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1 en due to resident macrophages that form the mononuclear phagocyte system.
2 a conserved organization of human and mouse mononuclear phagocyte system.
3 to unravel the functional complexity of the mononuclear phagocyte system.
4 of immune complexes (ICs) bearing C3 by the mononuclear phagocyte system.
5 ndency to be removed from circulation by the mononuclear phagocyte system.
6 its role to traffic immune complexes to the mononuclear phagocyte system.
7 inite period in tissues rich in cells of the mononuclear phagocyte system.
8 ted tissue, most often localized in cells of mononuclear phagocyte system.
9 dence that dendritic cells are a part of the mononuclear phagocyte system and are derived from a comm
10 show minimal uptake of pegylated NCPs by the mononuclear phagocyte system and excellent blood circula
11 an ontogenically distinct population in the mononuclear phagocyte system and have implications for t
12 ays in which nanoparticles interact with the mononuclear phagocyte system and impact its function dur
13 on of liposomes and silicon particles in the mononuclear phagocyte system and improved tumoritropic a
14 in in circulation, minimize clearance by the mononuclear phagocyte system, and limit uptake in health
15 process in immunobiology, with cells of the mononuclear phagocyte system being critical in mediating
16 the complexity of a central component of the mononuclear phagocyte system by using a new in vivo appr
19 Brucella melitensis chronically infects the mononuclear phagocyte system in BALB/c mice, but it caus
20 sis, thus compromising the efficiency of the mononuclear phagocyte system in dealing with infection.
23 endritic cells (DCs) from other cells of the mononuclear phagocyte system is complicated by the share
24 nduced depression in IL-12 production by the mononuclear phagocyte system may promote T-cell commitme
25 ffect of polymer structure in modulating the mononuclear phagocyte system (MPS) accumulation of polyi
28 -1 particles effectively avoid uptake by the mononuclear phagocyte system (MPS) in vivo with a long b
30 Ps and AuNPs were primarily deposited in the mononuclear phagocyte system (MPS) such as the liver and
31 he innate immune system, particularly of the mononuclear phagocyte system (MPS), its ontogeny and pot
34 vivo and their rapid uptake by cells of the mononuclear phagocyte system on intravenous administrati
36 factor receptor GFP transgene throughout the mononuclear phagocyte system), quantitative analysis of
37 ted hemoglobin modulates the response of the mononuclear phagocyte system to endotoxin, possibly thro
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