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1  more closely approaching the Fe(III)(NO(-)) resonance structure.
2  the larger contribution of the zwitterionic resonance structure.
3 ical regions defined by the nuclear magnetic resonance structure.
4  evolves aromaticity in open-shell diradical resonance structures.
5  the LSi horizontal linePH <--> LSi(+)-PH(-) resonance structures.
6  which gives rise to significantly different resonance structures.
7 form should be replaced by two more accurate resonance structures.
8 wed us to examine the energies of individual resonance structures.
9 to anion, and Fe(II) keto pi neutral radical resonance structures.
10  reduced forms of FMN-Na being stabilized by resonance structures.
11 ere, we report the solution nuclear magnetic resonance structure and dynamics of Sma0114 from the bac
12 ed as the difference between the most stable resonance structure and that of the delocalized species.
13 esult, ylide-like, rather than carbene-like, resonance structures are most important in the anions de
14                                              Resonance structures based on quintuple M-M bonding domi
15                                Although many resonance structures contribute to the resonance hybrid
16 ure determination including nuclear magnetic resonance structure determination and comparative model
17               This work highlights that more resonance structures do not always lead to a more stabil
18           Theoretical studies of 2 suggest a resonance structure having dominant Ti-C triple-bond cha
19             This behavior is rationalized by resonance structures hindering fast radical reactions.
20    This chromophore possesses a zwitterionic resonance structure in the ground state, as evidenced by
21 s supported by a three dimensional (3D) HCGs resonance structure in the microwave regime is presented
22 s; rather, it is composed of a collection of resonance structures in a dynamic equilibrium.
23                         The validity of this resonance structure is discussed in terms of experimenta
24                                The preferred resonance structure is Fe(II)<--{:C(X)Y}(0) and not Fe(I
25 y a strong contribution of the triply bonded resonance structure [LnMn identical withSnR]Cl and were
26                         The nuclear magnetic resonance structure of [C117S]YmoB and the homology mode
27        Here we describe the nuclear magnetic resonance structure of a region encompassing the second
28 ed model generated from the nuclear magnetic resonance structure of a related protein, NK lysin, sugg
29                      In the nuclear magnetic resonance structure of an archaeal HAMP domain, residues
30    Previous modeling on the nuclear magnetic resonance structure of CCP15-16 in the serum C3 converta
31                   Since the nuclear magnetic resonance structure of MA showed that these Thr residues
32          Here, the solution nuclear magnetic resonance structure of ParG is reported.
33 as constructed based on the nuclear magnetic resonance structure of PMP-C.
34 esent the three-dimensional nuclear magnetic resonance structure of the CBP bromodomain in complex wi
35          Here we report the nuclear magnetic resonance structure of the complex between the regulator
36                         The nuclear magnetic resonance structure of the lipid-bound state of this cyt
37          We report here the nuclear magnetic resonance structure of the major intramolecular G-quadru
38                         The nuclear magnetic resonance structure of the major VEGF G-quadruplex shows
39    We describe the solution nuclear magnetic resonance structure of the Moloney murine leukemia virus
40 ations of a recent micellar nuclear magnetic resonance structure of the natural killer (NK) cell-acti
41                         The nuclear magnetic resonance structure of the prohead RNA E-loop hairpin, r
42 urpose, we first solved the nuclear magnetic resonance structure of the RING domain of TRIM5alpha and
43         We present here the nuclear magnetic resonance structure of the TRIM5 B-box 2 domain and iden
44 sistent with the crystal or nuclear magnetic resonance structure of these or related interactions.
45                             Nuclear magnetic resonance structures of 9 of 12 designed 7- to 10-residu
46                             Nuclear magnetic resonance structures of apolipoprotein-detergent complex
47 -resolution radiographic or nuclear magnetic resonance structures of isolated components into lower r
48 re, we describe crystal and nuclear magnetic resonance structures of KaiB-KaiC,KaiA-KaiB-KaiC, and Ci
49  at ca. 1200 K, sulfinyl isocyanate, bearing resonance structures of O=C-N=S=O and O=C=N-S=O, has bee
50             The crystal and nuclear magnetic resonance structures of p16 from Escherichia coli and Ba
51 etworks within the nanoclusters resemble the resonance structures of polycyclic aromatic hydrocarbons
52 l analysis of the available nuclear magnetic resonance structures of PrP(C), we explore the propensit
53                                          The resonance structures of the derivatives rationalize thei
54 ps to reconcile the crystal/nuclear magnetic resonance structures of the TonB carboxy terminus with c
55 bution of all the 38 native nuclear magnetic resonance structures on the obtained FES, analyzing inte
56  these and related derivatives delineate the resonance structures predominant in these molecules.
57  in cyclic ketones with and without aromatic resonance structure representations, in tautomers and pe
58 mbrane (PM), and a previous nuclear magnetic resonance structure showed that both tyrosines of the CD
59 u-H)W] core can be described by a variety of resonance structures, some of which possess multiple bon
60 The indolo[3,2-b]carbazole core has a larger resonance structure that includes 3 phenyl rings, and th
61 species by disrupting the equilibrium of the resonance structures that constitutes the proposed CR mo
62 nalized by evaluating the aromaticity of the resonance structures that contribute to spin-delocalizat
63 s, and capable of supporting tunable plasmon resonance structures that span the entire visible spectr
64 ed in these transformations are described by resonance structures that suggest beta-elimination.
65                    In these charge-separated resonance structures, the uranium center is oxidized to
66     In the CheA(S) 'P1-CheZ nuclear magnetic resonance structure, these residues form an interaction
67 sures the stabilization from the most stable resonance structure to the delocalized energy-minimum st
68 rpes virus zinc ring domain nuclear magnetic resonance structure was used for homology-based modeling
69 (one pi and three sigma MOs), an analysis of resonance structures was performed for the O(h)Al(6)(2-)
70 g Na(V)1.5 carboxy terminus nuclear magnetic resonance structure, we construct a model of the predict
71  preferential oxidation of a cyclohexadienyl resonance structure with the unpaired electron localized

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