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1  identifying LDN5-like T cells as a distinct T cell type.
2    All of the lymphoid tumors tested were of T cell type.
3 gain represented the predominant gamma delta T cell type.
4 and delta chains is critical for determining T cell type.
5 g diagnosed with lymphoma, especially of the T-cell type.
6 t stem, hematopoietic stem and primary human T cell types.
7 nt effects on TFH cells and, possibly, other T cell types.
8 e shown to activate TGF-beta1 in several non-T cell types.
9 R beta mRNA expression were observed in both T-cell types.
10 siveness in transient assays in monocyte and T-cell types.
11 and increased T helper type 1 (Th1)/Th17 and T cell type 1 (Tc1)/Tc17 skin infiltration.
12          In multimarker analysis, the helper T cell type 1 (TH1)-related markers interferon-gamma, IL
13 ansion of antigen-specific regulatory CD4(+) T cell type 1 (TR1)-like cells in different mouse models
14 tion from a helper T cell Type 2 to a helper T cell Type 1 cytokine-biased profile in bronchoalveolar
15 IFN-gamma-dependent networks (perhaps helper T cell type 1 responses) while minimizing the effect of
16 ree groups of genes associated with a CD4(+) T-cell type-1 (Th1) immune response and three clusters l
17 in-10 (IL-10) is an anti-inflammatory helper T cell type 2 (Th2) cytokine that modulates Th1-type cyt
18                              IL-13, a helper T cell type 2 (Th2) cytokine, transforms cultured airway
19 as immune deviation in childhood to a helper T cell type 2 (Th2) subtype of CD4(+) cells.
20 ading to the generation of Th2 and cytotoxic T cell type 2 cells but not for IL-4 expression in cells
21 f CD8+ T cells into IL-4-secreting cytotoxic T cell type 2 cells.
22 cumsporozoite protein (CSP) ratios, a helper T cell type 2 cytokine, correlated with higher odds of m
23                                       Helper T cell type 2 responses in IFN-gamma(-/-) mice correspon
24 s associated with a transition from a helper T cell Type 2 to a helper T cell Type 1 cytokine-biased
25 increased and sustained production of helper T cell Type 2-associated cytokines by splenocytes of HDM
26                 Conversely, eosinophils, Th2 T cells, type 2 innate lymphoid cells, and possibly Foxp
27 eated DCs containing naive allogeneic CD4(+) T cells: type 2 cytokines (IL-6 and IL-13) increased whi
28 lighting the underappreciated role of helper T-cell type 2-related pathways.
29 that the role of each pathway depends on the T cell type and differentiation stage.
30 DC) subsets in initial activation of the two T cell types and their co-operation.
31 ly increased risk for NHL, especially of the T-cell type and primarily localized in the gut (EATL); (
32 risk for non-Hodgkin lymphoma, especially of T-cell type and primarily localized in the gut.
33 renewing tissues, terminally differentiated (TD) cell types are typically specified through the actio
34 risk for B-cell tumors at all or even to all T-cell types but only to a particular type of T-cell tum
35 tor induction of nuclear factor of activated T cells type c-1 and cathepsin K expression is defective
36 tional activator nuclear factor of activated T cells type c-1, associated with increased gene promote
37  induced lung eosinophilia and type 2 helper T-cell-type cytokines in orally sensitized mice.
38 rstand why X4 HIV-1 strains infection affect T-cell types differently during AIDS development and ind
39 d week 5, the predominance of one particular T cell type emerged, supporting the conclusion that tran
40 ely to be critical in various differentiated T cell types, even when triggered by the same stimulus.
41  destabilizes TCRalpha proteins in all other T cell types examined.
42 reactive T cells, these apparently disparate T cell types generally show simplified patterns of T cel
43 roenvironment is characterized by regulatory T cells, type II macrophages, myeloid-derived suppressor
44  subset, which represents a major gammadelta T cell type in the lymphoid organs and blood of mice, to
45 ongoing cross-talk between distinct effector T cell types in the lungs may contribute to a protective
46 level ratio, consistent with a type 2 helper T-cell-type inflammatory response, and subacute fibrosis
47  the induction of the IL-17-producing CD8(+) T cell type is largely epitope specific and that this sp
48 on with TGF-beta1, generating another CD8(+) T-cell type lacking both NKG2D and 4-1BB.
49               Brain biopsy confirmed active, T-cell type MS.
50 opathological analysis revealed lymphomas of T-cell type, often comprising a minor B-cell component.
51                                         Both T-cell types produced IL-17, IL-22, and IFN-gamma, but o
52 ) correlated with the disease resistance and T-cell-type response.
53 ther than the currently proposed specialized T-cell types that have a known lifespan of days.
54 dy aims to clarify the contributions of each T cell type to the regulation of squamous cell carcinoma
55  the disease induced by each of the effector T cell types to suppression by polyclonal regulatory T c
56 robe the temporal secretion patterns of each T cell type using real-time binding analyses for direct
57  and the level determines the development of T cell types, which are either protective or pathogenic.
58 sion pattern of GRAIL in other murine CD4(+) T cell types with a described anergic phenotype.

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