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The radiotracer binding data were compared to results obtained with TUNEL staining and clonogenic survival.
The generated RXRα binding data were compared with the data for RARα, PXR, LXR, FXR, and PPARα.
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However, when the receptor-binding data were compared with circulating levels of gonadal steroids separately for each phase of the cycle, several significant correlations emerged.
Cytological and physiological data were compared.
Averaged data were compared using t-test.
We therefore strongly recommend that the ChIP data be compared with the corresponding input data to decrease identification of false-positive protein-binding sites.
So data are compared to this state.
Using Encode ChIP-Seq data, the transcription factor binding sites were compared to the DHS sites, which showed highly overlapping percentage.
All binding data are summarized in Table S1.
Simulation results for stationary insulin receptor activation and insulin binding were compared to experimental data sets [ 57].
Two different binding methods were compared by specular reflectance measurements.
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