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1 he junction centre were strongly reactive to potassium permanganate.
2 m of the junction, as shown by reaction with potassium permanganate.
3  thymines in the transcription bubble toward potassium permanganate.
4 ction reaction between hydrogen peroxide and potassium permanganate.
5 symmetric oxidation reaction of alkenes with potassium permanganate.
6  DNA for possible unwinding in vivo by using potassium permanganate, a chemical that reacts with unpa
7                                              Potassium permanganate and dimethyl sulfate interference
8                                              Potassium permanganate and dimethyl sulfate interference
9 3 (fimbrial subunit), using gel retardation, potassium permanganate and DNase I footprinting, cleavag
10  repeats, were probed with dimethylsulphate, potassium permanganate and S1 nuclease.
11 a dispersion medium, a dehydrating agent for potassium permanganate, and an intercalant.
12                                       Use of potassium permanganate as a probe for unpaired bases in
13  complex formation has been determined using potassium permanganate as a probe.
14 en peroxide and oxidized thymines created by potassium permanganate, at a single-base resolution.
15 edrone (methcathinone), involving the use of potassium permanganate, became a new cause of intoxicati
16 midine-specific agents such as hydrazine and potassium permanganate, but not the DNA sugar-specific p
17  DNA melting and promoter clearance by using potassium permanganate, diethylpyrocarbonate and methidi
18 ted with these promoters in heterochromatin; potassium permanganate experiments showed a loss of Pol
19 7,8-tetrahydronaphthalen-1-yl)acetamide with potassium permanganate followed by acidic hydrolysis gav
20 ion was tested by using dimethyl sulfate and potassium permanganate footprinting analyses.
21       Transcription experiments in vitro and potassium permanganate footprinting analysis show that M
22                                              Potassium permanganate footprinting experiments indicate
23                                              Potassium permanganate footprinting on the nontemplate a
24                         In vitro DNase I and potassium permanganate footprinting revealed that Rns bi
25                                              Potassium permanganate footprinting revealed that the oc
26                                 We have used potassium permanganate footprinting to monitor DNA stran
27                                 Here we used potassium permanganate footprinting, DNase I footprintin
28                               Oxidation with potassium permanganate gave good yields of related diols
29 how that osmium tetroxide can be replaced by potassium permanganate, giving the same spectrum of muta
30 uclease or the single-strand-selective agent potassium permanganate included the major promoters P1 a
31 alactosidase histochemistry using 0.1% to 1% potassium permanganate incubation for 1 minute to 2 hour
32                                   The use of potassium permanganate is compatible with solid phase ca
33 th chloroacetaldehyde, dimethyl sulfate, and potassium permanganate is consistent with the formation
34                                        Using potassium permanganate (KMnO(4)) modification, we have i
35  report real-time hydroxyl radical (*OH) and potassium permanganate (KMnO4) footprints obtained under
36                                      We used potassium permanganate (KMnO4) to identify unpaired thym
37  reactivity of the top and bottom strands to potassium permanganate (KMnO4).
38 ulfuric acid with a strong oxidizer, such as potassium permanganate, leads to the formation of graphe
39                                 Here we used potassium permanganate modification to show that the avi
40                                 Furthermore, potassium permanganate probing shows that the conformati
41 Dehydrogenation of the indoline aminals with potassium permanganate produced the corresponding cyclic
42                                       Simple potassium permanganate proved to be the most efficient,
43    Here, we use protein-DNA crosslinking and potassium permanganate reactivity to explore the base-fl
44 benzothiazoline-6-sulfonic acid) (ABTS), and potassium permanganate reduction (PPR) leaf disc assays.
45 Tafel kinetics and mass diffusivities during potassium permanganate reduction from only one potential
46                                 Probing with potassium permanganate reveals that the bis-PNA complexe
47                                        After potassium permanganate sensitivity of unpaired thymine r
48                    Arsine is absorbed into a potassium permanganate solution, the discoloration of wh
49 etermination based on the discoloration of a potassium permanganate solution.
50  accessibility of PSE and type I elements to potassium permanganate suggests that origin regions are
51 arison of CCM with osmium tetroxide and with potassium permanganate, tested on a complete set of sing
52 present study we utilized the chemical probe potassium permanganate to identify sites of DNA distorti
53                                 We have used potassium permanganate to probe contacts between vaccini
54                                        Using potassium permanganate, which preferentially modifies si
55 er was an active layer containing pumice and potassium permanganate, while the skin layer was the bar
56                     The specific reaction of potassium permanganate with thymine in single-stranded D