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1 t, a COOH-terminal-deletion mutant of TRUSS (TRUSS(1-723)) was found to inhibit NF-kappaB activation
2 biquitous scaffolding and signaling protein (TRUSS), a 90.1 kDa TNF-R1-associated scaffolding protein
3 biquitous scaffolding and signaling protein (TRUSS), a novel TNF-R1-interacting protein of 90.7 kDa.
5 ography, we produced and characterized micro-truss and -shell structures made from alumina-polymer co
6 glected aspects of hernia management such as trusses, antibiotic cover, return to work and activity,
7 8) and central (residues 249-440) regions of TRUSS are required to form a docking interface that supp
10 co-immunoprecipitation assays revealed that TRUSS can interact with TRADD, TRAF2, and components of
11 terface, and (iii) the assembly of homomeric TRUSS complexes may contribute to its role in TNF-R1 sig
13 e entire N-terminal half (residues 1-440) of TRUSS, (ii) the binding interface for TNF-R1 is closely
14 ce, highly branched inflorescences and fruit trusses, indeterminate shoots in place of determinate fl
15 eletion mutagenesis of TNF-R1 indicated that TRUSS interacts with both the membrane-proximal region a
20 ak allele of the florigen gene SINGLE FLOWER TRUSS (SFT) and two mutations affecting a bZIP transcrip
21 and how the FLOWERING LOCUS T/SINGLE FLOWER TRUSS (SFT)-like and TERMINAL FLOWER1/SELF-PRUNING (SP)-
24 ystematically investigate (i) the regions of TRUSS that interact with TNF-R1 and TRAF2 and (ii) the a
26 ith TNF-R1 and TRAF2 and (ii) the ability of TRUSS to self-associate to form higher-order complexes.
27 contrast, a COOH-terminal-deletion mutant of TRUSS (TRUSS(1-723)) was found to inhibit NF-kappaB acti
28 l, subfamily C, member 4-associated protein)/TRUSS (tumor necrosis factor receptor-associated ubiquit
29 -immunoprecipitation experiments showed that TRUSS was constitutively associated with unligated TNF-R
30 on repeating unit cells composed of webs or trusses, when made from materials of high elastic stiffn
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