ライフサイエンスコーパス: monocytoid

1 ctivated monocytes/macrophages, and CD11c(+) monocytoid and CD11c(-) plasmacytoid dendritic cells (mD

2 al zone lymphoma (14 of 14 cases) and in the monocytoid and plasmacytic cells in extranodal marginal

3 sfected cells and elicited the chemotaxis of monocytoid and T-lymphoid cells.

4 Lesional DC subsets, CD11c(+) (monocytoid) and CD11c(-) (plasmacytoid), expressed activ

5 Monocytoid B cells showed weak expression, whereas plasm

6 homorphologic features included monocytosis, monocytoid blasts, aberrant expression of phosphoSTAT5,

7 Toll-like receptors, antimicrobial peptides, monocytoid cell activation markers, and numerous genes a

8 ry mononuclear phagocytes, as well as in the monocytoid cell line U937.

9 blocks binding of WEHI78/24 cells, a murine monocytoid cell line, to inflamed lymph node HEV and inh

10 XCL17-responsive monocytes, and in the THP-1 monocytoid cell line.

11 ther examined by in vitro experiments with a monocytoid cell line.

12 tly transduced marker genes into human T and monocytoid cell lines and, in contrast to a murine leuke

13 he effects of adhesion of the representative monocytoid cell lines, THP-1 and U937, to purified extra

14 ere studied by coculturing human Mo or human monocytoid cell lines, U937 and THP-1, with porcine EC.

15 e expression in latently infected T-cell and monocytoid cell lines.

16 human immunodeficiency virus type 1-infected monocytoid cell lines.

17 Apoptosis of monocytoid cells (human monocytes and U937 cells) was in

18 l vein endothelial cells (ECV 304) and human monocytoid cells (THP-1) were studied in a functional bi

19 s, phorbol ester-stimulated adhesion of U937 monocytoid cells and culturing of peripheral blood neutr

20 t annexin II on the surface of both cultured monocytoid cells and monocyte-derived macrophages promot

21 n was a potent inhibitor of adhesion of U937 monocytoid cells and neutrophils to fibrin gel and immob

22 ated anaerobic bacteria on HIV expression in monocytoid cells and T cells were examined.

23 derate)CD11c(-)CD123(-) cells that resembled monocytoid cells but failed to acquire a DC phenotype up

24 51 prevents adhesion of normal monocytes and monocytoid cells to intact aortic endothelium from chole

25 hat HDL no longer decreased adhesion of U937 monocytoid cells to tumor necrosis factor (TNF)alpha-sti

26 THP-1 monocytoid cells were activated to comparable extents by

27 When human or murine monocytoid cells were induced to differentiate into macr

28 Following an initial expansion of myeloid/monocytoid cells within the initial 2 wk, CD19+/pre-BCR-

29 Endothelial cells were exposed to human monocytoid cells, and adherent cells were quantitated us

30 as demonstrable with blood neutrophils, U937 monocytoid cells, and genetically engineered alphaMbeta2

31 ng nonactivated and activated U937 and THP-1 monocytoid cells, and neutrophils.

32 tic adhesiveness for monocytes and WEHI78/24 monocytoid cells, and this adhesion is inhibited by L11.

33 cles was enhanced in IFN-alpha-treated THP-1 monocytoid cells, and this enhancement was primarily dep

34 types, including T and B lymphoid cells and monocytoid cells, the expression of HIV-1 tat results in

35 revotella bivia stimulated HIV expression in monocytoid cells, whereas Bacteroides ureolyticus, Pepto

36 plasminogen binding is markedly increased on monocytoid cells.

37 ted RON in astrocytes, cortical neurons, and monocytoid cells.

38 to significantly stimulate HIV expression in monocytoid cells.

39 cells, including activated and non-activated monocytoid cells.

40 penia, splenomegaly, and the accumulation of monocytoid cells.

41 uced NF-kappa B translocation in THP-1 human monocytoid cells.

42 anes of human peripheral blood monocytes and monocytoid cells.

43 virus replication in chronically infected U1 monocytoid cells; these observations also suggest a pote

44 t an early progenitor stage with lymphoid or monocytoid characteristics.

45 the activation marker CMRF44 on circulating monocytoid dendritic cell (mDC) and plasmacytoid dendrit

46 In TOL patients, monocytoid dendritic cell (mDC) but not plasmacytoid den

47 TLR-activated freshly isolated monocytes and monocytoid dendritic cells from patients with XLA produc

48 plasmacytoid dendritic cells, monocytes, and monocytoid dendritic cells were activated with TLR-4, TL

49 plasmacytoid DCs but not myeloid-derived and monocytoid-derived DCs via a direct interaction that did

50 oRNAs that are active in aberrant macrophage/monocytoid function and differentiation.

51 was also achieved using lysates of the human monocytoid line MonoMac 6 as sources of MAPKKs and visua

52 motility of osteoclast precursor-containing monocytoid populations in vivo.

53 However, monocytoid precursors in chronic myelomonocytic leukemia

54 Finally, virions were derived from monocytoid THP-1 cells that constitutively display low l

55 inding that SAMHD1 is hyperphosphorylated in monocytoid THP-1 cells under nonrestrictive conditions.

56 THP-1 cells, a human monocytoid tumor line, were cocultured with Ureaplasma p

57 ion, we investigated the response of a human monocytoid (U-937) cell line to platelet MP stimulation.

58 chemokine receptors CCR1, CCR3, and CCR5 in monocytoid U937 cells as detected by cell surface molecu