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1 ineage potential was largely associated with interleukin 7 receptor alpha (IL-7R(alpha)) expression a
4 n of a polymorphism in the gene encoding the interleukin 7 receptor alpha chain (IL7R) as a significa
5 o1 deficiency resulted in a severe defect in interleukin 7 receptor alpha-chain (IL-7Ralpha) expressi
6 udy we show that increased expression of the interleukin 7 receptor alpha-chain (IL-7Ralpha) identifi
9 only high levels of PD-1 but also decreased interleukin-7 receptor alpha (CD127), an exhausted pheno
10 factor receptor (G-CSFR); and were uniformly interleukin-7 receptor alpha (IL-7Ralpha(-)) AA4.1(Lo),
11 e memory cells without undergoing changes in interleukin-7 receptor alpha (IL-7Ralpha) expression, di
13 (Th) cell subsets, ILC subsets positive for interleukin-7 receptor alpha (IL-7Ralpha) produce distin
15 ular or to the transmembrane domain (TMD) in interleukin-7 receptor alpha (IL7R) or cytokine receptor
16 elayed T cell responses and decreased CD127 (interleukin-7 receptor alpha [IL-7Ralpha] chain) convers
17 onstrated to regulate the gene expression of interleukin-7 receptor alpha chain (IL-7Ralpha) and post
18 t critically regulates the expression of the interleukin-7 receptor alpha chain (IL-7Ralpha) in T cel
20 increased MS risk is the soluble form of the interleukin-7 receptor alpha chain gene (sIL7R) produced
21 of CD45RB and upregulated expression of the interleukin-7 receptor alpha chain, indicating a transit
23 x10(-8)), as were a nonsynonymous SNP in the interleukin-7 receptor alpha gene (IL7RA) (P=2.94x10(-7)
24 , a c-Kit(hi) progenitor subset positive for interleukin 7 receptor-alpha (IL-7Ralpha) emerged that h
26 vitamin D(3), including genetic variants in interleukin-7 receptor-alpha (IL7RA*C), interleukin-2 re
27 ated STAT5 and high expression levels of the interleukin-7 receptor-alpha and interleukin-15 receptor
29 d- (CD62L-) CC chemokine receptor 7- (CCR7-) interleukin-7 receptor alphaLo (IL-7RalphaLo) phenotype.
30 cells had markedly reduced expression of the interleukin 7 receptor and exhibited shorter survival.
31 memory precursors (expressing high levels of interleukin-7 receptor and low levels of killer cell lec
32 cell expansion is driven by signals from the interleukin-7 receptor and the pre-B-cell receptor and i
36 have demonstrated that downregulation of the interleukin-7 receptor (CD127) distinguishes Treg cells
37 e show that neonatal thymi transplanted into interleukin 7 receptor-deficient hosts harbor population
39 f PU.1 as a transcriptional regulator of the interleukin-7 receptor has established one mechanism by
40 haracterized by selective down-regulation of interleukin-7 receptor, heightened apoptosis, and poor a
41 We show that activating mutations in the interleukin-7 receptor identified in human pediatric ETP
42 set by the proper signaling function of the interleukin 7 receptor (IL-7R) and the pre-T-cell antige
44 he pre-B cell antigen receptor (pre-BCR) and interleukin 7 receptor (IL-7R) coordinate pre-B cell pop
49 hed by progressively lower expression of the interleukin-7 receptor (IL-7R alpha) and by lower IL-7 r
50 One unexpected result was the high level of interleukin-7 receptor (IL-7R) gene expression in HS-27a
52 group is enriched for genes involved in the interleukin-7 receptor (IL-7R) pathway and T cell recept
59 apid apoptosis, and failed to upregulate the interleukin-7 receptor, known to be important for T cell
60 , effector CD8(+) T cells differentiate into interleukin-7 receptor(lo) (IL-7R(lo)) short-lived effec
62 ated polyfunctional T helper cells with high interleukin-7 receptor, rapid clonal expansion, and pote
63 ), a linchpin in the pre-B-cell receptor and interleukin 7 receptor signaling pathways critical to B-
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