ライフサイエンスコーパス: nonpermissive

1 missive for infection, while A172 cells were nonpermissive.

2 are present that make the local environment nonpermissive.

3 strain, including strains previously deemed nonpermissive.

4 cle between transcriptionally permissive and nonpermissive.

5 that the failure of B19V DNA replication in nonpermissive 293 cells can be overcome by adenovirus in

6 nfection under permissive (33 degrees C) and nonpermissive (37 degrees C) temperatures.

7 hromosome (BAC) transgenic line expressing a nonpermissive allele of Naip5 exhibits a reduction in ma

8 imary LCs harvested from mouse epidermis was nonpermissive, although a viral reporter protein was exp

9 In the lungs of nonpermissive BALB/c mice, L. pneumophila does not repli

10 Dot/Icm-dependent activation of caspase-1 in nonpermissive BALB/c mouse-derived macrophages, caspase-

11 y passaging wild-type VACV in cells that are nonpermissive because of A56/K2 expression.

12 viral activity of ISGs or whether cells were nonpermissive because of translation defects.

13 s in antiviral signaling, but a minority are nonpermissive because the virus infection aborts before

14 e generated new cdc13-ts reagents, which are nonpermissive below 34 degrees , to allow examination of

15 but resides in a low molecular mass form in nonpermissive, blood-derived naive CD4 T cells.

16 B-cell intrinsic defects and patients with a nonpermissive bone marrow environment.

17 ncorporating [(35)S]methionine into Atp8p at nonpermissive but not at the permissive temperature.

18 tes and several leukemic T-cell lines termed nonpermissive, but not in other cells termed permissive.

19 an unopposed innate response in replication-nonpermissive bystander cells.

20 it(+) cardiac progenitors and suggest that a nonpermissive cardiac milieu, rather than minimal cardio

21 d how abortive infection of resting and thus nonpermissive CD4 T cells in lymphoid tissues triggers a

22 A549), one semi-permissive (786-0), and one nonpermissive cell line (PANC-1).

23 runcated and chimeric forms of fJAM-A into a nonpermissive cell line and assayed binding by flow cyto

24 y to infect and replicate in this previously nonpermissive cell line.

25 the protein synthesis profile in previously nonpermissive cell lines, as well as early U(S)11 transc

26 he permissive cell functions required by the nonpermissive cell to ensure infectious virus production

27 HSV-1), is required for viral replication in nonpermissive cell types and for expression of a class o

28 us envelope gene allowing virus entry into a nonpermissive cell.

29 t were not explainable by a failure to enter nonpermissive cells and were not complemented in an ICP2

30 G35-2-pseudotyped virus when introduced into nonpermissive cells but did not render these cells permi

31 increased B19V capsid protein production in nonpermissive cells by codon optimization.

32 ike particles were successfully generated in nonpermissive cells by transient transfection of a plasm

33 a JAM-A mutant lacking a cytoplasmic tail in nonpermissive cells conferred full susceptibility to reo

34 Here, we describe serially passaging VACV in nonpermissive cells expressing A56/K2 as an unbiased app

35 ry (CHO) cells are traditionally regarded as nonpermissive cells for herpes simplex virus type 1 (HSV

36 leaved internal scaffold, were purified from nonpermissive cells infected with UL17, UL25, or UL6 nul

37 Expression of the feline SLC35F2 cDNA in nonpermissive cells renders the cells susceptible to inf

38 -1 integrase mutant replication in otherwise nonpermissive cells suggests alternative approaches to s

39 ut was not mutated in permissive cells or in nonpermissive cells that block secondary viral spread.

40 ol transporter 1 (mSMIT1) allowed previously nonpermissive cells to be infected by HEMV, indicating t

41 RhoC protein in EBOV and VSV permissive and nonpermissive cells were consistent with the cDNA gene a

42 Transfection of nonpermissive cells with alphav or beta1 cDNAs confers h

43 ary blood lymphocytes, certain T-cell lines (nonpermissive cells), and most likely in vivo is highly

44 evels of plasma-membrane-associated Env than nonpermissive cells, and Env internalization from the pl

45 ceptibility to FeLV-A when reintroduced into nonpermissive cells, but it did not render these cells p

46 orced by heterologous replication systems in nonpermissive cells, enhanced readthrough of (pA)p and t

47 a key factor in capsid protein production in nonpermissive cells.

48 ity to cell-to-cell transmission compared to nonpermissive cells.

49 r fusion on HCMV-permissive cells but not on nonpermissive cells.

50 V)-permissive phenotype when introduced into nonpermissive cells.

51 other parvoviruses inhibit proliferation of nonpermissive cells.

52 n and integration appear to be unimpaired in nonpermissive cells.

53 sufficient to mediate viral entry into ALV-J nonpermissive cells.

54 ly studied in populations of susceptible but nonpermissive cells.

55 d MNV virions in permissive cells but not in nonpermissive cells.

56 Vif protein are replication incompetent in 'nonpermissive' cells, such as primary T cells and the T-

57 n cDNA, along with a cDNA encoding JAM-A, in nonpermissive chicken embryo fibroblasts conferred susce

58 directed pathogenic hantavirus infection of nonpermissive CHO cells expressing chimeric alphavbeta3

59 These repressive effects of nonpermissive chromatin cannot be completely countered b

60 Moreover, nonpermissive chromatin progressively silences a transge

61 K4 methylation at a transgenic promoter in a nonpermissive chromatin region are stochastic, leading t

62 thyl-H3-K9 ratio to that characteristic of a nonpermissive chromatin state.

63 edicated loci but also promotes shaping of a nonpermissive chromatin through its capacity to recruit

64 ontrast to HIV-1 permissive clone 10 (plus), nonpermissive clone 17 (minus) was adherent to coverslip

65 cell-surface HLE expression on HLE null, HIV nonpermissive clones permits HIV infectivity.

66 differentiation in liquid medium, a normally nonpermissive condition.

67 lows growth of the E. coli fabG strain under nonpermissive conditions and restores in vitro fatty aci

68 of each unsuppressed mutant to divide under nonpermissive conditions correlated with the presence of

69 ene transcript levels between permissive and nonpermissive conditions for E. chaffeensis growth.

70 Growth of Lud135 under nonpermissive conditions is restored by the presence of

71 wever, possible low-level L2 synthesis under nonpermissive conditions led to ambiguity in interpretat

72 A:dT) tract-stimulated gene expression under nonpermissive conditions led to shifts of positioned nuc

73 ion, B104-5 cells with a dispersed ERC under nonpermissive conditions were more resistant to cisplati

74 ssive conditions, permissive conditions, and nonpermissive conditions with wild-type EBNA3C transcomp

75 However, under nonpermissive conditions, all stages of virus morphogene

76 At nonpermissive conditions, although trafficking of secret

77 s in DNA replication and morphogenesis under nonpermissive conditions, depending upon the experimenta

78 membrane proteins appeared unaffected under nonpermissive conditions, distinguishing the phenotype o

79 and pta rec mutants are not killed under the nonpermissive conditions, exemplifying a case of synthet

80 After shift to nonpermissive conditions, however, ten1-ts mutants accum

81 though the L2 protein was not detected under nonpermissive conditions, minute amounts could account f

82 ll wall compared with wild-type plants under nonpermissive conditions, no indications were found for

83 Under nonpermissive conditions, our conditional mutants of YNL

84 NAs were assayed for each EBNA3CHT LCL under nonpermissive conditions, permissive conditions, and non

85 is known to exhibit a runaway cell death in nonpermissive conditions, proves to be more tolerant to

86 Under nonpermissive conditions, spindles in td-kip3 doc1Delta

87 onditional effect on root architecture under nonpermissive conditions, suggesting they are also diffe

88 the LCLs specifically sustained growth under nonpermissive conditions, whereas EBNA3B or EBNA3C expre

89 complementation with EBNA3C for growth under nonpermissive conditions.

90 chaperonin, GroEL, helps proteins fold under nonpermissive conditions.

91 DNA replication occurs in these cells under nonpermissive conditions.

92 vision block seen in all shape mutants under nonpermissive conditions.

93 egmatis 628-53 undergoes filamentation under nonpermissive conditions.

94 oth dnaE and Deltathy mutants filament under nonpermissive conditions.

95 on, was synthesized by the G5R mutants under nonpermissive conditions.

96 ctive internal structures are produced under nonpermissive conditions.

97 ition to being a swarming cue under normally nonpermissive conditions.

98 due to depletion of the mutant protein under nonpermissive conditions.

99 low slow growth of pta recBC(Ts) cells under nonpermissive conditions; all three are in or near genes

100 ated protein folding were carried out under "nonpermissive" conditions, where the chaperonin system w

101 While U2AF(59) inactivation (nonpermissive) conditions inhibit splicing of some intro

102 Phenotypic analysis of nonpermissive Cts11 infections indicated that these amin

103 ants to sustain ongoing DNA synthesis during nonpermissive Cts24 infections, only a wtD5 allele suppo

104 sed to recombinant TGF-beta1 (or TGF-beta2), nonpermissive culture podocytes switch to G2/M arrest an

105 duces G0/G1 arrest and differentiation under nonpermissive culture through Smad3-dependent induction

106 er via exosomes drives antiviral immunity in nonpermissive DCs.

107 In contrast, a nonpermissive dimethyl-H3-K4/dimethyl-H3-K9 chromatin st

108 his issue of Blood, Pidala et al report that nonpermissive DPB1 allele mismatch is associated with in

109 1 also prevented AcMNPV-induced apoptosis in nonpermissive Drosophila melanogaster cells.

110 ailure of these integrins to be activated on nonpermissive ECM is because of active suppression by th

111 elongation is principally attributed to the nonpermissive environment and reduced intrinsic growth c

112 of the reduced intrinsic growth capacity and nonpermissive environment for axonal elongation.

113 We identified the postnatal cardiac ECM as a nonpermissive environment for cardiomyocyte cytokinesis

114 factors and underexpress others, creating a nonpermissive environment for cocultured motor neurons.

115 These metabolic shifts created a nonpermissive environment for the Enterobacteriaceae rec

116 cumulate at demyelinating lesions creating a nonpermissive environment that impairs axon regeneration

117 o direct cell autonomous growth even in this nonpermissive environment.

118 t, but in defective B-cell repopulation in a nonpermissive environment.

119 These results suggest that nonpermissive expression of RUNX3 protein is restricted

120 o at pH 5.2 and also at pH 6.8, a pH that is nonpermissive for assembly of L1 protein alone.

121 vored in cells which are both permissive and nonpermissive for B19 viral replication.

122 Hepatocytes are nonpermissive for B19 virus replication.

123 tified a human cell line (HeLa-USU) that was nonpermissive for fusion and virus infection.

124 n, were expressed in the cytoplasm, and were nonpermissive for HCV infection.

125 te differentiation into macrophages that are nonpermissive for HIV-1 infection.

126 In resting CD4(+) T cells which are nonpermissive for HIV-1 replication, the levels of Cycli

127 viral translation under conditions that are nonpermissive for host cell translation.

128 ied under conditions that are permissive and nonpermissive for hr1.

129 ired for viral replication in cells that are nonpermissive for ICP22 mutants.

130 most cell lines and primary human cells are nonpermissive for integrase mutant growth.

131 crophages from most inbred mouse strains are nonpermissive for intracellular replication and allow li

132 Dendritic cells from both strains were nonpermissive for L. pneumophila intracellular growth, s

133 al forebrain regions neighboring the MGE are nonpermissive for MGE cell migration, whereas the dorsal

134 Although the normal host microenvironment is nonpermissive for neoplastic progression, tumor-reactive

135 s of the RNA polymerase beta' subunit and is nonpermissive for plating of bacteriophage P2.

136 ve infection with HSV-2 but were selectively nonpermissive for productive infection with HSV-1, a phe

137 t the nonpermissive neuronal subtype is also nonpermissive for reactivation.

138 ell receptor ligation in conditions that are nonpermissive for replication.

139 rion assembly and renders the infected cells nonpermissive for secondary infections.IMPORTANCE Superi

140 er proteins (Yops) under conditions that are nonpermissive for synthesis and secretion in wild-type s

141 uman cells with genomic deletion of RFC were nonpermissive for TG35-2-pseudotyped virus infection, bu

142 nes distinct chromatin regions permissive or nonpermissive for transgene expression.

143 s, but Chinese hamster ovary (CHO) cells are nonpermissive for vaccinia virus (VACV).

144 Xrn1 KO A549 cells were viable but nonpermissive for VACV; however, wild-type and mutant vi

145 ivity and suggest a means to render the host nonpermissive for viral replication.

146 se bacteriophages to plaque on the otherwise nonpermissive groES or groEL mutant hosts in an allele-s

147 NiV infection-permissive cells but not to a nonpermissive HeLa cell line clone, suggesting that it b

148 esis at 34 degrees C in permissive (BHK) and nonpermissive (HEp-2) cells, but D1671V reduced in vitro

149 plit segment were impaired in replication at nonpermissive high temperatures, whereas high viral tite

150 Nonpermissive HLA-DPB1 allele mismatch was associated wi

151 related donor HCT survival, and avoidance of nonpermissive HLA-DPB1 mismatches in otherwise HLA-match

152 ovel concept of DeltaFD sheds new light onto nonpermissive HLA-DPB1 mismatches in unrelated HCT.

153 Here, we investigated this question in nonpermissive HLA-DPB1 T-cell epitope (TCE) mismatches r

154 ive hosts of its parental viruses but also a nonpermissive host (Spodoptera litura).

155 within macrophages and tissues from mice, a nonpermissive host.

156 When introduced into nonpermissive human 293T cells and quail QT6 cells, chNH

157 ession of human, but not mouse, FcRn renders nonpermissive human and mouse cells sensitive to echovir

158 and APOBEC3G are extensively coexpressed in nonpermissive human cells, including primary lymphocytes

159 ression of the putative HCV receptor CD81 on nonpermissive human hepatic but not murine cells enabled

160 ns, resulting in abortive HIV replication in nonpermissive human T cells.

161 e vectors for permissive (i.e., poultry) and nonpermissive (i.e., mammals, including humans) species,

162 ypes, such as production of cholera toxin in nonpermissive LB medium, reduced resistance to high osmo

163 Nonpermissive ligands indirectly inhibited TCR binding b

164 arrying foreign Ags, permissive ligands, and nonpermissive lipid ligands clarifies the molecular basi

165 GP1 fragment nor that of ebolavirus bound a nonpermissive lymphocyte cell line.

166 We isolated a BVDV-nonpermissive MDBK cell clone that harbored a 1.2-kb ins

167 y to promote swarming when added to normally nonpermissive media.

168 the most sensitive, showing rapid killing in nonpermissive medium.

169 ch that allowed the immune reconstitution of nonpermissive mice following injection of human hematopo

170 from myeloma-permissive mice, into otherwise nonpermissive mice resulted in myeloma development, asso

171 cue entry into an undifferentiated, normally nonpermissive monocytic cell line.

172 onitis virus (FIPV) WSU 79-1146 and DF2 into nonpermissive mouse 3T3 cells can be rescued by the expr

173 into mouse fibroblasts allowed the normally nonpermissive mouse cells to become productively infecte

174 activation of caspase 1 and pyropoptosis in nonpermissive mouse macrophages.

175 ther caspase-3 is activated in permissive or nonpermissive mouse macrophages.

176 opism of HSV1716 was also evident in another nonpermissive mouse melanoma cell line and is an exclusi

177 In AWT experiments employing the nonpermissive murine model, C57BL/6 mice given adult wor

178 Here we show that HCMV transiently protects nonpermissive myeloid cells from chemical and virus entr

179 ing CSPG and control substrata confirmed the nonpermissive nature of CSPGs for OPC adhesion and morph

180 om non-A5(+) neurons, demonstrating that the nonpermissive neuronal subtype is also nonpermissive for

181 ulibacter in cells from permissive (CGD) and nonpermissive (normal) hosts and identifies potentially

182 feature is that the permissive cells, unlike nonpermissive ones, have ceased to proliferate in vivo a

183 Macrophage/microglia formed a nonpermissive OV barrier, preventing dissemination of oH

184 by the Lgn1 gene locus, which expresses the nonpermissive phenotype in cells from BALB/c mice but th

185 ive activation of the enzyme under otherwise nonpermissive physiological redox potentials.

186 ependent compensatory interferon response in nonpermissive plasmacytoid dendritic cells (pDCs).

187 MT and ST in both permissive mouse cells and nonpermissive rat cells.

188 cient to mediate the entry of HCoV-HKU1 into nonpermissive RD cells.

189 3 K4 methylation and H3 acetylation, while a nonpermissive region is poor in or depleted of these two

190 epulsive interactions between the kinase and nonpermissive residue(s).

191 ification of sequence contextual effects and nonpermissive residues.

192 arcoma virus (RSV) genome association with a nonpermissive rodent host cell genome.

193 ion acts as a barrier to infection for other nonpermissive small-animal species, namely, ferret, guin

194 We demonstrate that the nonpermissive state exhibited by the majority of resting

195 d normally permissive CEMss cells to adopt a nonpermissive state, able to resist an HIV-1Deltavif cha

196 d long-term SSC cultures were derived from a nonpermissive strain that showed limited self-renewal di

197 ost inbred strains, as well as a variant for nonpermissive strains.

198 These results identify CSPGs as a nonpermissive substrate for OPCs and oligodendrocytes, a

199 osed by the spatiotemporal distribution of a nonpermissive substrate provided by versican, an extrace

200 AC6) was shown to support axon growth on the nonpermissive substrates myelin-associated glycoprotein

201 accelerates axon growth over permissive and nonpermissive substrates, including major CNS inhibitors

202 markedly facilitates axon regeneration over nonpermissive substrates.

203 (HIV-1/Delta vif) from an acute infection of nonpermissive T cells and performed a thorough examinati

204 showed a significantly higher percentage of nonpermissive TCE mismatches for DeltaFD >2.665, compare

205 Although dhc1b-3 flagella at the nonpermissive temperature (34 degrees C) showed a dramat

206 When shifted to the nonpermissive temperature (37 degrees C), TRF2ts cells s

207 y synthesized lipid A was not cleaved at the nonpermissive temperature (44 degrees C).

208 At the nonpermissive temperature (NPT), tsB7 capsids accumulate

209 Dts38], Dts12, and Dts56) and shown that at nonpermissive temperature all of the tsD5 viruses exhibi

210 Incubation at the nonpermissive temperature also precluded coimmunoprecipi

211 Ad2ts1 was prepared at a nonpermissive temperature and contains the precursor for

212 mutations was inhibited upon a shift to the nonpermissive temperature and in the latter case decline

213 ks PBP1b and has a thermosensitive PBP1a, at nonpermissive temperature and induced a mild cell-chaini

214 a temperature-sensitive VSV-M mutant at the nonpermissive temperature both substantially reversed th

215 e temperature and after several hours at the nonpermissive temperature but display aberrant organizat

216 Apoptosis also was suppressed at the nonpermissive temperature by constitutively active Akt a

217 e protected from cell death on incubation at nonpermissive temperature by mutation in the cydA gene c

218 synthesis, and thus lack of function at the nonpermissive temperature cannot be attributed to a lack

219 plasm of cells that had been infected at the nonpermissive temperature contained large granular areas

220 strong mouse-specific defect of PV1(RIPO) at nonpermissive temperature correlated with the translatio

221 Virions produced at the nonpermissive temperature do not assemble capsids, altho

222 cdc5-1 mutants arrest at telophase at the nonpermissive temperature due to the failure of CDK inac

223 e mutant proteins were largely stable at the nonpermissive temperature except the A68T/N73D mutant pr

224 cantly reduced if assayed at 30 degrees C, a nonpermissive temperature for Ty1 retrotransposition, or

225 This transcript is also absent at nonpermissive temperature in a 10-1 mouse cell line lack

226 risingly, certain ftsZ84 strains lyse at the nonpermissive temperature instead of filamenting, and in

227 infection is initiated and maintained at the nonpermissive temperature of 39.5 degrees C.

228 ibits a loss of silencing when raised to the nonpermissive temperature regardless of cell-cycle posit

229 Passage of tsS133A and tsF219L at the nonpermissive temperature resulted in emergence of multi

230 xamination of ts1249 capsids produced at the nonpermissive temperature revealed that, in comparison w

231 mutations were more rapidly degraded at the nonpermissive temperature than were the wild-type protei

232 rat8-2p localized to cytoplasmic granules at nonpermissive temperature that are distinct from P-bodie

233 We demonstrated that at the nonpermissive temperature the DnaB(A116V) mutant arreste

234 At the nonpermissive temperature these mutations have drastic e

235 cdc13-1 yeast grown at the nonpermissive temperature undergo G2/M arrest, progressi

236 shown that these cells enter mitosis at the nonpermissive temperature upon incubation with okadaic a

237 her (i) a temperature-sensitive virus at its nonpermissive temperature which does not inject viral DN

238 ressors of dnaN5 that restored growth at the nonpermissive temperature while maintaining an increase

239 s mutant ceased after one cell doubling at a nonpermissive temperature, 37 degrees C.

240 120/R273K mutant suppressed apoptosis at the nonpermissive temperature, a phenotype correlated with i

241 Upon a shift to a nonpermissive temperature, both large and small-ribosoma

242 At nonpermissive temperature, bub3 clb5-ts cells showed def

243 or olsA gene products supported growth at a nonpermissive temperature, exhibited AGPAT activity in v

244 lication immediately halts upon a shift to a nonpermissive temperature, growth and DNA replication of

245 hibited upon shift of mutant cultures to the nonpermissive temperature, indicating blockage of the sy

246 1% at the permissive temperature, and at the nonpermissive temperature, it renders further deteriorat

247 in virus-infected cells showed that, at the nonpermissive temperature, MHV-Brtsc31 was not able to p

248 of temperature-sensitive E. coli Y815 at the nonpermissive temperature, supporting its biological act

249 At the nonpermissive temperature, the capsids accumulate at the

250 At the nonpermissive temperature, this virus, designated ts8-22

251 At the nonpermissive temperature, vA6L-mut2 was normal at viral

252 At the nonpermissive temperature, viral gene expression and DNA

253 cause thermolability of the protein; at the nonpermissive temperature, virion morphogenesis arrests

254 pendent leader peptidase is inhibited at the nonpermissive temperature, whereas the insertion of the

255 MHV-Brts31-infected cells is reduced at the nonpermissive temperature.

256 ts showed reduced nuclear proteasomes at the nonpermissive temperature.

257 ented E. coli strain sensitive to GFZ at the nonpermissive temperature.

258 partial restoration of nsp5 activity at the nonpermissive temperature.

259 host cell but had an uncoating defect at the nonpermissive temperature.

260 dentical to that of Alb/ts/nsp5/V148A at the nonpermissive temperature.

261 d fewer myxospores than the wild type at the nonpermissive temperature.

262 is mutant also fails to enter S phase at the nonpermissive temperature.

263 pro, blocking its function completely at the nonpermissive temperature.

264 5 with the U(L)28 and U(L)33 proteins at the nonpermissive temperature.

265 m10 in mcm10-1 mutants that are grown at the nonpermissive temperature.

266 nts after 24 h of incubation in LB medium at nonpermissive temperature.

267 ants, even after prolonged incubation at the nonpermissive temperature.

268 ally assumes that the protein is inactive at nonpermissive temperature.

269 mutant FabG proteins may be disrupted at the nonpermissive temperature.

270 in mutant, and the VSV-G ts045 mutant at the nonpermissive temperature.

271 rain JN394top2-4 expressing betaE522K at the nonpermissive temperature.

272 ured in vivo was inhibited upon shift to the nonpermissive temperature.

273 undergo rapid apoptosis after a shift to the nonpermissive temperature.

274 ject its virion DNA into the nucleus at this nonpermissive temperature.

275 islocalized to the vacuole in neo1-ts at the nonpermissive temperature.

276 2 viral DNA replication is unimpaired at the nonpermissive temperature.

277 ast-acting mei-1(ts) mutant was shifted to a nonpermissive temperature.

278 nsp5-mediated polyprotein processing at the nonpermissive temperature.

279 ty to substrate stiffness during upshifts to nonpermissive temperatures in temperature-sensitive muta

280 ous ts alleles of spe-9, loss of function at nonpermissive temperatures is not due to protein misloca

281 plating analysis performed at permissive and nonpermissive temperatures revealed that changes in the

282 formed growth-based selection experiments at nonpermissive temperatures using a library of random bet

283 layed a modestly increased Cse4 half-life at nonpermissive temperatures, suggesting that turnover of

284 At nonpermissive temperatures, they fail to splice, resulti

285 use dramatic cellular phenotypes observed at nonpermissive temperatures.

286 NA (rnpB709) subunits lead to inviability at nonpermissive temperatures.

287 generate the TS phenotype at permissive and nonpermissive temperatures.

288 cally defective in Sir2-Sir4 interactions at nonpermissive temperatures.

289 itro, but only the rice isoforms denature at nonpermissive temperatures.

290 and the cellular signals in the surrounding nonpermissive tissue microenvironment that maintain the

291 lectively permissive environment, flanked by nonpermissive tissues.

292 ation and assembly, thereby rendering a cell nonpermissive to a specific class or species of viruses.

293 quiescent "bystander" CD4 T cells, which are nonpermissive to HIV infection, is a principal driver of

294 that fully assembled basement membranes are nonpermissive to smooth muscle cell (SMC) replication an

295 nous ligands, while other lipid ligands were nonpermissive to TCR binding.

296 radation was detected in cells permissive or nonpermissive to the ICP0-null virus; (ii) the loss of a

297 strains carried the Xpr1(n) receptor variant nonpermissive to XMRV and xenotropic murine leukemia vir

298 Expression of hVRK1 during nonpermissive ts2 infections restored virus production a

299 the A30 and G7 proteins are unstable during nonpermissive tsH5 infections, suggesting that the loss

300 esistance to exogenous infection is due to a nonpermissive variant of the XPR1 gammaretrovirus recept