In our study, we also consider human factors to regulate a selection process.
Biomaterial researchers have immobilized ECM, cell adhesion factors, and growth factors to regulate the cell functions.
Targeting the ETS1 interface might have great therapeutic value because ETS1 dimerizes itself or with other transcription factors to regulate target genes.
Likewise, targeting ETS1 interface might have great therapeutic promise because ETS1 dimerizes itself or other transcription factors to regulate transcriptional target genes.
Some members of OFPs have been shown to function as transcription factors to regulate plant growth and development, but little is known about the function of AtOFP8.
These biomimetic scaffolds may serve as blueprints for synthetical biological scaffolds including adhesive and physical factors to regulate cell adhesion, proliferation, tissue architecture, and function.
We also demonstrate effective targeting of artificial transcription factors to regulate gene expression from three different constitutive viral promoters (SV40, CMV, RSV).
While much effort has been focused on using biological factors to regulate stem cell differentiation, recently interest in the contribution of physical factors has increased.
The physiological functions of mature cells depend on the microenvironment/niche surrounding which can provide proper factors to regulate cell proliferation and differentiation.
These observations indicate that Sp1 interacts with Sp3, but not with the other transcription factors, to regulate resistin gene expression.
One such gene, Hmga2, encodes a small chromatin-associated protein that cooperates with other factors to regulate gene expression.
