(iii) regulating mixing proportion Fig. 5 Regulation of inter-specific competition by spatial separation of tree species.
Differential regulation of inter-MT spacing could in principle offer an intriguing mechanism to control the binding of MT-regulating MAPs and motor proteins.
Whether or not this reflects a consistent difference between the neural regulation of inter-temporal choice in rats and humans is a question that awaits further investigation.
As a TJ scaffolding protein anchored to the actin cytoskeleton, ZO-1 is crucial for the regulation of inter-endothelial TJ complexes and BBB structural integrity [ 42, 43].
Two structures that have been implicated in the regulation of inter-temporal choice are the core of the nucleus accumbens (AcbC) and the orbital prefrontal cortex (OPFC).
One group (marked Blue in Figure 3) mainly regulates linear intra-H2H gene pairs and the other (marked Red in Figure 3) is involved in the spatial regulation of inter-H2H pairs.
To comprehensively reveal the RNA expressional regulation of inter-genic regions, it was necessary to make a clear distinction between transcripts that were associated with known housekeeping genes (e.g. untranslated region), and the transcripts that were not associated with these gene features.
However, an evident up-regulation of inter-trafficking transcripts such as WD40, Grlp and ALP was observed which requires detailed investigation to decipher their possible role.
Furthermore, Ang-2 facilitates up-regulation of inter-cellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule -1 (VCAM-1), and E-selectin [ 3, 7, 10, 11].
The present study identified an important role for both SULTR1 3 and PHR1 in the regulation of sulfate inter-organ flux upon Pi starvation in Arabidopsis.
The mechanism of transcriptional regulation of intra- and inter-H2H gene pairs is still poorly understood and deserves considerable attention.
