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1                                              IKK gamma/NEMO is the essential regulatory subunit of th
2                                              IKK gamma/NEMO was demonstrated to shuttle between the c
3                                              IKK-gamma interacts preferentially with IKK-beta and is
4                                              IKK-gamma is required for the activation of the transcri
5                                           An IKK gamma mutant, which interacts with Hsp70, competitiv
6                                           An IKK-gamma carboxy-terminal truncation mutant that still
7 ing pathway that is independent of Bcl10 and IKK gamma.
8 appaB kinase beta (IKK-beta), IKK-alpha, and IKK-gamma/N, leading to changes in NF-kappaB-dependent g
9                                 IKK-beta and IKK-gamma are critical for cytokine-induced NF-kappaB fu
10 genes coding for the CD40 ligand (CD40L) and IKK-gamma (NEMO) genes, both X-linked; and mutations of
11 ppaB essential modulator NEMO (also known as IKK-gamma), which is the regulatory subunit of the Ikapp
12 paB essential modifier (NEMO), also known as IKK-gamma, is a member of the I-kappaB kinase complex re
13 and cells from IP patients exhibit defective IKK gamma/NEMO expression but normal expression of IKK c
14                 Thus, our findings establish IKK-gamma as a key molecule for adapting an oncoprotein-
15                      Expression of exogenous IKK gamma in the mutant cells restored NF-kappa B activa
16 eucine-repeat region of Tax is important for IKK gamma binding.
17 oiled-coil domain of I kappa B kinase gamma (IKK gamma) to inhibit IKK activity and consequently inhi
18 with Hsp70, competitively inhibits the Hsp70-IKK gamma interaction and relieves heat-mediated NF-kapp
19 erestingly, all the Tax mutants defective in IKK gamma binding failed to engage the IKK complex or st
20                       Recently, mutations in IKK-gamma (NEMO) have been shown to cause familial incon
21 308 effectively suppressed TNF-alpha-induced IKK-gamma and IkappaB-alpha phosphorylation and degradat
22 rminal putative zinc finger domains of NEMO (IKK gamma) are critical for UV-induced NF-kappa B activa
23 s caused by mutations in a gene called NEMO (IKK-gamma).
24 ecently demonstrated that mutations in NEMO (IKK-gamma), which encodes a critical component of the NF
25                                         NEMO/IKK gamma is indispensable for activation of the IKKs in
26 r-associated NF-kappa B activator) as a NEMO/IKK gamma-interacting protein via yeast two-hybrid analy
27          The TANK binding domain within NEMO/IKK gamma is required for proper functioning of this IKK
28 aB activation phases, requiring ATM and NEMO/IKK-gamma: The first phase induced TNF-alpha-TNFR1 feedf
29 tion required IKK alpha and IKK beta but not IKK gamma, the regulatory subunit of the IKK complex.
30 y, this mutant cell line lacks expression of IKK gamma, a non-catalytic component of the IKK complex.
31 vide genetic evidence for the requirement of IKK gamma in NF-kappa B signaling triggered by both T-ce
32 ndicate that, in addition to the key role of IKK gamma/NEMO in regulating cytokine-induced IKK activi
33 med NEMO (NF-kappa B essential modulator) or IKK gamma.
34 subunit, and requires the regulatory subunit IKK gamma (NEMO).
35 lpha and IKK beta and the regulatory subunit IKK gamma/nuclear factor-kappa B (NF-kappa B) essential
36  associates with the IKK regulatory subunit, IKK gamma, although the underlying biochemical mechanism
37 entially processed forms of a third subunit, IKK-gamma.
38 tripartite protein-protein interaction, Tax, IKK gamma, and PP2A form a stable ternary complex.
39                         We show that the Tax-IKK gamma interaction requires two homologous leucine zi
40 o and in vivo analysis, we demonstrated that IKK gamma/NEMO competed with p65 and IKK alpha for bindi
41             Our data support the notion that IKK gamma-associated PP2A is responsible for the rapid d
42 lecular cloning and sequencing indicate that IKK-gamma is composed of several potential coiled-coil m
43                          We propose that the IKK gamma/NEMO-deficient cells trigger an inflammatory r
44 , a human genodermatosis, synthenic with the IKK gamma/NEMO locus.
45 ns affecting the carboxy-terminal end of the IKK-gamma protein, a domain believed to connect the IKK
46  can be rescued by fusing the Tax mutants to IKK gamma.
47 ax, has been shown to interact directly with IKK gamma and activates IKK via a mechanism not fully un
48               Despite their interaction with IKK gamma, PP2A-interaction-defective Tax mutants failed
49 IKK-beta but instead complexes directly with IKK-gamma, a newly characterized component of the IKK co
50                 This direct interaction with IKK-gamma correlates with Tax-induced IkappaB-alpha phos
51 logous leucine zipper domains located within IKK gamma.

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