# |
PMID |
Sentence |
1 |
23768205
|
In addition, immunization with MCS/pGRP nanoparticles could suppress the growth of tumor cells.
|
2 |
23768205
|
Cell binding and cellular uptake results indicated that MCS/pGRP nanoparticles bound with C-type lectin receptors on macrophages.
|
3 |
23768205
|
In addition, immunization with MCS/pGRP nanoparticles could suppress the growth of tumor cells.
|
4 |
23768205
|
Cell binding and cellular uptake results indicated that MCS/pGRP nanoparticles bound with C-type lectin receptors on macrophages.
|
5 |
26353473
|
In this study, using gastrin-releasing peptide as a model plasmid (pGRP), the binding of MCS/pGRP nanoparticles to macrophages and the intracellular trafficking of MCS/pGRP nanoparticles in macrophages were investigated.
|
6 |
26353473
|
Observation with a confocal laser scanning microscope indicated the cellular uptake of MCS/pGRP nanoparticles were more than that of CS/pGRP nanoparticles in macrophages.
|
7 |
26353473
|
MCS/pGRP nanoparticles were taken up by macrophages and most of them were entrapped in endosomal/lysosomal compartments.
|
8 |
26353473
|
In this study, using gastrin-releasing peptide as a model plasmid (pGRP), the binding of MCS/pGRP nanoparticles to macrophages and the intracellular trafficking of MCS/pGRP nanoparticles in macrophages were investigated.
|
9 |
26353473
|
Observation with a confocal laser scanning microscope indicated the cellular uptake of MCS/pGRP nanoparticles were more than that of CS/pGRP nanoparticles in macrophages.
|
10 |
26353473
|
MCS/pGRP nanoparticles were taken up by macrophages and most of them were entrapped in endosomal/lysosomal compartments.
|