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These binding events should be verified by further ChIP experiments.
First, as with many biological processes, TF-gene binding events should be regarded as a quantitative and continuous variable rather than a simple on/off switch model.
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The results of our study suggest that the loss of a binding site because of obstruction by new steric constraints from the initial binding event should be avoided in GluA drug design and suggest that more effort in thiazide design could prove useful in cognitive enhancer development.
The events should be rather familiar.
Adverse events should be expected.
These events should be scored differently.
All adverse events should be reported.
The event should be unforgettable.
(f) Any adverse event should be restated. .
Any adverse event should be restated.
Therefore a monitoring event should be generated.
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