コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 y perivascular spaces and reduced numbers of recent thymic emigrants.
2 he identification of truly naive T cells and recent thymic emigrants.
3 (+) T cells showed the highest percentage of recent thymic emigrants.
4 lcium flux was also observed in adult CD4(+) recent thymic emigrants.
5 cells were found to be functionally immature recent thymic emigrants.
6 ent, egress from the thymus, and survival of recent thymic emigrants.
7 led the ready identification and analysis of recent thymic emigrants.
8 the collection of CD62L(high) and CD69(low) recent thymic emigrants.
9 erity of GVHD but positively correlated with recent thymic emigrants.
10 enrich within the CD25(-) subset and are not recent thymic emigrants.
11 involves both transferred mature T cells and recent thymic emigrants.
12 ce of CD4+CD25+ regulatory T cells among the recent thymic emigrants.
13 In contrast, thymectomy eliminated LN recent thymic emigrants.
14 ing diabetes only after the removal of CD25- recent thymic emigrants.
15 n circulating TCR excision circles and CD31+ recent thymic emigrants and a substantial expansion of t
16 sential elements of immune responses such as recent thymic emigrants and dendritic cells strongly rel
17 taCD44high cells, we traced the phenotype of recent thymic emigrants and found that most were CD44low
18 chitecture and thymocyte numbers, increasing recent thymic emigrants and improving TCR diversity of p
19 natures, low in vivo numbers of naive CD4(+) recent thymic emigrants and peripheral dendritic cells c
20 l expression of FasR on the vast majority of recent thymic emigrants and resting peripheral T lymphoc
22 udied thymopoiesis by CD31(+) naive T cells (recent thymic emigrants) and homeostatic proliferation b
23 rcle (TREC)-containing CD4 T cells (presumed recent thymic emigrants) and the counts of total T cells
26 -7/15), inflammatory signals, and priming of recent thymic emigrants are not sufficient to maintain v
27 op into either Th1 or Th2 cells and were not recent thymic emigrants as they were present in mice thy
28 thymocytes and continues in the periphery in recent thymic emigrants, before these newly produced T c
30 nto lethally irradiated hosts suggested that recent thymic emigrants can undergo homeostatic prolifer
32 s most likely originate from CD31(+)CD4(+) T recent thymic emigrants, CD31 was downregulated prior to
33 d with monoclonal anti-CD4 and anti-CD31 and recent thymic emigrants (CD4+recently emigrated from the
34 (CD4N) and CD8 (CD8N) T lymphocytes and CD4 recent thymic emigrants (CD4RTE) were quantified in the
35 ent excision circles (TRECs) as a measure of recent thymic emigrant cells in peripheral blood lymphoc
37 D45RA isoform indicating that the cells were recent thymic emigrants derived from immature progenitor
38 CD4 thymocytes, with the characteristics of recent thymic emigrants, failed to move away from CXCR4-
40 hymic longevity, resulting in a frequency of recent thymic emigrants in aged mice that is similar to
41 developed an assay to quantify the number of recent thymic emigrants in blood based on the detection
42 ha1 circle) showed that the concentration of recent thymic emigrants in blood decreased with age over
46 common in newly arising T cells (so-called "recent thymic emigrants") in adults, as well as in babie
47 ajority of HDAC3-deficient naive T cells are recent thymic emigrants, indicating a block in T cell ma
48 t signaling was important for integration of recent thymic emigrants into the mature naive compartmen
50 functionally heterogeneous subsets including recent thymic emigrants, mature naive phenotype cells, m
51 (range, 536/mm(3)-1574/mm(3)), a mean of 437 recent thymic emigrants/mm(3) (range, 196/mm(3)-785/mm(3
52 lary thymocytes, but appears abruptly in the recent thymic emigrant population, suggesting that the l
53 naive CD4(+) T cell response are apparent in recent thymic emigrant populations, additional defects d
55 dministration increased peripheral naive and recent thymic emigrant (RTE) populations, demonstrating
56 tions provides insight into the frequency of recent thymic emigrants (RTE) and, therefore, into thymi
60 As no markers have been identified for these recent thymic emigrants (RTE), it is presently impossibl
63 In this study we show that murine CD4(+) recent thymic emigrants (RTEs) are programmed to facilit
70 ircles (TRECs) have been used as markers for recent thymic emigrants (RTEs) in assessing human thymic
74 ally regulated levels of alpha4beta7 endowed recent thymic emigrants (RTEs) of unconventional types w
77 how that CD4(+)CD8(-)Foxp3(-) thymocytes and recent thymic emigrants (RTEs), contrarily to peripheral
78 he subjects' age as naive T cells, including recent thymic emigrants (RTEs), expanded preferentially,
87 poiesis can be assessed by quantification of recent thymic emigrants, T-cell receptor excision circle
88 hypothesized that TCR revision is limited to recent thymic emigrants that have maintained RAG express
89 llowing thymic maturation, T cells egress as recent thymic emigrants to peripheral lymphoid organs wh
91 on, the relative contribution of CD4 and CD8 recent thymic emigrants was modulated as they entered th
92 ation activating gene 2 promoter to identify recent thymic emigrants, we now show that T cell differe
94 nd tissues the main subset consists of naive recent thymic emigrants, with effector memory T cells (T
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。