ライフサイエンスコーパス: inactivated

1 ording to the last vaccine type (live and/or inactivated).

2 appens in the SC when the FEF is temporarily inactivated.

3 reas genes of metazoan origin were primarily inactivated.

4 tood, little is known about how Igo/Ensa are inactivated.

5 family are mono-O-glucosylated and, thereby, inactivated.

6 trimer, and as a consequence the DHO is also inactivated.

7 bait in which the rabies vaccine was already inactivated.

8 after all three kinases were simultaneously inactivated.

9 ity disappeared when pxpA, pxpB, or pxpC was inactivated.

10 nucleotide translocator isoform 1 (ANT1) was inactivated.

11 e not nearly as catastrophic as when Mps1 is inactivated.

12 oniae cells when the aPBP synthase PBP1a was inactivated.

13 n the enzymatic activity of uricase had been inactivated.

14 disrupted when the medial frontal cortex is inactivated.

15 s in which endogenous Piezo1 was CRISPR/Cas9 inactivated.

16 ow clefts, mutant channels were incompletely inactivated.

17 ludge and sludge where the protozoa had been inactivated.

18 (VGKC) complex proteins, leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-2

19 extracellular domains of leucine-rich glioma-inactivated 1 (LGI1) and contactin-associated protein-li

20 imbic encephalitis with leucine-rich, glioma-inactivated 1 (LGI1) antibodies is one of the most frequ

21 esults from mutations in leucine-rich glioma-inactivated 1 (LGI1), a soluble glycoprotein secreted by

22 omplex related proteins (leucine-rich glioma-inactivated 1 and contactin-associated protein-like 2),

23 ction mutations in LGI4 (leucine-rich glioma-inactivated 4).

24 four seminal studies that microstimulated or inactivated a key attention-related midbrain structure,

25 e site cysteine as the sulfide source and is inactivated after a single turnover.

26 Using CRISPR-Cas9, we inactivated all of the PERVs in a porcine primary cell l

27 ho received live vaccine alone compared with inactivated alone or concurrent live and inactivated vac

28 When inactivated along with ExoI in Escherichia coli, or Sae2

29 Binding of inactivated and fluorescently labeled Sin Nombre virus (

30 The robot rehabilitation system can be inactivated and the skills that were learned persist.

31 While rabies vaccines are inactivated and thus have an excellent safety profile an

32 ion from the lysogenic to lytic state, CI is inactivated, and the two lytic promoters are de-represse

33 monstrates the successful production of PERV-inactivated animals to address the safety concern in cli

34 n the FRC environment where Cox-2 is genetic inactivated are more sensitive and rapidly activated upo

35 ned the full binding affinity to Im7 but was inactivated as a DNase.

36 Vaccination in pregnancy with a monovalent inactivated AS03-adjuvanted split virion influenza A(H1N

37 Then, we inactivated Ascaris eggs through exposure to these carbo

38 hat carboxylic acids at these concentrations inactivated Ascaris eggs when the pH was below the pKa f

39 The crystal structure of this inactivated assembly provides first insight into the bin

40 High FA doses inactivated ATM via its covalent dimerization and format

41 We genetically inactivated atypical E2Fs in epithelial and mesenchymal

42 rigenesis was similar whether p16(INK4a) was inactivated before or after exposure to IR.

43 When we vaccinated mice, chemically inactivated BNSP333-S1 induced high-titer neutralizing a

44 ner (Control-NP) and a commercial adjuvanted inactivated BVDV vaccine (IAV), all inoculated subcutane

45 by light, transduce the signal, and are then inactivated by a GPCR kinase and arrestin.

46 nocytogenes unless the pathway was partially inactivated by AFN-1252 treatment.

47 Complex II activity was inactivated by blue light in mitochondria from strains e

48 Nitric oxide (NO) is inactivated by cell-free hemoglobin in a dioxygenation r

49 Additionally, integrins can be inactivated by CSPGs, and this inhibition can be overcom

50 and carbon dioxide reduction are completely inactivated by cyanide.

51 tile ring constriction and thus specifically inactivated by CYK-4 at the division plane.

52 g iron regulatory proteins IRP1 and IRP2 are inactivated by either Fe-S cluster insertion or protein

53 e response to HSV-1 and are also degraded or inactivated by ICP0, here we further investigate the rol

54 Our results also suggest that virus inactivated by LJ001 induces an immune response, showing

55 ation of NAD(P)H, is upregulated when p16 is inactivated by looking at gene expression profiling stud

56 HSV is inactivated by low-pH preexposure, and gB, a class III f

57 kinases for cyclin D-CDK4 complexes that are inactivated by p21-mediated stabilization.

58 cific sites at their activation loop and are inactivated by phosphatases.

59 MTs) in Arabidopsis thaliana are efficiently inactivated by phosphorylation to avoid toxic accumulati

60 we show that Atonal outlives its mRNA but is inactivated by phosphorylation.

61 ly inhibits a subset of Wnts, but is further inactivated by proteolytic cleavage.

62 These proteins are inactivated by Rho-selective GTPase-activating proteins

63 embles a nuclear export signal, and could be inactivated by site-directed mutagenesis.

64 res of wild-type PRF and a sulfurtransferase-inactivated C314S mutant with and without glutathione we

65 Of note, H2O2 also inactivated CBP21, but the second-order rate constant fo

66 nt and functioning in vivo, we concomitantly inactivated CD4 and CD8 genes in mice with intact MHC cl

67 Here, we describe a mouse model in which we inactivated Cic by selectively disabling its DNA-binding

68 trol channel gating via stability of a novel inactivated closed state.

69 filter backbone in its collapsed deep C-type inactivated conformation, highlighting the close interac

70 structures allow completion of a closed-open-inactivated conformational cycle in a single voltage-gat

71 alation to A. fumigatus viable conidia, heat-inactivated conidia (HIC), or HEPA-filtered air twice a

72 nmt3a-Dnmt3L construct fused to the nuclease-inactivated dCas9 programmable targeting domain to intro

73 mistry, against inactivation and rescues MCM inactivated during catalytic turnover by using the GTP-b

74 To study the role of these six BDs, we inactivated each of the six BDs of PBRM1 and re-expresse

75 nce with previous results, MDMs treated with inactivated EBOV and Ebola virus-like particles (VLPs) i

76 ained from uninfected donors and spiked with inactivated EBOV.

77 Pox-W263I activity and could reactivate heat-inactivated enzyme.

78 When RADX is inactivated, excessive RAD51 activity slows replication

79 reviously immunized with a nonlive, formalin-inactivated (FI)-RSV vaccine has been associated with se

80 cultured using a combination of mitotically inactivated fibroblasts and Rho-associated protein kinas

81 ed antihemagglutinin antibodies and seasonal inactivated flu vaccine (TIV) can elicit broadly protect

82 T-independent 2 (TI-2) antigenic response to inactivated FMDV capsid.IMPORTANCE We have demonstrated

83 he sequential inoculation of three different inactivated FMDV serotypes (O, A, and Asia1 serotypes) a

84 sponse following homologous and heterologous inactivated FMDV vaccination regimes.

85 eric PntAB in Synechocystis sp. PCC 6803 was inactivated, followed by phenotypic and biophysical char

86 d and unwinged aphids challenged with a heat-inactivated fungal pathogen, and found that immune costs

87 In pregametes, gametes and dark-inactivated gametes, aCRY is localized over the cell bod

88 e generated genetically engineered mice with inactivated Gas2.

89 ranscription and protein expression from the inactivated gene and the recovered organisms also expres

90 1 year later, after a booster with an inactivated H5N1 vaccine (part 2), 39 (98%) of 40 partic

91 lation was induced in cells infected with UV-inactivated HCMV, it was subsequently reduced, but not e

92 hole-inactivated-virus vaccine (formaldehyde-inactivated HSV-2 [FI-HSV-2]).

93 icial DNA and RNA both in buffer and in heat-inactivated human blood serum.

94 mportantly, our data also suggest that LJ001-inactivated IHNV elicited an innate immune response in t

95 a major tumor suppressor that is mutated and inactivated in 50% of all human cancers.

96 S. bayanus cells were completely inactivated in 10 passes without temperature control (co

97 PPO was completely inactivated in 20min at 85 degrees C, however, after 30m

98 of these genes (SLC39A14) was biallelically inactivated in a potentially treatable form of hypermang

99 CIC is inactivated in a variety of human tumors and has been im

100 d a mouse line in which Pax6 was selectively inactivated in beta cells by crossing animals with floxe

101 studies identify ADIPOR1 signaling, which is inactivated in both obesity and human cancers, as a key

102 (foxl/flox) (cKO) mice, in which Fam20C was inactivated in cells expressing Type I collagen.

103 The STAG2 gene encoding SA2 is often inactivated in human cancer, but not in in a manner asso

104 diated apoptosis, for example, is frequently inactivated in human cancers via multiple mechanisms suc

105 that lung-specific TFs become preferentially inactivated in lung cancer and precursor lung cancer les

106 which, unlike AHRR hypomethylation, are also inactivated in lung cancer itself.

107 g a major impact in neuronal morphology when inactivated in mice.

108 e only gene that was recurrently somatically inactivated in multiple tumors.

109 rotein p53, the "guardian of the genome", is inactivated in nearly all cancer types by mutations in t

110 I/SNF (BAF) chromatin-remodeling complex, is inactivated in nearly all pediatric rhabdoid tumors.

111 Liver kinase B1 (LKB1) is mutationally inactivated in Peutz-Jeghers syndrome and in a variety o

112 We identify subsets of TFs which become inactivated in precursor cells.

113 ers have shown that the cystatin E/M gene is inactivated in primary human tumors, pointing to its rol

114 of the products of a PKS mutant specifically inactivated in the dehydratase domain of extension-modul

115 We identify TFs, such as AHR, which become inactivated in the earliest stages of lung cancer and wh

116 se The von Hippel-Lindau tumor suppressor is inactivated in the majority of clear cell renal cell car

117 Hippel-Lindau (VHL) tumor suppressor gene is inactivated in the majority of clear cell renal cell car

118 enerated mice in which Gata6 is specifically inactivated in the pancreas.

119 anscriptional repressor that is specifically inactivated in the presence of formaldehyde, permitting

120 ction is dependent on p53, a protein that is inactivated in the vast majority of SCC tumors, leaving

121 nsgenic mice in which Tcf7l2 was selectively inactivated in their pancreatic pericytes exhibited impa

122 ne of these core target genes are frequently inactivated in tumors expressing wild-type TP53.

123 pdk1 and pdk2 were inactivated individually by transposon insertions, and b

124 imate the effectiveness of current and prior inactivated influenza A(H1N1)pdm09 vaccination from infl

125 to four groups and received a single dose of inactivated influenza vaccine (fluvirin: 18 mug of haema

126 ive attenuated influenza vaccine (LAIV) over inactivated influenza vaccine (IIV) among children aged

127 n 2011 and 2012 on the efficacy of trivalent inactivated influenza vaccine (IIV) during pregnancy wer

128 luenza vaccine (LAIV) is more effective than inactivated influenza vaccine (IIV) in providing both di

129 ing to evaluate vaccine efficacy of seasonal inactivated influenza vaccine (IIV) is controversial.

130 th a standard-dose, egg-grown, quadrivalent, inactivated influenza vaccine (IIV4) during the A/H3N2-p

131 ith a standard-dose, egg-grown, quadrivalent-inactivated influenza vaccine (IIV4) for immunogenicity

132 coadministered with a quadrivalent seasonal inactivated influenza vaccine (IIV4) was investigated in

133 are worker; or received a single dose of (4) inactivated influenza vaccine by microneedle patch self-

134 cacy of maternal immunisation with trivalent inactivated influenza vaccine for protection of infants

135 Vaccination of pregnant women with trivalent inactivated influenza vaccine in Mali-a poorly resourced

136 to receive seasonally recommended trivalent inactivated influenza vaccine or saline placebo in block

137 Among children 2 to 17 years of age, the inactivated influenza vaccine was 60% effective (95% CI,

138 to receive vaccine or placebo (all received inactivated influenza vaccine).

139 enuated influenza vaccine, 11 (7 cRCTs) used inactivated influenza vaccine, and 5 (1 cRCT) compared b

140 ances otherwise compromised Ab production to inactivated influenza vaccine.

141 not be used in 2016-17 and to switch to the inactivated influenza vaccine.

142 Currently, only inactivated influenza vaccines (IIVs) are available for

143 To date, only inactivated influenza vaccines (IIVs) are available to p

144 Current inactivated influenza vaccines are strain specific and n

145 Inactivated influenza vaccines confer protection by indu

146 In summary, inactivated influenza virus delivered through PLGA-NPs r

147 poly (I:C) was coated on a microneedle with inactivated influenza virus, and then immunized into BAL

148 rams using live-attenuated oral (OPV) and/or inactivated (IPV) PV vaccines have systematically reduce

149 en who had received a JE-CV booster after an inactivated JE vaccine primary immunization.

150 however, an ATP-driven proton pump (Pma1) is inactivated, leading to a marked decrease in cytoplasmic

151 /MST1 and STK3/MST2 in mammals), which, when inactivated, leads to considerable tissue overgrowth.

152 We develop conditionally inactivated LINC complexes in which the conserved SUN-do

153 the colon environment, with the presence of inactivated microbiota resulting in a higher bioaccessib

154 ivated at more hyperpolarized potentials and inactivated more slowly than it is in postnatal and adul

155 The inactivated mutant displays reduced virulence in vivo, i

156 describe the first substrate complex in the inactivated mutant form of PcCgkA at 1.7 A resolution.

157 after further digestion, as the irreversible inactivated myrosinase under gastric conditions caused n

158 tein (KpsC D160A) containing a catalytically inactivated N-terminal domain.

159 We inactivated neuroligins by stereotactic viral expression

160 required for the growth and survival of LKB1-inactivated NSCLC cells.

161 s LINC00473 as a therapeutic target for LKB1-inactivated NSCLC.

162 ctivated vaccines concurrently compared with inactivated-only (HR, 0.64; 95% CI, 0.58, 0.70).

163 However, when APC/C is inactivated or cyclin B1 is overexpressed, CRL2(ZYG11A/B

164 roxidase (POD) is an enzyme that needs to be inactivated or inhibited because of its deleterious effe

165 both EBNA3A and EBNA3C can be conditionally inactivated or using virus completely lacking the EBNA3

166 porcine primary cell line and generated PERV-inactivated pigs via somatic cell nuclear transfer.

167 nding protein) is inserted into functionally-inactivated point mutants of two target proteins (staphy

168 ndomly assigned to receive tOPV (n = 315) or inactivated polio vaccine (IPV) (n = 299) at 39 weeks.

169 The synchronized introduction of the inactivated polio vaccine (IPV) and the switch from triv

170 Both Uganda and Indonesia have introduced inactivated polio vaccine (IPV) as part of the Global Po

171 enhance immunity through the introduction of inactivated polio vaccine (IPV) in combination with OPV.

172 he globally coordinated efforts to introduce inactivated polio vaccine (IPV) into all countries that

173 Albania introduced inactivated polio vaccine (IPV) into its immunization sy

174 Kano State, Nigeria, introduced inactivated polio vaccine (IPV) into its routine immuniz

175 cine (OPV) only introduce at least 1 dose of Inactivated Polio Vaccine (IPV) into routine immunizatio

176 d for the introduction of at least 1 dose of inactivated polio vaccine (IPV) into the routine immuniz

177 o vaccine (OPV) introduce at least 1 dose of inactivated polio vaccine (IPV) into their routine immun

178 3 oral polio vaccine (bOPV) and one dose of inactivated polio vaccine (IPV) where available.

179 tion systems using polio assets, introducing inactivated polio vaccine (IPV), and replacing trivalent

180 third dose, and some vaccines, including the inactivated polio vaccine (IPV), must be injected more t

181 constraints are key challenges in the use of inactivated polio vaccine (IPV).

182 Introduction of inactivated polio vaccine creates challenges in maintain

183 virus-containing vaccine and introduction of inactivated polio vaccine in routine immunization to mit

184 in storage and transportation capacity after inactivated polio vaccine introduction, but temperature

185 The largest effects were observed for inactivated polio vaccine, where 2-fold higher maternal

186 ses to booster doses of acellular pertussis, inactivated polio, and diphtheria vaccines at 12 to 24 m

187 an 2013-2018-to introduce at least 1 dose of inactivated poliomyelitis vaccine (IPV); withdraw oral p

188 immunity induced by oral poliovirus (OPV) or inactivated poliovirus (IPV) vaccines and mixed schedule

189 y and safety of a novel monovalent high-dose inactivated poliovirus type 2 vaccine (mIPV2HD) in infan

190 A fractional dose of inactivated poliovirus vaccine (fIPV) administered by th

191 Fractional-dose administration of inactivated poliovirus vaccine (fIPV) could increase IPV

192 (one-fifth, 0.1 mL) intradermal doses of the inactivated poliovirus vaccine (ID fIPV) is positively c

193 grammatic adaptations and infants' uptake of inactivated poliovirus vaccine (IPV) after its introduct

194 In 2014, 2 studies showed that inactivated poliovirus vaccine (IPV) boosts intestinal i

195 The introduction of the inactivated poliovirus vaccine (IPV) represents a crucia

196 ries required regulatory approval for use of inactivated poliovirus vaccine and bivalent OPV in routi

197 ome differences in approach observed between inactivated poliovirus vaccine and bivalent OPV.

198 y lessons learned during the introduction of inactivated poliovirus vaccine in 3 countries that would

199 18, namely, (1) introduction of >/=1 dose of inactivated poliovirus vaccine in all 126 countries usin

200 g with the type 2 component, introduction of inactivated poliovirus vaccine, strengthening of routine

201 PV) will eventually need to be replaced with inactivated poliovirus vaccines (IPV).

202 cine (diphtheria-tetanus-acellular pertussis-inactivated poliovirus/Haemophilus influenzae type b vac

203 ATP-inactivated potassium channel block has no effect on PVE

204 Because block of stretch-sensitive ATP-inactivated potassium channels curtailed VF occurrence i

205 , combined with pharmacological block of ATP-inactivated potassium or stretch-activated cation-nonsel

206 as the remarkable capability to survive with inactivated production of lipid A biosynthesis and the a

207 f whom were positive for leucine-rich glioma-inactivated protein 1 [LGI1] Ab), and 4 (3.6%) had N-met

208 antly enhance the function of DCs to present inactivated PRRSV antigen through TRIF/MyD88-NF-kappaB s

209 ead-to-head comparison of recombinant versus inactivated quadrivalent influenza vaccines in 18-49 yea

210 To address this need, we developed an inactivated rabies virus (RABV) that contains the MERS-C

211 Here we show that inactivated rabies virus particles containing the MERS-C

212 Here we generated recombinant inactivated rabies viruses that carry one of the CDV gly

213 These data establish that an inactivated RABV-MERS S-based vaccine may be effective f

214 approach, we preferentially and efficiently inactivated RAF/ERK, upregulated BIM and down-regulated

215 unization of ferrets with beta-propiolactone-inactivated recombinant virus particles elicited protect

216 not the case in cells exposed to live RESTV, inactivated RESTV, or VLPs containing RESTV GP, indicati

217 In this study, we immunized mice with whole inactivated reverse genetics reassortant (RG) viruses ex

218 containing gamma2-subunit phosphorylated and inactivated RNA Pol I (polymerase I)-associated transcri

219 rat challenge model compared to formaldehyde inactivated RSV (FI-RSV) and live RSV experimental infec

220 observed in animals immunized with formalin-inactivated RSV.

221 infected intranasally with either RSV or UV-inactivated RSV.

222 positioning remains unchanged when nmy-2 is inactivated, seam cell loss occurs through inappropriate

223 Antibody responses to the inactivated seasonal influenza vaccine in patients with

224 genomes contain an incomplete and apparently inactivated set of genes encoding the upper branch of me

225 th the structures associated with the closed-inactivated state (C/I) and in the well-known closed con

226 ctures of the KcsA channel suggest that this inactivated state corresponds to a "constricted" conform

227 s unusual in binding selectively to the slow-inactivated state of sodium channels, in contrast to dru

228 filter corresponds to the functional C-type inactivated state of the KcsA.

229 iated with the irreversible transition to an inactivated state, as suggested by the Lumry-Eyring mode

230 sts that this receptor can exist in a deeply inactivated state, not responsive to ATP, and that its d

231 transition to accelerate entry into the slow inactivated state, resulting in use-dependent block.

232 are minimally essential for maintaining the inactivated state.

233 nformation does not correspond to the C-type inactivated state.

234 uctive (O/O) and the stable open deep C-type inactivated states (O/I), respectively.

235 esults suggest that lacosamide binds to fast-inactivated states in a manner similar to other antiseiz

236 ther, our data suggest that the stability of inactivated states is under tight evolutionary control,

237 l, more consistent with slow binding to fast-inactivated states than selective binding to slow-inacti

238 The cycling of Navs through open, closed and inactivated states, and their closely choreographed rela

239 ivated states than selective binding to slow-inactivated states.

240 second prepulses, suggesting binding to fast-inactivated states.

241 de access to closed, open, and fast- or slow-inactivated states.

242 ed on apparent affinities for the respective inactivated states.

243 ne and phenytoin, which bind tightly to fast-inactivated states.

244 tiepileptic drugs that bind to and stabilize inactivated states.

245 ignals were obtained in the resting and slow inactivated states.

246 m samples from adults who received a dose of inactivated subunit vaccine (ISV) targeting monovalent 2

247 In this study, inactivated SwIV H1N2 antigens (KAg) encapsulated in PLG

248 b5(+) endosomes is severely altered in Meis1-inactivated sympathetic neurons.

249 onsible for this phenotype, we insertionally inactivated the 14 annotated PTS EIIC-encoding genes in

250 To disinhibit SST(+) interneurons, we inactivated the gamma2 subunit gene of GABAA receptors s

251 In this study, we inactivated the glucocorticoid receptor (GR) specificall

252 The S1565D phosphomimetic substitution also inactivated the kinase but did so without interfering wi

253 Although H936A inactivated the lipid kinase activity without affecting

254 s on outcomes in the brain, we conditionally inactivated the murine Pten gene in neonatal neural stem

255 test this hypothesis, we pharmacogenetically inactivated the rhesus monkey amygdala, a subcortical re

256 While RABV vaccines are inactivated, the live-attenuated CDV vaccines retain res

257 We inactivated these candidate genes in cell line models to

258 Mechanistically, NUDT15 inactivated thiopurine metabolites and decreased thiopur

259 g a CRISPR-based approach, we systematically inactivated three of the most commonly mutated chromatin

260 we confirm that UBA, UCA, and UEA are indeed inactivated through genetic defects at the promoter, whe

261 led by phosphorylation; in particular, it is inactivated through phosphorylation by the TORC1 kinase

262 at both Syt1 and Syt2 need to be genetically inactivated to cause a significant reduction of activity

263 v1.7) that splicing modifies the return from inactivated to deactivated states, and the differences b

264 d immunosuppression that can be targeted and inactivated to improve the anticancer efficacy of PLN-de

265 ch the nuclear localization signal (NLS) was inactivated to prevent nuclear translocation of nBMP2 wh

266 inhibitory synapses and must be genetically inactivated together with Syt2 to achieve a significant

267 quences at their breakpoints and recurrently inactivated tumor-suppressor genes.

268 arallel mechanisms and at proteasomes, RA190-inactivated Uch37 cannot disassemble hRpn13-bound ubiqui

269 lethal disease in N. vectensis and that heat-inactivated V. coralliilyticus and bacterial flagellin c

270 nd its priming immune responses with an H5N1 inactivated vaccine boost.

271 ve among children in a year with substantial inactivated vaccine effectiveness.

272 onstrated that mice receiving a conventional inactivated vaccine followed by a skin-applied dissolvin

273 was 63% (95% CI, 45 to 75; P<0.001) for the inactivated vaccine, as compared with -19% (95% CI, -113

274 last vaccine received was live compared with inactivated vaccine, as well as concurrent receipt compa

275 candidate for the development of novel PRRS inactivated vaccine.

276 as well as concurrent receipt compared with inactivated vaccine.

277 ith inactivated alone or concurrent live and inactivated vaccines (HR, 0.50; 95% confidence interval

278 Separate estimates were calculated for the inactivated vaccines and the live attenuated vaccine.

279 cally not as efficient as live attenuated or inactivated vaccines at inducing protective immune respo

280 etter cross-protective immune responses than inactivated vaccines by eliciting local mucosal immunity

281 ctively) and for those who received live and inactivated vaccines concurrently compared with inactiva

282 In contrast, the inability of inactivated vaccines to replicate enhances safety at the

283 However, traditional inactivated vaccines used in animals are costly and have

284 ity but have reduced safety when compared to inactivated vaccines.

285 We show that in mice H7 whole inactivated virus vaccines (WIVs) were as immunogenic as

286 nucleic acid (DNA and messenger RNA), whole-inactivated virus, live-attenuated or chimeric virus, an

287 L40, and we compared this vaccine to a whole-inactivated-virus vaccine (formaldehyde-inactivated HSV-

288 mutants revealed that four of the five genes inactivated were required for stress survival.

289 Virus was inactivated when all three Env protomers were occupied b

290 dates have recently been described which use inactivated whole virus, DNA or RNA that express the vir

291 Inactivated whole virus, DNA, RNA, and vectored vaccine

292 riptome uncovered immune molecules activated/inactivated with aging and identified the silencing of t

293 telangiectasia mutated (ATM)-p53 pathway is inactivated with relatively high frequency, leading to t

294 pores, show that each pore can be separately inactivated without blocking F(-) conduction through its

295 H3K27me3 and Xist RNA, only a subset of the inactivated X-linked genes is derepressed in Eed (-/-) T

296 hat one of the two X chromosomes is randomly inactivated, X-SPINK1 mice exhibit mosaic pattern of SPI

297 conductive (E71A, at 2.25 A) and deep C-type inactivated (Y82A at 2.4 A) conformations.

298 These ready-to-use inactivated yeast interfering RNA tablets may one day fa

299 We developed a purified formalin-inactivated Zika virus vaccine (ZPIV) candidate that sho

300 Immunogenicity and safety of inactivated zoster vaccine (ZVIN) were evaluated in adul