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1 xic T lymphocytes, natural killer cells, and lymphokine-activated killer cells.
2  cytotoxic T-lymphocytes, natural killer, or lymphokine-activated killer cells.
3  IL-4 was required to limit the induction of lymphokine-activated killer cells.
4 d in perforin- and granzyme-resistant CTL or lymphokine-activated killer cells.
5 ed to stimulate lymphocyte proliferation and lymphokine-activated killer cell activation.
6  cytotoxic T lymphocyte, natural killer, and lymphokine-activated killer cell activities compared wit
7 hocyte activity, and both natural killer and lymphokine-activated killer cell activities of graft non
8 oxic assay of PBL indicated the induction of lymphokine-activated killer cell activity, but no eviden
9 induction of Ag-independent MHC-unrestricted lymphokine-activated killer cell activity.
10 traction of CD8+ T cells, and stimulation of lymphokine-activated killer cell activity.
11  exhibited a marked decrease in IL-2-induced lymphokine-activated killer cell activity.
12 ions in T cell differentiation, induction of lymphokine-activated killer cells, and regulation of imm
13 eral downstream orphan granzyme genes in the lymphokine-activated killer cell compartment.
14 otoxic lymphocytes, natural killer cells and lymphokine-activated killer cells depend primarily on th
15  actions of different human effector cells, (lymphokine-activated killer cells, gammadelta T cells, c
16 ytotoxic T lymphocytes and natural killer or lymphokine-activated killer cells is not blocked by BCR-
17                 We now show that NO inhibits lymphokine-activated killer cell killing of K562 target
18 or T cell fraction derived from heterologous lymphokine activated killer cells kills those tumor cell
19 delivered into living tumor cells and during lymphokine-activated killer cell-mediated attack.
20 tion of murine and human T cell-mediated and lymphokine-activated killer cell-mediated cytotoxicity,
21 uces production of IFN-gamma and augments NK/lymphokine-activated killer cell proliferation and funct
22 mC and F genes in their MLR-derived CTLs and lymphokine-activated killer cells; removal of the PGK-ne
23 ndothelium and cytotoxicity against tumor by lymphokine-activated killer cells were not affected by P
24                                              Lymphokine-activated killer cells were sorted into diffe
25 cid mice previously reconstituted with human lymphokine-activated killer cells, whereas treatment wit

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