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1 pe generated by ionizing radiation and other radiomimetics.
2 utations confer only weak sensitivity to the radiomimetic agent methyl methane sulfonate (MMS) but co
5 also analyzed the PCNA complex induced by a radiomimetic agent, Bleomycin (BLM), which produces pred
9 ifest increased sensitivity to radiation and radiomimetic agents and show defects in DSB damage repai
12 phosphorylation at Ser1981, yet unlike other radiomimetics and IR, DNA breaks induced by C-1027 resul
13 hese proteins was required for resistance to radiomimetics, and many were required for resistance to
14 ontrasted cell responses to IR and C-1027, a radiomimetic antibiotic that induces DNA strand breaks.
16 are formed in DNA by ionising radiation and radiomimetic anticancer agents and are thought to be bio
17 que characteristic of ionizing radiation and radiomimetic anticancer drugs is the induction of cluste
21 Bs), such as those produced by radiation and radiomimetics, are amongst the most toxic forms of cellu
23 such as ionizing radiation and conventional radiomimetics because their mechanisms require oxygen to
24 eatments with cobalt-60 gamma irradiation or radiomimetic bleomycin, except after high bleomycin dose
27 itivity to DNA-damaging agents, particularly radiomimetic chemicals inducing DNA double-strand breaks
28 e of the transgenic cells to UV light or the radiomimetic chemicals methyl methanesulfonate and mitom
29 uction of DSBs utilize ionizing radiation or radiomimetic chemicals, such as neocarzinostatin (NCS),
30 oma cells to UV-, ribotoxic (anisomycin) and radiomimetic chemicals-induced programmed cell death in
33 ms, DNA damage-induced GDR elicited by IR or radiomimetic chemotherapy was monitored in the presence
34 the UV mimetic compound oxaliplatin and the radiomimetic compound doxorubicin promoted apoptosis by
38 ase Chinese hamster ovary CHO cells with the radiomimetic DNA double-strand cleaving agent neocarzino
39 q, we determine numbers of DSBs induced by a radiomimetic drug and replication stress, and reveal two
41 mal human cells to gamma-irradiation and the radiomimetic drug neocarzinostatin had no effect on ATM
42 rmore, BGT226 sensitizes cancer cells to the radiomimetic drug neocarzinostatin, suggesting that BGT2
45 rtemis-deficient ES cells are sensitive to a radiomimetic drug, but less sensitive to ionizing radiat
47 slocations induced by ionizing radiation and radiomimetic drugs are thought to arise by incorrect joi
48 osure of cells to ionizing radiation (IR) or radiomimetic drugs induces Chk2 phosphorylation by ATM,
49 agents, such as ionizing radiation (IR) and radiomimetic drugs is crucial in maintaining genomic int
50 Delta cells are hypersensitive to a range of radiomimetic drugs that share the feature of creating le
51 rgeted DNA and RNA damages from radicals and radiomimetic drugs to design DNA cleaving molecules for
52 recombination, sensitivity to radiation and radiomimetic drugs, and failure to repair a subset of DN
53 are usually caused by ionizing radiation and radiomimetic drugs, but can also occur under normal phys
54 reaks are produced by ionizing radiation and radiomimetic drugs, but it was not known whether they ca
55 t uniquely induced by ionizing radiation and radiomimetic drugs, but their level of production by UVB
56 o DSBs induced by ionizing radiation (IR) or radiomimetic drugs, including bleomycin, in living cells
58 e that is activated by ionizing radiation or radiomimetic drugs, whereas p95/nbs1 is part of a protei
69 ound maintains the characteristic ability of radiomimetics to cleave DNA in cell-free systems, varyin