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1 wnregulation of the T-cell effector cytokine interleukin 21.
2 expression is regulated by interleukin-6 and interleukin-21.
3 ecules interferon-gamma, interleukin-17, and interleukin-21.
4 tched to IgG1 and IgG2b when stimulated with interleukin-21.
6 de-pulsed dendritic cells in the presence of interleukin-21 and enriched by peptide-major histocompat
8 specialization of CD4(+) T cells to produce interleukin-21 and promote antibody-mediated immunity an
9 pression was associated with interleukin 27, interleukin 21, and interferon gamma expression, rather
10 scriptional regulator Bcl6, the receptor for interleukin-21, and the ancestral polarity protein atypi
11 pecific CXCR5(+) CD4(+) T cells that secrete interleukin-21 are strongly associated with B cell memor
12 mediated by the cytokines interleukin-6 and interleukin-21 but is independent of TH1, TH2, and TH17
13 ls, IgM+CD21-/low-memory B cells, CD4+CXCR5+ interleukin 21+ cells, and T-helper 17 cells, compared w
15 ), CD4+IL17A+ cells (P < .01), and CD4+CXCR5+interleukin 21+ follicular T-helper (Tfh) cells (P < .01
16 ophages were also analyzed for expression of interleukin 21 (IL-21) and negative regulators of immune
18 antigen-primed plasma cells failed to induce interleukin 21 (IL-21) or the transcriptional repressor
19 uantification of human and cynomolgus monkey interleukin 21 (IL-21) was developed, qualified, and imp
20 zed proximally to mutating B cells, secreted interleukin 21 (IL-21), induced expression of the transc
21 nsforming growth factor beta1 (TGFbeta1) and interleukin 21 (IL-21), produced by follicular helper T
22 efficacy of CD20-targeted therapy, we fused interleukin 21 (IL-21), which induces direct lymphoma cy
24 lly, Foxp1 directly and negatively regulated interleukin 21 (IL-21); Foxp1 also dampened expression o
25 was shown to be implicated in regulation of interleukin-21 (IL-21) and IL-17 secretion in mice and h
26 t specialized in helping B lymphocytes, with interleukin-21 (IL-21) and inducible costimulatory molec
27 ighlights the recent identification of human interleukin-21 (IL-21) and interleukin-21 receptor (IL-2
28 mmac-dependent cytokine expression indicated interleukin-21 (IL-21) as a primary candidate optimizing
29 ould be treated by eliminating production of interleukin-21 (IL-21) by donor T cells or IL-21 recepto
31 ronic HIV-1 control, it is not known whether interleukin-21 (IL-21) contributes to early HIV-1 immuni
37 and indirect immune cell-mediated effects of interleukin-21 (IL-21) in mantle cell lymphoma (MCL), pr
38 y, we have examined the role of the cytokine interleukin-21 (IL-21) in regulating humoral immunity du
46 hronic viral infection, we demonstrated that interleukin-21 (IL-21) is an essential component of CD4+
49 phocytic leukemia (B-CLL) cells treated with interleukin-21 (IL-21) produce low levels of granzyme B.
53 teractions, was maintained by T-cell-derived interleukin-21 (IL-21), and promoted repeated rounds of
54 L) expressed on B cells and was dependent on interleukin-21 (IL-21), IL-6, and signal transducer and
56 of chronic viral infection demonstrate that interleukin-21 (IL-21), produced primarily by CD4 T cell
57 found that a small subset of gp120-specific interleukin-21 (IL-21)-secreting CXCR5(+) CD4(+) T cells
65 issue of Immunity have identified a role for interleukin-21 in the development of these specialized c
66 se 1 dose-escalation study of membrane-bound interleukin 21 (mbIL21) expanded donor NK cells infused
68 fication of human interleukin-21 (IL-21) and interleukin-21 receptor (IL-21R) deficiencies as novel e
69 homozygous loss-of-function mutations in the interleukin-21 receptor gene (IL21R; c.G602T, p.Arg201Le
72 unction, which was not enhanced by exogenous interleukin 21 supplementation in HIV-infected, older va
73 ly competent "Tfh-like" cells that expressed interleukin-21, Tfh cell markers, and Bcl6 and rescued G
74 Active production of both interleukin 27 and interleukin 21, together with production of interferon g
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