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These findings suggesting that individual Maml coactivators may regulate molecular specificity of Notch receptor functions remains to be confirmed.
CPNE2 (copine II) codes a calcium-dependent membrane-binding protein that may regulate molecular events at the interface of the cell membrane and cytoplasm.
Given the primary purpose of this clinical trial, in this discussion, we focus primarily on how TPM may regulate molecular pathways of synaptic plasticity underlying METH's reward and reinforcing effects that influence abstinence.
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Mechanical unfolding and refolding may regulate the molecular elasticity of modular proteins with mechanical functions.
This challenge is compounded because a given gene may regulate several molecular events in different cell types during different developmental stages.
We have placed these genes in a Foxa2-dependent genetic regulatory network and we hypothesize how Foxa2 may regulate a molecular program of Spemann/Mangold organizer development.
Equally important is knowing how an organism's experiences, social interactions and environment regulate molecular biology and gene function.
A transactivation inhibitory domain at its C-terminus with high homology to the vertebrate p63 may regulate nvp63 on a molecular level.
Our analysis of the genome-wide map of p53-NF-κB binding sites suggests that the molecular complex may regulate gene expression more widely, although the exact mechanism by which it operates in each location is not identical.
These findings are reviewed in the context of future research on RLS, with an emphasis on fundamentally conserved molecular pathways that may regulate sleep architecture across species.
Next, we performed global gene expression profiling studies to identify specific genetic targets and molecular pathways that may regulate T-Ag-induced changes in cellular motility.
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