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miRNAs in bursa and spleen of developing chicken embryo have been recently identified, and diverse expression patterns of these miRNAs between different immune organs were observed, suggesting that miRNAs may function as dynamic regulators of the vertebrate immune system [ 45].
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It is widely accepted that critical genes involved in transforming mammary epithelial cells encode proteins that function as dynamic regulators of signal transduction pathways that regulate cell cycle, differentiation, proliferation and survival [ 14].
Somatostatin receptors (SSTR) have been recognised as dynamic regulators of tumour development, cell proliferation and apoptosis (Ruscica et al, 2012).
It is therefore paramount that the interface between the central nervous system and the peripheral circulatory system (that is, the BBB) functions as a dynamic regulator of ion balance, as a facilitator of nutrient transport, and as a barrier to potentially harmful molecules.
The interface between CNS and the peripheral circulatory system functions as a dynamic regulator of ion balance, a nutrient transport, and molecular trafficking is historically known as blood-brain barrier (BBB) [ 1].
Within the AB loop, residues normally act to either stabilise or function as negative regulators of the interaction.
The specific structural characteristics of both the protein cores and GAG types provide the structural basis for the plethora of their biological functions which include acting as structural components in tissue organization or dynamic regulators of cellular behaviour [ 3].
The authors identified Btbd7 as a dynamic regulator of branching morphogenesis through its highly focal expression leading to local regulation of E-cadherin and epithelial cell motility [ 15].
Our data provide first insights of S100A10 function as a regulator of the filamentous actin network.
However, chromatin is a highly dynamic regulator of gene expression.
SPL genes are negatively regulated by miR156 and function as positive regulators of MIR172 genes.
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