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CD1 molecules function to present lipid-based antigens to T cells.
MHC molecules function to present foreign antigens.
In general, these molecules function to regulate gene expression at the transcriptional and post-transcriptional level.
Specifically, N-glycans molecules function to maintain the structural integrity of the cell walls.
Candidate molecules for this activity include the chemokines, IP-10 and MIP-1, although it is not completely clear how these molecules function to suppress angiogenesis.
These molecules function to promote B cell maturation by directing B cell localization to the germinal centers as well as the localization of B cells to sites of inflammation [ 39].
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The CCN1 molecule functions to support many key biological processes necessary for tissue repair and thus presents a promising target for bioengineering applications.
The lower expression of CD1a is probably not of any functional importance in the context of mRNA loaded DC to be used as cancer vaccines, since this molecule functions to present bacterial lipids to T cells.
They may also be less tightly bound to enzyme catalysts as coenzymes, detachable molecules that function to carry chemical groups or electrons between molecules.
Collective results identify XRCC4 and XLF filaments suitable to align DNA molecules and function to facilitate LigIV end joining required for DSB repair in vivo.
MicroRNAs (miRNAs) are short (18 25 nt) non-coding single-stranded RNA molecules that function to post-transcriptionally regulate gene expression [13].
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