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1 profiles, the pursuit of inhibitors for both aggrecanase 1 (a disintegrin and metalloproteinase with
6 lu(373)-Ala(374) site is cleaved in vitro by aggrecanase-1 (ADAMTS4) and aggrecanase-2 (ADAMTS5), whe
7 iption-polymerase chain reaction analyses of aggrecanase-1, aggrecanase-2 (ADAM-TS4, ADAM-TS5, respec
10 NF-kappaB activity resulting in induction of aggrecanase-1 and aggrecanase-2 expression, with consequ
11 n or expression of the two key aggrecanases (aggrecanase-1 and aggrecanase-2) in synovial tissue (ST)
14 other TIMPs, is a strong inhibitor of human aggrecanases 1 and 2, with K(i) values in the subnanomol
16 2), which has extensive homology to ADAMTS4 (aggrecanase-1) and the inflammation-associated gene ADAM
18 of matrix metalloproteinases-3, -9, and -13, aggrecanase-1, and the matrix protease regulator cycloox
19 SP-1) motif located within the C terminus of aggrecanase-1 binds to the glycosaminoglycans of aggreca
20 gions of the TSP-1 motif effectively blocked aggrecanase-1 cleavage of aggrecan by preventing the enz
21 toward the target substrate in a commercial aggrecanase 1 enzyme-linked immunosorbent assay and was
25 , these data suggest that the TSP-1 motif of aggrecanase-1 is critical for substrate recognition and
31 rom patients with arthritis, suggesting that aggrecanase-1 may be important in diseases involving car
34 everal studies indicate that this binding of aggrecanase-1 to aggrecan through the TSP-1 motif is nec
36 pological substrate specificity of ADAMTS-4 (aggrecanase-1) was examined using triple-helical or sing
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