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1 liferative response to specific alloantigen (clonal anergy).
2 e progression and promote the development of clonal anergy.
3 genes involved in pathways leading to T cell clonal anergy.
4 kade do not escape the ultimate induction of clonal anergy.
5 (Mls-1(a)) induces tolerance to Mls-1(a) by clonal anergy.
6 T lymphocytes that prevents the induction of clonal anergy.
7 stemic tolerance by both clonal deletion and clonal anergy.
8 factor interleukin-2 (IL-2), a state called clonal anergy.
9 contributes to defective IL-2 production in clonal anergy.
11 is state resulted from a combination of both clonal anergy and cytokine-mediated immunosuppression.
12 ) nondeletional T-cell tolerance mediated by clonal anergy and dependent on the structure, location,
13 hus, Ndrg1 contributes to the maintenance of clonal anergy and inhibition of T-cell-mediated inflamma
14 ral tolerance has generally been ascribed to clonal anergy and/or active immunoregulatory states.
16 duced T-cell hyporesponsiveness as a form of clonal anergy, and they supported an important role for
17 monstrate that T cell adaptive tolerance and clonal anergy are distinct biochemical states, possibly
18 s by tumor cells to T lymphocytes may induce clonal anergy as a mechanism of escape from immune surve
19 ligand-mediated apoptosis and the resulting clonal anergy as the mechanisms of high dose AChR alpha
20 proposed to inhibit the induction of T cell clonal anergy by either directly antagonizing negative s
23 c cells, but may instead induce a persistent clonal anergy capable of blocking subsequent immunity.
24 ession by Th2 or TGF-beta-secreting cells or clonal anergy/deletion, depending on the Ag dose used, w
30 progression and facilitate the induction of clonal anergy in nearby responder CD25(-)CD4(+) T cells.
32 ith reduced Ikaros activity are resistant to clonal anergy induced by TCR ligation in the absence of
33 ction signaling defect as the sole basis for clonal anergy induction and document the presence of a d
34 therefore explored the relationship between clonal anergy induction and the avoidance of autoimmune
42 T-cell hyporesponsiveness can be caused by clonal anergy or adaptive tolerance, but the pathophysio
44 ory mechanisms, such as receptor editing and clonal anergy, preventing the activation of B cells expr
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