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Specific Ablation of Antiviral Gene Expression in Macrophages by Antibody-Dependent Enhancement of Ross River Virus Infection

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Figure

TABLE 1. Primer sequences used in the RT-PCR studies of RRV-infected RAW 264.7 cellsa
TABLE 2. Comparison of in vitro RRV growth and percentRRV cell infectivity at 24 h postinfection in RAW 264.7cells cultured with or without LPSa
FIG. 2. LPS-stimulated (250 ng/ml) TNF (A) and RNI (B) production inRAW 264.7 cultures infected with RRV at an MOI of 0.1
FIG. 4. Analysis of general de novo protein synthesis in LPS-treated (1.0ng/ml) RAW 264.7 cultures at 24 h post-RRV infection (MOI of 0.1; plus

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