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1 ctivity of ADA and inhibits proliferation of lymphocytic cells.
2 DP expression differs between epithelial and lymphocytic cells.
3 vely regulate Syk in COS-7 cells and Ramos B lymphocytic cells.
4 pression in U937 monocytic cells or in CEM T lymphocytic cells.
5  lymphoid population that comprises distinct lymphocytic cells and accessory cells.
6 sion of the CD43 promoter by 35% in Jurkat T lymphocytic cells and by 52% in the pre-erythroid/pre-me
7                          HLTF is degraded in lymphocytic cells and macrophages infected with Vpr-expr
8    The expression of anti-IN SFvs in human T-lymphocytic cells and peripheral blood mononuclear cells
9                       Increased numbers of T-lymphocytic cells and T-helper cells in the junctional e
10 tase activity production in HDAC4(+) ACH-2 T-lymphocytic cells but not in HDAC4(-) U1 promonocytic ce
11 he CD11c gene reduced promoter activity in T lymphocytic cells by 47%.
12                                              Lymphocytic cell death was significantly lower (P < 0.00
13      Further analysis of chemokine action on lymphocytic cells has shown the potent migration-promoti
14  T cells, dendritic cells (DC) and/or innate lymphocytic cells (ILC2).
15 CR3, an IP-10/Mig receptor, was expressed on lymphocytic cells in virtually every perivascular inflam
16 granules was confirmed in infections of H9 T-lymphocytic cells, indicating that gag localization was
17 ssed in the thymus, spleen (predominantly in lymphocytic cells), intestine, and testes.
18  peripheral blood lymphocytes (PBLs) and a B lymphocytic cell line (B-LCL).
19 increased expression of Fas ligand; the E6-1 lymphocytic cell line also released soluble FasL.
20 rties were evaluated against the murine P388 lymphocytic cell line and a minipanel of human cancer ce
21 riptional regulation of RORgammaT in a human lymphocytic cell line and Th17 differentiated from naive
22 g activity was present in the EBV-negative B-lymphocytic cell line DG75, the EBV-positive B-lymphocyt
23 s induced by cytokine withdrawal in a murine lymphocytic cell line via a receptor-dependent mechanism
24 K562 erythroleukemic cell line, but not in a lymphocytic cell line.
25 ies analyzed viruses produced by transformed lymphocytic cell lines chronically infected with HTLV-1,
26 icant cytoprotection activity on three human lymphocytic cell lines exposed to an aggressive H(2)O(2)
27 mphocytic cell line DG75, the EBV-positive B-lymphocytic cell lines GG68 and 721, the cervical cell l
28 Moreover, we identified two adherent primate lymphocytic cell lines that bind RBR at their surface an
29 gly, APOBEC3G occurs specifically in human T lymphocytic cell lines that contain this antiviral defen
30 rus is maintained in these cells, four human lymphocytic cell lines that support the entire virus lif
31   Fibroblast, kidney, hepatoma, and leukemic lymphocytic cell lines were unaffected.
32 o apoptotic cells from starved or irradiated lymphocytic cell lines, an observation extended to insec
33 in is normally or over-expressed in some non-lymphocytic cell lines, such as prostate cancer, ovarian
34 taining EBV latency in some epithelial and B-lymphocytic cell lines.
35  T lymphocytes and in several IL2-responsive lymphocytic cell lines.
36 g responses of genetically manipulated human lymphocytic cell lines.
37     CCR5, a RANTES receptor, was detected on lymphocytic cells, macrophages, and microglia in activel
38 expression in thymus and spleen cells within lymphocytic cells, moderate expression in the epithelial
39              We measure the growth of single lymphocytic cells, mouse and human T cells, primary huma
40               Functional studies in Jurkat T lymphocytic cells point to the importance of both the E2
41 e level of ADP expression determines whether lymphocytic cells proceed with a lytic or a persistent a
42 sive corpus callosum demyelination without a lymphocytic cell response.
43 ddition of morphine sulfate to human CEMx174 lymphocytic cells resulted in increased expression of mi
44 says utilizing luciferase reporter cells and lymphocytic cells revealed the ability of whole SP to pr
45 reduced Cdk6 activity, and hematopoietic and lymphocytic cells show high expression and significant d
46           The expression of anti-RT SFv in T-lymphocytic cells specifically neutralizes the RT activi
47  high levels of TIL and assess variations in lymphocytic cell subsets across breast cancer subtypes.
48                         Expression of YAP in lymphocytic cells that normally do not support TEAD-depe
49                             FL5.12 cells are lymphocytic cells that undergo apoptosis following inter
50             Although >95% of HIV-infected H9 lymphocytic cells were producing HIV antigens by immunof
51  neutrophils and decreased marrow B220(+) (B-lymphocytic) cells, which were normalized by PTH.