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2 ign and synthesis of a water-soluble 1,3-bis(diphenylene)-2-phenylallyl (BDPA) radical via the conjug
4 g(H)-V) relationship was shifted -43 mV, and diphenylene iodinium (DPI)-inhibitable inward current re
11 th ebselen (3.6 +/- 0.2 versus 1.1 +/- 0.2), diphenylene iodonium (3.6 +/- 0.2 versus 1.0 +/- 0.1), a
12 ion was inhibited by NADPH oxidase inhibitor diphenylene iodonium (DPI) and mitochondria electron cha
15 cking the activity of the NADPH oxidase with diphenylene iodonium (DPI) inhibits ROS formation and ph
16 cells could be attenuated in the presence of diphenylene iodonium (DPI), an inhibitor of the NADPH ox
17 inhibited by an inhibitor of NADPH oxidase, diphenylene iodonium (DPI), and by antioxidants, N-acety
18 ed by NADPH oxidase inhibitors, apocynin and diphenylene iodonium (DPI), but not the xanthine/xanthin
19 as inhibited by the NADPH oxidase inhibitors diphenylene iodonium (DPI), imidazole, and pyridine.
20 gene expression was inhibited by antioxidant diphenylene iodonium (DPI), which is consistent with the
21 nd Tiron (5 mmol/L) and the flavin-inhibitor diphenylene iodonium (DPI, 20 micromol/L) abolished nore
22 tion in LPS-stimulated HMs were inhibited by diphenylene iodonium (nonspecific inhibitor for flavin-c
23 ial cells with the NAD(P)H oxidase inhibitor diphenylene iodonium abolishes RSV-induced STAT activati
25 vious studies with NADPH oxidase inhibitors, diphenylene iodonium and apocynin, suggested that NADPH
26 hils treated with the flavoprotein inhibitor diphenylene iodonium and in neutrophils from patients wi
28 trast, inhibitors of NADPH oxidase activity, diphenylene iodonium and staurosporine, as well as antio
30 t ascorbate, or the ROS-generation inhibitor diphenylene iodonium attenuated gravitropism while enhan
32 ocalized near nectary pores and inhibited by diphenylene iodonium but not by cyanide or azide, sugges
35 Cu) and inhibitors of NADPH oxidases (e.g., diphenylene iodonium chloride), enzymes responsible for
36 s, and in wild-type plants by treatment with diphenylene iodonium chloride, an inhibitor of hydrogen
37 endent production of hydrogen peroxide via a diphenylene iodonium chloride-sensitive calcium-dependen
38 en, catalase, and the flavoprotein inhibitor diphenylene iodonium each attenuated PDGF- and Rac1-medi
39 dies and inhibition experiments using CO and diphenylene iodonium indicate that only the low spin hem
40 wever, the antioxidants N-acetylcysteine and diphenylene iodonium inhibited both AA- and Ang II-induc
42 etylcysteine or the flavin protein inhibitor diphenylene iodonium is demonstrated to reduce oxidant l
43 e, which generates superoxide and H2O2, with diphenylene iodonium or apocynin decreased Ang II-induce
44 reatment of rat VSMCs with the NOX inhibitor diphenylene iodonium or the antioxidants N-acetylcystein
47 alone, 5.0+/-1.1-fold; NAC, 1.8+/-0.2-fold; diphenylene iodonium, 1.4+/-0.3-fold migration; and ebse
52 (ROS) dependent because it was inhibited by diphenylene iodonium, an inhibitor of NADPH oxidase, and
53 and was inhibited by 1-methylcyclopropene or diphenylene iodonium, an inhibitor of NADPH oxidase.
54 s H2O2 activates only p38MAPK (14-fold), and diphenylene iodonium, an NADH/NADPH oxidase inhibitor, a
56 inhibited by the NAD(P)H oxidase inhibitor, diphenylene iodonium, as well as by overexpression of do
57 nhibitor of flavoprotein-dependent oxidases, diphenylene iodonium, but not by inhibitors of various o
58 eine, the flavin-containing enzyme inhibitor diphenylene iodonium, or the glutathione peroxidase mime
59 NADPH oxidase function through the inhibitor diphenylene iodonium, the superoxide dismutase mimetic M
60 two inhibitors of ROS generation, azide and diphenylene iodonium, we found that perxoxidases generat
61 as abrogated by N-acetyl cysteine but not by diphenylene iodonium, which displayed prooxidant activit
62 an Arabidopsis thaliana azide-sensitive but diphenylene iodonium-insensitive apoplastic oxidative bu
63 njury correlated with the acute induction of diphenylene iodonium-sensitive NADPH-dependent superoxid
64 n (IL)-1beta stimulation of SMCs resulted in diphenylene iodonium-sensitive ROS production within int
71 nd mouse HSCs by the NADPH oxidase inhibitor diphenylene-iodonium (DPI) and in HSCs lacking the NADPH
72 mplex, which contains a catalytically active diphenylene squaramide moiety and two hydrogen-bond-acce
74 ule, such as poly(para-phenylene), poly(4,4'-diphenylene vinylene) or polyfluorene through alpha- or
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