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2 ineage potential was largely associated with interleukin 7 receptor alpha (IL-7R(alpha)) expression a
5 n of a polymorphism in the gene encoding the interleukin 7 receptor alpha chain (IL7R) as a significa
6 o1 deficiency resulted in a severe defect in interleukin 7 receptor alpha-chain (IL-7Ralpha) expressi
7 udy we show that increased expression of the interleukin 7 receptor alpha-chain (IL-7Ralpha) identifi
10 only high levels of PD-1 but also decreased interleukin-7 receptor alpha (CD127), an exhausted pheno
11 factor receptor (G-CSFR); and were uniformly interleukin-7 receptor alpha (IL-7Ralpha(-)) AA4.1(Lo),
12 e memory cells without undergoing changes in interleukin-7 receptor alpha (IL-7Ralpha) expression, di
14 (Th) cell subsets, ILC subsets positive for interleukin-7 receptor alpha (IL-7Ralpha) produce distin
16 ular or to the transmembrane domain (TMD) in interleukin-7 receptor alpha (IL7R) or cytokine receptor
17 previously described activating mutations in interleukin-7 receptor alpha (IL7RA) in poor-prognosis "
18 elayed T cell responses and decreased CD127 (interleukin-7 receptor alpha [IL-7Ralpha] chain) convers
19 onstrated to regulate the gene expression of interleukin-7 receptor alpha chain (IL-7Ralpha) and post
20 t critically regulates the expression of the interleukin-7 receptor alpha chain (IL-7Ralpha) in T cel
22 increased MS risk is the soluble form of the interleukin-7 receptor alpha chain gene (sIL7R) produced
23 of CD45RB and upregulated expression of the interleukin-7 receptor alpha chain, indicating a transit
25 x10(-8)), as were a nonsynonymous SNP in the interleukin-7 receptor alpha gene (IL7RA) (P=2.94x10(-7)
26 Moreover, we determined that dex upregulated interleukin-7 receptor alpha on CAR T cells and increase
27 , a c-Kit(hi) progenitor subset positive for interleukin 7 receptor-alpha (IL-7Ralpha) emerged that h
29 vitamin D(3), including genetic variants in interleukin-7 receptor-alpha (IL7RA*C), interleukin-2 re
30 ated STAT5 and high expression levels of the interleukin-7 receptor-alpha and interleukin-15 receptor
33 D4+ T cells lacking autophagy show increased interleukin-7 receptor-alpha surface expression, while n
35 d- (CD62L-) CC chemokine receptor 7- (CCR7-) interleukin-7 receptor alphaLo (IL-7RalphaLo) phenotype.
36 cells had markedly reduced expression of the interleukin 7 receptor and exhibited shorter survival.
37 memory precursors (expressing high levels of interleukin-7 receptor and low levels of killer cell lec
38 cell expansion is driven by signals from the interleukin-7 receptor and the pre-B-cell receptor and i
42 have demonstrated that downregulation of the interleukin-7 receptor (CD127) distinguishes Treg cells
43 e show that neonatal thymi transplanted into interleukin 7 receptor-deficient hosts harbor population
45 f PU.1 as a transcriptional regulator of the interleukin-7 receptor has established one mechanism by
46 haracterized by selective down-regulation of interleukin-7 receptor, heightened apoptosis, and poor a
47 We show that activating mutations in the interleukin-7 receptor identified in human pediatric ETP
48 set by the proper signaling function of the interleukin 7 receptor (IL-7R) and the pre-T-cell antige
50 he pre-B cell antigen receptor (pre-BCR) and interleukin 7 receptor (IL-7R) coordinate pre-B cell pop
56 hed by progressively lower expression of the interleukin-7 receptor (IL-7R alpha) and by lower IL-7 r
57 sident memory (TRM) cells, but low levels of interleukin-7 receptor (IL-7R) and are functionally less
58 4(+) T cells and in reduced abundance of the interleukin-7 receptor (IL-7R) encoded by the NF-kappaB
60 One unexpected result was the high level of interleukin-7 receptor (IL-7R) gene expression in HS-27a
63 group is enriched for genes involved in the interleukin-7 receptor (IL-7R) pathway and T cell recept
72 of normal and malignant thymocytes carrying interleukin-7 receptor (IL7R) gain-of-function mutations
73 apid apoptosis, and failed to upregulate the interleukin-7 receptor, known to be important for T cell
74 , effector CD8(+) T cells differentiate into interleukin-7 receptor(lo) (IL-7R(lo)) short-lived effec
77 ated polyfunctional T helper cells with high interleukin-7 receptor, rapid clonal expansion, and pote
78 ), a linchpin in the pre-B-cell receptor and interleukin 7 receptor signaling pathways critical to B-
80 ry receptors (inducible T-cell costimulator, interleukin 7 receptor), whereas inhibitory receptors (p