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1                                              TCR gamma delta cells, as well as alpha beta TCR-NKT cel
2                                              TCR gamma delta T cells are considered important in the
3 n RI gamma-chain in TCR-gamma delta cells, a TCR-gamma delta transgenic mouse (G8) has been crossed w
4 eptor alpha/beta chain (TCR alpha beta), and TCR gamma delta.
5            These results suggest that CD8(+) TCR gamma delta IELs do not require class I MHC for deve
6                 Unlike TCR-alpha beta cells, TCR-gamma delta cells express a distinct member of the z
7                                 In contrast, TCR gamma delta IEL development occurred efficiently in
8                                 In contrast, TCR-gamma delta + DETC were normal in number and appeara
9  as the absolute number of thymic dendritic, TCR-gamma delta and NK1.1 T cells were equivalent to con
10 a(-/-) mice, no development of graft-derived TCR gamma delta cells occurred, indicating that extrathy
11                      Donor- and host-derived TCR gamma delta cells were recovered from thymus grafts,
12 d intrathymically, distinguishable by either TCR-gamma delta or -alpha beta surface expression.
13 as sufficient for development of extrathymic TCR gamma delta IEL.
14                                           In TCR gamma delta cells, IL-2-producing cells are a subset
15 netics of endogenous IL-2 RNA degradation in TCR gamma delta cells.
16 the role of the Fc epsilon RI gamma-chain in TCR-gamma delta cells, a TCR-gamma delta transgenic mous
17 intraepithelial lymphocytes (IEL), including TCR gamma delta cells, can develop extrathymically.
18 uced TCR expression, because intraepithelial TCR-gamma delta cells from the zeta-deficient mice did n
19                 In contrast, intraepithelial TCR-gamma delta cells of G8.zeta-/- mice expressed high
20  B and TCR alpha beta cells, but lack mature TCR gamma delta cells.
21                                  Analysis of TCR gamma delta gene usage in the CNS showed that the on
22  TCR alpha beta cells and the development of TCR gamma delta cells are partially independent of the T
23 te the role of thymic IL-7 in development of TCR gamma delta cells, newborn TCR beta-deficient (TCR b
24 demonstrated that extrathymic development of TCR gamma delta IEL required extrathymic IL-7 production
25             These structural requirements of TCR gamma delta recognition of prenyl pyrophosphates dis
26 eric form of CD8 is exclusively expressed on TCR gamma delta IELs and on subsets of NK cells and TCR
27                                   Peripheral TCR gamma delta cells accumulate GFP RNA faster than end
28 R gamma delta and NKT cells, as well as skin TCR gamma delta-dendritic epidermal T cells, indicate th
29 f transgene expression in thymic and splenic TCR gamma delta and NKT cells, as well as skin TCR gamma
30 cating that extrathymic IL-7 did not support TCR gamma delta IEL generation from newborn thymic precu
31 d intestine synthesize IL-7, suggesting that TCR gamma delta cell development could occur in either s
32 sing the TCR alpha beta receptor and not the TCR gamma delta cells, which exclusively express CD8 alp
33 c epsilon RI gamma-chain associates with the TCR-gamma delta complex in the absence of the zeta-chain
34  IL-7 was required for development of thymic TCR gamma delta cells, while peripheral IL-7 was suffici
35 a/BoyEg mice were found to be susceptible to TCR gamma delta+ cell mediated GVHD-induced lethality ch
36 ndogenous IL-2 gene expression in transgenic TCR gamma delta cells may be explained by subset-specifi
37 rts describing thymic differentiation in two TCR gamma delta transgenic mouse models have suggested t

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