<p>MDCK cells were inoculated with influenza A viruses (MOI 0.001), then treated with ATA for 48 h. Media were collected and released viruses were quantified by ELISA. The columns represent the means of triplicates and error bars represent standard deviations. * = corrected p-value <0.05.</p
<p>Confluent MDCK cells in 6 well plates were infected with 0.001 MOI of influenza A PR8 virus and i...
<p>U87MGs were pre-treated with DMSO or BAY-11-7082 (1 µM) for 2 hours. The conditioned media (media...
<p>(a) CEF cells were incubated with individual peptide or mixed peptide in pair at concentration of...
<p>MDCK cells infected with influenza A viruses (MOI 0.001) were treated with ATA for 48 h. Cell via...
<p>Viruses in culture supernatants were detected by ELISA 48 h following treatment with ATA, AH or b...
<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>MDCK cells were infected with influenza A PR8 virus and treated with the indicated concentrations...
<p>Influenza PR8, NC, NY and B viruses were pre-incubated with ATA (0, 50, 100 µg/ml) for 30 min, th...
<p>MDCK cells were infected with influenza A PR8 virus and exposed to DMSO, AH or ATA, then processe...
<p>Cells were infected with rWSN at MOI of 1, then cultured in the absence or presence of PGA1 for t...
<p>A: Cytopathic effect assay of CsA on the influenza virus replication. Monolayers of MDCK cells on...
<p>BV42 managed to inhibit the attachment of influenza virus (A/Texas/1/77) to MDCK host cells. The ...
<p>ATA inhibits enzymatic activity of NA (A) derived from PR8, NC, NY and B viruses, (B) recombinant...
<p>(A) The viral infectivity was titrated directly via a plaque assay on MDCK cells. Values represen...
<p>Confluent MDCK cells in 6 well plates were infected with 0.001 MOI of influenza A PR8 virus and i...
<p>U87MGs were pre-treated with DMSO or BAY-11-7082 (1 µM) for 2 hours. The conditioned media (media...
<p>(a) CEF cells were incubated with individual peptide or mixed peptide in pair at concentration of...
<p>MDCK cells infected with influenza A viruses (MOI 0.001) were treated with ATA for 48 h. Cell via...
<p>Viruses in culture supernatants were detected by ELISA 48 h following treatment with ATA, AH or b...
<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>MDCK cells were infected with influenza A PR8 virus and treated with the indicated concentrations...
<p>Influenza PR8, NC, NY and B viruses were pre-incubated with ATA (0, 50, 100 µg/ml) for 30 min, th...
<p>MDCK cells were infected with influenza A PR8 virus and exposed to DMSO, AH or ATA, then processe...
<p>Cells were infected with rWSN at MOI of 1, then cultured in the absence or presence of PGA1 for t...
<p>A: Cytopathic effect assay of CsA on the influenza virus replication. Monolayers of MDCK cells on...
<p>BV42 managed to inhibit the attachment of influenza virus (A/Texas/1/77) to MDCK host cells. The ...
<p>ATA inhibits enzymatic activity of NA (A) derived from PR8, NC, NY and B viruses, (B) recombinant...
<p>(A) The viral infectivity was titrated directly via a plaque assay on MDCK cells. Values represen...
<p>Confluent MDCK cells in 6 well plates were infected with 0.001 MOI of influenza A PR8 virus and i...
<p>U87MGs were pre-treated with DMSO or BAY-11-7082 (1 µM) for 2 hours. The conditioned media (media...
<p>(a) CEF cells were incubated with individual peptide or mixed peptide in pair at concentration of...