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1 e a new group of anticancer drugs with tumor selective toxicity.
2 evaluated in cell culture to delineate their selective toxicity.
3 ine atovaquone-binding affinity, and thereby selective toxicity.
5 ions include: (a) tirapazamine having a high selective toxicity against hypoxic cells; (b) the nature
6 inhibitors (BXI-61 and BXI-72) that exhibit selective toxicity against lung cancer cells compared wi
7 t disulfiram (DSF) is shown to have a highly selective toxicity against melanoma in culture, inducing
9 inhibitor does not consistently produce the selective toxicity and pathological hallmarks characteri
15 n-binding drug combretastatin A-4 exhibits a selective toxicity for proliferating endothelial cells i
16 ative, the antimalaria drug quinacrine, have selective toxicity for tumor cells and can simultaneousl
18 has focused on genomic expression related to selective toxicity in chiral pesticide, nor on epigeneti
20 e (GSH) depletion induces ROS production and selective toxicity in HL60 cells that overexpress Bcl-2
22 ytotoxic drug cargo, exhibited M2 macrophage-selective toxicity not observed in monovalent M2pep trea
26 important implications for understanding the selective toxicity of anti-cancer drugs in tumor cells.
27 nderstanding of the structural basis for the selective toxicity of atovaquone could help in designing
35 ition alone is not sufficient to explain the selective toxicity of MPP(+) to dopaminergic neurons.
37 abotropic glutamate receptors attenuates the selective toxicity of rotenone on DA neurons by activati
39 Here we show a completely new mechanism of selective toxicity of superparamagnetic nanoparticles (S
40 ysis of Msh2+/+ and Msh2-/- cells shows that selective toxicity of the halogenated nucleotide analogu
46 ity of rotenone plays a critical role in its selective toxicity on tyrosine hydroxylase-positive (TH+
48 experiments indicate hydrogel surfaces show selective toxicity to bacterial versus mammalian cells.
49 M2pep]4-Biotin and [M2pep]2-[KLA]2 exhibited selective toxicity to both M2-like TAMs and malignant ce
50 ygen species drive pharmacologic ascorbate's selective toxicity to cancer cells in vitro, in mice, an
54 otenone, another complex I inhibitor, causes selective toxicity to dopamine neurons, and Ndufs4 inact
55 n of BPNT-1 in the nervous system, can cause selective toxicity to specific neurons, resulting in cor
56 poxic cytotoxic agent tirapazamine exhibited selective toxicity to the primitive stem cell subset.
58 clinical trials demonstrate the feasibility, selective toxicity, tolerability, and potential efficacy
60 offer a promising therapeutic strategy with selective toxicity toward malignant but not normal cells
64 or related compounds, might exhibit greater selective toxicity toward tumor cells that overexpress t
65 anti-cancer drugs due to their demonstrated selective toxicity towards cancer cells relative to norm
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