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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
10 ed LPS-dependent activation of NF-kappaB and IkappaB kinase beta activity, protected against LPS acti
11 [inhibitor of transcription factor NFkappaB (IkappaB) kinase beta; an upstream kinase responsible for
13 r NF-kappaB due to spontaneous activation of IkappaB kinase beta and degradation of the NF-kappaB inh
14 ominant negative mutants of IkappaBalpha and IkappaB kinase beta and electrophoretic mobility shift a
16 plicating a possible link with the defective IkappaB kinase beta and IkappaBalpha phosphorylation in
17 splenic B cells are defective in BCR-induced IkappaB kinase beta and IkappaBalpha phosphorylation.
18 tracellular signal-regulated kinase 1/2, and IkappaB kinase beta appear to contribute to the anti-apo
19 -dead mutant of NF-kappaB-inducing kinase or IkappaB kinase-beta but not IkappaB kinase-alpha signifi
20 was inhibited by dominant-negative AP-1 and IkappaB kinase-beta, but stimulated by WT AP-1 and Ikapp
21 an inducible, constitutively active form of IkappaB kinase beta (CA-IKKbeta), a key kinase in the ca
22 capable of expressing constitutively active IkappaB kinase beta (CAIKKbeta) in airway epithelium wer
23 iciency also abrogated the formation of TAB1.IkappaB kinase beta complexes in 4T1 breast cancer cells
24 kinases, IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta, components involved in IkappaBalpha
25 or of NF-kappaB expressed in C2C12 cells and IkappaB kinase beta-deficient embryonic mouse fibroblast
26 on of ABCA1 by TNFalpha is reduced by 65% in IkappaB kinase beta-deficient macrophages and by 30% in
27 r-associated factor 6 (TRAF6) and attenuates IkappaB kinase beta-dependent (IKKbeta-dependent) phosph
28 t pathway involves NF-kappaB-inducing kinase-IkappaB kinase beta/gamma-dependent phosphorylation and
29 on of CD28, which involves activation of the IkappaB-kinase beta/IkappaB/NF-kappaB-signaling cascade.
30 nsults activate a kinase complex composed of IkappaB kinase beta (IKK-beta), IKK-alpha, and IKK-gamma
31 oteins, IkappaB kinase alpha (IKK-alpha) and IkappaB kinase beta (IKK-beta), that are present in a tu
35 s involves hypothalamic immunity mediated by IkappaB kinase-beta (IKK-beta), nuclear factor kappaB (N
36 appaB (NF-kappaB) and its upstream activator IkappaB kinase-beta (IKK-beta, encoded by Ikbkb) in the
37 nduces activation of inhibitor of NF-kappaB (IkappaB) kinase-beta (IKK-beta), a protein kinase that p
38 , IL-1 receptor-associated kinase 4 (IRAK4), IkappaB kinase beta (IKKB), IkappaB kinase iota (IKKI),
39 eta-resistant variants, genetic depletion of IkappaB kinase beta (IKKbeta) (activated during hyperamm
40 nvolves an increased nuclear accumulation of IkappaB kinase beta (IKKbeta) and an increased recruitme
41 anonical and noncanonical NF-kappaB pathways IkappaB kinase beta (IKKbeta) and IKKalpha to activate N
42 cross-linking resulted in phosphorylation of IkappaB kinase beta (IKKbeta) and the phosphorylation an
43 kinases IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta (IKKbeta) as RelB interacting partne
46 sgenic mice expressing constitutively active IkappaB kinase beta (IKKbeta) in intestinal epithelial c
48 -theta is mediated through the activation of IkappaB kinase beta (IKKbeta) in the absence of detectab
49 perrepressor and a dominant-negative form of IkappaB kinase beta (IKKbeta) inhibited NF-kappaB bindin
50 otein kinase C-theta (PKC-theta), Bcl10, and IkappaB kinase beta (IKKbeta) into lipid rafts of the im
56 a) mice in which NF-kappaB signaling through IkappaB kinase beta (IKKbeta) is selectively ablated in
57 of Inhibitor of kappaB (IkappaB) proteins by IkappaB Kinase beta (IKKbeta) leads to IkappaB degradati
59 pression enhances LPA-induced MEKK3-mediated IkappaB kinase beta (IKKbeta) phosphorylation and NF-kap
60 via the alternate pathway is accompanied by IkappaB kinase beta (IKKbeta) phosphorylation, IkappaBal
62 d that knockdown or blocking the activity of IkappaB kinase beta (IKKbeta) prevented the aggregation
63 t indomethacin, inhibited the activity of an IkappaB kinase beta (IKKbeta) that is required to activa
64 Tax expression increases the activity of IkappaB kinase beta (IKKbeta) to enhance phosphorylation
68 teracts with and promotes the degradation of IkappaB kinase beta (IKKbeta), a component of the Ikappa
70 beta(Deltahep) mice, which specifically lack IkappaB kinase beta (IKKbeta), an activator of NF-kappaB
71 hances TNFalpha-induced RIP1 ubiquitination, IkappaB kinase beta (IKKbeta), and NF-kappaB phosphoryla
72 luding p65, IkappaB kinase alpha (IKKalpha), IkappaB kinase beta (IKKbeta), and NF-kappaB-inducing ki
73 trast, the phosphorylation of ERK, p38 MAPK, IkappaB kinase beta (IKKbeta), and nuclear NFkappaB acti
74 complex, IkappaB kinase alpha (IKKalpha) and IkappaB kinase beta (IKKbeta), are required for NF-kappa
75 phosphorylation of IkappaBalpha by activated IkappaB kinase beta (IKKbeta), but the activities of oth
77 fer marginally in their very poor binding to IkappaB kinase beta (IKKbeta), only wt NIK is able to bi
78 NF-kappaB pathway with UTC, an inhibitor of IkappaB kinase beta (IKKbeta), or transfection of CLL ce
80 lates sensitize insulin action by inhibiting IkappaB kinase beta (IKKbeta), the detailed mechanisms r
81 n of receptor-interaction proteins (RIP) and IkappaB kinase beta (IKKbeta), the key components of the
82 ownstream of the T-cell receptor (TCR) or of IkappaB kinase beta (IKKbeta), we demonstrate that NF-ka
83 We also demonstrate that IFN-gamma activates IkappaB kinase beta (IKKbeta)-dependent NF-kappaB to reg
84 a novel scenario of the proapoptotic role of IkappaB kinase beta (IKKbeta)-NF-kappaB, which can act a
85 hysiological basis of canonical or classical IkappaB kinase beta (IKKbeta)-nuclear factor kappaB (NF-
90 ced interleulin-8 production, and diminished IkappaB kinase beta (IKKbeta)/IKKgamma coimmunoprecipita
93 ritive and genetic inhibition of the central IkappaB kinase beta (IKKbeta)/nuclear factor-kappaB (NF-
94 was abolished by a dominant-negative form of IkappaB kinase beta (IKKbeta, K44A) or a null mutation o
95 ells overexpressing a kinase-mutated form of IkappaB kinase beta (IKKbeta-KM), the activation of NF-k
100 f screening hits identified as inhibitors of IkappaB kinase-beta (IKKbeta), a key regulatory enzyme i
101 tween the carboxyl terminus of beta-ENaC and IkappaB kinase-beta (IKKbeta), the kinase that phosphory
102 ty of a recently identified cellular kinase, IkappaB kinase-beta (IKKbeta), was significantly elevate
103 NF-kappaB is regulated from the cytoplasm by IkappaB kinase-beta (IKKbeta), which earmarks inhibitors
106 ARD11)-TAK1 (MAP3K7)-inhibitor of NF-kappaB (IkappaB) kinase-beta (IKKbeta) module is a switch mechan
108 ty of a key kinase of the NF-kappaB cascade, IkappaB-kinase beta (IKKbeta) subunit, as a function of
111 sgenic mice expressing constitutively active IkappaB kinase beta in airway epithelium (IKTA (IKKbeta
112 r, ubiquitin-dependent mechanism to activate IkappaB kinase-beta in response to TNF-alpha and TLR3 li
114 NIK (NF-kappaB-inducing kinase) or IKKbeta (IkappaB kinase beta) inhibited the activity of NF-kappaB
116 and in vitro kinase assays demonstrated that IkappaB kinase beta is a key serine/threonine kinase act
119 -specific transgenic expression of activated IkappaB kinase beta (MIKK), causes profound muscle wasti
124 100 also requires IKKalpha, but not IKKbeta (IkappaB kinase beta) or IKKgamma (IkappaB kinase gamma).
125 ibitor of nuclear factor kappaB kinase beta (IkappaB kinase beta, or IKKbeta) has emerged as a key re
126 , PACAP, and VIP suppress phosphorylation of IkappaB kinase beta (P-IKKbeta), prevent degradation of
127 ivation of the kinases IkappaB kinase alpha, IkappaB kinase beta, p38, Akt, and extracellular recepto
129 uclear factor-kappaB-alpha level and reduced IkappaB kinase-beta phosphorylation, suggesting a suppre
133 of CD4+ T cells with the NF-kappaB-inducing IkappaB kinase beta showed that NF-kappaB activation is
134 ding domain (NBD) of IkappaB kinase alpha or IkappaB kinase beta specifically inhibit the induction o
135 B kinase-beta, but stimulated by WT AP-1 and IkappaB kinase-beta, suggesting that PKC-theta stimulate
136 es between TAK1-binding protein 1 (TAB1) and IkappaB kinase beta that enabled TGF-beta to activate p6