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1 exing this cytokine to its soluble receptor, IL-15R alpha.
2 L-2, and an IL-15-specific receptor subunit, IL-15R alpha.
3 completely on parenchymal cell expression of IL-15R alpha and IL-15 but not IL-15R beta.
4 ne unique roles for macrophage expression of IL-15R alpha and show that NK cells rely upon distinct I
5 common gamma (C gamma ) chain, IL-7R alpha , IL-15R alpha; and proliferative responses of T cells in
6 ion most likely involved the alpha receptor (IL-15R alpha) because this high affinity receptor would
7 tion and maturation, expression of IL-15 and IL-15R alpha by both parenchymal and hematopoietic cells
8                     We therefore studied the IL-15R alpha chain expression in human gamma delta T cel
9                                        Since IL-15R alpha chain is necessary and sufficient for IL-15
10 s of the IL-2R in combination with an unique IL-15R alpha chain.
11 ctional similarities between IL-2R alpha and IL-15R alpha chains, the activation-triggered mechanisms
12             To study the expression of human IL-15R alpha chains, we have utilized tagged human IL-15
13  NK cells, and CD4+ and CD8+ T cells express IL-15R alpha chains.
14 provide novel insights into the use of IL-15/IL-15R alpha complexes to relieve tumor-resident T cells
15 re, we report that in vivo delivery of IL-15/IL-15R alpha complexes triggers rapid and significant re
16 ipheral blood following treatment with IL-15/IL-15R alpha complexes, the destruction of solid tumors
17 ha and show that NK cells rely upon distinct IL-15R alpha dependent IL-15 signals than memory CD8(+)
18 a and IL-2R gamma c in the presence of IL-2, IL-15R alpha did not co-precipitate with the IL-2R beta/
19 sue expression of IL-2/IL-2R alpha and IL-15/IL-15R alpha differ.
20   We analyzed the requirements for IL-15 and IL-15R alpha expression by bone marrow-derived or parenc
21        Naive CD8 T cell development required IL-15R alpha expression by both bone marrow-derived and
22                             However, whether IL-15R alpha expression by these subsets is necessary fo
23  sufficient for IL-15 binding, regulation of IL-15R alpha expression may represent a new target for T
24                                 By contrast, IL-15R alpha expression on cells other than T cells is a
25  After memory CD8(+) T cell differentiation, IL-15R alpha expression on DCs selectively supports cent
26                                 We find that IL-15R alpha expression on macrophages but not dendritic
27 ports central memory CD8(+) T cells, whereas IL-15R alpha expression on macrophages supports both cen
28 hereas memory-phenotype CD8 T cells required IL-15R alpha expression only by hematopoietic cells.
29 ed cell proliferation following knockdown of IL-15R alpha expression.
30 sporine or rapamycin, blocks mitogen-induced IL-15R alpha expression.
31         Despite secretion of IL-15, LCs lack IL-15R-alpha for surface presentation of IL-15.
32 vity increased over time in correlation with IL-15R alpha gene expression.
33 induces proliferation of cells co-expressing IL-15R alpha, IL-2R beta, and IL-2R gamma chains.
34 n of antigenic peptides, which together with IL-15R-alpha/IL-15, break tolerance against WT1 by stimu
35 we have generated four lines of mice lacking IL-15R alpha in various cell types.
36               Interleukin-15 receptor alpha (IL-15R alpha) is a pleiotropically expressed molecule th
37                                     We found IL-15R alpha mRNA expression in IL-15-stimulated and Ag-
38        LCs synthesize the highest amounts of IL-15R-alpha mRNA and protein, which binds IL-15 for pre
39                    By contrast, mice lacking IL-15R alpha on macrophages, DCs, or both, exhibit equiv
40 ffinity receptors, supports the existence of IL-15R alpha on these cells.
41 ion of the high-affinity receptor for IL-15, IL-15R alpha, on T cells is dispensable for the generati
42 genes encoding interferon- alpha , IL-2, and IL-15R alpha (P < .05, for each).
43                       To investigate whether IL-15R alpha presented by different cells perform distin
44             These findings may be related to IL-15R alpha's ability to present IL-15 in trans to low-
45 The results suggest the existence of a human IL-15R alpha subunit, although physical evidence of this
46 unexpected results provide insights into how IL-15R alpha supports memory CD8(+) T cells.
47 kin (IL)-15, and IL-15 receptor alpha chain (IL-15R alpha ) were associated with the magnitude of the

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