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1 sed to examine the conformational effects of echinomycin, a DNA bis-intercalating antibiotic, on line
4 mplexes containing different drugs including echinomycin, actinomycin-D, ethidium bromide, Hoechst 33
5 tranded DNA is not inhibited indicating that echinomycin acts by interacting with the DNA and not the
6 ts that direct molecular recognition between echinomycin and DNA, mediated by hydrogen bonding and va
7 respectively, L1210 cell line) comparable to echinomycin and one analogue, which bears the luzopeptin
9 mportantly, in mice with complete remission, echinomycin appeared to completely eliminate LICs becaus
10 portantly, in X.laevis embryos injected with echinomycin at the two-cell stage the drug specifically
11 which the 2-amino group that is crucial for echinomycin binding has been added or removed, respectiv
12 The structural perturbations induced when echinomycin binds to closed circular duplex pBR322 DNA w
13 available among the different DNA fragments; echinomycin binds to TpD sites much more tightly than to
14 high-affinity bisintercalation analogous to echinomycin, but with little or no perceptible sequence
15 poxia-inducible factor (HIF)1alpha inhibitor echinomycin can be used to treat relapsed AML without af
21 One of the most potent compounds identified, echinomycin (NSC-13502), a small-molecule known to bind
23 t in a mouse model of relapsed AML, low-dose echinomycin selectively targets LICs and spares normal h
24 rcalating antibiotics (e.g., triostine A and echinomycin), the detailed interactions between those tw
25 ve examined the binding of actinomycin D and echinomycin to artificial DNA molecules asymmetrically s
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