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1 virus (DENV) using methylene blue (MB) as an intercalating agent.
2 d 1.4-2.8-fold when the TFO was linked to an intercalating agent.
3 leases and increased interaction of DNA with intercalating agents.
4 ellipticine alkaloids and could serve as DNA-intercalating agents.
5 re T cells to apoptotic death induced by DNA intercalating agents.
6 ytoxic and/or cytostatic effects of some DNA intercalating agents.
7 compensated for by conjugating the TFO to an intercalating agent (30-350-fold stabilization) or by ad
8 - or 13-fold, whereas an aminohexyl group or intercalating agent (acridine or psoralen) increased tri
10 ersensitive to inhibition by mAMSA and other intercalating agents and exhibited elevated levels of mA
13 llipticine, but confer resistance to the non-intercalating agents etoposide, teniposide and merbarone
14 en challenged with the discovery of powerful intercalating agents formed by unfused aromatic molecule
15 receive doxorubicin as therapy, but this DNA-intercalating agent has relatively low tumor specificity
17 DNA by covalently attaching a DNA-targeting intercalating agent (i.e., ethidium bromide) resulted in
18 tested the hypothesis that certain membrane-intercalating agents increase the chemical activity of c
21 sed anticancer drug, Doxorubicin (DOX, a DNA intercalating agent), LB-1.2 also causes marked GBM xeno
22 ch forms covalent adducts with DNA, a duplex intercalating agent (methylene blue), and a cytotoxic me
23 II that resulted in hypersensitivity to the intercalating agent N-[4-(9-acridinylamino)-3-methoxy-ph
24 and A/T-rich regions, respectively, and the intercalating agent nogalamycin, which binds G/C-rich se
25 agents (i.e. proteins, nanoparticles (NPs), intercalating agents) or artificial DNAs, often coupled
26 both proteins, as it is abolished by the DNA intercalating agents propidium iodide and ethidium bromi
27 immature thymocytes to survive DNA-damaging intercalating agents reflects their tolerance of double-
29 leavage is not affected by actinomycin D, an intercalating agent that does not bind dsRNA; (iii) the
31 -carboxamides form a class of known DNA mono-intercalating agents that exhibit cytotoxic activity aga
32 ells in a microtiter well format to identify intercalating agents that increase or decrease the activ
33 Arginine-rich peptides and small-molecule intercalating agents utilize distinct molecular mechanis
34 ship between the site(s) of covalently bound intercalating agents, whose solution conformations in DN
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