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1 ic cells, Langerhans cells, and interstitial dermal dendritic cells.
2 , which was brief but sufficient to activate dermal dendritic cells.
3 ers of lymph node-resident but not migratory dermal dendritic cells.
4 en by pMHCII presentation by local CD11b(hi) dermal dendritic cells.
5 mal injection by LECs was similar to that of dermal dendritic cells.
6 ere revealed to be T-cells, macrophages, and dermal dendritic cells.
10 ells, infiltrating epidermal CD8(+) T cells, dermal dendritic cells and macrophages, and increased ex
11 ection of Langerhans cells, macrophages, and dermal dendritic cells, and these cells emigrated from s
13 ection of Langerhans cells, macrophages, and dermal dendritic cells by 75-90% and reduced the overall
16 es occur via 'cooperation' between migratory dermal dendritic cells (DCs) and basophils positive for
17 ed by CD31(+) endothelial cells and CD11c(+) dermal dendritic cells (DCs) in lesional psoriatic skin.
18 sease, P. gingivalis associates in situ with dermal dendritic cells (DCs), many of which express DC-S
19 inducible elimination of LCs and Langerin(+) dermal dendritic cells (dDCs) after administration of di
20 harbours specialized immune cells, including dermal dendritic cells (DDCs) and interleukin (IL)-17-pr
21 avital two-photon microscopy, we report that dermal dendritic cells (DDCs) and Langerhans cells (LCs)
22 of human skin migratory CD1a+ LCs and CD11c+ dermal dendritic cells (DDCs) demonstrated significant d
23 capacity of human Langerhans cells (LCs) and dermal dendritic cells (DDCs) to induce antigen-specific
25 l lipid antigens to specific T cells whereas dermal dendritic cells express much less CD1a molecules
26 rhans cells, expressing CD1a and HLA-DR, and dermal dendritic cells, expressing HLA-DR, are known to
27 difference in the migration of hapten-laden dermal dendritic cells (FITC+, CD11c+, Langerin-) into t
29 of CD1 was detected on cortical thymocytes, dermal dendritic cells in the skin, follicular dendritic
30 onal and monocyte derived) but not migratory dermal dendritic cells in the skin-draining lymph nodes
31 y taken up by epidermal Langerhans cells and dermal dendritic cells in the vicinity of the MCs or tra
32 in the number of resident (but not migratory dermal) dendritic cells in the lymph node but showed no
33 ls, including Langerhans cells, macrophages, dermal dendritic cells, mast cells, fibroblasts, and lym
34 eration of contact hypersensitivity and that dermal dendritic cells may play a more important role.
35 fection of Langerhans cells and interstitial dermal dendritic cells results in an impaired ability to
36 A to the skin can target distinct subsets of dermal dendritic cells to confer a superior immune respo
38 yte-derived dendritic cells and interstitial dermal dendritic cells, yet the virus fully replicates o
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