Exact(1)
Combined with the fact that PWX (L/V) motif might be important for the peptide binding mentioned above, it is possible that the Trp, Pro and Leu residues form a hydrophobic environment which can be recognized by certain cell surface proteins.
Similar(59)
Recent studies, however, provide evidence for the existence within this niche of smaller precursor stem cell populations that exhibit extensive proliferative and multilineage differentiative capacity and can be distinguished by their expression of certain cell surface antigens [ 11, 12].
TGF-β inhibits the expression of MMP-1 and MMP-3 by binding to a certain cell surface receptor complex (TGF-β receptor proteins: TβR I/II/III), thus preventing the breakdown of collagens.
As the cytotoxicity assays were performed in consecutive two days, the variation in the spontaneous cytotoxicity was unlikely to be due to the propagation of cytotoxic cells but is more likely to be affected by the expression of certain cell surface adherent molecules.
These morphological changes are accompanied by an orchestrated compartmentalization of certain cell surface associated molecules [4], [5], [6].
It could be due to the presence of different alleles of a certain cell surface protein targeted by specific parasite effector molecules.
The distinct property of lectins to bind specific carbohydrates makes them capable of recognising certain cell surface glycoproteins and detecting alterations on that, by using histochemical techniques.
Recent studies have indicated that certain cell surface markers can be used to locate and enrich neural precursor cells.
Three groups of patients were identified based on the presence of certain cell surface antigens.
Such a mechanism could theoretical be mediated by the oncoprotein MDM2, which interacts with p53 but has recently also been found to associate with certain cell surface receptors and regulate their functions (Shenoy et al, 2001).
Signaling through RAGE is clearly responsible for biological effects induced by extracellular S100A4 in certain cell systems, but other cell surface molecules have also been suggested to be involved in S100A4 signaling.
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