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1 d activation-regulated chemokine) and CCL22 (macrophage-derived chemokine).
2 ated chemokines CCL11 (eotaxin-1) and CCL22 (macrophage-derived chemokine).
3 such as RANTES, stroma-derived factor-1, and macrophage-derived chemokine.
4 a) but lower levels of the anti-inflammatory macrophage-derived chemokine.
5 m, i.e., the inhibition of the production of macrophage-derived chemokines.
8 gulation of mRNA for the receptors CCR4 (for macrophage-derived chemokine and thymus and activation-r
9 ct the entire lung and induce high levels of macrophage-derived chemokines and cytokines, which resul
10 ry and activation-regulated chemokine, CCL22/macrophage-derived chemokine, and CCL26/eotaxin-3), T(H)
11 axin-3, interferon gamma-induced protein 10, macrophage-derived chemokine, and macrophage inflammator
13 mus-expressed chemokine, eotaxin, eotaxin 2, macrophage-derived chemokines, and C10 were also induced
15 ed CD169(+)marginal zone macrophages and the macrophage-derived chemokine CCL22 to increase splenic C
16 sion of macrophage inflammatory proteins and macrophage-derived chemokine (CCL22) in the synovial tis
17 p-regulation of CCR4 and one of its ligands, macrophage-derived chemokine (CCL22), and that tolerance
18 s toxin, neutralization of the CC chemokine, macrophage-derived chemokine (CCL22), or by desensitizat
19 and activation-regulated chemokine/CCL17 and macrophage-derived chemokine/CCL22 in the lung after all
20 L, the production of the Th2-chemokines MDC (macrophage-derived chemokine/CCL22) and TARC (thymus and
24 (thymus and activation-regulated chemokine, macrophage-derived chemokine) correlated with airway eos
26 L-6, IL-8, CD38, and CD69 and down-regulated macrophage-derived chemokine, human leukocyte antigen DR
27 38, and CD69 were reduced, whereas levels of macrophage-derived chemokine, human leukocyte antigen DR
28 ymus- and activation-regulated chemokine and macrophage-derived chemokine, ligands for CCR4, were mea
29 ruiting chemotactic factors, including IL-8, macrophage-derived chemokine, macrophage inflammatory pr
30 ed pigment epithelium-derived factor (PEDF), macrophage derived chemokine (MDC), systolic blood press
31 Interleukin 1 receptor antagonist (IL-1ra), macrophage-derived chemokine (MDC) and macrophage inflam
34 skin were found to up-regulate expression of macrophage-derived chemokine (MDC) during maturation int
40 nd activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC)), CD (10 proteins), a
43 (IL)-12, tumor necrosis factor (TNF)-alpha, macrophage-derived chemokine (MDC), and C10, known to en
44 crophage colony-stimulating factor (GM-CSF), macrophage-derived chemokine (MDC), and macrophage infla
45 induce the release of CC chemokines, RANTES, macrophage-derived chemokine (MDC), macrophage inflammat
46 actant protein (MCP)-1, MCP-2, MCP-3, MCP-4, macrophage-derived chemokine (MDC), macrophage migration
48 arily as a mixture of three beta chemokines [macrophage-derived chemokine (MDC), thymus and activatio
49 and I-309 were induced by LPS; in addition, macrophage-derived chemokine (MDC), thymus and activatio
53 induced protein of 10-kDa (IP-10)/CXCL10 and macrophage-derived chemokine (MDC)/CCL22 production were
54 activation-regulated chemokine (TARC)/CCL17, macrophage-derived chemokine (MDC)/CCL22, I-309/CCL1) an
56 te chemoattractant protein-3 (MCP-3/CCL7) or macrophage-derived chemokine (MDC/CCL22), elicited anti-
57 kine/CC chemokine ligand 17 (TARC/CCL17) and macrophage-derived chemokine (MDC/CCL22), which preferen
60 CP-4, IL-8, interferon-inducible protein-10, macrophage-derived chemokine [MDC], and platelet factor-
61 d T cell chemoattractant protein-1 (STCP-1) (macrophage-derived chemokine; MDC), a recently described
62 ion regulated chemokine; TARC) and CCL22 (or macrophage-derived chemokine; MDC), in Th2-type cytokine
63 A-specific IgE responses, but have defective macrophage-derived chemokine-mediated CD4+ T cell migrat
64 platelet aggregation induced by SDF-1alpha, macrophage-derived chemokine, or thymus and activation-r
65 d other inflammatory diseases by suppressing macrophage-derived chemokine production via the EP4 rece
66 ial paracrine effect of endogenous PGE(2) on macrophage-derived chemokine production, we co-cultured
69 ducible chemokines such as C10, eotaxin, and macrophage-derived chemokine were significantly lower in
70 A)R expression was increased in macrophages, macrophage-derived chemokines were reduced in response t