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To understand these processes better, we need to start with the basics of transcriptional control.
Transcriptional start sites have also been assigned based on alignment data.
The gene order is therefore a simple but effective form of transcriptional regulation.
Transcriptional gene profiles have not been considered in making such recommendations.
The transcriptional factor Pax8 binds in two of these sites.
YgfY was also thought to be involved in transcriptional regulation.
In fig 3B, we examined the transcriptional activity of these p53 constructs.
Transcriptional regulation (bottom portion of figure) occurs in several ways.
Genes are regulated at either the transcriptional stage, or later, before translation.
Where are the transcriptional regulatory elements for the downstream gene?
Their presence is regulated at the transcriptional level of the respective genes.
On the basis of this function, p300 is called a transcriptional coactivator.
A predictive model for transcriptional control of physiology in a free living cell.
It is thus not surprising that this region has a complex set of transcriptional regulatory sites.
Sp140 associates with certain bodies and appears to be involved in transcriptional activation.
However, acetylation is not always associated with enhanced transcriptional activity.
This project aims to establish the roadmap of these transcriptional states.
The model represents individuals as networks of interacting transcriptional regulators.
It is a nuclear protein and functions as a transcriptional regulator.
In mammals, three miR-34 precursors are produced from two transcriptional units.
One of the nuclear dot proteins appears to be involved in transcriptional active regions.
Conclusions Predicting and understanding transcriptional regulation is a fundamental problem in biology.
The exact start transcriptional sites for either gene has not been definitively established.
Our data may therefore help point to one important feature of the transcriptional program that sets the stage for these signaling events.
Thus, transcriptional regulators and their downstream targets can be identified simultaneously.
