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3 he TCRbeta locus in gammadelta cells and the TCRgamma and delta loci in alphabeta cells were undertak
5 parable to those of mice transgenic for both TCRgamma and TCRdelta chains, and numbers of alphabeta t
7 oughput TCR-sequencing approach to study the TCRgamma and TCRdelta repertoires of naive ex vivo PBMC,
10 pression of functionally rearranged TCRbeta, TCRgamma, and TCRdelta chains by means of transgenes.
12 induced DP cell development, indicating that TCRgamma can associate with pTalpha and CD3 to form a no
13 g-TCRdelta rearrangements are expressed with TCRgamma, canonically found in the TCRdelta heterodimer.
14 and Vgamma4 genes, located downstream in the TCRgamma Cgamma1 gene cluster, are expressed by the earl
16 avy, T-cell receptor (TCR)alpha, TCRbeta, or TCRgamma chains expressed in a population of lymphocytes
18 number of DP thymocytes, demonstrating that TCRgamma chains were expressed on the cell surface in th
19 ed IL-7 induced sterile transcripts from the TCRgamma constant region in cultured thymocytes from IL-
21 allelic dosage was used to detect FLASH and TCRgamma deletions, which were interpreted in conjunctio
24 onstrated that the development of intestinal TCRgamma delta IEL, regardless of location, shares commo
25 ed alleles, supporting a role for functional TCRgamma/delta rearrangements in the gammadelta divergen
26 cell types, including conventional T cells, TCRgamma/delta T cells, regulatory T cells, and NK cells
27 +,CD4+,CD8-, express either TCRalpha/beta or TCRgamma/delta, and produce mainly type 2 cytokines.
29 containing additional regulatory sequences, TCRgamma expression was down-regulated in DP cells, and
30 T cell development correlated with increased TCRgamma gene rearrangement involving primarily Vgamma1.
31 thymocyte subsets, but only modestly reduces TCRgamma gene rearrangement, while deletion of each elem
33 elta genes, which paired with the Vgamma2(+) TCRgamma gene to generate the Vgamma2/Vdelta7(+) skin ga
34 required for embryonic thymocyte production, TCRgamma gene transcription, and Peyer's patch developme
35 oductive rearrangements of both TCRdelta and TCRgamma genes among CD44highCD25+ thymocytes, suggestin
37 ed by the transcriptional down-regulation of TCRgamma genes that normally accompanies DP cell develop
39 ccessful identified the absence of biallelic TCRgamma locus deletion (ABD), a characteristic of early
41 this receptor, whereas rearrangement of the TCRgamma locus may require a signal that is not shared b
49 d expression of T-cell receptor gamma chain (TCRgamma) mRNA in human prostate and have shown that it
50 pecific form of T cell receptor gamma chain (TCRgamma) mRNA in the human prostate and demonstrated th
51 the thymus with the result that TCRalpha and TCRgamma proteins are not expressed in the same cell at
53 Rdelta-/- mice display random proportions of TCRgamma rearranged alleles, supporting a role for funct
54 What prevents these cells from continuing TCRgamma rearrangement and adopting the gammadelta T cel
56 ne segment, suggesting that ordered waves of TCRgamma rearrangement exist in the adult mouse thymus a
57 sitive quantitative PCR method, we show that TCRgamma rearrangements are present in CD44(+)CD25(+) Pr
58 expression of TCRgammadelta, TCRdelta and/or TCRgamma rearrangements but no complete TCRbeta variable
62 TCR repertoires in cattle, demonstrating the TCRgamma repertoire to be clonally stratified and essent
67 r, HsA and 3'E(Cgamma1), severely diminishes TCRgamma transcription, selectively impairs development
69 at expression of the productively rearranged TCRgamma transgene competitively inhibits alphabeta thym
71 er ORF encodes a 13-kDa truncated version of TCRgamma, whereas the shorter alternative reading frame