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1 AK1, TAB1 (TAK1 binding protein), and TRAF6 (TNF receptor-associated factor 6).
2 isolated NASPs act either via or upstream of TNF receptor-associated factor 6.
3 terleukin-1 receptor-activated kinase-1, and TNF receptor-associated factor 6.
4 luding IL-1 receptor-associated kinase 4 and TNF-receptor associated factor 6.
5 Lys-34 and required the E3 ubiquitin ligase TNF receptor-associated factor 6 after stimulation of ce
6 se-pair with sequences in the 3' UTRs of the TNF receptor-associated factor 6 and IL-1 receptor-assoc
7 ys-63-linked polyubiquitination at Lys-34 by TNF receptor-associated factor 6 and is thereby activate
8 ase) and subsequently integrates with TRAF6 (TNF receptor-associated factor 6) and/or c-fos signaling
9 involving MyD88, IL-1R-associated kinase 1, TNF receptor-associated factor 6, and IkappaB kinase and
10 ts of myeloid differentiation protein, IRAK, TNF receptor-associated factor 6, and NF-kappaB-inducing
11 t signaling by disrupting the recruitment of TNF receptor-associated factor 6/c-Src complex to lipid
12 nd prevents the dissociation of, IRAK-IRAK-4-TNF receptor-associated factor 6 from the TLR signaling
13 cells, is dependent upon a MyD88-dependent, TNF receptor-associated factor-6-independent signaling p
14 ukin-1 receptor-associated kinase)1/4-TRAF6 (TNF receptor-associated factor 6), leading to integrin a
15 d expression of the signal transducer TRAF6 (TNF receptor-associated factor 6), leading us to conside
17 ly interacts with IL-1R-associated kinase-1, TNF receptor-associated factor-6, TGF-beta-activated kin
18 otein interactions with IKK-alpha, IKK-beta, TNF receptor-associated factor 6, TNF receptor-associate
19 ependent upon binding of the adapter protein TNF receptor-associated factor 6 to the cytoplasmic doma
21 found to activate NF-kappaB in concert with TNF receptor associated factor 6 (TRAF6), we propose tha
22 l analyses revealed that DAB2 interacts with TNF receptor-associated factor 6 (TRAF6) and attenuates
24 NKL-induced NF-kappaB activation and delayed TNF receptor-associated factor 6 (TRAF6) deubiquitinatio
25 completely understood, but ubiquitination of TNF receptor-associated factor 6 (TRAF6) has recently be
30 Upon LPS challenge, CREBH interacts with TNF receptor-associated factor 6 (TRAF6), an E3 ubiquiti
33 urthermore, NOSTRIN interacted directly with TNF receptor-associated factor 6 (TRAF6), leading to the
34 1 receptor-associated protein kinase (IRAK), TNF receptor-associated factor 6 (TRAF6), phosphatidylin
35 rectly interacting with the TRAF-C domain of TNF receptor-associated factor 6 (TRAF6), resulting in i
40 he CINC promoter by IL-17 in IEC-6 cells was TNF receptor-associated factor-6 (TRAF6), but not TRAF2,
41 the molecular adaptor tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6) exhibit a spec
44 es demonstrated that tumour necrosis factor (TNF) receptor-associated factor 6 (TRAF6) plays a key ro
45 estigated the role of tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6), an adaptor pr
46 Here we show that tumour necrosis factor (TNF) receptor-associated factor 6 (TRAF6), an adaptor pr
47 d kinase (IRAK-1) and tumor-necrosis factor (TNF) receptor-associated factor 6 (TRAF6), which are kno
48 We also found that tumor necrosis factor (TNF) receptor-associated factor 6 (TRAF6), which mediate
49 r gene activity was 16-fold higher following TNF receptor-associated factor-6 transfection after IL-1
50 leukin (IL)-1 receptor-associated kinase and TNF receptor-associated factor 6, two key adaptor/scaffo
51 e system of IKK complex activation by TRAF6 (TNF receptor-associated factor 6), we show that these pe
52 luding MyD88, IL-1R-associated kinase 4, and TNF receptor-associated factor 6, while it inhibited the
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