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1  with negatively charged fluorescent label 8-aminopyrene-1,2,6-trisulfonate (APTS) were separated to
2 le, mixture of oligosaccharides labeled by 8-aminopyrene-1,3,6-trisulfonate (APTS) was separated by c
3  addition, CE-MS was used to confirm major 8-aminopyrene-1,3,6-trisulfonate (APTS)-labeled glycans re
4 or resolution over the commonly used label 8-aminopyrene-1,3,6-trisulfonic acid (APTS) in both the CE
5 ans based on ceramide glycanase digestion, 8-aminopyrene-1,3,6-trisulfonic acid (APTS) labeling, and
6  from these samples were then reacted with 8-aminopyrene-1,3,6-trisulfonic acid (APTS) to provide a f
7  laser-induced fluorescence (CE/LIF) using 8-aminopyrene-1,3,6-trisulfonic acid (APTS)-labeled glycan
8                                            8-Aminopyrene-1,3,6-trisulfonic acid (APTS)-labeled maltoo
9 t, CGE-LIF relies on the green fluorophore 8-aminopyrene-1,3,6-trisulfonic acid (APTS).
10 en derivatized with a charged fluorophore, 8-aminopyrene-1,3,6-trisulfonic acid and further separated
11 glycans that are subsequently reacted with 8-aminopyrene-1,3,6-trisulfonic acid to add charge and a f
12 , the glycan samples were derivatized with 8-aminopyrene-1,3,6-trisulfonic acid to impart needed char
13  activity was also detected when the APTS (8-aminopyrene-1,3,6-trisulfonic acid, trisodium salt)-labe
14 ccharides labeled with a novel fluorophore 1-aminopyrene-3,6,8-trisulfonate (APTS) at the reducing te
15 een used for structure characterization of 1-aminopyrene-3,6,8-trisulfonate (APTS)-derivatized oligos
16 oresis separations of glycans labeled with 1-aminopyrene-3,6,8-trisulfonic acid were achieved with se
17 hangeable and nonexchangeable protons of the aminopyrene and the nucleic acid were assigned following
18 cts, the 1-NP-induced DNA adduct contains an aminopyrene (AP) moiety covalently linked to the C8 posi
19 synalignment at the N-(deoxyguanosin-8-yl)-2-aminopyrene ([AP]dG) adduct site positioned opposite dC
20 lix glucan, laminarin, doubly labeled with 1-aminopyrene as donor probe and fluorescein-5-isothiocyan
21 ructural studies have been undertaken on the aminopyrene-C(8)-dG ([AP]dG) adduct in the d(C5-[AP]G6-C
22 cifically placed 8-(deoxyguanosin-N(2)-yl)-1-aminopyrene (dG(1,8)), one of the DNA adducts derived fr
23 a major DNA adduct, N-(deoxyguanosin-8-yl)-1-aminopyrene (dGAP), both in vitro and in vivo.
24  form predominantly N-(deoxyguanosin-8-yl)-1-aminopyrene (dGAP).
25  was crosslinked by a conjugated molecule (1-aminopyrene-disuccinimidyl suberate, AD).
26 ropyrene, 9(10)-hydroxy-4-nitropyrene, and 4-aminopyrene from 4-NP.
27 han the major 1-NP adduct, N-(guanin-8-yl)-1-aminopyrene (Gua-C8-AP).
28 hangeable and nonexchangeable protons of the aminopyrene moiety and the nucleic acid were assigned fo
29 tween the active site residues of Dpo4 and 1-aminopyrene moiety at the first pause site.
30             In summary, intercalation of the aminopyrene moiety is accompanied by displacement of bot
31 Dpo4.DNA-dG(1,8).dCTP ternary structure, the aminopyrene moiety of the dG(1,8) lesion, is sandwiched
32 .DNA-dG(1,8) binary structure shows that the aminopyrene moiety of the lesion stacks against the prim
33 cal electron donor-acceptor triads having an aminopyrene primary donor (APy) and a p-diaminobenzene s
34 AP]dG.dA 11-mer duplex containing the larger aminopyrene ring (reported in this study) relative to th
35 ard the major groove as a consequence of the aminopyrene ring intercalation into the helix.
36                                          The aminopyrene ring of [AP]dG6 is intercalated into the DNA
37                                          The aminopyrene ring of [AP]dG6 is intercalated into the DNA
38 agenesis induced by N-(deoxyguanosin-8-yl)-1-aminopyrene, the major DNA adduct formed by the carcinog
39 ectrophoresis (CE)-ESI-MS in the analysis of aminopyrene-trisulfonate labeled linear maltooligosaccha
40 ctive metabolism leading to the formation of aminopyrene was evident only with 4-NP.