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1 ion +5 with the chemical cleavage agent 1,10-o-phenanthroline.
2 ferent organic complexing ligands, EDTA, and o-phenanthroline.
3 nucleases are inhibited by the zinc chelator o-phenanthroline.
4                 Three colorimetric reagents, o-phenanthroline, 2,4,6-tri(2-pyridyl)-s-triazine (TPTZ)
5 m the growth medium with the chelating agent o-phenanthroline (20 microM) mimics aerobiosis or combin
6                                              o-Phenanthroline (250 microM), a selective chelator of F
7                         N-acetylcysteine and o-phenanthroline abolished ERK activation by BHTOOH, con
8                           In the presence of o-phenanthroline, an inhibitor of mitochondrial processi
9 n of zinc acetate or the zinc chelators 1,10-o-phenanthroline and EDTA.
10                 The metal was complexed with o-phenanthroline and eosin at pH 7.5 in Tris; a piece of
11 ited by metal ion chelators such as EDTA and o-phenanthroline and partially inhibited by myxothiazol
12 ter by Cu(II) neocuproine (compared with the o-phenanthroline and terpyridine complexes) better allow
13  peptide libraries was completely blocked by o-phenanthroline and thus required metallopeptidases.
14  sensitivity to inhibition of DNA binding by o-phenanthroline, and immunological properties of the li
15 ic RNA cleavage when compared with analogous o-phenanthroline- and terpyridine-derived reagents.
16 uorescent emission of 8-hydroxyquinoline and o-phenanthroline at lambda(em) = 360 nm (lambda(exc) = 2
17  environment, when complexed with Cu2+, 1,10-o-phenanthroline causes cleavage of nearby nucleic acids
18       We have linked the DNA cleaving moiety o-phenanthroline-copper to eight different sites within
19                 Moreover, in the presence of o-phenanthroline-copper, a Cys residue at position 42 in
20 is study utilizes a chemical nuclease, 1, 10-o-phenanthroline-copper, to localize regions of 16S rRNA
21 d p-phenanthroline inhibit import similar to o-phenanthroline, indicating that inhibition of import i
22              High concentrations of EDTA and o-phenanthroline inhibit import of iron-sulfur protein i
23 of the cleavage reagent 5-iodoacetamido-1,10-o-phenanthroline (IoP).
24                      The results showed that o-phenanthroline is the optimal reagent due to its high
25     Pharmacological inhibition of Rpn11 with O-phenanthroline (OPA) blocks cellular proteasome functi
26 p56(lck) dimers with the Zn2+ chelators 1,10-O-phenanthroline or 8-hydroxyquinoline-5-sulfonic acid r
27  pretreatment with either N-acetyl-cysteine, o-phenanthroline, or mannitol, indicating that metal-cat
28 ation of actin monomer (G-actin) with copper o-phenanthroline resulted in a rapid, high yield of disu
29                            The Zn2+ chelator o-phenanthroline reverses the blockade.
30                                  Conversely, o-phenanthroline reversibly impaired the PS-direct of ac
31                           In the presence of o-phenanthroline, S-nitrosocysteine decomposition follow
32 were degraded rapidly by a process involving o-phenanthroline-sensitive metallopeptidases.
33  inhibited by the zinc-chelating agent, 1,10-o-phenanthroline, suggesting it might be a zinc finger p
34 ytic processing of the presequence, and that o-phenanthroline together with EDTA inhibits import of i
35                    The inhibitory effects of o-phenanthroline were related to suppression of S-nitros
36 bited by the same concentrations of EDTA and o-phenanthroline which inhibit import of the wild-type p
37                  In addition, the effects of o-phenanthroline (which removes Ni but not Cu) and neocu