<p>(A) Anti-VSV activities of ChIFNs at different time points. Cells were pretreated with serial four-fold dilutions of ChIFN-α or ChIFN-β for different durations (2, 4, 8, 12, or 24 h) before VSV infection and then stained with crystal violet. (B) Antiviral titration curves of the ChIFNs. DF-1 cells were untreated or treated with 10-fold serial dilutions of ChIFN-α or ChIFN-β for 12 h before VSV infection and then stained with crystal violet. The relative survival percentage was calculated as the ratio of OD values between IFN-treated wells and untreated wells. (C) Antiviral activities of ChIFNs against VSV, NDV and AIV. Cells were treated with serial four-fold dilutions of ChIFN-α or ChIFN-β for 12 h, followed by VSV, NDV or AIV infection...
<p>(<b>a–f</b>) Cells were pretreated with cycloheximide (CHX), ammonium chloride (NH<sub>4</sub>Cl)...
A selection of antiherpes compounds including bromovinyldeoxyuridine (BVDU), acyclovir (ACV), and fl...
A set of 20 nucleoside analogs were examined for their inhibitory effects on the cytopathogenicity a...
<p>(A) WISH cells were treated with the antagonists, YNS, IFNα2 or left untreated for four hours. VS...
<p>Dose dependent reduction of CHIKV-induced CPE by (A) 3-deaza-adenosine, (B) 6-aza-uridine, (C) ch...
<p>(A) U87 cells were treated with DMSO or inhibitors, stimulated with 100 ng/ml IFN-λ1 or 500 U/ml ...
<p>Confluent monolayer of HuH-7 cells were infected with 50 pfu CHIKV-118-GFP in the presence of com...
An immunofluorescent assay (IFA) for Pichinde virus (PCV), a member of the family Arenaviridae, was ...
<p><b>A</b>) U87MG astrocytes were pretreated for 2 hours with DMSO or various BIO derivatives at 1 ...
<p>(a) Demonstration of expression of different morbillivirus V proteins in the stable cell lines us...
<p><b>(A)</b> ELISA-like cell-based assay was used to evaluate the antiviral activity of the drugs. ...
(A) Antiviral activity of HsIFNλ4 variants against HCVcc infection in Huh7 cells measured by RT-qPCR...
<p>Serial twofold dilutions of IFN-β standard (starting with 100 pg/ml) and of two different test sa...
(A-B) Colon organoids were pre-treated with the indicated concentrations of type I IFN (β) or type I...
<p>Neutralizing activity was determined by FRNT on Vero or NIH 3T3 cells with increasing concentrati...
<p>(<b>a–f</b>) Cells were pretreated with cycloheximide (CHX), ammonium chloride (NH<sub>4</sub>Cl)...
A selection of antiherpes compounds including bromovinyldeoxyuridine (BVDU), acyclovir (ACV), and fl...
A set of 20 nucleoside analogs were examined for their inhibitory effects on the cytopathogenicity a...
<p>(A) WISH cells were treated with the antagonists, YNS, IFNα2 or left untreated for four hours. VS...
<p>Dose dependent reduction of CHIKV-induced CPE by (A) 3-deaza-adenosine, (B) 6-aza-uridine, (C) ch...
<p>(A) U87 cells were treated with DMSO or inhibitors, stimulated with 100 ng/ml IFN-λ1 or 500 U/ml ...
<p>Confluent monolayer of HuH-7 cells were infected with 50 pfu CHIKV-118-GFP in the presence of com...
An immunofluorescent assay (IFA) for Pichinde virus (PCV), a member of the family Arenaviridae, was ...
<p><b>A</b>) U87MG astrocytes were pretreated for 2 hours with DMSO or various BIO derivatives at 1 ...
<p>(a) Demonstration of expression of different morbillivirus V proteins in the stable cell lines us...
<p><b>(A)</b> ELISA-like cell-based assay was used to evaluate the antiviral activity of the drugs. ...
(A) Antiviral activity of HsIFNλ4 variants against HCVcc infection in Huh7 cells measured by RT-qPCR...
<p>Serial twofold dilutions of IFN-β standard (starting with 100 pg/ml) and of two different test sa...
(A-B) Colon organoids were pre-treated with the indicated concentrations of type I IFN (β) or type I...
<p>Neutralizing activity was determined by FRNT on Vero or NIH 3T3 cells with increasing concentrati...
<p>(<b>a–f</b>) Cells were pretreated with cycloheximide (CHX), ammonium chloride (NH<sub>4</sub>Cl)...
A selection of antiherpes compounds including bromovinyldeoxyuridine (BVDU), acyclovir (ACV), and fl...
A set of 20 nucleoside analogs were examined for their inhibitory effects on the cytopathogenicity a...