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1 udies focus on type I NKT cells that express semi-invariant aB T cell receptors (TCR) and recognize a
3 Natural killer T cells express a conserved, semi-invariant alphabeta T cell receptor that has specif
6 ural killer T cells (NKT cells) expressing a semi-invariant CD1d-reactive T cell receptor (invariant
7 caque spleen-derived Valpha24(+) T cells are semi-invariant double-negative cells with effector memor
9 T TCR/MR1 complex structure explains how the semi-invariant MAIT-TCR engages the nonpolymorphic MR1 p
10 MR1 presenting a variety of ligands, how the semi-invariant mouse MAIT TCR binds mouse MR1-ligand rem
16 mammalian phospholipids, demonstrating that semi-invariant NKT TCRs have a capacity for private Ag s
17 and that they recognize; their expression of semi-invariant or diverse T cell receptors; the structur
18 cells (NKT cells) characterized by either a semi-invariant T cell antigen receptor (TCR) repertoire
19 ted invariant T cells (MAIT cells) express a semi-invariant T cell receptor (TCR) alpha-chain, TRAV1-
20 ssociated invariant T (MAIT) cells express a semi-invariant T cell receptor (TCR) that detects microb
23 (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-cla
24 natural killer T (NKT) cells expressing the semi-invariant T cell receptor V(alpha)14J(alpha)18 requ
25 iated invariant T (MAIT) cells use canonical semi-invariant T cell receptors (TCR) to recognize micro
28 osal-associated invariant T (MAIT) cells are semi-invariant T cells specifically recognizing riboflav
29 rved alphabeta T-cell lineage that express a semi-invariant T-cell receptor (TCR) restricted to the M
30 ry T cells that comprise type I (express the semi-invariant T-cell receptor [TCR] and can be detected
32 itive CD4+CD8+ thymocytes that rearrange the semi-invariant T-cell receptor found on mature NKT cells
33 l-associated invariant T (MAIT) cells have a semi-invariant T-cell receptor that allows recognition o
34 ond to intra-hepatic cytokines, and (via the semi-invariant T-cell receptor) to bacteria translocated
35 population characterized by expression of a semi-invariant T-cell receptor, rapidly produce copious
37 ell-characterized type I NKT cells express a semi-invariant TCR and can recognize both alpha- and bet
38 -associated invariant T (MAIT) cells express semi-invariant TCR and restriction by nonclassical MHC c
40 , posing the interesting question of how the semi-invariant TCR can bind to such structurally distinc
41 ulation characterized by the expression of a semi-invariant TCR capable of recognizing bacterial prod
42 ls, or invariant NKT (iNKT) cells, express a semi-invariant TCR characterized by its unique Valpha14-
43 They are an innate-like subset featuring a semi-invariant TCR repertoire that drives their well-rec
44 tudies on NKT cells focused on a subset with semi-invariant TCR termed invariant NKT cells, the major
45 l-associated invariant T (MAIT) cells have a semi-invariant TCR Valpha-chain, and their optimal devel
48 ided into two groups: type I NKT cells use a semi-invariant TCR, whereas type II express a relatively
49 ecognize self-glycolipids by virtue of their semi-invariant TCR, which triggers NKT cell lineage comm
50 KT) cells have at least two subsets: type I, semi-invariant TCRalpha chain-expressing (Valpha14Jalpha
52 hilin family they interact with, whereas the semi-invariant TCRs of iNKT and mucosal-associated invar
53 Contrastingly, Vdelta2(+) T cells express semi-invariant TCRs, which are present at birth and shar
55 availability of potent Ags and tetramers for semi-invariant/type I NKT cells allowed this population
61 KTgammadelta T cells uses TCRs composed of a semi-invariant Vdelta6.3/6.4-Ddelta2-Jdelta1 chain toget