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1 inflammatory protein-1alpha and -1beta, and interferon-inducible protein-10.
2 emotactic protein-3, and the C-X-C chemokine interferon-inducible protein-10.
6 ression construct repressed the iNOS, COX-2, interferon-inducible protein 10 and interferon-gamma mRN
8 tor-alpha and interferon-gamma), chemokines (interferon-inducible protein-10 and monocyte chemoattrac
9 nokine induced by gamma interferon), CXCL10 (interferon-inducible protein 10), and CCL5 (RANTES) were
10 ractant protein-1, CCL5/RANTES, CXCL10/gamma interferon inducible protein-10, and kerotinocyte cytoki
11 e synthase (iNOS), cyclooxygenase-2 (COX-2), interferon-inducible protein 10, and interferon-gamma in
12 ciated with elevated interleukin (IL) 12p40, interferon-inducible protein 10, and monocyte chemoattra
13 -alpha), monocyte chemoattractant protein 1, interferon-inducible protein 10, and RANTES, are upregul
15 crophage colony-stimulating factor, eotaxin, interferon-inducible protein 10, cytokine-induced neutro
16 nterferon regulatory factor 7, CXCL10 [gamma interferon-inducible protein 10], gamma interferon, and
17 chemoattractant protein 1 (MCP-1), and gamma interferon-inducible protein 10 (gammaIP-10) mRNA transc
18 ymus-and-activation-regulated chemokine, and interferon-inducible protein 10 in their serum than did
22 n of a T-cell chemoattractant, CXCL10 (gamma interferon-inducible protein 10) in response to viral in
24 induced by interferon-gamma (MIG, CXCL9) and interferon inducible protein-10 (IP-10, CXCL10) during H
25 study, we examined the roles of CXCL10/gamma interferon-inducible protein 10 (IP-10) and CCL2/monocyt
26 -inducible genes; however, the expression of interferon-inducible protein 10 (IP-10) and interferon c
28 l expressed and secreted (RANTES), and gamma interferon-inducible protein 10 (IP-10) expression indep
29 IL-8) and for angiostatic chemokines such as interferon-inducible protein 10 (IP-10) has been difficu
30 )-normalized measures of CD3epsilon mRNA and interferon-inducible protein 10 (IP-10) mRNA, and 18S rR
32 yte chemoattractant protein 1 (MCP-1), gamma-interferon-inducible protein 10 (IP-10), and RANTES comp
33 ing, RSV-induced beta interferon (IFN-beta), interferon-inducible protein 10 (IP-10), chemokine ligan
34 xf1 +/- livers exhibited decreased levels of interferon-inducible protein 10 (IP-10), delayed inducti
35 onocyte chemotactic protein 1 (MCP-1), gamma-interferon-inducible protein 10 (IP-10), macrophage infl
36 solateral secretion of interleukin 8 (IL-8), interferon-inducible protein 10 (IP-10), monocyte chemot
37 feron beta (IFN-beta), interleukin 6 (IL-6), interferon-inducible protein 10 (IP-10), RANTES, and IL-
40 ma (IFN-gamma) and the downstream chemokines interferon-inducible protein-10 (IP-10) and monokine ind
41 NF-alpha), interleukin-1beta (IL-1beta), and interferon-inducible protein-10 (IP-10) by murine macrop
42 ack of induction of TNF-alpha, IL-1beta, and interferon-inducible protein-10 (IP-10) genes by CD14KO
44 hat expression of the murine alpha-chemokine interferon-inducible protein-10 (IP-10) was higher in th
45 ong a large panel of chemokines tested, only interferon-inducible protein-10 (IP-10), interferon-gamm
47 ic protein-1 (MCP-1), and RANTES) and C-X-C (interferon-inducible protein-10 (IP-10), MIP-2, and cyto
49 hemokines that lack the ELR motif, including interferon-inducible protein 10 [IP-10 (CXCL10)] and mon
50 The expression of 3 ELR- CXC chemokines (interferon-inducible protein 10 [IP-10], monokine induce
51 cted chemokines (interleukin-8 [IL-8], gamma interferon-inducible protein 10 [IP-10], RANTES, monocyt
52 nterferon [HuMig], interleukin-8 [IL-8], and interferon-inducible protein-10 [IP-10]) and CC (macroph
54 age inflammatory protein 1 alpha/beta, gamma interferon-inducible protein 10, macrophage chemotaxic p
55 chemotactic protein-3 [MCP-3], MCP-4, IL-8, interferon-inducible protein-10, macrophage-derived chem
56 eceptor antagonist, IL-4, IL-6, IL-8, IL-10, interferon-inducible protein-10, monocyte chemoattractan
57 lating factor, interleukin-6, interleukin-8, interferon-inducible protein-10, monocyte chemotactic pr
58 hat were upregulated included Eotaxin; gamma-interferon-inducible protein 10; monocyte chemoattractan
59 a subset of immune-related genes, including interferon-inducible protein 10, monokine induced by gam
60 viously that the ELR-negative CXC chemokines interferon-inducible protein 10, monokine induced by gam
61 e of 18S ribosomal RNA, CD3epsilon mRNA, and interferon-inducible protein-10 mRNA outperformed the me
62 ithout affecting IL-2, IL-12, IFN-gamma, and interferon-inducible protein 10 production in CD3/CD28-s
64 eak JNK activation, resulting in high IP-10 (interferon-inducible protein 10), tumor necrosis factor
65 fect was observed, with alpha interferon and interferon-inducible protein 10 undergoing significant e
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