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1 alpha in the cytosol of cells overexpressing TGase 2.
2 e as well as I-kappaBalpha polymerization by TGase 2.
3 minor extent by TGase 1, and probably not by TGase 2.
4                             TGase-1, but not TGase-2, -5, and -7, was expressed in RPTC.
5                                              TGase 2 activates NF-kappaB via a novel pathway.
6                                We found that TGase 2 activates the transcriptional activator nuclear
7 l lines, whereas the expression of wild-type TGase-2 and the GTP hydrolysis-defective mutant was sust
8 ies that in fact three members, the TGase 1, TGase 2, and TGase 3 enzymes, and are differentially exp
9 mer's patients, encoding a truncated form of TGase-2 (called TGase-S), shows strong apoptotic activit
10 y shown that calcium-activated TGase 3, like TGase 2, can bind, hydrolyze, and is inhibited by GTP de
11 bust and facile detection of the radiotracer-TGase 2 complex by autoradiography of thin layer plates
12           A number of point mutants of human TGase-2 defective for binding GTP, as well as a mutant t
13                                          The TGase 2 enzyme cross-linked SPR1 proteins poorly.
14                                          The TGase 2 enzyme is known to be present in neuronal tissue
15                          Transglutaminase 2 (TGase 2) expression is increased in inflammatory disease
16 ata on the expression profile of activatable TGase 2 in mouse organs and selected tumors were obtaine
17 yme isoforms known in the human genome, only TGase 2 is known to bind and hydrolyze GTP to GDP; bindi
18 transamidase activity of transglutaminase 2 (TGase 2) is considered to be important for several patho
19        Western blotting and experiments with TGase 2 knock-out (KO) mice ruled out the possibility th
20  the expression of the GTP-binding-defective TGase-2 mutants in different cell lines, whereas the exp
21          Moreover, the GTP-binding-defective TGase-2 mutants induced cell death.
22      However, the precise mechanism by which TGase 2 promotes inflammation remains unclear.
23 e demonstrated previously that inhibitors of TGase 2 reduce nitric oxide (NO) generation in a lipopol
24 hat enable the highly sensitive detection of TGase 2, such as application of radiolabeled activity-ba
25 chondrial/mitoplast TGase activity is due to TGase 2, the TGase isoform responsible for the majority
26 s, at least three of which, namely, TGase 1, TGase 2 (tissue transglutaminase), and TGase 3, are pres
27 in and gene expression for transglutaminase (TGase 2; tissue transglutaminase (tTG)) in hippocampus a
28                     Tissue transglutaminase (TGase-2), which binds GTP and catalyzes the cross-linkin
29  GTP-binding capability of full-length human TGase-2 would prevent it from conferring protection agai