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1 armony with previous comparisons obtained by crystallographic analyses.
2 e enzyme is known from high resolution x-ray crystallographic analyses.
3 ce using site-directed mutagenesis and x-ray crystallographic analyses.
4 ructure on the basis of proton NMR and X-ray crystallographic analyses.
5 e identified from other studies, with recent crystallographic analyses.
6 in solution as suggested by 1H NMR and X-ray crystallographic analyses.
7 t surfaces were retained as was confirmed by crystallographic analyses.
8 ata, DP4+ probability calculation, and X-ray crystallographic analyses.
9 d (13) C NMR, infrared, elemental, and X-ray crystallographic analyses.
10 m of inhibition using mass spectrometric and crystallographic analyses.
11 of 1 were studied by spectroscopic and X-ray crystallographic analyses.
12 on on protein crystals, complementary to the crystallographic analyses.
13  these modifications were confirmed by x-ray crystallographic analyses.
14 ter was addressed through elegantly designed crystallographic analyses.
15 c (1)H and (13)C NMR spectroscopic and X-ray crystallographic analyses.
16 t of the active site), as supported by X-ray crystallographic analyses.
17 vable in typical medium- and high-resolution crystallographic analyses.
18 sis and chemical cross-linking, coupled with crystallographic analyses.
19 ed conformations identified in earlier X-ray crystallographic analyses.
20 K and characterized by biochemical and X-ray crystallographic analyses.
21  SA*+ are probed by the combination of X-ray crystallographic analyses and density functional theoret
22                                    We report crystallographic analyses and ligand-binding experiments
23 -free P protein required for high resolution crystallographic analyses and may be useful for the prep
24               Atomic-scale characterization, crystallographic analyses and molecular dynamics simulat
25                                         Both crystallographic analyses and quantum mechanical calcula
26 ructures were experimentally proven by X-ray crystallographic analyses and the electronic configurati
27  conformational changes not seen in previous crystallographic analyses, and a quantitative analysis r
28 tor to InhA, as shown by enzymatic and X-ray crystallographic analyses, and establishes InhA as the p
29 y, NOE experiments, mass spectrometry, X-ray crystallographic analyses, and isothermal titration calo
30 ed by solution and solid-state NMR and X-ray crystallographic analyses, and provided insight into the
31          The results of single-crystal X-ray crystallographic analyses are given for four of the comp
32 e unusual interactions are documented, X-ray crystallographic analyses are reported, and theoretical
33 ng development of in vitro assays as well as crystallographic analyses both in the absence and presen
34                                              Crystallographic analyses confirm that 1 and 2 adopt C(2
35 ar magnetic resonance spectroscopy and X-ray crystallographic analyses confirm that a Tyr8 to Phe mut
36                                        X-ray crystallographic analyses confirm that the side chains o
37                             Peptide maps and crystallographic analyses confirm the presence of the 10
38 ar magnetic resonance spectroscopy and X-ray crystallographic analyses demonstrate that the covalent
39                                              Crystallographic analyses demonstrate that the surface a
40 tudies, mass spectrometric measurements, and crystallographic analyses demonstrate that these inhibit
41  the BtuCD and BtuF preparations used in the crystallographic analyses for both ATPase and transport
42                                     Based on crystallographic analyses for others RTKs, TrkB tyrosine
43                                          The crystallographic analyses further evidence the lattice c
44                                              Crystallographic analyses have been unsuccessful in reso
45 yme complexes may be more flexible than most crystallographic analyses have implied.
46                        High resolution x-ray crystallographic analyses have shown that, remarkably, t
47 ent issue of PLOS Biology reveal by means of crystallographic analyses how the Rap proteins of bacill
48                           REAP combined with crystallographic analyses identified 35 sites where repl
49                               Previous x-ray crystallographic analyses identified distinct binding si
50                                        X-ray crystallographic analyses identify the consistent format
51                                              Crystallographic analyses of 11 PelC-Ca(2+) complexes, f
52 lpha-substituted tropanes, as shown by X-ray crystallographic analyses of 11, 12, and 19.
53             Here we report physiological and crystallographic analyses of a calcium selectivity filte
54               We report here the first X-ray crystallographic analyses of a Fab fragment from a rat a
55 tion, have been largely revealed by detailed crystallographic analyses of a number of haemoglobin mol
56                                              Crystallographic analyses of a shared HSPG-CSPG binding
57                               Finally, X-ray crystallographic analyses of a spectrum of analogues cle
58                                   Subsequent crystallographic analyses of AChE complexes with the TZ2
59                                              Crystallographic analyses of CocE-L169K/G173Q, determine
60                                              Crystallographic analyses of four distinct structures (a
61     Evidence for such a mechanism comes from crystallographic analyses of fragments of VP4, the rotav
62                              By carrying out crystallographic analyses of full-length H6N6-NS1 (A/blu
63 F-RNA we carried out thermodynamic and X-ray crystallographic analyses of fully and partially 2'-F-mo
64                                     Previous crystallographic analyses of GlpG, a bacterial rhomboid
65                                              Crystallographic analyses of H-2K(b)-peptide complexes s
66                                              Crystallographic analyses of HA from the recent H1N1 vir
67                                    We report crystallographic analyses of human JMJD5 complexed with
68 nscription complexes of a bacterial RNAP and crystallographic analyses of its backtracked and Gre-fac
69              Biophysical analyses, including crystallographic analyses of JMJD6(Delta344-403) in comp
70                                  A series of crystallographic analyses of Leishmania major PTR1 are r
71                            Comparative X-ray crystallographic analyses of MDMX and of pTyr99 MDMX in
72 e phosphatase activity of NSP2, we performed crystallographic analyses of native NSP2 and a functiona
73                                              Crystallographic analyses of product and substrate compl
74  mapping in a human helminth parasite, while crystallographic analyses of protein-drug interactions i
75                                        X-ray crystallographic analyses of Q425 in the presence of Ca(
76                                              Crystallographic analyses of Ras bound to the catalytic
77                                              Crystallographic analyses of representative structures r
78                                        X-ray crystallographic analyses of ribosomal complexes have re
79                                              Crystallographic analyses of SC-2 and HS-2 show that SC-
80 eraction at the atomic level, we carried out crystallographic analyses of Sp-Nup37 alone and in a com
81                                          The crystallographic analyses of such enzyme-DNA complexes h
82                           We performed x-ray crystallographic analyses of the 6-aminohexanoate oligom
83                                        X-ray crystallographic analyses of the 8-, 9-, and 10-membered
84                        IR spectral and X-ray crystallographic analyses of the [ArH,NO+] complexes rev
85                                              Crystallographic analyses of the antibodies, in many cas
86                                              Crystallographic analyses of the complexes revealed very
87                        Structural as well as crystallographic analyses of the cross-linked species, B
88                                  Kinetic and crystallographic analyses of the EcoRV E45A mutant enzym
89 d-containing bacteriophage PM2 determined by crystallographic analyses of the entire approximately 45
90  molecule-1, have been investigated by X-ray crystallographic analyses of the individual components a
91                            Here, we describe crystallographic analyses of the mechanism of inhibition
92                                        X-ray crystallographic analyses of the new cores were used to
93                                              Crystallographic analyses of the paired-end complex (PEC
94        However, recent high-resolution X-ray crystallographic analyses of the protein from Escherichi
95 putational model of the nucleosome, based on crystallographic analyses of the structure and elasticit
96                                NMR and X-ray crystallographic analyses of the tetrafluorinated methyl
97                                        X-ray crystallographic analyses of the three parent ligands (1
98                              Here we present crystallographic analyses of the virally hijacked form o
99                                              Crystallographic analyses of this construct show the bas
100                              Biochemical and crystallographic analyses of this factor, which we term
101                         Single-crystal X-ray crystallographic analyses of three alpha/beta-peptide ca
102                                        X-ray crystallographic analyses of three different examples ha
103          Spectroscopic and atomic resolution crystallographic analyses of three representatives, mOra
104                                              Crystallographic analyses of two compounds demonstrated
105 ally different from that proposed from x-ray crystallographic analyses of two-domain fragments, in wh
106 ased on solution fluorescence, kinetics, and crystallographic analyses of wild-type and mutant polyme
107                              Our kinetic and crystallographic analyses offer the molecular basis for
108  line with important conclusions of previous crystallographic analyses, particularly the ZZEssa confi
109                                     Electron crystallographic analyses provide little information abo
110                                              Crystallographic analyses provided a rationale for their
111                                              Crystallographic analyses reveal inhibition by 2OG cosub
112                                     Detailed crystallographic analyses reveal quantitively the flexib
113                                        X-ray crystallographic analyses reveal that the backbone of 5
114                                              Crystallographic analyses reveal that the N-terminal dom
115                        Biochemical and X-ray crystallographic analyses reveal that the properties of
116                                     Notably, crystallographic analyses reveal that the unusual dimeri
117                                              Crystallographic analyses reveal that the UTY(KDM6C) act
118                                    While the crystallographic analyses revealed only one structure, I
119                                        X-ray crystallographic analyses revealed that GRL-142 interact
120                              Biochemical and crystallographic analyses revealed that hormone binding
121                                        X-ray crystallographic analyses revealed that the phase transi
122                                        X-ray crystallographic analyses revealed that, similar to 8-ox
123                                              Crystallographic analyses revealed two binding modes for
124         We report cellular, biochemical, and crystallographic analyses revealing that Pseudomonas pro
125 ese enzymes are homologous, and recent X-ray crystallographic analyses show the active sites of the t
126                               Previous x-ray crystallographic analyses showed that the GAT region is
127                          The results support crystallographic analyses showing the importance of hydr
128 sis experiments, enzymatic assays, and x-ray crystallographic analyses suggest that His(49) functions
129          Amide hydrogen exchange studies and crystallographic analyses suggest that this substrate-bi
130                            Atomic resolution crystallographic analyses suggest that two important fac
131                   We show in biochemical and crystallographic analyses that PHF2 recognizes histone H
132 2+ and the MIDAS region have been defined by crystallographic analyses, the role of cation in I domai
133 richia coli genome, has been solved by X-ray crystallographic analyses to a resolution of 1.85 A for
134 l angle X-ray scattering and 2 were shown by crystallographic analyses to be in close agreement with
135                    We used thermodynamic and crystallographic analyses to compare the I:s(2)C and A:s
136 nary complexes have been determined by X-ray crystallographic analyses to high resolution.
137                                Here, through crystallographic analyses we show that the SUMO E2 Ubc9
138 hemical and biophysical tools, LC-MS/MS, and crystallographic analyses, we identified key residues es
139 ing biochemical, spectroscopic and anaerobic crystallographic analyses, we showed that formaldehyde r
140                                        X-ray crystallographic analyses were performed on ureas 1, 3,
141  for the inhibition of elastase, kinetic and crystallographic analyses were undertaken to identify th
142 erminal domain of RNase E is consistent with crystallographic analyses, which indicate that the tetra
143                                              Crystallographic analyses with five inhibitors imply ind
144                                              Crystallographic analyses with succinate, fumarate, L-ma

 
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