ライフサイエンスコーパス: interferon-inducible protein 10

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.

3 Two chemokines, interferon inducible protein 10 and monocyte chemotactic

4 CXC chemokines (particularly CXCL10/interferon-inducible protein 10 and CXCL8/interleukin-8)

5 Furthermore, vasopressin decreased interferon-inducible protein 10 and granulocyte colony-s

6 ression construct repressed the iNOS, COX-2, interferon-inducible protein 10 and interferon-gamma mRN

7 CXCR3 ligands interferon-inducible protein 10 and monokine-induced by

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 uch as macrophage colony-stimulating factor, interferon-inducible protein 10, and interleukin-1 recep

13 ciated with elevated interleukin (IL) 12p40, interferon-inducible protein 10, and monocyte chemoattra

14 -alpha), monocyte chemoattractant protein 1, interferon-inducible protein 10, and RANTES, are upregul

15 In those with SVR, interferon-inducible protein 10, ATX, and Mac2BP levels

16 g factor, chemokine CXC ligand (CXCL) 1, and interferon inducible protein 10/CXCL10.

17 latory factor 2 module expression and plasma interferon-inducible protein-10/CXCL10 negatively correl

18 crophage colony-stimulating factor, eotaxin, interferon-inducible protein 10, cytokine-induced neutro

19 nterferon regulatory factor 7, CXCL10 [gamma interferon-inducible protein 10], gamma interferon, and

20 chemoattractant protein 1 (MCP-1), and gamma interferon-inducible protein 10 (gammaIP-10) mRNA transc

21 ymus-and-activation-regulated chemokine, and interferon-inducible protein 10 in their serum than did

22 flammatory chemokines CCL5/RANTES and CXCL10/interferon-inducible protein 10 in vitro.

23 ith the expression of CCL5/RANTES and CXCL10/interferon-inducible protein 10 in vivo.

24 chemoattractant protein (MCP)-1, MCP-2, and interferon-inducible protein-10 in the pancreas.

25 n of a T-cell chemoattractant, CXCL10 (gamma interferon-inducible protein 10) in response to viral in

26 e factors is the ELR-negative CXC chemokine, interferon inducible protein-10 (IP-10).

27 induced by interferon-gamma (MIG, CXCL9) and interferon inducible protein-10 (IP-10, CXCL10) during H

28 study, we examined the roles of CXCL10/gamma interferon-inducible protein 10 (IP-10) and CCL2/monocyt

29 -inducible genes; however, the expression of interferon-inducible protein 10 (IP-10) and interferon c

30 Because the human interferon-inducible protein 10 (IP-10) can also inhibit

31 l expressed and secreted (RANTES), and gamma interferon-inducible protein 10 (IP-10) expression indep

32 IL-8) and for angiostatic chemokines such as interferon-inducible protein 10 (IP-10) has been difficu

33 )-normalized measures of CD3epsilon mRNA and interferon-inducible protein 10 (IP-10) mRNA, and 18S rR

34 In addition, interferon-inducible protein 10 (IP-10) was identified a

35 yte chemoattractant protein 1 (MCP-1), gamma-interferon-inducible protein 10 (IP-10), and RANTES comp

36 ing, RSV-induced beta interferon (IFN-beta), interferon-inducible protein 10 (IP-10), chemokine ligan

37 xf1 +/- livers exhibited decreased levels of interferon-inducible protein 10 (IP-10), delayed inducti

38 onocyte chemotactic protein 1 (MCP-1), gamma-interferon-inducible protein 10 (IP-10), macrophage infl

39 solateral secretion of interleukin 8 (IL-8), interferon-inducible protein 10 (IP-10), monocyte chemot

40 feron beta (IFN-beta), interleukin 6 (IL-6), interferon-inducible protein 10 (IP-10), RANTES, and IL-

41 Mig is related functionally to interferon-inducible protein 10 (IP-10), with which it s

42 inflammatory protein-1alpha (MIP-1alpha) and interferon-inducible protein 10 (IP-10).

43 ma (IFN-gamma) and the downstream chemokines interferon-inducible protein-10 (IP-10) and monokine ind

44 NF-alpha), interleukin-1beta (IL-1beta), and interferon-inducible protein-10 (IP-10) by murine macrop

45 ack of induction of TNF-alpha, IL-1beta, and interferon-inducible protein-10 (IP-10) genes by CD14KO

46 Interferon-inducible protein-10 (IP-10) is a member of t

47 hat expression of the murine alpha-chemokine interferon-inducible protein-10 (IP-10) was higher in th

48 ong a large panel of chemokines tested, only interferon-inducible protein-10 (IP-10), interferon-gamm

49 The human cytokine, interferon-inducible protein-10 (IP-10), is a small glyc

50 ic protein-1 (MCP-1), and RANTES) and C-X-C (interferon-inducible protein-10 (IP-10), MIP-2, and cyto

51 IFN-gamma, interferon-inducible protein-10 (IP-10), tumor necrosis

52 hemokines that lack the ELR motif, including interferon-inducible protein 10 [IP-10 (CXCL10)] and mon

53 The expression of 3 ELR- CXC chemokines (interferon-inducible protein 10 [IP-10], monokine induce

54 cted chemokines (interleukin-8 [IL-8], gamma interferon-inducible protein 10 [IP-10], RANTES, monocyt

55 nterferon [HuMig], interleukin-8 [IL-8], and interferon-inducible protein-10 [IP-10]) and CC (macroph

56 e secretion of chemokines, including CXCL10 (interferon-inducible protein 10 kDa [IP-10]).

57 age inflammatory protein 1 alpha/beta, gamma interferon-inducible protein 10, macrophage chemotaxic p

58 chemotactic protein-3 [MCP-3], MCP-4, IL-8, interferon-inducible protein-10, macrophage-derived chem

59 eceptor antagonist, IL-4, IL-6, IL-8, IL-10, interferon-inducible protein-10, monocyte chemoattractan

60 lating factor, interleukin-6, interleukin-8, interferon-inducible protein-10, monocyte chemotactic pr

61 hat were upregulated included Eotaxin; gamma-interferon-inducible protein 10; monocyte chemoattractan

62 a subset of immune-related genes, including interferon-inducible protein 10, monokine induced by gam

63 viously that the ELR-negative CXC chemokines interferon-inducible protein 10, monokine induced by gam

64 e of 18S ribosomal RNA, CD3epsilon mRNA, and interferon-inducible protein-10 mRNA outperformed the me

65 ithout affecting IL-2, IL-12, IFN-gamma, and interferon-inducible protein 10 production in CD3/CD28-s

66 Plasma HCV, soluble CD14 (sCD14), interferon-inducible protein 10, soluble CD163 (sCD163),

67 Levels of chemokine mRNA (gamma interferon-inducible protein 10, T-cell activation gene

68 eak JNK activation, resulting in high IP-10 (interferon-inducible protein 10), tumor necrosis factor

69 fect was observed, with alpha interferon and interferon-inducible protein 10 undergoing significant e