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1 treating hydrazinoazines with (15)N-labeled nitrous acid.
2 sor to ammonia, hydrazine, hydroxylamine and nitrous acid.
3 ophila HS by selective depolymerization with nitrous acid.
4 cts of chemical reactions between indole and nitrous acid.
5 at is formed directly by the condensation of nitrous acid.
6 dylinositol-specific phospholipase C but not nitrous acid.
7 oth cellular resistance to and mutability by nitrous acid.
8 These tetrasaccharides were analyzed using nitrous acid and enzymatic degradation combined with mat
10 ctive nitrogen species involved derives from nitrous acid and is most probably the nitronium cation.
11 lysis in deliquesced aerosol particles forms nitrous acid and nitrate and thus impacts air quality, c
12 lysis mainly sustains the observed levels of nitrous acid and nitrogen oxides at midday under typical
13 idence for rapid recycling of nitric acid to nitrous acid and nitrogen oxides in the clean marine bou
17 d much of the resistance of alpha- spores to nitrous acid and restored full resistance of alpha- spor
19 is would have been converted into nitric and nitrous acids and delivered to the early oceans as acid
21 to reduce the nitro groups and cyclized with nitrous acid, and the corresponding 4-position was funct
22 heat, formaldehyde, HCl, hydrogen peroxide, nitrous acid, and UV radiation than wild-type spores did
24 cells was released from plasma membranes by nitrous acid, as expected for GPI and its PI-PLC resista
25 gradients of DO, pH, free ammonia, and free nitrous acid, associated with aerated and nonaerated pha
27 tive bias in the simulated concentrations of nitrous acid by 28% on average when compared to field ob
28 dition to providing the first structure of a nitrous acid cross-link in DNA, these studies could be o
29 data available for lesion 2 originating from nitrous acid cross-linked DNA to synthetic 2 supports it
30 identical to that of lesion 1 obtained from nitrous acid cross-linked DNA, thus providing a proof of
31 , we described the solution structure of the nitrous acid cross-linked dodecamer duplex [d(GCATCCGGAT
32 ce to the understanding of the mechanisms of nitrous acid cross-linking and mutagenicity, as well as
33 sequence context effect on the structure of nitrous acid cross-links in [d(CG)]2 and the factors all
35 results of the disaccharide analysis of the nitrous acid-degraded [35S]HS suggested that 3-OST-2 tra
36 or quantification of both enzyme-derived and nitrous acid depolymerization products for structural an
37 e utility of PGC-MS for quantification of HS nitrous acid depolymerization products for structural an
40 a novel pretreatment strategy based on free nitrous acid (FNA or HNO2) to enhance methane production
42 ter (BTF) through free ammonia (FA) and free nitrous acid (FNA) inhibition on nitrite-oxidizing bacte
43 ng communities to free ammonia (FA) and free nitrous acid (FNA) would stabilize nitritation by select
44 5-45 mg of N/L) that was established by free nitrous acid (FNA)-based sludge treatment was not higher
50 o-N-2-phenylcyclopropyl-N-methylaniline with nitrous acid gave 4-chloro-N-methyl-N-nitrosoaniline (76
51 a pH lower than 7, implicating formation of nitrous acid (HNO2) and NO, that adds NO equivalents to
52 zing bacteria were not further detected, but nitrous acid (HNO2) was still removed through chemical d
53 in the plasma phase and the solution lead to nitrous acid (HNO2), nitric acid (HNO3), and hydrogen pe
56 hich the nitrosonium ion (NO+)and water form nitrous acid (HONO) and a hydrated proton cluster in the
59 labile nighttime radical reservoirs, such as nitrous acid (HONO) and nitryl chloride (ClNO(2)), contr
60 kappa(1)-O(2)N complex with p-TolSH produces nitrous acid (HONO) and the corresponding dicopper thiol
62 ycling of NO(x) in various environments with nitrous acid (HONO) as an intermediate based on synthesi
64 adiated nitrophenols can produce nitrite and nitrous acid (HONO) in bulk aqueous solutions and in vis
73 us reactivity studies showing that gas-phase nitrous acid (HONO) is released from the protonation of
74 ve importance of common activities on indoor nitrous acid (HONO) mixing ratios was explored during hi
75 (HA) is thought to promote NO2 conversion to nitrous acid (HONO) on soil surfaces during the day.
77 ion of SO(2) by nitrogen dioxide (NO(2)) and nitrous acid (HONO) takes place, the latter producing ni
78 orbed to indoor surfaces reacts with ambient nitrous acid (HONO) to form carcinogenic tobacco-specifi
82 tic converter has been developed to quantify nitrous acid (HONO), a photochemical precursor to NO and
84 rising finding is the formation of gas-phase nitrous acid (HONO), a species known to be a major photo
86 HOx production rates from the photolysis of nitrous acid (HONO), hydrogen peroxide (H2O2), ozone (O3
89 ts, in addition to elevated mixing ratios of nitrous acid (HONO), VOCs, and nitrogen oxides (NO(X)).
91 [NO] + nitrogen dioxide [NO(2)]) and NO(z) (nitrous acid [HONO] + nitric acid [HNO(3)] + nitrogen tr
92 yl radicals (OH) in the gas phase to produce nitrous acid, HONO, but essentially nothing is known abo
93 as been synthesized, and their reaction with nitrous acid in aqueous acetic acid at 0 degrees C was e
94 of the aniline into an aryl diazonium, using nitrous acid in aqueous conditions, was performed in sit
95 NO(2) hydrolysis also enhances the levels of nitrous acid in other polluted regions such as North Ind
97 ion events leading to high concentrations of nitrous acid in the atmosphere contributed to an observe
98 ntaining mixtures, HgCl2-mediated release of nitrous acid in the presence of 2,3-diaminonaphthalene i
99 ants or the double mutant nor any changes in nitrous acid-induced mutagenesis for rdgB mutant strains
100 ontaneous mutagenesis spectra, as well as in nitrous acid-induced mutagenesis spectra, in wild-type c
105 recycling route reproduces levels of gaseous nitrous acid, NO, and NO2 within the model and measureme
106 treating the [3H]heparan sulfate chains with nitrous acid or bacterial heparin lyases, which cut the
107 may be formed either by the condensation of nitrous acid or by the autooxidation of nitric oxide, bo
108 stituted diaminopyrimidines or -pyridines by nitrous acid, orthoester, or acyl halide treatment.
110 ction of 3-amino-5-nitro-1,2,4-triazole with nitrous acid produces the corresponding diazonium salt.
111 le formed between 2,3-diaminonaphthalene and nitrous acid released from S-nitrosothiols by treatment
112 reaction between 2,3-diaminonaphthalene and nitrous acid released from the S-NO bond by HgCl2 approa
115 onase, NaOH/NaBH(4), heparinase I, or low pH nitrous acid showed that each HS-glycosaminoglycan regio
116 at internal N-sulfoglucosamine residues with nitrous acid then creates a set of fragments of defined
119 contrast, mutagenesis of nongrowing cells by nitrous acid was unaffected by an nirB mutation, suggest
120 ompletely abolished following treatment with nitrous acid, which digests heparan sulfate glycosaminog
121 g microorganisms with the antimicrobial free nitrous acid, which is generated in situ from calcium ni
122 f nitrate is converted in the acid medium to nitrous acid, which leads to the nitrosation of the indo
123 The reaction of 6 with in situ generated nitrous acid yielded the primary explosive bis(4-diazo-5