ライフサイエンスコーパス: cytopathic effect

1 fully examined how MVC infection induces the cytopathic effect.

2 on kinetics and demonstrated only a moderate cytopathic effect.

3 ndothelial cells but without a virus-induced cytopathic effect.

4 o inhibit cellular transcription and cause a cytopathic effect.

5 ine (LLC-MK2) with the appearance of typical cytopathic effect.

6 cellular transcription and development of a cytopathic effect.

7 ollections of infected cells causing minimal cytopathic effect.

8 tion did not cause Schwann cell apoptosis or cytopathic effect.

9 ters, increased production of RNA, and total cytopathic effect.

10 lytic KSHV replication, resulting in foci of cytopathic effect.

11 for 3 days completely reversed virus-induced cytopathic effect.

12 ntracellular multiplication and a diminished cytopathic effect.

13 ing factor enhances reovirus replication and cytopathic effect.

14 by passage on cells and evaluation for viral cytopathic effect.

15 such as the observation of hemadsorption or cytopathic effect.

16 ial and epithelial cells without causing any cytopathic effect.

17 is and not extent of tubular injury or viral cytopathic effect.

18 a variety of insect cells with little overt cytopathic effect.

19 hology, single-step replication kinetics and cytopathic effect.

20 out a lengthy infectious cycle with minimal cytopathic effects.

21 calcium stores correlate with appearance of cytopathic effects.

22 ates poorly in HeLa cells and does not cause cytopathic effects.

23 rows to high titers in HeLa cells and causes cytopathic effects.

24 concomitant with lack of visually detectable cytopathic effects.

25 tants were able to replicate without causing cytopathic effects.

26 y low levels of HIV-1 p24 and HIV-associated cytopathic effects.

27 ovirus (Sf-RV) that does not cause any overt cytopathic effects.

28 inhibited plaque formation and virus-induced cytopathic effects.

29 tering cell susceptibility to viral-mediated cytopathic effects.

30 infected with HCMV exhibited characteristic cytopathic effects.

31 d as the mechanism through which Pet induces cytopathic effects.

32 he 4070A amphotropic MLV did not produce any cytopathic effects.

33 ad slower replication kinetics and caused no cytopathic effects.

34 ented IE72 and ICAM-1 protein expression and cytopathic effects.

35 it any unusual phenotypic characteristics or cytopathic effects.

36 he nucleus and the rates of virus-associated cytopathic effects.

37 from accumulating to high levels and causing cytopathic effects.

38 living animals in the absence of significant cytopathic effects.

39 s by cytolytic T lymphocytes (CTLs) or viral cytopathic effects.

40 ells, resulting in increased replication and cytopathic effects.

41 in three fates: 1) cell death due to a viral cytopathic effect, 2) cell death due to immune clearance

42 SVV-infected Vero cells at the height of the cytopathic effect (3 days after infection) and chemilumi

43 n bronchial epithelial Calu-3 cells, causing cytopathic effects, a process reflective of its natural

44 lized sample and evaluating the cultures for cytopathic effect after 14 days incubation.

45 uggested that the delay in the production of cytopathic effects after transfection may have been due

46 II-expressing glioblastoma multiforme but no cytopathic effect against normal cells.

47 e-derived macrophages can themselves mediate cytopathic effects against resident host T cells in skin

48 tious virus on the basis of a tissue culture cytopathic effect, an increase in virus genome copy equi

49 and formation of NS1 tubules, a decrease in cytopathic effect, an increased release of infectious vi

50 -challenged macrophages include an apoptotic cytopathic effect, an innate antiviral response, and a m

51 ssion of dominant negative Akt induced early cytopathic effect and caspase-mediated cell death in ade

52 ction decreased TER before the appearance of cytopathic effect and cell death and resulted in an incr

53 d stress conditioned mice lacked significant cytopathic effect and clearance was demonstrated in 95%

54 ed concentration-dependent inhibition of CMV cytopathic effect and CMV plaque formation in both human

55 linical isolate and examined in situ for CMV cytopathic effect and immediate-early and early antigens

56 irulence, as indicated by decreased observed cytopathic effect and inflammatory biomarker production.

57 s (Ed MeV) transcription caused an increased cytopathic effect and mortality in transgenic hsp70-over

58 U/ml) in mosquito cells, producing extensive cytopathic effect and plaques, but they do not appear to

59 transfected into both cell types resulted in cytopathic effect and recovery of functional virus, indi

60 ent reduced the number of cells displaying a cytopathic effect and the accumulation of immediate earl

61 ophin further inhibited the virally mediated cytopathic effect and viral release.

62 ular virus exhibited a significantly reduced cytopathic effects and apoptosis in infected cells, impl

63 all cases, virus infection induced classical cytopathic effects and apoptotic cell death.

64 Macrophages resist viral cytopathic effects and CD8(+) T-cell killing.

65 y, DC infected with WT rSV5 showed extensive cytopathic effects and increased levels of active caspas

66 ivalent to that of rOka, causing significant cytopathic effects and infectious virus production by da

67 ine 40 of NEDD8 to glutamate (Q40E), causing cytopathic effects and inhibiting cell proliferation.

68 state that protects cells from virus-induced cytopathic effects and inhibits virus replication.

69 nhibitor to DC infected with WT rSV5 reduced cytopathic effects and resulted in higher surface expres

70 on (MV-Edm) and wtF (MV-wtF) confer distinct cytopathic effects and strengths of hemagglutinin (H) in

71 ycle and a main viral factor responsible for cytopathic effects and subversion of antiviral defense.

72 tease activity is critical for TcdB-mediated cytopathic effects and TcdB systemic toxicity, highlight

73 dl1520 was tested for in vitro cytopathic effects and viral replication in the human HC

74 tion, protect resting CD4 T cells from these cytopathic effects and, primarily through this protectio

75 permissivity for adenoviral gene expression, cytopathic effects and/or burst size.

76 plicity of infection leads to no discernible cytopathic effect, and low virus titers are produced.

77 s determined using hemagglutinin expression, cytopathic effect, and neuraminidase activity.

78 icantly lowering viral load and direct viral cytopathic effects, and aborting the potential downstrea

79 exogenous lox sites caused decreased growth, cytopathic effects, and chromosomal aberrations.

80 for viral propagation, enteroviral-mediated cytopathic effects, and the development of cardiomyopath

81 , starting at 24 h, RAW264.7 cells exhibited cytopathic effects, annexin V staining, and cleaved casp

82 ecause of their relative resistance to viral cytopathic effects, APC can provide an alternative reser

83 Cytopathic effects are currently believed to contribute

84 In contrast, the cytopathic effects are not affected in MV-infected cells

85 (ii) Apoptosis, the calcium stores, and cytopathic effects are regulated by Bcl-2.

86 eins and released virus are reduced, and the cytopathic effects are strongly impaired.

87 ese cell types include direct infection with cytopathic effects as a consequence of replication.

88 ed and tested against EV-D68 using the viral cytopathic effect assay.

89 aluated in a plaque reduction assay and in a cytopathic effect assay.

90 tion was monitored using a series of assays (cytopathic effects assay, Ad5 hexon enzyme-linked immuno

91 of these siRNAs to prevent or reduce certain cytopathic effects associated with HCMV infection was al

92 understand the role of TVB receptors in the cytopathic effects associated with infection by specific

93 tem eliminates the negative influence of the cytopathic effects associated with replication of SIVMne

94 orms generated particles capable of inducing cytopathic effects at levels distinct from those observe

95 reshold level of viral replication, at which cytopathic effects begin to be seen, exists for HIV-1 in

96 pe 1 (HIV-1) envelope glycoproteins mediates cytopathic effects, both syncytium formation and single-

97 were rescued, 3 mutant viruses generated no cytopathic effect but were competent to synthesize viral

98 proach, infected cells will not die of viral cytopathic effects, but might be eliminated if HIV-speci

99 he concentration of acyclovir that inhibited cytopathic effect by 50% (EC50) was > or = 3 microg/mL w

100 The viruses display a characteristic cytopathic effect by forming syncytia in susceptible cel

101 The generation of cytopathic effects by murine leukemia viruses (MLVs) in

102 steine proteases were identified as enabling cytopathic effects by promoting adhesion of T. foetus to

103 Although direct cytopathic effects can contribute to disease severity, m

104 Direct virus-mediated cytopathic effects cannot explain the phenotypes of brai

105 pression of miR-155 rescued cells undergoing cytopathic effect caused by infection with subgroup B av

106 atitis C viral load in vitro and reduced the cytopathic effect caused by the fully replicating flaviv

107 hanced interferon-mediated resistance to the cytopathic effect caused by VSV and Sindbis virus (SNV).

108 uch more resistant than control cells to the cytopathic effects caused by influenza virus infection.

109 MOIs 0.1, 1, and 10 resulted in significant cytopathic effect consisting of excessive syncycial form

110 Cytopathic effects could be completely blocked by additi

111 However, rSV5deltaSH causes increased cytopathic effect (CPE) and apoptosis in MDBK cells and

112 ogy and ultimately leads to development of a cytopathic effect (CPE) and cell death.

113 usion and ionic exchange and then tested for cytopathic effect (CPE) and collagenolytic activity in v

114 myxovirus simian virus 5 (SV5) causes little cytopathic effect (CPE) and infection continues producti

115 ir replication and their ability to generate cytopathic effect (CPE) and to interfere with other vira

116 In this study, we carried out cytopathic effect (CPE) assays using ONYX-015 on five hu

117 The observed antiviral activities from the cytopathic effect (CPE) based assay were confirmed throu

118 protection against the Acanthamoeba-induced cytopathic effect (CPE) by an additional mechanism that

119 ith a greater percentage of cells exhibiting cytopathic effect (CPE) compared to nontransfected contr

120 No cytopathic effect (CPE) developed in neurons infected wi

121 displayed extensive syncytium formation and cytopathic effect (CPE) following infection with MV, con

122 lular transcription and rapid induction of a cytopathic effect (CPE) in cells of vertebrate origin.

123 to cause disease can be correlated to their cytopathic effect (CPE) in tissue culture characterized

124 the V protein (rSV5VDeltaC) induces a severe cytopathic effect (CPE) in tissue culture whereas wild-t

125 to adhesion, the parasites produce a potent cytopathic effect (CPE) leading to target cell death.

126 rneal epithelium, express MBP, and produce a cytopathic effect (CPE) on host cells.

127 The cytopathic effect (CPE) seen with some subgroups of avia

128 ltiplicity of infection does not result in a cytopathic effect (CPE) within 14 days postinfection (dp

129 rom this clade was found to induce a variant cytopathic effect (CPE), different from the canonical ar

130 DA) and monitored infected cell cultures for cytopathic effect (CPE), intra- and extracellular viral

131 rtebrate origin, is the rapid development of cytopathic effect (CPE), which is strongly dependent upo

132 However, we have found cytopathic effect (CPE)-inducing particles in 2 out of m

133 in Vero C1008 cells and inspected daily for cytopathic effect (CPE).

134 cked collagenolytic activity, migration, and cytopathic effects (CPE) against corneal cells in vitro.

135 creased dramatically in NPSCs with resultant cytopathic effects (CPE) and eventual cell death.

136 fected with TR showed delayed development of cytopathic effects (CPE) and replication centers and she

137 F-1, but RCASBP M2C (4070A) caused extensive cytopathic effects (CPE) in DF-1 cells whereas RCASBP M2

138 Cytopathic effects (CPE) induced by DENV-2 New Guinea C

139 protein is also responsible for most of the cytopathic effects (CPE) observed in infected cells.

140 this paradox, we studied the replication and cytopathic effects (CPE) of late-stage R5 HIV-1 biologic

141 TcsL cytopathic effects (CPE) were blocked by bafilomycin A1

142 This study found that typical polyomavirus cytopathic effects (CPE) were present and SV40 T antigen

143 er number of stock isolates at or past tube (cytopathic effect [CPE]) culture (TC) end points.

144 The virus causes cytopathic effects (CPEs) of extensive syncytial formati

145 3k and Akt, we show that VSV replication and cytopathic effects do not require activation of these ki

146 esting CD4(+) T cells survived despite viral cytopathic effects, even in the presence of autologous c

147 with replicating CCR5-tropic HIV-1, without cytopathic effect, exhibit selective attenuation of the

148 heless, A28-deficient virions did not induce cytopathic effects, express early genes, or initiate a p

149 y as a discipline has depended on monitoring cytopathic effects following virus culture in vitro.

150 the selectivity of ONYX-015 replication and cytopathic effects for the first time in humans, we carr

151 N or poly I:C prior to infection limited the cytopathic effect from Vesicular stomatitis virus (VSV),

152 e eliminated by the immune response or viral cytopathic effect have failed, indicating the need for a

153 Different forms of cytopathic effects have been associated with the virulen

154 Following the observation of cytopathic effect in a striped-snakehead fish cell line,

155 -irradiated PyV did not display any enhanced cytopathic effect in adar1(-/-) cells.

156 s wild-type adenovirus promotes a widespread cytopathic effect in all infected cells, E1A- and E1A/E1

157 als based on the alleviation of HCV-mediated cytopathic effect in an engineered cell line-n4mBid.

158 6, and MA104 cells, but there was no visible cytopathic effect in Caco-2, Mv 1 Lu, or PK(15) cells.

159 Amino acid 208 of mu2 also influences the cytopathic effect in cardiac myocytes after spread.

160 er, the mechanism by which cp viruses induce cytopathic effect in cell culture remains unknown.

161 the basis for investigating the role of this cytopathic effect in CMV pathogenesis.

162 or the recovery of FCV with a characteristic cytopathic effect in feline kidney cells.

163 observed previously, HCMV induced a typical cytopathic effect in human aortic endothelial cells (HAE

164 g that the SV5 P/V mutant has both a reduced cytopathic effect in human DC compared to WT SV5 and an

165 Because ribavirin treatment reduces the cytopathic effect in infected cells, we used high-densit

166 iate little to no microscopically observable cytopathic effect in mammalian cells and have a good bio

167 SVV produces a cytopathic effect in monkey kidney cells in tissue cultu

168 n of infectious particles, and a more potent cytopathic effect in permissive cells.

169 ute virus of canines (MVC) produces a strong cytopathic effect in permissive Walter Reed/3873D (WRD)

170 Ad.TK(RC)(II), generated a more efficiently cytopathic effect in proliferating cells, independently

171 n compound 5o that inhibited a virus-induced cytopathic effect in the entry stage of infection (EC(5)

172 Cytopathic effect in the infected brains was proportiona

173 leading to higher virus yields and enhanced cytopathic effect in tumor cells.

174 rporation into virus particles and increased cytopathic effect in Vero cells.

175 lly characterized the MVC infection-produced cytopathic effect in WRD cells, namely, the cell death a

176 The cytopathic effects in a malignant glioma cell line were

177 it ileal loop assay but did produce atypical cytopathic effects in cell culture assay.

178 Viruses lacking A55 or C2 have altered cytopathic effects in cultured cells and altered patholo

179 litis virus, which produced relatively minor cytopathic effects in fibroblasts, circumvented the need

180 educed viral proliferation and virus-induced cytopathic effects in glial cell lines and human astrocy

181 Class 1 SPATEs induce cytopathic effects in numerous epithelial cell lines, an

182 lones causes their increased replication and cytopathic effects in SCID-hu mice and likely contribute

183 d and gentamicin-killed CA180 did not induce cytopathic effects in the macrophage.

184 MV-Edm infection induced potent cytopathic effects in these myeloma cells, resulting in

185 ve this threshold level correlates best with cytopathic effects in this model system.

186 d that cholesterol supplementations increase cytopathic effects in tissue culture and also intensify

187 as been implicated in the induction of viral cytopathic effects in vitro, contributes to the capacity

188 protein is responsible for several important cytopathic effects, including the inhibition of host gen

189 Cell rounding is a hallmark of the cytopathic effect induced by cytomegaloviruses.

190 Apoptosis plays a major role in the cytopathic effect induced by reovirus following infectio

191 SAPI suppressed the cytopathic effects induced by DENV2 infection as well as

192 identify vif and vpr as necessary for T cell cytopathic effects induced by HIV-1.

193 erleukin-6 and -8 production, as well as the cytopathic effects induced by RSV.

194 factor 3 formation, and block the antiviral cytopathic effects induced by type I IFNs.

195 D614G natural mutation, that modulate viral cytopathic effects, infectivity and sensitivity to inhib

196 A cytopathic effect inhibition assay was used to determine

197 ters in human lung grafts and caused similar cytopathic effects irrespective of the presence of human

198 results in 50% protection from virus-induced cytopathic effect is approximately 2.2 microM, with a th

199 The cytopathic effect is characterized as necrotic rather th

200 on of transgene expression without resulting cytopathic effects is useful.

201 of the E1B-19K protein resulted in enhanced cytopathic effect, large plaques on cell monolayers, fra

202 g virus clearance without the development of cytopathic effect, may prove crucial in the design of ne

203 it does in B cells, but instead resulted in cytopathic effects more commonly associated with product

204 in the in vitro replication, plaque size, or cytopathic effect morphology of HVP2ap versus HVP2nv iso

205 ed coincident with the onset of an extensive cytopathic effect not observed with wt rHPIV1.

206 Le-(U5C, A14G) induced cytopathic effects not seen with WT SV5, and the extent

207 rus (ZIKV) replication and is central to the cytopathic effects observed in infected cells.

208 enhanced toxin production and increased the cytopathic effect of C. difficile on cultured fibroblast

209 Viral replication and the cytopathic effect of CG8840 were evaluated by virus yiel

210 a protein responsible for the characteristic cytopathic effect of clinical HCMV strains that also pro

211 e dystrophin in cultured cells decreased the cytopathic effect of enteroviral infection and the relea

212 thesized and evaluated for inhibition of the cytopathic effect of HIV-1(RF) in CEM-SS cell culture an

213 cromolar EC(50) values for inhibition of the cytopathic effect of HIV-1(RF) in CEM-SS cells.

214 ne thymus protects human thymocytes from the cytopathic effect of HIV-1, suggesting a possible approa

215 inhibit HIV-1 reverse transcriptase and the cytopathic effect of HIV-1RF and HIV-1IIIB at submicromo

216 e most potent of the new ADAMs inhibited the cytopathic effect of HIV-1RF in CEM-SS cell culture with

217 We observed that the cytopathic effect of lymphomagenic MLVs was restricted t

218 e treatment can increase gene expression and cytopathic effect of neurotropic paramyxoviruses, includ

219 produce type I IFN and are resistant to the cytopathic effect of the infection.

220 FCH, hepatocytes may be injured by a direct cytopathic effect of the virus rather than by the host i

221 on of apoptosis in host cells is a prominent cytopathic effect of vesicular stomatitis virus (VSV) in

222 lar edema and ionic changes are hallmarks of cytopathic effects of a viral infection, the tonicity-dr

223 Mature and not immature DCs resisted the cytopathic effects of canarypox virus and elicited stron

224 y E. coli with urinary tract disease and the cytopathic effects of CNF1 on cultured urinary tract cel

225 IV infection may not depend solely on direct cytopathic effects of HIV replication, but that effects

226 , and 40, which exhibit EC(50)'s against the cytopathic effects of HIV-1 of 9.0, 1.0, and 4.0 nM, res

227 ls, unlike lymphocytes, are resistant to the cytopathic effects of HIV.

228 d tissue was examined to see whether in vivo cytopathic effects of human immunodeficiency virus (HIV)

229 rations of recombinant proteins or by direct cytopathic effects of replicating virus.

230 eplicated readily in cell culture, producing cytopathic effects of rounding, detachment, and syncytiu

231 Instead, direct cytopathic effects of SIV resulting in chronic immune ac

232 n immunodeficiency virus (SIV) suggests that cytopathic effects of SIV resulting in chronic immune ac

233 apoptosis in such cells, suggesting that the cytopathic effects of SIVagm vpr are species specific.

234 whereas E3 intrabody completely blocked the cytopathic effects of TcdB holotoxin.

235 l production was partially due to the severe cytopathic effects of the X4 virus.

236 ly indirect in nature and possibly linked to cytopathic effects of these robustly replicating viruses

237 Cytopathic effects of ts1 infection in cultured astrocyt

238 fected host appear to result from the direct cytopathic effects of viral infection and the effects of

239 l population that is less susceptible to the cytopathic effects of virus infection.

240 of other viral components causes many of the cytopathic effects of VSV, including an inhibition of ho

241 V protein expression or the induction of the cytopathic effects of VSV.

242 trophozoites or cysts induced a significant cytopathic effect on corneal epithelial cells compared w

243 ive isolates were tested and shown to have a cytopathic effect on HeLa cell monolayers.

244 We also showed that mycolactone causes a cytopathic effect on mouse fibroblast L929 cells that is

245 esis of Acanthamoeba keratitis by inducing a cytopathic effect on the corneal epithelial and stromal

246 more slowly in Vero cells and had less of a cytopathic effect on tissue culture cells but caused sev

247 demonstration of Clostridium sordellii-like cytopathic effect on Vero cells.

248 No acute cytopathic effects on any homogeneous cell line, or cons

249 e cell-associated and purified form elicited cytopathic effects on cultured kidney and bladder epithe

250 this disorder apparently result from direct cytopathic effects on the atrial and ventricular myocard

251 uch, has serine protease activity and causes cytopathic effects on various cell types.

252 Analysis of SAFV-2 revealed virus growth and cytopathic effect only in human cell lines, with large p

253 to their elimination through a virus-induced cytopathic effect or host anti-HIV immunity.

254 C is primarily attributable to direct viral cytopathic effect or to an immune-mediated response.

255 There is no cytopathic effect or viral DNA expansion when infected T

256 genic mice that displayed both antiviral and cytopathic effects, presumably because they displayed hi

257 ng a surrogate cell entry system resulted in cytopathic effect rates similar to those of other LCTs a

258 lebbing also frequently occur as part of the cytopathic effect seen during many different viral infec

259 Furthermore, AdTyrdelta24 showed a cytopathic effect similar to the wild-type E1A containin

260 combinant vectors exhibited virus yields and cytopathic effects similar to the parental G47Delta.

261 lular expression of the protein could induce cytopathic effects similar to those observed when the to

262 tions in SPI-1, SPI-2, or spvB induced these cytopathic effects similar to wild-type bacteria.

263 er by a permeable membrane did not produce a cytopathic effect, suggesting contact-dependent cytotoxi

264 e protease inhibitors do not abolish the Cif cytopathic effect, suggesting that another enzymatic act

265 n of SRSF2 enhanced reovirus replication and cytopathic effect, suggesting that T1L mu2 modulation of

266 ortive infection in limited cell lines and a cytopathic effect suggestive of herpes simplex virus.

267 mer mediates virus entry into host cells and cytopathic effects (syncytium formation).

268 V protein is capable of inducing more severe cytopathic effects than the wild type, implicating measl

269 n vitro tests were conducted to evaluate the cytopathic effect, the minimum inhibitory concentration

270 l become transcriptionally inactive prior to cytopathic effects, the viral genome might be maintained

271 cleaved spectrin, only Pet and Sat elicited cytopathic effects; the remaining SPATEs did not cause a

272 f genome and antigenome RNAs and a change in cytopathic effect to a more syncytium-forming phenotype.

273 le dilution of antiserum, and observation of cytopathic effect to determine the adenovirus serotype.

274 re that HIV type 1 (HIV-1) exerts a profound cytopathic effect upon peripheral blood CD4(+) T lymphoc

275 ed by evaluating inhibition of virus induced cytopathic effect, virus plaque formation, and virus gen

276 sed production of inflammatory cytokines and cytopathic effects visible under microscopy.

277 caused apoptotic death of the cells, and its cytopathic effect was blocked by Humanin.

278 V-IFNbeta was greatly reduced and diminished cytopathic effect was observed due to the production of

279 A high cytopathic effect was observed for the isolates positive

280 No viral RNA replication or cytopathic effect was observed in cells transfected with

281 A cytopathic effect was observed in virus cultures of the

282 The cytopathic effect was observed with macrophages at multi

283 became immunoreactive for viral antigens and cytopathic effect was observed.

284 A virus that caused overt cytopathic effects was isolated, but it did not infect v

285 range of anogenital HPV genotypes to induce cytopathic effects, we examined the influences of HPV ty

286 iral protein synthesis, plaque diameter, and cytopathic effect were significantly reduced.

287 0-fold by the U51 siRNA, and virally induced cytopathic effects were also inhibited.

288 cells through an extracellular matrix before cytopathic effects were detected.

289 he E1A and E1B genes, virus replication, and cytopathic effects were examined by Northern blot, Weste

290 permissive to EBOV replication, significant cytopathic effects were not observed.

291 However, RNA synthesis and cytopathic effects were observed following serial passag

292 cat with chronic sinusitis and rhinitis when cytopathic effects were observed in Crandall-Reese felin

293 , viral protein synthesis and development of cytopathic effects were suppressed.

294 Macrophages are resistant to HIV cytopathic effects, which contributes to viral persisten

295 can perturb nuclear architecture and induce cytopathic effects, which ultimately lead to disease pat

296 nolayers infected with UL24-betagluc yielded cytopathic effect with syncytium formation.

297 virus was isolated from BHK21 cells, causing cytopathic effects with syncytial formation.

298 mmalian cells in culture results in a severe cytopathic effect within 24 to 48 h postinfection manife

299 producing infectious virions and significant cytopathic effects within 14 days of inoculation.

300 NA can persist for weeks in the absence of a cytopathic effect, yet viral RNA remains detectable.