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1 ng that this effect is specific to the human IL-15 receptor.
2 ated upregulation of interleukin (IL)-15 and IL-15 receptor.
3 122, the beta-subunit shared by the IL-2 and IL-15 receptors.
4 on of IL-12, IL-15, and IL-18 or the IL-2 or IL-15 receptors.
5  is shared by the IL-2, IL-4, IL-7, IL-9 and IL-15 receptors.
6 mma chain of the IL-2, IL-4, IL-7, IL-9, and IL-15 receptors.
7  is distinct from known components of T-cell IL-15 receptors.
8 ht NK cells from MM patients primed with the IL-15 receptor agonist ALT-803 in vivo displayed enhance
9          Additionally, our data suggest that IL-15 receptor agonists may be useful tools in treating
10               Interleukin 15 (IL-15) and the IL-15 receptor alpha (IL-15Ralpha) chain are both requir
11              We show that endogenous soluble IL-15 receptor alpha (IL-15Ralpha) derived from epiderma
12 expression of the single-chain IL-15 and the IL-15 receptor alpha (IL-15Ralpha) in the same cell allo
13  co-expression of interleukin 15 (IL-15) and IL-15 receptor alpha (IL-15Ralpha) in the same cell allo
14                                              IL-15 receptor alpha (IL-15Ralpha) is a component of the
15 ion proteins have been engineered to provide IL-15 receptor alpha (IL-15Ralpha) mediated trans-presen
16 n 3 (MCP-3), IL-2 receptor beta (IL-2Rbeta), IL-15 receptor alpha (IL-15Ralpha), interferon receptor
17 s, and determined that these cells expressed IL-15 receptor alpha (IL-15Ralpha).
18 e treated T. gondii immune mice with soluble IL-15 receptor alpha (sIL-15Ralpha) to block the host en
19 ent as a heterodimer associated with soluble IL-15 receptor alpha (sIL-15Ralpha).
20 lls, possibly by affecting the expression of IL-15 receptor alpha and IL-15.
21           These are all tissues that express IL-15 receptor alpha but not IL-2 receptor alpha.
22 ing molecule (Bim), interleukin (IL)-15, and IL-15 receptor alpha chain (IL-15R alpha ) were associat
23                  Significantly, mRNA for the IL-15 receptor alpha chain was not expressed in NK cells
24 ed that these tolerant T cells expressed the IL-15 receptor alpha chain, and could be induced to prol
25  using mice deficient in either IL-15 or the IL-15 receptor alpha chain.
26                            Expression of the IL-15 receptor alpha on cancer cells was needed to effic
27                                          The IL-15 receptor alpha subunit (IL-15Ralpha) mediates high
28 ferred is through trans-presentation via the IL-15 receptor alpha subunit.
29 timulatory cytokine trans-presented with the IL-15 receptor alpha-chain to the shared IL-2/IL-15Rbeta
30 , whereas intratubular CD8 T cells expressed IL-15 receptor alpha.
31             We now report that IL-15 and the IL-15 receptor (alpha, beta, gamma chains) are constitut
32 ation of CD40 led to increased expression of IL-15 receptor-alpha by dendritic cells, an action that
33                        IL-15 precomplexed to IL-15 receptor-alpha was used in immunotherapy experimen
34 anscription factors for development, but not IL-15 receptor-alpha, indicating that intraepithelial IL
35  by treating mice with IL-15 precomplexed to IL-15 receptor-alpha, which induced the development of e
36 in (IL)-15 superagonist mutant and a dimeric IL-15 receptor alphaSu/Fc fusion protein, was found to e
37 unts of the antiapoptotic protein Bcl-2, the IL-15 receptor and the receptor CD27, and little homeost
38              These expressed the common IL-2/IL-15 receptors and another subset of APOBEC3G anti-vira
39 noclonal antibodies targeting either IL-2 or IL-15 receptors and safer than inhibitors of downstream
40 increase in CD4(+) T cells was recorded with IL-15 receptors, APOBEC3G and CC chemokines, the latter
41  flt3/flk2, CXCR4, the IL-7 receptor and the IL-15 receptor - are known to promote the expansion and
42 characterized by high expression of the IL-2/IL-15 receptor beta (CD122).
43  receptor alpha chain (IL-15Ralpha) and IL-2/IL-15 receptor beta chain (IL-2Rbeta) knockout mice.
44 of the transcription factors T-bet, the IL-2/IL-15 receptor beta chain CD122, and suppression of eome
45 etal thymus were activated and expressed the IL-15 receptor beta chain, skin-homing receptors, and th
46 er signaling via CD122 (interleukin-2 [IL-2]/IL-15 receptor beta-chain) plays a role in regulating th
47 alpha production by IL-15 required the (IL-2/IL-15) receptor beta chain, as demonstrated by receptor
48          Neutralisation of the high-affinity IL-15 receptor binding subunit, IL-15ralpha in elderly m
49                               Peritransplant IL-15 receptor blockade does not prolong allograft survi
50                                              IL-15 receptor blockade in mouse cardiac and islet allot
51      This study investigated the efficacy of IL-15 receptor blockade using Mut-IL-15/Fc in an outbred
52 KG2A(+)KLRG1(+) CD8 T cells express IL-7 and IL-15 receptors, can survive long-term without cognate A
53 d Nfil3) as well as one of the components of IL-15 receptor, CD122.
54 ntified a gene-gene interaction between IL-2/IL-15 receptor common beta chain and IL-2/IL-7/IL-15 rec
55 -15 receptor common beta chain and IL-2/IL-7/IL-15 receptor common gamma chain.
56 estigated for defects in the interleukin-15 (IL-15) receptor complex because functional IL-15 signali
57 CH1 and RBPJ, as well as the interleukin-15 (IL-15) receptor complex, the latter enhancing IL-15 auto
58 he interleukin (IL) 2, IL-4, IL-7, IL-9, and IL-15 receptor complexes remains undefined.
59                                          The IL-15 receptor consists of IL-15Ralpha, IL-2Rbeta, and t
60 he interleukin (IL)-2, IL-4, IL-7, IL-9, and IL-15 receptors, contributes to both cytokine binding an
61 igh affinity alpha-chain of the interleukin (IL)-15 receptor exists not only in membrane-anchored but
62 -cell survival but rather repressed IL-7 and IL-15 receptor expression, STAT5 phosphorylation, and BC
63                     Interleukin-2 (IL-2) and IL-15 receptors have been detected on some murine neopla
64      To inhibit IL-15 function and to target IL-15 receptor (IL-15R) bearing cells, we have generated
65 ion are regulated by IL-15, the influence of IL-15 receptor (IL-15R)-mediated signaling at the cellul
66                                IL-15 and the IL-15 receptor (IL-15R)alpha chain are essential for nor
67  previously described unique features of the IL-15 receptor (IL-15R)alpha.
68               The high affinity interleukin (IL)-15 receptor, IL-15Ralpha, is essential for supportin
69  mice lacking the high affinity interleukin (IL)-15 receptor, IL-15Ralpha, surprisingly results in th
70    Interleukin (IL)-15 and its high affinity IL-15 receptor, IL-15Ralpha, support NK cell homeostasis
71 ibody recognizing a signaling subunit of the IL-15 receptor, IL-2/15Rbeta, had a significant ( approx
72 n in cells that expressed the heterotrimeric IL-15 receptor in cis.
73 counter in vivo and engagement of the TCR or IL-15 receptor in vitro leads to the down-regulation of
74  interfering with the signal of the IL-2 and IL-15 receptors in a primate model of experimental autoi
75                        In T and NK cells the IL-15 receptor includes IL-2/15R beta and gamma c subuni
76 homeostatic pathway defined by IL-15/IL-15R (IL-15 receptor) interaction and the inflammasome pathway
77 alpha was not co-precipitated from the [125I]IL-15 receptor-ligand complex, demonstrating that IL-15
78    New forms of therapy directed at IL-2 and IL-15 receptors may be effective against certain neoplas
79 mbinant cytokines (rIL-15, rTNFalpha) and an IL-15 receptor neutralising antibody.
80 ility of exploiting reagents that impact the IL-15 receptor pathway to facilitate construction of hum
81                                    Mast cell IL-15 receptors recruit JAK-2 and STAT-5, instead of JAK
82 anscripts for the CD122 interleukin 2 (IL-2)/IL-15 receptor required by NK-lineage precursors.
83 ta chain, a shared component of the IL-2 and IL-15 receptors required for receptor function.
84        However, IL-15Ralpha is not merely an IL-15 receptor subunit, as mice lacking either IL-15 or
85 zed that differential expression of IL-2 and IL-15 receptor subunits on cycling T cells in vivo may d
86  T-cell divisions and expression of IL-2 and IL-15 receptor subunits, we demonstrate that IL-15 is a
87 lated cytokine receptors, including IL-7 and IL-15 receptors, that mediate nonredundant or critical s
88  vascular endothelial cells (VECs) expressed IL-15 receptors, the present study was undertaken to inv
89 modulate expression of the beta-chain of the IL-15 receptor, thus establishing a central axis between
90 and expressed reduced levels of the IL-7 and IL-15 receptors, thus providing a possible mechanism for
91 s of IL-12 and IL-15 mRNAs and the IL-12 and IL-15 receptors were also increased.

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