel

237 rmaldehyde incubation of infected cells also inactivated the virus.

238 ancer progression: most carcinoma cells have inactivated their epithelial antiproliferative response

239 some molecules of their protective catalase inactivated, these tumor cells allow locally surviving c

240 h plays a crucial role in gene silencing, is inactivated through recurrent mutations in core subunits

241 Mice homozygous for an inactivated Tmem189 gene lacked plasmanylethanolamine de

242 In mice with a conditionally inactivated Tsc1 gene in glia, 8 significantly reduced t

243 FBXW7 targeted the frequently inactivated tumor suppressor KMT2D for protein degradati

244 For the most frequently inactivated tumor suppressor p53, genetic mouse models h

245 CNL1 has been inactivated twice independently by point mutations in C.

246 t not cleavage, and another group encodes an inactivated type V variant.

247 e transcriptional repressor role of SerRS is inactivated under hypoxia through phosphorylation by ata

248 ll number of bacterial genes are known to be inactivated upon IGE integration and reactivated upon ex

249 ain (H1/stalk) following trivalent influenza inactivated vaccine (IIV3) immunization in pregnant wome

250 accine (n = 20), live-attenuated followed by inactivated vaccine (n = 15), twice AS03-adjuvanted inac

251 ated vaccine (n = 15), twice AS03-adjuvanted inactivated vaccine (n = 16) or placebo (n = 5, intranas

252 live-attenuated followed by AS03-adjuvanted inactivated vaccine (n = 20), live-attenuated followed b

253 a single-dose immunization of ZIKV purified inactivated vaccine (ZPIV)(4-7) in a dengue virus (DENV)

254 his vaccine response, we immunized mice with inactivated vaccine and injected Ag-pulsed activated APC

255 ine on day 85; the same regimen but with the inactivated vaccine being adjuvanted with AS03; and an A

256 Our results using inactivated vaccine candidates from the human pandemic p

257 03-adjuvanted, chimeric H8/1, intramuscular, inactivated vaccine followed by an AS03-adjuvanted, chim

258 on-adjuvanted, chimeric H5/1, intramuscular, inactivated vaccine on day 85; the same regimen but with

259 This suggests that CD4 effectors induced by inactivated vaccine require high levels of cognate Ag re

260 The adjuvanted inactivated vaccine, but not the live-attenuated vaccine

261 sus nonadjuvanted H5N1 avian influenza virus inactivated vaccine.

262 se (HD) and the standard-dose (SD) trivalent inactivated vaccine.

263 03-adjuvanted, chimeric H5/1, intramuscular, inactivated vaccine.

264 Vaccination with inactivated vaccines is safe after transplantation and i

265 e, through strategies that included seasonal inactivated vaccines, Flumist, and synthetic peptides de

266 ein vaccines are a desirable alternative for inactivated vaccines.

267 otected against a respiratory challenge than inactivated vaccines.

268 to investigate the efficacy and safety of an inactivated varicella zoster virus (VZV) vaccine for her

269 ety and interchangeability of a single dose, inactivated Vero-cell derived, JENVAC(R) to the live att

270 ty, and interchangeability of a single-dose, inactivated, Vero-cell derived, JENVAC to the live-atten

271 Pitman Moore rabies virus) and heterologous (inactivated vesicular stomatitis virus) antigens and acc

272 sponsive enhancer that becomes progressively inactivated via Polycomb-mediated silencing as discs mat

273 ctures of Env trimers on aldrithiol-2 (AT-2)-inactivated virions in ligand-free, antibody-bound and C

274 e culture infective dose (TCID(50))/ml using inactivated virus and 25 copies/ml (c/ml) using syntheti

275 intranasal LTA1 enhanced immune responses to inactivated virus antigen and subsequent protection agai

276 icient to induce HLA upregulation because UV-inactivated virus had no effect.

277 At the present time, vaccination with inactivated virus vaccine produced from embryonated chic

278 In contrast, immunization with an inactivated virus vaccine, even when enhanced by additio

279 Vaccination with inactivated virus vaccines has been applied for several

280 wed similar limits of detection (LODs) using inactivated virus, with 100% detection, ranging from 500

281 uential cross-infection, or vaccination with inactivated virus.

282 inic for gene therapy and immunotherapy, and inactivated viruses or virus-like particles have long be

283 her than motor response targets, were in the inactivated visual field.

284 Animals with procaine-inactivated VLs had tortuous paths and were unable to fi

285 l patients who received at least one dose of inactivated VZV vaccine or placebo and had follow-up dat

286 The inactivated VZV vaccine was well tolerated and efficacio

287 s (CMV)-cre strain, Wasf3 constitutively was inactivated, which led to viable mice with no visible mo

288 compared live infection with influenza to an inactivated whole influenza vaccine.

289 available, the only protection is a formalin-inactivated whole virus vaccine.

290 Q-Vax, a formalin-inactivated whole-bacteria vaccine, is currently the onl

291 Q-Vax, a formalin-inactivated whole-bacteria vaccine, is currently the onl

292 The formalin-inactivated whole-cell vaccine (WCV) confers long-term p

293 est parenteral administration of adjuvanted, inactivated whole-cell vaccines for O157 can induce O157

294 are rapidly activated with near-infrared and inactivated with far-red light.

295 Urease is first inactivated with silver ions and printed onto paper micr

296 LRP5-deficiency in osterix-expressing cells inactivated Wnt signaling in the nucleus pulposus by 95%

297 Wwp2 and mice in which the Wwp2 E3 enzyme is inactivated (Wwp2-C838A) exhibit aggravated spontaneous

298 ect of the pre-harvest treatment by specific inactivated yeasts (YE) on the qualitative parameters an

299 of an aluminum hydroxide adjuvanted purified inactivated Zika vaccine (PIZV) against challenge with Z

300 Notably, inactivated ZIKV vaccination enhanced dengue disease sev