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1 nts of TRAF2, NIK, IkappaB kinase alpha, and IkappaB kinase beta.
2 bind TRAF6, TAK1, IkappaB kinase alpha, and IkappaB kinase beta.
3 wnstream kinases c-Jun N-terminal kinase and IkappaB kinase beta.
4 modulator (NEMO), and the catalytic subunit, IkappaB kinase beta.
5 ing the activation and intrinsic activity of IkappaB kinase-beta.
6 kappaB degradation) and was found to involve IkappaB-kinase beta.
7 reduced phosphorylative activation, reducing IkappaB kinase-beta activation and intrinsic activity, t
8 of RelA/p65 in a manner that is dependent on IkappaB kinase beta activity and on the mitogen-activate
9 ed LPS-dependent activation of NF-kappaB and IkappaB kinase beta activity, protected against LPS acti
10 [inhibitor of transcription factor NFkappaB (IkappaB) kinase beta; an upstream kinase responsible for
12 r NF-kappaB due to spontaneous activation of IkappaB kinase beta and degradation of the NF-kappaB inh
13 ominant negative mutants of IkappaBalpha and IkappaB kinase beta and electrophoretic mobility shift a
15 plicating a possible link with the defective IkappaB kinase beta and IkappaBalpha phosphorylation in
16 splenic B cells are defective in BCR-induced IkappaB kinase beta and IkappaBalpha phosphorylation.
17 tracellular signal-regulated kinase 1/2, and IkappaB kinase beta appear to contribute to the anti-apo
18 -dead mutant of NF-kappaB-inducing kinase or IkappaB kinase-beta but not IkappaB kinase-alpha signifi
19 was inhibited by dominant-negative AP-1 and IkappaB kinase-beta, but stimulated by WT AP-1 and Ikapp
20 an inducible, constitutively active form of IkappaB kinase beta (CA-IKKbeta), a key kinase in the ca
21 capable of expressing constitutively active IkappaB kinase beta (CAIKKbeta) in airway epithelium wer
22 iciency also abrogated the formation of TAB1.IkappaB kinase beta complexes in 4T1 breast cancer cells
23 kinases, IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta, components involved in IkappaBalpha
24 or of NF-kappaB expressed in C2C12 cells and IkappaB kinase beta-deficient embryonic mouse fibroblast
25 on of ABCA1 by TNFalpha is reduced by 65% in IkappaB kinase beta-deficient macrophages and by 30% in
26 r-associated factor 6 (TRAF6) and attenuates IkappaB kinase beta-dependent (IKKbeta-dependent) phosph
27 t pathway involves NF-kappaB-inducing kinase-IkappaB kinase beta/gamma-dependent phosphorylation and
28 on of CD28, which involves activation of the IkappaB-kinase beta/IkappaB/NF-kappaB-signaling cascade.
29 nsults activate a kinase complex composed of IkappaB kinase beta (IKK-beta), IKK-alpha, and IKK-gamma
30 oteins, IkappaB kinase alpha (IKK-alpha) and IkappaB kinase beta (IKK-beta), that are present in a tu
34 s involves hypothalamic immunity mediated by IkappaB kinase-beta (IKK-beta), nuclear factor kappaB (N
35 appaB (NF-kappaB) and its upstream activator IkappaB kinase-beta (IKK-beta, encoded by Ikbkb) in the
36 nduces activation of inhibitor of NF-kappaB (IkappaB) kinase-beta (IKK-beta), a protein kinase that p
37 , IL-1 receptor-associated kinase 4 (IRAK4), IkappaB kinase beta (IKKB), IkappaB kinase iota (IKKI),
38 nvolves an increased nuclear accumulation of IkappaB kinase beta (IKKbeta) and an increased recruitme
39 anonical and noncanonical NF-kappaB pathways IkappaB kinase beta (IKKbeta) and IKKalpha to activate N
40 cross-linking resulted in phosphorylation of IkappaB kinase beta (IKKbeta) and the phosphorylation an
41 kinases IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta (IKKbeta) as RelB interacting partne
44 sgenic mice expressing constitutively active IkappaB kinase beta (IKKbeta) in intestinal epithelial c
46 -theta is mediated through the activation of IkappaB kinase beta (IKKbeta) in the absence of detectab
47 perrepressor and a dominant-negative form of IkappaB kinase beta (IKKbeta) inhibited NF-kappaB bindin
48 otein kinase C-theta (PKC-theta), Bcl10, and IkappaB kinase beta (IKKbeta) into lipid rafts of the im
54 a) mice in which NF-kappaB signaling through IkappaB kinase beta (IKKbeta) is selectively ablated in
56 pression enhances LPA-induced MEKK3-mediated IkappaB kinase beta (IKKbeta) phosphorylation and NF-kap
57 via the alternate pathway is accompanied by IkappaB kinase beta (IKKbeta) phosphorylation, IkappaBal
59 d that knockdown or blocking the activity of IkappaB kinase beta (IKKbeta) prevented the aggregation
60 t indomethacin, inhibited the activity of an IkappaB kinase beta (IKKbeta) that is required to activa
61 Tax expression increases the activity of IkappaB kinase beta (IKKbeta) to enhance phosphorylation
65 teracts with and promotes the degradation of IkappaB kinase beta (IKKbeta), a component of the Ikappa
67 beta(Deltahep) mice, which specifically lack IkappaB kinase beta (IKKbeta), an activator of NF-kappaB
68 hances TNFalpha-induced RIP1 ubiquitination, IkappaB kinase beta (IKKbeta), and NF-kappaB phosphoryla
69 luding p65, IkappaB kinase alpha (IKKalpha), IkappaB kinase beta (IKKbeta), and NF-kappaB-inducing ki
70 trast, the phosphorylation of ERK, p38 MAPK, IkappaB kinase beta (IKKbeta), and nuclear NFkappaB acti
71 complex, IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta (IKKbeta), are required for NF-kappa
72 phosphorylation of IkappaBalpha by activated IkappaB kinase beta (IKKbeta), but the activities of oth
74 fer marginally in their very poor binding to IkappaB kinase beta (IKKbeta), only wt NIK is able to bi
75 NF-kappaB pathway with UTC, an inhibitor of IkappaB kinase beta (IKKbeta), or transfection of CLL ce
77 lates sensitize insulin action by inhibiting IkappaB kinase beta (IKKbeta), the detailed mechanisms r
78 n of receptor-interaction proteins (RIP) and IkappaB kinase beta (IKKbeta), the key components of the
79 ownstream of the T-cell receptor (TCR) or of IkappaB kinase beta (IKKbeta), we demonstrate that NF-ka
80 We also demonstrate that IFN-gamma activates IkappaB kinase beta (IKKbeta)-dependent NF-kappaB to reg
81 a novel scenario of the proapoptotic role of IkappaB kinase beta (IKKbeta)-NF-kappaB, which can act a
82 hysiological basis of canonical or classical IkappaB kinase beta (IKKbeta)-nuclear factor kappaB (NF-
87 ced interleulin-8 production, and diminished IkappaB kinase beta (IKKbeta)/IKKgamma coimmunoprecipita
90 ritive and genetic inhibition of the central IkappaB kinase beta (IKKbeta)/nuclear factor-kappaB (NF-
91 was abolished by a dominant-negative form of IkappaB kinase beta (IKKbeta, K44A) or a null mutation o
92 ells overexpressing a kinase-mutated form of IkappaB kinase beta (IKKbeta-KM), the activation of NF-k
97 f screening hits identified as inhibitors of IkappaB kinase-beta (IKKbeta), a key regulatory enzyme i
98 tween the carboxyl terminus of beta-ENaC and IkappaB kinase-beta (IKKbeta), the kinase that phosphory
99 ty of a recently identified cellular kinase, IkappaB kinase-beta (IKKbeta), was significantly elevate
100 NF-kappaB is regulated from the cytoplasm by IkappaB kinase-beta (IKKbeta), which earmarks inhibitors
103 ARD11)-TAK1 (MAP3K7)-inhibitor of NF-kappaB (IkappaB) kinase-beta (IKKbeta) module is a switch mechan
105 ty of a key kinase of the NF-kappaB cascade, IkappaB-kinase beta (IKKbeta) subunit, as a function of
108 sgenic mice expressing constitutively active IkappaB kinase beta in airway epithelium (IKTA (IKKbeta
109 r, ubiquitin-dependent mechanism to activate IkappaB kinase-beta in response to TNF-alpha and TLR3 li
111 NIK (NF-kappaB-inducing kinase) or IKKbeta (IkappaB kinase beta) inhibited the activity of NF-kappaB
115 -specific transgenic expression of activated IkappaB kinase beta (MIKK), causes profound muscle wasti
120 100 also requires IKKalpha, but not IKKbeta (IkappaB kinase beta) or IKKgamma (IkappaB kinase gamma).
121 ibitor of nuclear factor kappaB kinase beta (IkappaB kinase beta, or IKKbeta) has emerged as a key re
122 , PACAP, and VIP suppress phosphorylation of IkappaB kinase beta (P-IKKbeta), prevent degradation of
123 ivation of the kinases IkappaB kinase alpha, IkappaB kinase beta, p38, Akt, and extracellular recepto
125 uclear factor-kappaB-alpha level and reduced IkappaB kinase-beta phosphorylation, suggesting a suppre
129 of CD4+ T cells with the NF-kappaB-inducing IkappaB kinase beta showed that NF-kappaB activation is
130 ding domain (NBD) of IkappaB kinase alpha or IkappaB kinase beta specifically inhibit the induction o
131 B kinase-beta, but stimulated by WT AP-1 and IkappaB kinase-beta, suggesting that PKC-theta stimulate
132 es between TAK1-binding protein 1 (TAB1) and IkappaB kinase beta that enabled TGF-beta to activate p6
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