<p>MDCK cells were infected with influenza A PR8 virus and exposed to DMSO, AH or ATA, then processed for electron microscopy. (A and B) Low and high magnification view, respectively, of MDCK cells infected with influenza A PR8 virus in the presence of DMSO only. (C and D) Low and high magnification view, respectively, of MDCK cells infected with influenza A PR8 virus in the presence of AH. (E and F) Low and high magnification view, respectively, of MDCK cells infected with influenza A PR8 virus in the presence of ATA.</p
I): uninfected cells; (II): cells infected with equine influenza A virus H3N8 (18 h p.i.); (III): ce...
<p>After adsorption for 1 h at 37°C, the inocula were removed and the cultures were washed 3 times. ...
<p>MDCK cells were inoculated with influenza A viruses (MOI 0.001), then treated with ATA for 48 h. ...
<p>Uninfected MDCK cells, or MDCK cells infected with influenza A strains were treated with either A...
<p>(A) Cytotoxicity of ATA in MDCK cells. MDCK cells were treated with ATA for 48 h at the indicated...
<p>Confluent MDCK cells in 6 well plates were infected with 0.001 MOI of influenza A PR8 virus and i...
Single-cell clones have been established from the MDCK cell line, characterized for their morphology...
<div><p>Single-cell clones have been established from the MDCK cell line, characterized for their mo...
<p>Viruses in culture supernatants were detected by ELISA 48 h following treatment with ATA, AH or b...
<p>(A) MDCK and BEAS-2B cells were infected with USSR H1N1 or H2N3 influenza viruses at 1.0 MOI (bas...
<p>MDCK cells were infected with influenza A PR8 virus and treated with the indicated concentrations...
<p>(A) The antiviral effect of selected aptamers on the viability of MDCK cells infected by the infl...
<p>MDCK cells infected with influenza A viruses (MOI 0.001) were treated with ATA for 48 h. Cell via...
<p>MDCK cells were infected at an MOI of 0.001 in the presence of 1 µg/ml TPCK-trypsin. After adsorp...
<p>(<b>A</b>) Macrophages were exposed to A(H1N1)pdm09 (MOI = 5) and, at different days after expos...
I): uninfected cells; (II): cells infected with equine influenza A virus H3N8 (18 h p.i.); (III): ce...
<p>After adsorption for 1 h at 37°C, the inocula were removed and the cultures were washed 3 times. ...
<p>MDCK cells were inoculated with influenza A viruses (MOI 0.001), then treated with ATA for 48 h. ...
<p>Uninfected MDCK cells, or MDCK cells infected with influenza A strains were treated with either A...
<p>(A) Cytotoxicity of ATA in MDCK cells. MDCK cells were treated with ATA for 48 h at the indicated...
<p>Confluent MDCK cells in 6 well plates were infected with 0.001 MOI of influenza A PR8 virus and i...
Single-cell clones have been established from the MDCK cell line, characterized for their morphology...
<div><p>Single-cell clones have been established from the MDCK cell line, characterized for their mo...
<p>Viruses in culture supernatants were detected by ELISA 48 h following treatment with ATA, AH or b...
<p>(A) MDCK and BEAS-2B cells were infected with USSR H1N1 or H2N3 influenza viruses at 1.0 MOI (bas...
<p>MDCK cells were infected with influenza A PR8 virus and treated with the indicated concentrations...
<p>(A) The antiviral effect of selected aptamers on the viability of MDCK cells infected by the infl...
<p>MDCK cells infected with influenza A viruses (MOI 0.001) were treated with ATA for 48 h. Cell via...
<p>MDCK cells were infected at an MOI of 0.001 in the presence of 1 µg/ml TPCK-trypsin. After adsorp...
<p>(<b>A</b>) Macrophages were exposed to A(H1N1)pdm09 (MOI = 5) and, at different days after expos...
I): uninfected cells; (II): cells infected with equine influenza A virus H3N8 (18 h p.i.); (III): ce...
<p>After adsorption for 1 h at 37°C, the inocula were removed and the cultures were washed 3 times. ...
<p>MDCK cells were inoculated with influenza A viruses (MOI 0.001), then treated with ATA for 48 h. ...