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1 32D cells expressing the wild-type human (hu)IL-2R beta.
2 ptosis in response to IL-2 as well as the wt IL-2R beta.
3 pha to the cytoplasmic domain of a truncated IL-2R beta.
4 active Akt mutants in BAF/3 cells expressing IL-2R beta[A0]delta S promotes the expression of Bcl-2 a
5 chromatography, followed by IL-2R alpha and IL-2R beta affinity chromatography and hydrophobic inter
6 FRET data from donor- and acceptor-labeled IL-2R beta-alpha, gamma-alpha, and gamma-beta pairs demo
7 Signals transduced via the S region of the IL-2R beta (amino acids 267-322) in BAF/3 cells activate
9 regulation, illustrating the specificity of IL-2R beta and gamma subunit signaling on the regulation
10 p12I stabilizes the immature forms of the IL-2R beta and gamma(c) chains and decreases their cell
16 -15 creates a less stable bridge between the IL-2R beta and IL-2R gamma c chains than does IL-2 on YT
17 precipitated through IL-2R beta showed that IL-2R beta and IL-2R gamma c co-precipitate in a 1:1 rat
18 While IL-2R alpha did co-precipitate with IL-2R beta and IL-2R gamma c in the presence of IL-2, IL
20 the interactions of IL-2 and IL-15 with the IL-2R beta and IL-2R gamma c subunits, as differences in
22 quired for high-affinity IL-2 binding, while IL-2R beta and IL-2R gamma(c) are required for the trans
23 eletion of JH7-6 impaired the association of IL-2R beta and IL-4R alpha chains with Jak1 but did not
24 e signals transduced via the S region of the IL-2R beta and is linked to the translocation of Akt to
25 (IL-2R alpha), a protein that together with IL-2R beta and the common cytokine receptor gamma chain
31 s analyzed, including phosphorylation of the IL-2R beta-associated kinase Jak1, expression of c-myc a
32 main binds a phosphopeptide derived from the IL-2R beta chain (corresponding to residues surrounding
34 ith a naive phenotype expressed little or no IL-2R beta chain, a shared component of the IL-2 and IL-
35 ed by IL-15 requires expression of an intact IL-2R beta chain, indicating that IL-15 operates in this
39 sisted of the extracytoplasmic domain of the IL-2R beta-chain and the cytoplasmic domain of IL-7R alp
41 7R alpha-chain and the cytoplasmic domain of IL-2R beta-chain in IL-2Rbeta(-/-) mice did not prevent
42 how that transgenic thymic expression of the IL-2R beta-chain in IL-2Rbeta-deficient mice prevents le
43 This suggests that the acidic domain of the IL-2R beta-chain plays an essential role in regulating I
44 is inhibited in mice treated with Ab to the IL-2R beta-chain that blocks signaling by either IL-2 or
45 BAF-B03 cells transfected with the wild-type IL-2R beta-chain undergo apoptosis when stimulated with
48 ast the p55IL-2R (IL-2R alpha) and p70IL-2R (IL-2R beta) components of the multimeric high affinity I
53 s on CIA using transgenic mice expressing an IL-2R beta/IL-4R alpha chimeric cytokine receptor transg
54 -mediated protection, CIA was exacerbated in IL-2R beta/IL-4R alpha chimeric receptor transgenic mice
57 Although IL-2-induced phosphorylation of IL-2R beta, JAK1, and STAT5 all required the presence of
58 risingly, IL-2R alpha makes no contacts with IL-2R beta or gamma(c), and only minor changes are obser
59 te oligonucleotides specific for IL-2, IL-4, IL-2R beta, or IL-2R gamma chains, added in culture, cou
60 endent of either the cytoplasmic tail of the IL-2R beta- or gamma c-subunits and their associated sig
61 uMik beta 1) Abs directed at IL-2R alpha and IL-2R beta, respectively, inhibit IL-2 binding and biolo
62 ated with IL-2 and then precipitated through IL-2R beta showed that IL-2R beta and IL-2R gamma c co-p
63 ation as well as cytolytic activity involves IL-2R beta signals that also up-regulate expression of t
66 due to cross-linking of the IL-2R alpha and IL-2R beta, thus blocking IL-2 binding and possibly impe
68 c co-precipitate in a 1:1 ratio, while only IL-2R beta was found in the immunoprecipitates of YT cel
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