ライフサイエンスコーパス: chemokine CXCL10

1 ent of the chemokine receptor CXCR3 with the chemokine CXCL10.

2 cking such a reentry by neutralizing the key chemokine CXCL10.

3 , but with increased mRNA for the T-cell Th1 chemokine CXCL10.

4 hment, which was mediated by the LEC-derived chemokine CXCL10.

5 ion of the type I interferon (IFN)-regulated chemokine CXCL10.

6 ntrol by the cytokine interleukin-13 and the chemokine CXCL10.

7 response genes, IFN-induced GTPases, and the chemokine CXCL10.

8 on of the transcription factor IRF1, and the chemokine, CXCL10.

9 f IL-12, IFN-gamma and the IFN-gamma induced chemokine, CXCL10.

10 cterized by significant up-regulation of the chemokine, CXCL10.

11 ion of an IFN-inducible and STAT-1-dependent chemokine, CXCL10.

12 N-gamma transcript and the IFN-gamma-induced chemokine, CXCL10.

13 latelet-derived growth factor (PDGF) and the chemokine, CXCL10.

14 interferon regulatory factor, IRF1, and the chemokine, CXCL10.

15 e highly upregulated downstream of CCL2; the chemokine CXCL10 and its cognate receptor, CXCR3, stood

16 crobial peptides beta-defensin 3, CRAMP, and chemokine CXCL10 and its receptor CXCR3 in corneal epith

17 ed that blocking the interaction between the chemokine CXCL10 and its receptor CXCR3 on activated CTL

18 ementia and demonstrated the presence of the chemokine CXCL10 and its receptor, CXCR3, in the neurons

19 ease of proinflammatory cytokines (IL-6) and chemokines (CXCL10 and CCL5).

20 BC), neopterin levels, and concentrations of chemokines CXCL10 and CCL2.

21 essential for IL-1-induced expression of the chemokines CXCL10 and CCL5, which recruit mononuclear ce

22 Immature myeloid cells in dLNs expressed the chemokines CXCL10 and CXCL16 in an IFN-gamma-dependent m

23 ymphocytes are recruited into the CNS by the chemokines CXCL10 and CXCL9.

24 nstrate that estradiol induces expression of chemokines CXCL10 and/or CXCL11 within human endometrium

25 osphorylation, production of type I IFN, the chemokine CXCL10, as well as caspase-9-mediated tumor ce

26 ne of CA-MRSA, and the related SPA-releasing chemokine CXCL10 bound to both cell wall and cell membra

27 us studies have shown that expression of the chemokine CXCL10 by West Nile virus (WNV)-infected neuro

28 patients with active cryptosporidiosis, four chemokines (CXCL10, CCL11 [eotaxin], CCL5 [RANTES], and

29 ha [TNF-alpha] and interleukin-6 [IL-6]) and chemokines (CXCL10, CCL2, CCL3, and CCL5) correlated wit

30 essed the expression of the genes encoding 3 chemokines, CXCL10, CCL2, and CCL20, and repressed CXCL1

31 The chemokine, CXCL10, chemotactic for NK cells, activated T

32 Levels of the chemokines CXCL10, CXCL11, CCL4, and CCL5 increased in b

33 Expression of the Th1-associated chemokines CXCL10, CXCL9, CCL5, and CXCL11 was elevated

34 alpha-toxin in the induction of Th1-related chemokine CXCL10 diversely, which could favour the recru

35 ti-photon microscopy to demonstrate that the chemokine CXCL10 enhances the ability of CD8+ T cells to

36 The chemokine CXCL10 has been associated with several autoim

37 report, we investigated the role of the CXC chemokine CXCL10 (IFN-gamma-inducible protein-10) in the

38 dition, the metastatic IECs also induced the chemokine CXCL10 in a TLR3-, TRIF-, and IRF3-dependent m

39 during viral infection through induction of chemokine CXCL10 in central nervous system epithelial an

40 ionally, coculture induced expression of the chemokine CXCL10 in MSCs and the cognate receptor CXCR3

41 ced an overactivation of the proinflammatory chemokine CXCL10 in PBMC from NCGS patients, and that th

42 Various cell types can produce the chemokine CXCL10 in response to IFN-gamma stimulation.

43 ts demonstrate an important role for the CXC chemokine CXCL10 in the recruitment and accumulation of

44 that PND patients harbor high levels of the chemokine CXCL10 in their CSF.

45 Mass spectrometry identified the potent chemokine, CXCL10, in the EVs, which was markedly enrich

46 The chemokines CXCL10/interferon-gamma-inducible protein of

47 The chemokine CXCL10 (IP-10) was significantly elevated (> 2

48 infection by upregulating expression of the chemokine CXCL10 (IP-10).

49 The chemokine CXCL10/IP-10 facilitates recruitment of Th1-ty

50 additional secreted proteins, including the chemokine CXCL10/IP10.

51 The chemokine CXCL10 is expressed early after virus infectio

52 eviously reported that the IFN-gamma-induced chemokine CXCL10 is expressed in lesional skin from viti

53 The chemokine CXCL10 is expressed within the CNS in response

54 e (AD) patients and in AD animal models, the chemokine CXCL10 is found in high concentrations, sugges

55 The chemokine CXCL10 is produced by many inflammatory cells

56 ht to investigate the mechanism by which the chemokine CXCL10 mediates bactericidal activity against

57 ion plasmids; 2) by inhibiting DMXAA-induced chemokine (CXCL10) mRNA and protein production in the AB

58 The non-ELR-CXC chemokine, CXCL10 or IP-10, is chemotactic for monocytes

59 otropic TG delivery of the T cell-attracting chemokine CXCL10 (pull), boosted the number and function

60 In contrast, the T-cell attractant chemokine CXCL10 showed an almost 10-fold higher express

61 ptor type 6 (CXCR6) on MSCs and MSCs secrete chemokine CXCL10 that binds to receptor CXCR3 on BCCs, d

62 The expression of the chemokine CXCL10 was initially detected in neurons as ea

63 cell-deficient mice with the IFN-I-dependent chemokine, CXCL10 was also sufficient to improve sepsis

64 sponse to infection-induced elevation of the chemokine CXCL10, which attracted CXCR3(+) memory CD8(+)

65 or levels of IFN-gamma and the IFN-inducible chemokine CXCL10, which is a ligand for CXCR3.

66 es leads to transcriptional induction of the chemokine CXCL10, which is considered an interferon (IFN

67 sponse to WNV infection, neurons secrete the chemokine CXCL10, which recruits effector T cells via th