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1 1000 mum), accompanied by tautomerization of cyanuric acid.
2 onsecutive deamination reactions to generate cyanuric acid.
3 ituents from the herbicide atrazine to yield cyanuric acid.
4  through the addition of a nucleobase mimic, cyanuric acid.
5 kes of melamine (16.9-30.6 ng/kg bw/day) and cyanuric acid (88.8-161 ng/kg bw/day) were calculated fo
6                                              Cyanuric acid, a common chlorine stabilizer, reacts reve
7 steps, encoded by the genes atzABC, to yield cyanuric acid, a nitrogen source for many bacteria.
8 in aquatic recreational facilities to remove cyanuric acid, a stabilizer for the chlorine.
9                                              Cyanuric acid also catalyzes NHCl(2) formation from NH(2
10  58% amino acid sequence identity to TrzD, a cyanuric acid amidohydrolase, from Pseudomonas sp. strai
11                     In this study, melamine, cyanuric acid, ammeline, and ammelide were analyzed in 1
12 of melamine and its three derivatives (i.e., cyanuric acid, ammeline, and ammelide) was determined in
13 y interacting low-molecular-weight monomers (cyanuric acid and a modified triaminopyrimidine) are sho
14 ometric hydrolysis of N-isopropylammelide to cyanuric acid and isopropylamine.
15 ly identical vesicular membranes composed of cyanuric acid and melamine functionalized phospholipids
16 y simple, unfunctionalized molecules such as cyanuric acid and melamine have so far been used in this
17 ng N-isopropylammelide stoichiometrically to cyanuric acid and N-isopropylamine.
18  the bacterial transformation of melamine to cyanuric acid and potentially contribute to the toxicity
19 bstances such as 1H-benzotriazole, melamine, cyanuric acid, and 1,4-dioxane are responsible for subst
20 her genes encoding the further catabolism of cyanuric acid, atzE and atzF, reside in a contiguous clu
21        Every year over 250 million pounds of cyanuric acid (CA) and chlorinated isocyanurates are pro
22                                              Cyanuric acid (CA) and melamine (M) functionalized lipid
23                                         When cyanuric acid (CA), a plausible ancestral nucleobase, is
24 wo monotelechelic polymers containing either cyanuric acid (CA)- or ureidoguanosine (UG)-end groups t
25 associations were noted between melamine and cyanuric acid concentrations and maternal/infant charact
26 le nucleic acids are formed from mixtures of cyanuric acid (Cy) and ribonucleotides (l-, d-pTARC) tha
27                                              Cyanuric acid (CYA) is a chlorine stabilizer used in swi
28 midine (TAP) and carboxylic acid substituted cyanuric acid (CyCo6 or R-4MeCyCo6) monomers self-assemb
29 mimics (2,4,6-triaminopyrimidine, TAP, and a cyanuric acid derivative, CyCo6) spontaneously assemble
30            The remarkable ability of TAP and cyanuric acid derivatives to self-assemble in water, and
31             Under simulated pool conditions, cyanuric acid enhanced micropollutant removal, suppresse
32                                 Melamine and cyanuric acid have been reported to occur in animal prod
33                     The chlorinated salts of cyanuric acid have found an important role in recreation
34 phyrin (2) by means of the Hamilton receptor/cyanuric acid hydrogen bonding motif into energy transdu
35 t, the published enzyme reaction products of cyanuric acid hydrolase are incorrectly identified as bi
36 dy, we report the X-ray structure of TrzD, a cyanuric acid hydrolase from Acidovorax citrulli.
37                                              Cyanuric acid hydrolase opens the cyanuric acid ring hyd
38 ctroscopy and mass spectrometry to show that cyanuric acid hydrolase releases carboxybiuret, which sp
39                                              Cyanuric acid hydrolases (AtzD) and barbiturases are hom
40 nificant because it revealed that homologous cyanuric acid hydrolases and barbiturases catalyze compl
41                                              Cyanuric acid hydrolases are of industrial importance be
42 assignment of individual sequences as either cyanuric acid hydrolases or barbiturases, and spurious c
43 i-O-Ac-2-deoxy-beta-D-erythro-pentofuranosyl)cyanuric acid, Ia.
44 t pertains to the occurrence of melamine and cyanuric acid in cattle feed and urine is lacking.
45 xposure patterns and sources of melamine and cyanuric acid in cattle.
46 tively) were developed to accurately measure cyanuric acid in swimming pools.
47 e-evaluates these constants and examines how cyanuric acid influences breakpoint reactions, focusing
48                        Degradation of excess cyanuric acid is necessary to maintain chlorine disinfec
49 sly combining the implementation of melamine-cyanuric acid (MCA) supramolecular aggregates and microw
50 preorganized, supramolecular hydrogen-bonded cyanuric acid-melamine (CAM) crystals.
51 d, hollow carbon nitride structures, using a cyanuric acid-melamine (CM) complex in ethanol as a star
52 siting terephthalic acid or trimesic acid on cyanuric acid/melamine, we have determined, using atomic
53            The coordination of polyamine and cyanuric acid modification endows MNNs with high adsorpt
54 other rigid, symmetrically trifunctionalized cyanuric acid moiety.
55 rk, we show that the addition of substituted cyanuric acid molecules can successfully program polyade
56 g eight silver atoms, four melamine and four cyanuric acid molecules, which generate 1D coordination
57 ules by insoluble complexes of melamine with cyanuric acid or uric acid.
58 esent in the soybean meal, such as melamine, cyanuric acid or whey powder (milk serum).
59                           In the presence of cyanuric acid, polyadenine strands assemble into triple
60 acting as chlorine reservoirs in the form of cyanuric acid, preventing the photolytic destruction of
61 ne-5,8-dione; alternatively, N-haloimides of cyanuric acid provided both oxidation and halogenation g
62  to understand the effect of the chlorine-to-cyanuric acid ratio on DBP mixture composition and calcu
63 replace two of the three hydrogen atoms from cyanuric acid resulting in the transformation from short
64 ises from C-dots with embedded fluorophores, cyanuric acid-rich C-dots, a blend of molecular fluoroph
65            Cyanuric acid hydrolase opens the cyanuric acid ring hydrolytically and subsequent decarbo
66 arrying out nucleophilic attack, opening the cyanuric acid ring, and the mobile lysine guides product
67 ustainable, solid-state, polyamine-appended, cyanuric acid-stabilized melamine nanoporous networks (M
68                    Recommended levels of the cyanuric acid stabilizer are in the 10-100 mg/L concentr
69  Escherichia coli expressing AtzD hydrolyzed cyanuric acid to biuret.
70 nsistent with the association of adenine and cyanuric acid units into a hexameric rosette, which brin
71       Urinary concentrations of melamine and cyanuric acid varied significantly among the three count
72 monas sp. strain ADP metabolizes atrazine to cyanuric acid via three plasmid-encoded enzymes, AtzA, A
73                                              Cyanuric acid was the major derivative, accounting for 7
74  from 4.2 to 5280 ng/mL (median: 370 ng/mL); cyanuric acid was the major derivative, accounting for 9
75 ted cumulative daily intakes of melamine and cyanuric acid were at least 10-fold below the current to
76                                              Cyanuric acid, while mitigating scavenging of *OH and ni
77  report the discovery that a small molecule, cyanuric acid, with three thymine-like faces, reprogramm