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1 treatment in cells grown in the presence of alpha-difluoromethylornithine.
2 s a more potent inhibitor of the enzyme than alpha-difluoromethylornithine.
3 ying exogenous putrescine in the presence of alpha-difluoromethylornithine.
4 , or by preventing putrescine formation with alpha-difluoromethylornithine.
5 TM activation is polyamine dependent because alpha-difluoromethylornithine, a specific inhibitor of O
9 In addition, in vivo inhibition of ODC with alpha-difluoromethylornithine also exacerbated the colit
11 ; (ii) depletion of cellular polyamines with alpha-difluoromethylornithine, an inhibitor of ornithine
15 itor of cationic amino acid transport, or by alpha-difluoromethylornithine, an ornithine decarboxylas
16 utrescine was inhibited by the ODC inhibitor alpha-difluoromethylornithine, and L-proline generation
19 roblastoma (NB) cells with the ODC inhibitor alpha-difluoromethylornithine (DFMO) depleted polyamine
20 Inhibition of polyamine biosynthesis with alpha-difluoromethylornithine (DFMO) has been shown to i
25 ned treatment with the Odc suicide inhibitor alpha-difluoromethylornithine (DFMO) or Odc heterozygosi
27 tic action of the NO donor agents as well as alpha-difluoromethylornithine (DFMO), a known ODC inhibi
28 tment of ODC/Ras double transgenic mice with alpha-difluoromethylornithine (DFMO), a specific inhibit
30 y to determine the chemopreventive effect of alpha-difluoromethylornithine (DFMO), an enzyme-activate
31 duced by zinc deficiency can be inhibited by alpha-difluoromethylornithine (DFMO), an enzyme-activate
32 n polyamine levels in COS-7 cells induced by alpha-difluoromethylornithine (DFMO), an inhibitor of or
33 were cultured in the presence or absence of alpha-difluoromethylornithine (DFMO), an inhibitor of th
37 itor of cationic amino acid transport, or by alpha-difluoromethylornithine (DFMO), an ODC inhibitor.
38 , i.e. N1,N11-diethylnorspermine (DENSPM) or alpha-difluoromethylornithine (DFMO), have synergistic e
44 ministration of the suicide inhibitor of ODC alpha-difluoromethylornithine (DFMO, 0.5% w/v) in the dr
45 s by inhibiting ornithine decarboxylase with alpha-difluoromethylornithine dramatically enhanced the
46 Treatment with the biosynthesis inhibitor alpha-difluoromethylornithine during tetracycline remova
48 position to that observed for putrescine and alpha-difluoromethylornithine in previous T. brucei ODC
49 nhibiting ornithine decarboxylase (ODC) with alpha-difluoromethylornithine increased the levels of AT
52 vation, the polyamine biosynthesis inhibitor alpha-difluoromethylornithine inhibits the ability of MT
53 either the ornithine decarboxylase inhibitor alpha-difluoromethylornithine or the S-adenosylmethionin
55 administration of the suicidal ODC inhibitor alpha-difluoromethylornithine reduced UVB-induced BCCs i
56 with the ornithine decarboxylase inhibitor L-alpha-difluoromethylornithine sensitized all of these le
57 nstream target of Akt, was also increased in alpha-difluoromethylornithine-treated cells, which was p
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