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1 cells, cortical thymic epithelial cells, and medullary thymic epithelial cells.
2 a transcription factor which is expressed in medullary thymic epithelial cells.
3 xpression, particularly in keratinocytes and medullary thymic epithelial cells.
4 ssues of patients with APECED, especially in medullary thymic epithelial cells.
5 ssion of MPO mRNA predominantly localized to medullary thymic epithelial cells.
6 effort to better define the heterogeneity of medullary thymic epithelial cells.
7 or superfamily members in the development of medullary thymic epithelial cells.
8 and recruited P-TEFb to target promoters in medullary thymic epithelial cells.
9 L2 is expressed on placental endothelium and medullary thymic epithelial cells.
10 restricted to B cells, dendritic cells, and medullary thymic epithelial cells.
11 ng T cells and autoimmune regulator-positive medullary thymic epithelial cells, a key process for cen
12 reduction of autoimmune receptor-expressing medullary thymic epithelial cells (Aire1 mTEC) and a dec
13 (+) T cells preferentially damaged recipient medullary thymic epithelial cells and impaired negative
14 function of NF-kappaB2 in the development of medullary thymic epithelial cells and, thus, the control
15 n of certain organ-specific self-antigens in medullary thymic epithelial cells, and has a role in the
17 ng pathways that regulate the development of medullary thymic epithelial cells are not fully understo
21 on is enriched, particularly in neonates, in medullary thymic epithelial cells expressing the autoimm
23 nt in the differentiation of Aire-expressing medullary thymic epithelial cells have been defined.
24 we found no evidence that TSAs presented by medullary thymic epithelial cells in Aire+TCRmini mice a
25 also induce IA-IE expression on cortical and medullary thymic epithelial cells in an IFN-gamma-depend
26 in negative selection, including the role of medullary thymic epithelial cells in displaying tissue s
27 lls that colocalize with dendritic cells and medullary thymic epithelial cells in the thymic medulla.
29 riptional regulator classically expressed in medullary thymic epithelial cells, monocytes, macrophage
31 tical role in T cell tolerance by regulating medullary thymic epithelial cell (mTEC) development.
32 o-step terminal differentiation model of the medullary thymic epithelial cell (mTEC) lineage from imm
33 hough the molecular mediators that stimulate medullary thymic epithelial cell (mTEC) maturation are p
34 sting of a branching structure that contains medullary thymic epithelial cell (mTEC) networks to supp
35 h cortical thymic epithelial cell (cTEC) and medullary thymic epithelial cell (mTEC) subsets take pla
36 ism, we have previously reported that mature medullary thymic epithelial cells (mTEC(high)) expressin
37 eral self-antigens (TRA), which is in mature medullary thymic epithelial cells (mTEC(high)) partly co
38 ize the developmental pathways that generate medullary thymic epithelial cells (mTEC) from their imma
40 in developing T cells is highly dependent on medullary thymic epithelial cells (mTEC), and mTEC devel
41 CD70 was expressed on Aire(-) and Aire(+) medullary thymic epithelial cells (mTECs) and on dendrit
42 d that Myh6 transcripts were absent in mouse medullary thymic epithelial cells (mTECs) and peripheral
43 ulate transcription of a battery of genes in medullary thymic epithelial cells (mTECs) and, consequen
46 ce of autoimmune regulator (Aire)-expressing medullary thymic epithelial cells (mTECs) during the emb
49 expression of peripherally restricted Ags by medullary thymic epithelial cells (mTECs) is associated
50 of tissue-restricted self antigens (TRAs) in medullary thymic epithelial cells (mTECs) is essential f
51 us tissue-restricted self-antigens (TRAs) in medullary thymic epithelial cells (mTECs) is essential t
52 ession of tissue-specific antigens (TSAs) by medullary thymic epithelial cells (Mtecs) leads to delet
53 roles for bone marrow (BM)-derived APCs and medullary thymic epithelial cells (mTECs) on the convent
58 plethora of tissue-restricted Ags (TRAs) by medullary thymic epithelial cells (mTECs) plays an essen
59 ular, autoimmune regulator (Aire)-expressing medullary thymic epithelial cells (mTECs) provide a spec
60 Aire functions in terminally differentiated medullary thymic epithelial cells (MTECs) to derepress t
63 f-tolerance in developing T cells depends on medullary thymic epithelial cells (mTECs), whose develop
64 ns2 gene specifically in the Aire-expressing medullary thymic epithelial cells (mTECs), without affec
65 neages--cortical thymic epithelial cells and medullary thymic epithelial cells (mTECs)--are yet to be
68 derived TEPs differentiate into cortical and medullary thymic epithelial cells, reconstitute the norm
69 nity by promoting self-antigen expression in medullary thymic epithelial cells, such that developing
71 y a marked reduction in the number of mature medullary thymic epithelial cells that express CD80 and
72 iated down-regulation of ICA69 expression in medullary thymic epithelial cells, thus providing a nove
74 2, Bcl-3 functions within stroma to generate medullary thymic epithelial cells, which are essential f
76 ngly autoimmune regulator-expressing, mature medullary thymic epithelial cells, which play a pivotal
77 expression of many tissue-specific genes in medullary thymic epithelial cells, which plays an import
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