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1 roliferation of allospecific CD8+ T cells in mixed lymphocyte culture.
2 BALB/c (H-2(d)) host spleen cells in a 5-day mixed lymphocyte culture.
3 , and in their ability to suppress a one-way mixed lymphocyte culture.
4 development of T cell hyporesponsiveness in mixed lymphocyte culture.
5 on to C57BL/6 splenocyte stimulator cells in mixed lymphocyte culture.
6 gglutinin, monoclonal antibodies to CD3, and mixed lymphocyte culture.
7 optive transfer assay and in vitro coculture mixed lymphocyte culture.
8 IFN-gamma-producing responses in allogeneic mixed lymphocyte cultures.
9 the generation of cytolytic T lymphocytes in mixed lymphocyte cultures.
10 ine-dependent cytotoxic T-cell generation in mixed lymphocyte cultures.
11 pairs based upon molecular tissue typing or mixed lymphocyte cultures.
12 not generate cytotoxic responses in primary mixed-lymphocyte cultures against MHC-disparate (allogen
13 splant recipients 2 years postoperatively in mixed lymphocyte culture and cell-mediated lympholysis r
14 poresponsiveness of residual CD8+ T cells in mixed lymphocyte culture and cytotoxic T lymphocyte to L
15 cyte responsiveness was measured by in vitro mixed lymphocyte culture and cytotoxic T lymphocyte.
17 absence of proliferation of CD4(+) T cells (mixed lymphocyte culture) and the description of an aber
18 were followed by inspection, serial biopsy, mixed lymphocyte culture, and alloantibody determination
21 demonstrated nonspecific suppression of the mixed lymphocyte culture assays at 90 and 200 days and a
24 utatively tolerant animals was examined with mixed lymphocyte cultures, cell-mediated lympholysis ass
25 bset (26-76%) of CD8+ CTL generated in human mixed lymphocyte cultures; cell sorting experiments conf
27 responses to postnatal boosts) and in vitro (mixed lymphocyte culture, cytotoxicity, and cytokine rel
28 CD4+ T cells cultured in short-term in vitro mixed lymphocyte cultures developed strong Ag-specific c
33 we tested two of the regulators for in vitro mixed lymphocyte culture (MLC) and cytotoxic T lymphocyt
34 myeloid cells, isolated from sex-mismatched mixed lymphocyte culture (MLC) nonreactive siblings, hav
36 nalloreactive T lymphocytes, by performing a mixed lymphocyte culture (MLC) stimulation of donor cell
37 Immunological responses were monitored by mixed lymphocyte culture (MLC), CML, skin graft rejectio
38 duction, as measured by in vitro analysis of mixed lymphocyte culture (MLC), T cell cytotoxicity, T h
40 this stimulatory activity of DBMC, in vitro mixed lymphocyte cultures (MLC) and cell-mediated lympho
41 ide was added either after the initiation of mixed lymphocyte cultures (MLC) or after interleukin-2 s
46 unophenotype profile, suppressive ability in mixed lymphocyte cultures, morphology, and ability to di
47 ning, using untreated bone marrow cells from mixed lymphocyte culture-nonreactive normal littermates.
49 ion by human T-cell populations generated in mixed lymphocyte cultures or isolated from transplant ne
50 ion inhibited donor-specific and third-party mixed lymphocyte culture proliferation in a dose-depende
54 rvival was monitored daily from day 10, with mixed lymphocyte culture responses measured on day 14 or
55 cine had no effect on IL-2 production in the mixed lymphocyte culture; therefore, the effect of glyci
56 Immunocompetence was assessed by one-way mixed lymphocyte culture using patients' peripheral bloo
59 ingle-peptide mice react strongly in primary mixed lymphocyte cultures with IAb molecules from wild-t
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