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1 aglandin transporter (PGT) and the enzyme 15-hydroxyprostaglandin dehydrogenase.
3 tory cytokine-dependent downregulation of 15-hydroxyprostaglandin dehydrogenase (15-PGDH) and subsequ
6 of the key prostaglandin catabolic enzyme 15-hydroxyprostaglandin dehydrogenase (15-PGDH) in breast c
10 requires the concomitant presence of the 15-hydroxyprostaglandin dehydrogenase (15-PGDH) tumor suppr
13 by ubiquitously abrogating expression of 15-hydroxyprostaglandin dehydrogenase (15-PGDH), a prostagl
15 c overexpression of PGE2-degrading enzyme 15-hydroxyprostaglandin dehydrogenase (15-PGDH), resulted i
20 chanisms, including up-regulation of both 15-hydroxyprostaglandin dehydrogenase (15-PGDH, the key pro
22 -2 (COX-2) and enhanced the expression of 15-hydroxyprostaglandin dehydrogenase, a physiologic COX-2
24 e identity with the NADPH-dependent human 15-hydroxyprostaglandin dehydrogenase/carbonyl reductase.
26 cyclooxygenase 2-regulated synthesis and 15-hydroxyprostaglandin dehydrogenase-driven degradation an
27 nthase-1, and inhibited the expression of 15-hydroxyprostaglandin dehydrogenase, leading to increased
29 Pretreatment of the R15L cells with the 15-hydroxyprostaglandin dehydrogenase (PGDH) inhibitor 5-[[
30 , is inactivated by the catabolic enzyme, 15-hydroxyprostaglandin dehydrogenase (PGDH), which has tum
31 15-oxo-ETE) as a product from rabbit lung 15-hydroxyprostaglandin dehydrogenase (PGDH)-mediated oxida
32 found the predominantly cytosolic markers 15-hydroxyprostaglandin dehydrogenase, prostaglandins PGE2
33 al prostaglandin E synthase-1 and reduces 15-hydroxyprostaglandin dehydrogenase, resulting in prostag
34 triol also up-regulated the expression of 15-hydroxyprostaglandin dehydrogenase, the enzyme initiatin
36 nd identified mutations in HPGD, encoding 15-hydroxyprostaglandin dehydrogenase, the main enzyme of p
37 (FZD6) and prostaglandin-metabolizing enzyme hydroxyprostaglandin dehydrogenase were increased in SCC
38 monocytes appears to be carried out by a 15-hydroxyprostaglandin dehydrogenase, which is present in
39 omise is illustrated by recent studies of 15-hydroxyprostaglandin dehydrogenase, which plays a critic
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