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Recruitment of STAT5 and CBP/P300 to the LTR in Primary Cells with RUNX1 binding inhibition. PBMC blasts from healthy donors were infected with ΔNef or ΔRUNX. (A) Viral replication was followed over time by p24 ELISA. After 48 h infection, PBMC cells were fixed and prepped for CHIP analysis with IP targeting (B) RUNX1 (C) STAT5 and (D) CBP/P300. **P ≤ 0.01, ***P ≤ 0.001.
