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1 nogens and to more variant sequences of CD8+ T lymphocyte epitopes.
2 f multiple escape mutations within cytotoxic T lymphocyte epitopes.
3  class I binding peptides comprise cytotoxic T lymphocyte epitopes.
4 es indicate that they all contain both B and T lymphocyte epitopes.
5 y complex (MHC) class I-associated cytolytic T lymphocyte epitopes.
6 leles and mutations within defined cytotoxic T-lymphocyte epitopes.
7 ation of CD8(+) cells with cognate cytotoxic T-lymphocyte epitopes also induced secretion of soluble
8 or determining whether selected MSP1a CD4(+) T-lymphocyte epitopes and selected MSP1a and MSP1b B-lym
9 s [aa] 580 to 623), comprising the cytotoxic T-lymphocyte epitope (AVERYLKDQQLL) and the cysteine loo
10                                Subsequently, T-lymphocyte epitope-bearing peptides of NcSRS2 were map
11 ell, 6 T cell proliferative, and 3 cytotoxic T lymphocyte epitopes derived from 9 stage-specific P. f
12 uses were constructed to express a cytotoxic T-lymphocyte epitope derived from chicken ovalbumin (SII
13 r gamma interferon, we identify a new CD4(+) T-lymphocyte epitope encoded within the Rev protein of S
14 t interestingly, the newly identified helper T lymphocyte epitopes encompass or lie proximal to previ
15 efficacy may be important for selecting CD8+ T lymphocyte epitopes for inclusion in future HIV vaccin
16                    To date, SIV-derived CD8+ T lymphocyte epitopes from only three high frequency mac
17 ope modification strategies can alter CD8(+) T-lymphocyte epitope immunodominance hierarchies elicite
18                 The ability to determine CD4 T lymphocyte epitopes in large cohorts of patients using
19 he sequence of commonly recognized cytotoxic T-lymphocyte epitopes in 25 posttransplant lymphoprolife
20 onstrated that E6 aa48-57 contains cytotoxic T-lymphocyte epitopes naturally presented by E6-expressi
21                                  A cytotoxic T lymphocyte epitope of the CS protein of P. falciparum,
22 the HIV-1 gp120 third variable loop, the CD4 T lymphocyte epitopes of 2 HIV-infected persons were map
23 the identification of a novel CD8+ cytotoxic T-lymphocyte epitope on the Plasmodium falciparum circum
24 e CD8 T-lymphocyte-stimulatory elements, CD8 T-lymphocyte epitopes on OmpB(689-744) and OmpB(739-848)
25 igen, the K(b)-restricted dominant cytotoxic T-lymphocyte epitope OVA(257-264).
26 ar avidities for an immunodominant cytotoxic T lymphocyte epitope peptide, implying that the response
27 iciency virus mac251 (SIV(mac251)) cytotoxic T-lymphocyte epitopes recognized by CD8(+) T cells of in
28       The first human RSV-specific cytotoxic T-lymphocyte epitope to be defined is described.
29 histocompatibility complex class I cytotoxic T-lymphocyte epitopes, was found.
30 h responses to several subdominant cytotoxic T lymphocyte epitopes, whereas their clade C variants we

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