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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
8 do the dominant negative forms of the common IL-2R beta and gamma chains.
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
11  this effect depends on the presence of both IL-2R beta and gamma(c) chains and Jak3.
12                                          The IL-2R beta and gamma(c) chains associated with p12I are
13                The interactions of p12I with IL-2R beta and gamma(c) may have important implications
14 , which nearly span the entire length of the IL-2R beta and gamma(c) subunits.
15       Helix A of IL-2 wedges tightly between IL-2R beta and gamma(c) to form a three-way junction tha
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
19  and immunoprecipitates that were probed for IL-2R beta and IL-2R gamma c on Western blots.
20  the interactions of IL-2 and IL-15 with the IL-2R beta and IL-2R gamma c subunits, as differences in
21                                  Inasmuch as IL-2R beta and IL-2R gamma subunits also serve as a comp
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
26  that were directed against the IL-2R alpha, IL-2R beta, and gamma(c) subunits of IL-2R.
27 zation of the receptor subunits IL-2R alpha, IL-2R beta, and gamma(c).
28 eration of cells co-expressing IL-15R alpha, IL-2R beta, and IL-2R gamma chains.
29 a R beta L, IFN-gamma R alpha, IL-10R alpha, IL-2R beta, and IL-4R alpha.
30                  Other cytokines sharing the IL-2R beta- and/or common gamma-chains (i.e., IL-15, IL-
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
33 ed T cell proliferation was dependent on the IL-2R beta chain but not the IL-2R alpha chain.
34      As increasing the IL-2 affinity for the IL-2R beta chain leads to better antitumor effect, we ge
35 ith a naive phenotype expressed little or no IL-2R beta chain, a shared component of the IL-2 and IL-
36 ed by IL-15 requires expression of an intact IL-2R beta chain, indicating that IL-15 operates in this
37                 A monoclonal antibody to the IL-2R beta chain, Mik beta 1, reduced CD69 expression an
38 , interacts with the tyrosine-phosphorylated IL-2R beta chain.
39  from different cytoplasmic tyrosines on the IL-2R beta-chain (IL-2Rbeta).
40 sisted of the extracytoplasmic domain of the IL-2R beta-chain and the cytoplasmic domain of IL-7R alp
41 essing different chemokine receptors and the IL-2R beta-chain but not the IL-2R alpha-chain.
42 7R alpha-chain and the cytoplasmic domain of IL-2R beta-chain in IL-2Rbeta(-/-) mice did not prevent
43 how that transgenic thymic expression of the IL-2R beta-chain in IL-2Rbeta-deficient mice prevents le
44  This suggests that the acidic domain of the IL-2R beta-chain plays an essential role in regulating I
45  is inhibited in mice treated with Ab to the IL-2R beta-chain that blocks signaling by either IL-2 or
46 BAF-B03 cells transfected with the wild-type IL-2R beta-chain undergo apoptosis when stimulated with
47                      Neither IL-2R alpha nor IL-2R beta chains are required for IL-15 binding.
48                         (ii) In vivo, mutant IL-2R beta chains lacking the acidic region of IL-2Rbeta
49 ast the p55IL-2R (IL-2R alpha) and p70IL-2R (IL-2R beta) components of the multimeric high affinity I
50                Fusion of the A region of the IL-2R beta cytoplasmic tail to IL-7R alpha enables IL-7
51 IL-15R alpha did not co-precipitate with the IL-2R beta/gamma c complex.
52 high enough to titrate intermediate-affinity IL-2R beta/gamma(c) receptors.
53 2/IL-2R alpha/IL-2R beta to IL-2/IL-2R alpha/IL-2R beta/gamma(c).
54 s on CIA using transgenic mice expressing an IL-2R beta/IL-4R alpha chimeric cytokine receptor transg
55 -mediated protection, CIA was exacerbated in IL-2R beta/IL-4R alpha chimeric receptor transgenic mice
56           Neutralizing IL-2, IL-2R alpha, or IL-2R beta inhibited AICD.
57 n CLPs are delivered via IL-2 receptor beta (IL-2R beta) intracellular domains.
58     Although IL-2-induced phosphorylation of IL-2R beta, JAK1, and STAT5 all required the presence of
59 risingly, IL-2R alpha makes no contacts with IL-2R beta or gamma(c), and only minor changes are obser
60 te oligonucleotides specific for IL-2, IL-4, IL-2R beta, or IL-2R gamma chains, added in culture, cou
61 endent of either the cytoplasmic tail of the IL-2R beta- or gamma c-subunits and their associated sig
62 uMik beta 1) Abs directed at IL-2R alpha and IL-2R beta, respectively, inhibit IL-2 binding and biolo
63 ated with IL-2 and then precipitated through IL-2R beta showed that IL-2R beta and IL-2R gamma c co-p
64 ation as well as cytolytic activity involves IL-2R beta signals that also up-regulate expression of t
65 IgG exhibited both anti-IL-2R alpha and anti-IL-2R beta specificities in binding assays.
66 en linked to a compromised expression of the IL-2R beta subunit (CD122) by old CD8+ T cells.
67  due to cross-linking of the IL-2R alpha and IL-2R beta, thus blocking IL-2 binding and possibly impe
68 ly from IL-2/IL-2R alpha to IL-2/IL-2R alpha/IL-2R beta to IL-2/IL-2R alpha/IL-2R beta/gamma(c).
69  c co-precipitate in a 1:1 ratio, while only IL-2R beta was found in the immunoprecipitates of YT cel
70                        Heterodimerization of IL-2R beta with either gamma c or the truncated erythrop
71 ing and possibly impeding the association of IL-2R beta with IL-15R.