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1 c blocking of the most reactive sites at the bay region.
2 al hazards for communities in the Chesapeake Bay region.
3 arrier to rotation of the aryl groups in the bay region.
4  new regional VLM solution of the Chesapeake Bay region.
5 f the remaining alkene at the phenanthrene's bay region.
6                         The structure of the bay region (1R,2S,3R,4S)-N6-[1-(1,2,3,4-tetrahydro-2,3,4
7 nzymatic activation to enantiomeric pairs of bay-region 7,8-diol 9, 10-epoxides (the benzylic 7-hydro
8                     The structure of the non-bay region (8S,9R,10S,11R)-N(6)-[11-(8,9,10, 11-tetrahyd
9 on adducts are readily bypassed in vivo, the bay region adducts are both blocking to approximately th
10                               While both non-bay region adducts are readily bypassed in vivo, the bay
11 s been linked to repair efficiency such that bay region adducts can be readily repaired while their f
12 nt intrinsic topologies of the rigid, planar bay region adducts versus the twisted, sterically hinder
13  complexation affinity than their respective bay region analogs B[a]P, chrysene, and phenanthrene.
14 ed from shorebirds and gulls in the Delaware Bay region and from ducks in Alberta, Canada, during >18
15 xy-derivatives of three important classes of bay-region and fjord-region PAHs whose diol-epoxides ext
16 benzylic carbocations formed by 1,2-epoxide (bay-region) and 5,6-epoxide (K-region) ring opening.
17 -K-region o-quinones (bay region, methylated bay region, and fjord region o-quinones) produced by AKR
18 ected at over 60 sites across the Chesapeake Bay region annually.
19 lication system, we have shown that both non-bay region anti-trans-benz[a]anthracene adducts are esse
20                             In contrast, the bay region anti-trans-benz[a]anthracene lesions do induc
21  is most efficient in the GSH conjugation of bay-region anti-diol epoxide of benzo(a)pyrene (anti-BPD
22  group) at the imide sites as well as at the bay regions are described in this study.
23                       This differed from the bay region BA RSRS (61,2) adduct, in which the lesion wa
24 orotation at A6 appears to be common to both bay region BA RSRS (61,3) and BP SRSR (61,3) adducts.
25 on BcPh amino tribenzoate as compared to the bay-region BaP amino tribenzoate.
26                         In contrast, the non-bay region benz[a]anthracene adduct was easily bypassed
27            The bay region benzo[a]pyrene and bay region benz[a]anthracene adducts were poorly replica
28 rison with the bay region benzo[a]pyrene and bay region benz[a]anthracene adducts with the correspond
29 try and at the same site shows that this non-bay region benz[a]anthracene lesion assumes different ba
30                                 This was the bay region benz[a]anthracene RSRS (61,3) adduct.
31                          Comparison with the bay region benzo[a]pyrene and bay region benz[a]anthrace
32                                          The bay region benzo[a]pyrene and bay region benz[a]anthrace
33  analogous stereoisomeric DNA adducts of the bay region benzo[a]pyrene diol epoxide (B[a]PDE), 10S (+
34 s-anti-[BP]dA.dT 11-mer duplex, containing a bay region benzo[a]pyrenyl [BP]dA adduct, is compared wi
35  striking contrast to earlier research with "bay" region benzo[a]pyrene-N2-guanine (designated (BP)G)
36 r their fjord-region benzo[c]phenanthrene or bay-region benzo[a]pyrene analogues.
37                             By contrast, the bay region BP-N2-G adducts are susceptible to repair, si
38  (HFP) mediated substitution reaction of the bay-region C10 acetoxy group in four stereoisomeric 7,8,
39 lization (Mallory photocyclization); the new bay region cyclization, with two radical iodine-mediated
40                               The Chesapeake Bay region (defined as longitudes - 78 degrees to -74 de
41 (5-MeC-1,2-diol), as well as 5-MeC-7,8-diol, bay region dihydrodiols, and phenols.
42 or metabolites of 6-MeC were 6-MeC-1,2-diol, bay region dihydrodiols, phenols, and 6-(hydroxymethyl)c
43  that DNA adducts formed from benzo[a]pyrene bay-region diol epoxides can markedly affect top1 activi
44 ate that the adenine adducts induced by both bay-region diol epoxides of DMBA lead to the mutation at
45 d anti-DMBADE), the two metabolically formed bay-region diol epoxides of DMBA, and we have also analy
46 tralis (diatom) was observed in the Monterey Bay region during the same period.
47 long the southern North Sea and the Kattegat Bay regions during the periods from 1930 and 1950 onward
48  of adducts derived from the highly reactive bay region enantiomeric (+)- and (-)-anti-7,8-diol-9,10-
49 e short 2.055 A interatomic distance between bay-region F-9 and H-8, downfield shift of H-8, and a 26
50 e carboxylic acid group is introduced to the bay region for the purpose of further bioconjugation.
51 ivative (10), relief of steric strain in the bay-region greatly favors ipso-protonation (10aH+).
52 ry, the Hampton Roads area of the Chesapeake Bay region has experienced one of the highest rates of r
53 ion of zethrene core and substitution at the bay region in one single step.
54 ructural differences between the non-bay and bay region lesions are correlated with site-specific mut
55             The mutagenic frequency of these bay region lesions is dependent on the stereochemistry a
56      Classes of PAH non-K-region o-quinones (bay region, methylated bay region, and fjord region o-qu
57 zation has been explored for grafting on the bay region of perylenediimide (PDI) different electro- a
58 ester and carboxylate functionalities at the bay region of the acenaphthene motif increases each liga
59                 The Pd shift occurred in the bay region of the dibenzo[g,p]chrysene building blocks,
60 ergies for Diels-Alder cycloadditions in the bay regions of periacenes should diminish monotonically
61 phenyl derivative, a region analogous to the bay regions of perylene and other periacenes.
62                        We also find that the bay region PAHs dibenzo[a,j]anthracene, dibenzo[a,c]anth
63 erred binding sites for the diol epoxides of bay region polycyclic aromatic hydrocarbons (PAH).
64 igenic potential of fjord region compared to bay region polycyclic aromatic hydrocarbons.
65                      The results suggest the bay region ring contributes to base stacking interaction
66 ifferences are attributed to the loss of the bay region ring.
67 n, new catalysts were prepared in which the "bay region" tert-butyl groups were replaced by trimethyl
68 of the two aryl substituents within the same bay region, the chiral peropyrene adopts a twisted backb
69 ementary APEX reactions that occur at K- and bay-regions to access a variety of previously untapped n
70        In major cities across the Chesapeake Bay region, VLM rates are - 1.1 +/- 1.6 mm/yr (1-sigma)
71  electron-deficient aryl substituents in the bay regions were synthesized via iridium-catalyzed C-H a
72 ls combine to form the congested angucycline bay region with control of regio-, diastereo-, and enant