ライフサイエンスコーパス: alpha-chemokine

1 dentified as a portion of the mob-1 gene, an alpha-chemokine.

2 uctural homology with an important domain on alpha chemokines.

3 activated by IL-8, GROalpha, and a few other alpha chemokines.

4 as opposing effects on the expression of two alpha-chemokines.

5 six-stranded sheet similar to that found in alpha-chemokines.

6 N-fragment depends on an ELR motif found in alpha-chemokines and conserved among mammalian TyrRSs, h

7 or, eg, interleukin 1, tumor necrosis factor alpha, chemokines, and cell adhesion molecules) pathways

8 any pro-inflammatory cytokines including TNF alpha, chemokines, and growth factors are expressed in d

9 alpha-Chemokines are known heparin-binding proteins.

10 IL-20, IL-21, IL-28A, tumor necrosis factor-alpha, chemokine C-C motif ligand [CCL]13, CCL26, chemok

11 (IL-1beta), tumor necrosis factor alpha (TNF-alpha), chemokine (C-C motif) ligand 5 (CCL 5), chemokin

12 increased secretion of tumor necrosis factor-alpha, chemokine (C-C motif) ligand 5, and monocyte chem

13 rominent expression of tumor necrosis factor-alpha; chemokine (C-X-C motif) ligand 1; stromal cell-de

14 alpha-Chemokines comprise a family of cytokines that are

15 The two alpha-chemokines, connective tissue activating peptide-I

16 ted increased levels of IFN-inducible T cell alpha-chemokine/CXCL11 mRNA in the CNS and decreased lev

17 GRO proteins are alpha-chemokine cytokines that attract neutrophils and s

18 ntial display to identify Mob-1, a member of alpha-chemokine family, as one of the immediate transcri

19 Induction of alpha-chemokine gene expression was quantitated by real-

20 role for differential induction of the three alpha-chemokine genes in corneal inflammatory processes

21 ES, MIP-1alpha, MIP-1beta, and MCP-1 nor the alpha-chemokine IL-8 had an effect on infection of eithe

22 nized cDNA expression cassettes encoding the alpha-chemokines IL-8 and SDF-1alpha and the beta-chemok

23 n 1 (MCP-1; CCL2), and I-309 (CCL1), and one alpha chemokine, IL-8 (CXCL8); all correlated with monoc

24 In this work we demonstrate that the CXC or alpha-chemokines, IL-8 and melanoma growth stimulatory a

25 de mice showed that expression of the murine alpha-chemokine interferon-inducible protein-10 (IP-10)

26 d secreted chemokine (RANTES) as well as the alpha-chemokines: interferon-gamma-inducible protein (IP

27 epatitis C virus (HCV) infection induces the alpha-chemokine interleukin-8 (CXCL-8), which is regulat

28 okines: interleukin-6, tumor necrosis factor-alpha; chemokine: keratinocyte stimulating factor) were

29 XCR4 receptors, similar to the physiological alpha-chemokine ligands, stromal cell-derived factor (SD

30 st activity on the related, but distinct rat alpha-chemokine macrophage-inflammatory protein 2.

31 ukin-1beta [IL-1beta], tumor necrosis factor alpha), chemokine (macrophage inflammatory protein 2), T

32 mma, interleukin 2, or tumor necrosis factor alpha), chemokine (macrophage inhibitory factor 1beta),

33 uggest that hIRH, although having the -CXC-, alpha chemokine motif, and exhibiting in vivo and in vit

34 5,ELR>AAR into CINC, we have developed a rat alpha-chemokine receptor antagonist (ra) analogous to a

35 pression of the alpha4beta7 integrin and the alpha-chemokine receptor CXCR2.

36 e-adapted strains of FIV are able to use the alpha-chemokine receptor CXCR4 for cell fusion.

37 Recently, the alpha-chemokine receptor CXCR4 has been reported to medi

38 The alpha-chemokine receptor CXCR4 has recently been shown t

39 The feline homolog of the alpha-chemokine receptor CXCR4 has recently been shown t

40 The alpha-chemokine receptor fusin (CXCR-4) and beta-chemoki

41 emonstrate for the first time that the CXCR4 alpha-chemokine receptor is expressed on cells of the me

42 pregulation of exodus 2 beta-chemokine, RDC1 alpha-chemokine receptor, and transforming growth factor

43 cells and observed robust expression of the alpha chemokine receptors CXCR-1 and CXCR-2.

44 transfected cells revealed that subfamily of alpha chemokine receptors CXCR5 and CXCR3 mediated the c

45 irst time constitutive expression of the CXC/alpha chemokine receptors, CXCR1, CXCR2 and CXCR3, on ol

46 phocyte chemotaxis to 6CK/SLC but not to the alpha chemokine SDF-1 (stromal cell-derived factor); and

47 ne marrow and lymph nodes, which secrete the alpha-chemokine SDF-1.

48 The alpha-chemokine stromal cell-derived factor (SDF)-1alpha

49 CXCR4 is the receptor for the alpha-chemokine stromal cell-derived factor 1 (SDF-1) an

50 de sharing sequence characteristics with the alpha-chemokine superfamily.

51 stromal cell-derived factor-1 (SDF-1) is an alpha chemokine that binds to the CXCR4 receptor.

52 However, in contrast to other alpha chemokines that induce neutrophil migration, IP-10

53 -cell alpha-chemoattractant) gene encodes an alpha-chemokine that is a potent chemoattractant for act

54 -CTAP is the longest defined structure of an alpha-chemokine to date.

55 e, which is a potent inhibitor of binding of alpha-chemokines to their receptors on neutrophils.

56 2 potential HCMV virulence genes that encode alpha -chemokines: UL146 and UL147.

57 As the first example of a virus-encoded alpha chemokine, vCXC-1 may ensure the active recruitmen

58 ifferential effects on the expression of two alpha-chemokines; whereas the Glu-Lys-Arg (ELR)(-) chemo

59 The two chemokine subfamilies are alpha(alpha)-chemokines, which primarily function as neutrophi