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1 g the luminal deposition of platelet-derived regulated on activation normal T cell expressed and secr
2 her chemokines (MCP-1, MCP-3, MCP-4, RANTES (regulated on activation normal T cell expressed and secr
3 ne induced by gamma-interferon), and RANTES (regulated on activation normal T cell expressed and secr
4 e natural chemokine ligands of CCR5, RANTES (regulated on activation normal T cell expressed and secr
5 ttractant protein-1), MIP-1beta, and RANTES (regulated on activation normal T cell expressed and secr
6 R848, and CpG-mediated production of RANTES (regulated on activation normal T cell expressed and secr
7 emokines and inflammatory cytokines, such as regulated on activation normal T cell expressed and secr
8 itors composed of one CCR5-targeting RANTES (regulated on activation normal T cell expressed and secr
9 and IL-10) and chemokines, including RANTES (regulated on activation normal T cell expressed and secr
10 MIP-1beta, and MIP-2 were increased, whereas regulated on activation normal T cell expressed and secr
11 IL-8, macrophage inflammatory protein-1beta, regulated on activation normal T cell expressed and secr
12 ammatory mediators interleukin (IL)-6, IL-8, regulated on activation normal T cell expressed and secr
13 to adaptive immunity (MIP-3alpha and RANTES (regulated on activation normal T cell expressed and secr
14 L triggered the accumulation of CCL5/RANTES (regulated on activation normal T cell expressed and secr
15                                      RANTES (regulated on activation normal T cell expressed and secr
16 -induced production of the chemokine RANTES (regulated on activation normal T cell expressed and secr
17 dingly, we found a rapid increase in RANTES (regulated on activation normal T cell expressed and secr
18 pha-induced interleukin-6 secretion, whereas regulated on activation normal T cell expressed and secr
19                        The chemokine RANTES (regulated on activation normal T cell expressed and secr
20 e IFNbeta augmented TNFalpha-induced RANTES (regulated on activation normal T cell expressed and secr
21                      However, high levels of Regulated on Activation Normal T cell Expressed And Secr
22 desensitized their responsiveness to RANTES (regulated on activation normal T cell expressed and secr
23                   In the presence of RANTES (regulated on activation normal T cell expressed and secr
24 o the promoter of the chemokine gene RANTES (regulated on activation normal T cell expressed and secr
25 roglobulin, IL-1alpha, Mcp-1 and -3, RANTES (regulated on activation normal T cell expressed and secr
26 , interferon gamma inducible protein-10, and regulated on activation normal T cell expressed and secr
27                                      RANTES (regulated on activation normal T cell expressed and secr
28 y mediators, including the chemokine RANTES (regulated on activation normal T cell expressed and secr
29                                      RANTES (regulated on activation normal T cell expressed and secr
30 feron A/B genes as well as chemokine RANTES (regulated on activation normal T cell expressed and secr
31 matory protein- (MIP) 1alpha, MIP-1beta, and regulated on activation normal T cell expressed and secr
32 ttractants, including the chemokines RANTES (regulated on activation normal T cell expressed and secr
33 l-Met-Leu-Phe and the beta-chemokine RANTES (regulated on activation normal T cell expressed and secr
34 matory cytokines and chemokines (IL-6, IL-8, regulated on activation normal T cell expressed and secr
35 protein (MIP)-1alpha, MIP-1beta, and RANTES (regulated on activation normal T cell expressed and secr
36 be secreted by activated CD8+ cells, RANTES (regulated on activation normal T cell expressed and secr
37 thelin-1 (ET-1), interleukin-10 (IL-10), and regulated on activation normal T cells expressed and sec
38 cation in the M/M system; (ii) antibodies to regulated on activation normal T-cell expressed and Secr
39 eta, B lymphocyte chemoattractant (BLC), and regulated on activation normal T-cell expressed and secr
40 itor of metalloproteinases 1/2], and RANTES [regulated on activation normal T-cell expressed and secr
41 d poly I:C) mainly induced the expression of regulated on activation normal T-cell expressed and secr
42 ined by real time RT-PCR and, in the case of regulated on activation normal T-cell expressed and secr
43  monocyte chemoattractant protein-1 (MCP-1), regulated on activation normal T-cell expressed and secr
44 r (TNF)-alpha, interleukin (IL)-6, IL-8, and regulated on activation normal T-cell expressed and secr
45 inflammatory protein-1alpha, or CCL5/RANTES (regulated on activation normal T-cell expressed and secr
46 ion levels of the ligands of CCR1 and/or -5, regulated on activation normal T-cell expressed and secr
47 mulated modestly lower production of RANTES (Regulated on Activation Normal T-cell Expressed and Secr
48 inducible nitric oxide synthase) and RANTES (regulated on activation normal T-cell expressed and secr
49 r-luciferase NF-kappaB responsive construct, regulated on activation normal T-cell expressed and secr
50 ucible T-cell alpha chemoattractant (I-TAC), regulated on activation normal T-cell expressed and secr
51 ucible-T cell alpha chemoattractant (I-TAC), regulated on activation normal T-cell expressed and secr
52 infection enhanced IL-8 mRNA levels, whereas regulated on activation normal T-cell expressed and secr
53 cells induced endothelial cell expression of regulated on activation normal T-cell expressed and secr
54 ge inflammatory protein (MIP)-1alpha, MIP-2, regulated on activation normal T-cell expressed and secr
55 , monocyte chemotactic protein-1 (MCP-1) and regulated on activation normal T-cell expressed and secr
56                       The expression of CCL5/regulated on activation normal T-cell expressed and secr
57 cted allografts, there was overexpression of regulated on activation normal T-cell expressed and secr
58 plasminogen activator inhibitor (PAI-1), and regulated on activation, normal T cell expressed and sec
59 ha, IL-1alpha (Interleukin-1 alpha), RANTES (regulated on activation, normal T cell expressed and sec
60       Several chemo-kines, including RANTES (regulated on activation, normal T cell expressed and sec
61                   The beta-chemokine RANTES (regulated on activation, normal T cell expressed and sec
62                     The CCR5 ligands RANTES (regulated on activation, normal T cell expressed and sec
63 e-2, monocyte chemoattractant protein-1, and regulated on activation, normal T cell expressed and sec
64 eated a series of chimeric MCP-1 and RANTES (regulated on activation, normal T cell expressed and sec
65 tentiates induction of the chemokine RANTES (regulated on activation, normal T cell expressed and sec
66  (IL-6), TNF-alpha, IL-8, MCP-1, and RANTES (Regulated on Activation, Normal T Cell Expressed and Sec
67 e chemotactic protein 1 (MCP-1), and RANTES (regulated on activation, normal T cell expressed and sec
68 C motif) receptor 5 inhibitors, 5P12-RANTES (regulated on activation, normal T cell expressed and sec
69 s, and suppressed expression of both RANTES (regulated on activation, normal T cell expressed and sec
70 t upregulation of mRNA and protein levels of regulated on activation, normal T cell expressed and sec
71 ated chemokines such as fractalkine, RANTES (regulated on activation, normal T cell expressed and sec
72                                              Regulated on activation, normal T cell expressed and sec
73  monocyte chemoattractant protein-1 (MCP-1), regulated on activation, normal T cell expressed and sec
74 ha and -beta and chemokines, such as RANTES (regulated on activation, normal T cell expressed and sec
75                  The beta-chemokines RANTES (regulated on activation, normal T cell expressed and sec
76                      SCH-C inhibited RANTES (regulated on activation, normal T cell expressed and sec
77 ate these pathways to induce IFN-alpha/beta, regulated on activation, normal T cell expressed and sec
78 ery of the platelet-derived chemokines CCL5 (regulated on activation, normal T cell expressed and sec
79 on and production of inflammatory cytokines: regulated on activation, normal T cell expressed and sec
80                                      RANTES (regulated on activation, normal T cell expressed and sec
81 ncrease CNS levels of the chemokines RANTES (regulated on activation, normal T cell expressed and sec
82                        The chemokine RANTES (regulated on activation, normal T cell expressed and sec
83                   The discovery that RANTES (regulated on activation, normal T cell expressed and sec
84 sis, the eosinophil chemotactic responses of regulated on activation, normal T cell expressed and sec
85 /microglia, that the beta-chemokines RANTES (regulated on activation, normal T cell expressed and sec
86                    The CC chemokines RANTES (regulated on activation, normal T cell expressed and sec
87 chemokines cytokine-response gene-2 (CRG-2), regulated on activation, normal T cell expressed and sec
88 rophage inflammatory protein 1beta-, RANTES (regulated on activation, normal T cell expressed and sec
89 protein (MIP)-1alpha, MIP-1beta, and RANTES (regulated on activation, normal T cell expressed and sec
90 uced tumor necrosis factor-alpha and RANTES (regulated on activation, normal T cell expressed, and se
91 age inflammatory protein-1alpha, and RANTES (regulated on activation, normal T cell expressed, and se
92 Important among these chemokines are RANTES (regulated on activation, normal T cell-expressed and -se
93 crophage inflammatory protein-1alpha/RANTES (regulated on activation, normal T cell-expressed and sec
94 macrophage-inflammatory protein-1 alpha, and regulated on activation, normal T cells expressed and se
95 on-gamma-inducible protein of 10 kd, KC, and regulated on activation, normal T-cell expressed and sec
96  macrophage inflammatory protein-1 alpha and regulated on activation, normal T-cell expressed and sec
97         Expression of MIP-1alpha; MIP-1beta; regulated on activation, normal T-cell expressed and sec
98  growth factor, interleukin-12 (p40/70), and regulated on activation, normal T-cell expressed and sec
99 ha), monocyte chemoattractant protein 1, and regulated on activation, normal T-cell expressed and sec
100 sed levels of the HIF-1-dependent chemokine, regulated on activation, normal T-cell expressed and sec
101 ng growth factor-beta(1), eotaxin-1, RANTES (regulated on activation, normal T-cell expressed and sec
102  concentrations of ligands for CCR5 (RANTES [regulated on activation, normal T-cell expressed and sec
103  chemoattractant protein-1) and CCR5/RANTES (regulated on activation, normal T-cell expressed and sec
104 of stromal cell-derived factor 1 (SDF-1) and regulated on activation, normal T-cell expressed and sec
105 okine induced by interferon-gamma (Mig); and regulated on activation, normal T-cell expressed and sec
106 age inflammatory protein-1 beta) and RANTES (regulated on activation, normal T-cell expressed and sec
107  of NF-kappaB ligand (RANKL), interleukin-6, Regulated on activation, normal T-cell expressed, and se
108 otein-2; monocyte chemotactic protein-1; and regulated on activation, normal T-cell expressed, and se
109 GF [platelet-derived growth factor], RANTES [regulated on activation, normal T-cell-expressed and sec
110               Whereas three beta chemokines, regulated-on-activation normal T-cell expressed and secr
111                                    Levels of regulated-on-activation, normal T cell-expressed and -se
112  and secretion of interleukin (IL)-6 and the regulated-on-activation, normal T-cell expressed and sec

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