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Cell entry was initiated by raising the incubation temperature to 37°C for the indicated time.
Stimulation was performed for the indicated time with 1.0 mM of freshly prepared CaCl2 for the indicated time.
Regression analysis was performed for the indicated outcomes.
Monocytes were incubated with IC for the indicated time-points.
Radiation sensitivity assays were conducted exposing cultures in a cesium irradiator for the indicated doses.
Cells were stimulated as described above for the indicated periods of time.
The cells were incubated under normoxia at 37°C for the indicated time.
Eight weeks after vector treatment, mice were sacrificed for the indicated analyses.
Protein lysates were harvested from cells incubated in normoxia or hypoxia for the indicated periods.
Fluorescence recovery was recorded for the indicated time.
The cells were infected with VSV for the indicated time.
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