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1             We assessed tumorigenicity using limiting dilution analysis.
2 herwise underestimated with the conventional limiting dilution analysis.
3 e of techniques exploiting the principles of limiting dilution analysis.
4  incorporation of [3H]thymidine into DNA and limiting dilution analysis.
5 xic (CTLf) T cells were enumerated by use of limiting dilution analysis.
6  because few cells score as LCMV specific in limiting dilution analysis.
7 ), and cytotoxic T cell precursors (pCTL) by limiting dilution analysis.
8 s of the clade B of HIV-1 were determined by limiting dilution analysis.
9 lopeptide reactive T cells was determined by limiting dilution analysis.
10 -lymphocyte precursor (CTLp) frequency using limiting dilution analysis.
11  the HIC and MLR populations, as assessed by limiting dilution analysis.
12 cine endothelial and lymphoblastoid cells by limiting dilution analysis and analyzed the responding T
13 re PR1-specific CTLs than were identified by limiting dilution analysis and correlated better with ly
14 esponses to all 3 viruses were quantified by limiting dilution analysis and staining with HLA-A*0201
15 L reactive to SIV proteins was determined by limiting-dilution analysis and demonstrated that the res
16 ells in peripheral blood were quantitated by limiting dilution analysis, and their effect on EBV load
17  antigen-specific memory B cells by means of limiting-dilution analysis, and we compared memory B-cel
18  as determined by in vitro proliferation and limiting dilution analysis (approximately equals 1:190,0
19 protein L6, were equivalent as determined by limiting dilution analysis (approximately equals 1:5,000
20 te with similarly high cloning efficiency in limiting dilution analysis as CD28(+) CD45RO(hi) cells o
21                         Furthermore, in vivo limiting dilution analysis assays revealed that LDN19318
22                                        Using limiting dilution analysis, CD8(+) T cells isolated duri
23 ontrols; because of low cell numbers, formal limiting dilution analysis could only be performed in 10
24                                              Limiting dilution analysis demonstrated a 10-fold increa
25                                              Limiting dilution analysis demonstrated that proliferati
26                                              Limiting dilution analysis-derived minimal frequency est
27                           All recipients had limiting dilution analysis-detectable, graft-reactive cy
28 equencies of 1 in 10(5)-10(6) as measured by limiting dilution analysis, estimates of the T cell freq
29  36 mo after transplantation were studied in limiting dilution analysis for allopeptide reactivity.
30  chromium release assay for CTL activity and limiting dilution analysis for CTL precursor frequency,
31                                              Limiting dilution analysis from these experiments showed
32              Using long-term BM cultures and limiting dilution analysis, G0CD34+ cells were found to
33                                              Limiting dilution analysis identified an expanded popula
34                                              Limiting dilution analysis identified one predominant CT
35                                              Limiting dilution analysis indicated that the frequency
36                                              Limiting dilution analysis indicated that the T cell pre
37                                              Limiting-dilution analysis indicates that Hem-End coloni
38 than, CTL precursor frequencies derived from limiting dilution analysis, indicating that this novel p
39 L responses against different virus strains, limiting dilution analysis is particularly appropriate t
40 panded in the presence of IL-2 and tested in limiting dilution analysis (LDA) for reactivity to synth
41                                              Limiting dilution analysis (LDA) of infiltrating cells r
42                                              Limiting dilution analysis (LDA) of SIC to determine pre
43                                              Limiting dilution analysis (LDA) results were also nonli
44 per T-lymphocyte proliferation was tested by limiting dilution analysis (LDA).
45 cellular interferon-gamma (IFN-gamma) and by limiting-dilution analysis (LDA) of cytotoxic T-cell pre
46 ecific CD8+ T cells has been accomplished by limiting dilution analysis of cytotoxic precursor cells.
47                  Similarly, as determined by limiting dilution analysis of IL-2-producing cells, T ce
48                                              Limiting dilution analysis of residual alloantigen-react
49                                              Limiting dilution analysis of TLR activated, latently in
50                                              Limiting dilution analysis of transduced Jurkat cells de
51                                              Limiting dilution analysis of unfractionated blood demon
52                                   Sequential limiting dilution analysis of virus-specific CD4+ T cell
53                                              Limiting-dilution analysis of lymphocytes from animals t
54 M+, IgG+, and RF+ B cells were determined by limiting-dilution analysis of purified peripheral blood
55 nd multiply spliced viral RNAs combined with limiting dilution analysis provided measurements of tran
56                                   Similarly, limiting dilution analysis revealed a greater frequency
57                                              Limiting dilution analysis revealed a high precursor fre
58 requencies of helper and cytotoxic cells, by limiting dilution analysis, serially measured in vitro c
59                                              Limiting dilution analysis showed a 5- to 6-fold higher
60                                   Results of limiting dilution analysis suggested that the increase i
61                                              Limiting dilution analysis suggests that the kidney marr
62                                              Limiting dilution analysis suggests that these cells can
63 l HCMV-specific CTL response, we have used a limiting-dilution analysis system to quantify HCMV-speci
64        The DNA material was quantified using limiting-dilution analysis; the mean concentration was d
65 e used monocyte-derived dendritic cells in a limiting dilution analysis to generate Mtb-specific CD8(
66 ral tissues have not been evaluated, we used limiting dilution analysis to measure the concentration
67 d distinguish patients at risk, we performed limiting dilution analysis to quantify anti-EBV cytotoxi
68 of keratinocytes into subcutis combined with limiting dilution analysis, to assess the long-term repo
69 equency of BCR-ABL(+) cells as determined by limiting dilution analysis was consistently higher in 38
70 CD1-, and nonclassically restricted cells, a limiting dilution analysis was performed.
71                                              Limiting dilution analysis was used to assess helper T-l
72                                              Limiting dilution analysis was used to characterize nume
73                                              Limiting dilution analysis was used to quantify the loca
74                                     Here, by limiting dilution analysis, we anatomically map the deve
75                                        Using limiting dilution analysis, we demonstrate that the abso
76                                      Using a limiting dilution analysis, we found the frequency of SR
77 ated cell sorting, cell transplantation, and limiting dilution analysis, we were able to identify the
78              Using bulk culture analysis and limiting-dilution analysis, we have shown that a replica
79 ong term immunologic memory as determined by limiting dilution analysis, with memory T cells displayi

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