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1 he identification of truly naive T cells and recent thymic emigrants.
2 (+) T cells showed the highest percentage of recent thymic emigrants.
3 lcium flux was also observed in adult CD4(+) recent thymic emigrants.
4 cells were found to be functionally immature recent thymic emigrants.
5 led the ready identification and analysis of recent thymic emigrants.
6 y perivascular spaces and reduced numbers of recent thymic emigrants.
7  the collection of CD62L(high) and CD69(low) recent thymic emigrants.
8 erity of GVHD but positively correlated with recent thymic emigrants.
9 enrich within the CD25(-) subset and are not recent thymic emigrants.
10 involves both transferred mature T cells and recent thymic emigrants.
11 ce of CD4+CD25+ regulatory T cells among the recent thymic emigrants.
12        In contrast, thymectomy eliminated LN recent thymic emigrants.
13 ing diabetes only after the removal of CD25- recent thymic emigrants.
14 ent, egress from the thymus, and survival of 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
21                     Whereas the frequency of recent thymic emigrants and the differentiation of induc
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
24 requency of naive CD45RA(+)/CCR7(+) T cells, recent thymic emigrants, and TCR excision circles.
25          Increased intrahepatic apoptosis of recent thymic emigrants appears in part responsible for
26                                              Recent thymic emigrants are newly generated T cells that
27 -7/15), inflammatory signals, and priming of recent thymic emigrants are not sufficient to maintain v
28                    Functional assays support recent thymic emigrants as the precursors of CD4 T(SCM).
29 op into either Th1 or Th2 cells and were not recent thymic emigrants as they were present in mice thy
30 thymocytes and continues in the periphery in recent thymic emigrants, before these newly produced T c
31                   A greater understanding of recent thymic emigrant biology has come with the develop
32 nto lethally irradiated hosts suggested that recent thymic emigrants can undergo homeostatic prolifer
33                All infants had fewer than 50 recent thymic emigrants (CD3(+)CD45RA(+)CD62L(+)) per cu
34 s most likely originate from CD31(+)CD4(+) T recent thymic emigrants, CD31 was downregulated prior to
35 d with monoclonal anti-CD4 and anti-CD31 and recent thymic emigrants (CD4+recently emigrated from the
36  (CD4N) and CD8 (CD8N) T lymphocytes and CD4 recent thymic emigrants (CD4RTE) were quantified in the
37 ent excision circles (TRECs) as a measure of recent thymic emigrant cells in peripheral blood lymphoc
38 curred after the cells left the transitional recent thymic emigrant compartment.
39 D45RA isoform indicating that the cells were recent thymic emigrants derived from immature progenitor
40                                 Besides MME+ recent thymic emigrants, effector-like clusters are iden
41          Within peripheral tissues iNKT cell recent thymic emigrants exhibit a different TCR repertoi
42 ls, as opposed to that of tissue resident or recent thymic emigrants, explained this increase, as see
43  CD4 thymocytes, with the characteristics of recent thymic emigrants, failed to move away from CXCR4-
44                   We hypothesized that DP-BB recent thymic emigrants have a shortened life span and d
45 hymic longevity, resulting in a frequency of recent thymic emigrants in aged mice that is similar to
46 developed an assay to quantify the number of recent thymic emigrants in blood based on the detection
47 ha1 circle) showed that the concentration of recent thymic emigrants in blood decreased with age over
48                                              Recent thymic emigrants in chickens transiently express
49 eneic HCT, including enhancing the number of recent thymic emigrants in circulation although direct t
50                               Measurement of recent thymic emigrants in the periphery thus provides a
51 o apoptosis than nondivided eGFP(hi)CD44(lo) recent thymic emigrants in the periphery.
52  common in newly arising T cells (so-called "recent thymic emigrants") in adults, as well as in babie
53 ajority of HDAC3-deficient naive T cells are recent thymic emigrants, indicating a block in T cell ma
54 t signaling was important for integration of recent thymic emigrants into the mature naive compartmen
55                           Here, we show that recent thymic emigrant maturation is a progressive proce
56 functionally heterogeneous subsets including recent thymic emigrants, mature naive phenotype cells, m
57 (range, 536/mm(3)-1574/mm(3)), a mean of 437 recent thymic emigrants/mm(3) (range, 196/mm(3)-785/mm(3
58 lary thymocytes, but appears abruptly in the recent thymic emigrant population, suggesting that the l
59 naive CD4(+) T cell response are apparent in recent thymic emigrant populations, additional defects d
60  T cells without affecting thymocytes and/or recent thymic emigrants remains unknown.
61                                              Recent thymic emigrant (RTE) cells are nascent T cells t
62 ng to reduced thymic output and a decline in recent thymic emigrant (RTE) naive T cells in circulatio
63 dministration increased peripheral naive and recent thymic emigrant (RTE) populations, demonstrating
64 tions provides insight into the frequency of recent thymic emigrants (RTE) and, therefore, into thymi
65                                              Recent thymic emigrants (RTE) are an important subpopula
66 gr1-deficient mice have poor accumulation of recent thymic emigrants (RTE) in the periphery.
67       We have used two approaches to isolate recent thymic emigrants (RTE) in young and aged mice and
68 As no markers have been identified for these recent thymic emigrants (RTE), it is presently impossibl
69 hese markers and their exact relationship to recent thymic emigrants (RTE).
70      In this study, we show levels of CD8(+) recent thymic emigrants (RTEs) accounted for the prognos
71     In this study we show that murine CD4(+) recent thymic emigrants (RTEs) are programmed to facilit
72                                              Recent thymic emigrants (RTEs) are the youngest peripher
73                                              Recent thymic emigrants (RTEs) are the youngest subset o
74                                              Recent thymic emigrants (RTEs) are the youngest T cells
75                                       CD4(+) recent thymic emigrants (RTEs) comprise a clinically and
76 ome of which depends on the context in which recent thymic emigrants (RTEs) encounter antigen.
77              After developing in the thymus, recent thymic emigrants (RTEs) enter the lymphoid periph
78 ircles (TRECs) have been used as markers for recent thymic emigrants (RTEs) in assessing human thymic
79                            Using GFP to mark recent thymic emigrants (RTEs) in mice carrying a GFP tr
80                       Analysis of gammadelta recent thymic emigrants (RTEs) indicated that most gamma
81              Here we demonstrate that CD8(+) recent thymic emigrants (RTEs) migrated directly into th
82                                              Recent thymic emigrants (RTEs) must undergo phenotypic a
83 ally regulated levels of alpha4beta7 endowed recent thymic emigrants (RTEs) of unconventional types w
84                                         Such recent thymic emigrants (RTEs) undergo both phenotypic a
85                                        These recent thymic emigrants (RTEs) underwent phenotypic matu
86 how that CD4(+)CD8(-)Foxp3(-) thymocytes and recent thymic emigrants (RTEs), contrarily to peripheral
87 he subjects' age as naive T cells, including recent thymic emigrants (RTEs), expanded preferentially,
88 ion leads to a decrease in the generation of recent thymic emigrants (RTEs), resulting in a reduced r
89            To explore the TCR sensitivity of recent thymic emigrants (RTEs), we triggered T cells wit
90 d signals, which are also characteristics of recent thymic emigrants (RTEs).
91 well as flow cytometry measurements of CD31+ recent thymic emigrants (RTEs).
92 D4+ compartment contains a high frequency of recent thymic emigrants (RTEs).
93 esponses of mature CD8 T cells with those of recent thymic emigrants (RTEs).
94 induced autologous graft-vs-host disease are recent thymic emigrants (RTEs).
95 noregulatory T cells in CSA-treated rats are recent thymic emigrants (RTEs).
96 ut and found an increase in the frequency of recent thymic emigrants (RTEs, CD4(+) CD31(+) ) at 12-mo
97             The youngest peripheral T cells (recent thymic emigrants [RTEs]) are functionally distinc
98 newly generated naive T cells (also known as recent thymic emigrants) (RTEs) in mice, and followed th
99              These T cells may not represent recent thymic emigrants, since naive T cells may maintai
100 s of T cell receptor (TCR) excision circles, recent thymic emigrant T cells and naive CD4+ T cells, a
101 in particular CD3(+)CD45RA(+)CD62L(+)CD31(+) recent thymic emigrant T cells and non-class-switched CD
102 poiesis can be assessed by quantification of recent thymic emigrants, T-cell receptor excision circle
103 versely correlated with CD4(+) T-cell count, recent thymic emigrants, TCR excision circles, and TCR d
104                                              Recent thymic emigrants that fail postpositive selection
105 hypothesized that TCR revision is limited to recent thymic emigrants that have maintained RAG express
106 llowing thymic maturation, T cells egress as recent thymic emigrants to peripheral lymphoid organs wh
107                            This enables some recent thymic emigrants to undergo LIP and convert into
108 completes the phenotype also found on mature recent thymic emigrant Treg cells.
109 numbers of CD3(+) CD45RA(+) CD62L(+) CD31(+) recent thymic emigrants was associated with a loss of se
110 on, the relative contribution of CD4 and CD8 recent thymic emigrants was modulated as they entered th
111 ation activating gene 2 promoter to identify recent thymic emigrants, we now show that T cell differe
112                         We hypothesized that recent thymic emigrants with regulatory function are imp
113 nd tissues the main subset consists of naive recent thymic emigrants, with effector memory T cells (T
114                                    Levels of recent thymic emigrants within the peripheral blood were

 
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