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1 prepared and characterized by single crystal X-ray analysis.
2 2.0]heptane was determined by single crystal X-ray analysis.
3 mplexes were characterized by single-crystal X-ray analysis.
4 py, X-ray diffraction, and energy-dispersive X-ray analysis.
5 that can be recalcitrant to high resolution X-ray analysis.
6 ulphur mapping by cryo-SEM/energy-dispersive X-ray analysis.
7 ives have been isolated and characterized by X-ray analysis.
8 sphatidylcholine that had been determined by X-ray analysis.
9 ding block 2 are confirmed by single-crystal X-ray analysis.
10 abicyclo[3.2.1]octane has been reassigned by X-ray analysis.
11 electron diffraction, and energy dispersive X-ray analysis.
12 c molecule, whose structure was confirmed by X-ray analysis.
13 eochemistry of an aldol product confirmed by X-ray analysis.
14 9, and 11 were unambiguously established by X-ray analysis.
15 lly characterized by means of single-crystal X-ray analysis.
16 g from the core that was deleted for NMR and X-ray analysis.
17 ization, electrospray mass spectrometry, and X-ray analysis.
18 e high-resolution structure of the enzyme by x-ray analysis.
19 ctivity filter (TVGYG) of KcsA identified by x-ray analysis.
20 ng diffraction-quality crystals suitable for x-ray analysis.
21 ton NMR spectroscopy, mass spectrometry, and X-ray analysis.
22 erivatives was prepared and characterized by X-ray analysis.
23 alline forms as determined by single-crystal X-ray analysis.
24 talline (reactive) salts suitable for direct X-ray analysis.
25 ng electron microscopy and energy dispersive X-ray analysis.
26 structure was confirmed on the basis of its X-ray analysis.
27 ion of 2D NMR experiments and single-crystal X-ray analysis.
28 les has been established by a single-crystal X-ray analysis.
29 borate (11c) was confirmed by single-crystal X-ray analysis.
30 adiazines were established by single-crystal X-ray analysis.
31 d characterized through NMR spectroscopy and X-ray analysis.
32 f the arms were determined by single-crystal X-ray analysis.
33 diphosphonate cavitand 13 by single-crystal X-ray analysis.
34 and 12 have been confirmed by single-crystal X-ray analysis.
35 unequivocally determined by a single-crystal X-ray analysis.
36 C NMR, mass spectrometry, and single-crystal X-ray analysis.
37 ctroscopic data as well as by single crystal X-ray analysis.
38 to a structure similar to those obtained by x-ray analysis.
39 l structure of PGHS-2 holoenzyme obtained by x-ray analysis.
40 pic methods, accurate mass measurements, and X-ray analysis.
41 enyldiimide N'-oxide as indicated by NMR and X-ray analysis.
42 btaining crystals with a volume suitable for x-ray analysis.
43 state for 5, as determined by single crystal X-ray analysis.
44 tively), whose structures were determined by X-ray analysis.
45 nfiguration was determined by single-crystal X-ray analysis.
46 e ligand and characterized by single crystal X-ray analysis.
47 oxynucleoside triphosphate, as determined by x-ray analysis.
48 2) also forms crystals that are suitable for X-ray analysis.
49 ructure, both of which were characterized by X-ray analysis.
50 re NMR (17.1 +/- 0.8 kcal/mol) estimates and X-ray analysis.
51 med by DFT quantum chemical calculations and X-ray analysis.
52 re isostructural according to single crystal X-ray analysis.
53 MR spectroscopy, intermediate isolation, and X-ray analysis.
54 RMS, HPLC, and in the cases of 2b and 5b, by X-ray analysis.
55 nd 5-15 H2O were confirmed by single-crystal X-ray analysis.
56 a diborane complex has been established from X-ray analysis.
57 f 3 was determined via 13a by single-crystal X-ray analysis.
58 hich was further confirmed by single-crystal X-ray analysis.
59 or into crystalline derivatives suitable for X-ray analysis.
60 key products are confirmed by single-crystal X-ray analysis.
61 Both structures are verified by X-ray analysis.
62 4)Cu accumulation sites by energy dispersive x-ray analysis.
63 s were determined by DFT calculations and/or X-ray analysis.
64 em have been characterized by single-crystal X-ray analysis.
65 formations were determined by single-crystal X-ray analysis.
66 nambiguously characterized by single-crystal X-ray analysis.
67 em have been characterized by single-crystal X-ray analysis.
68 n mass spectrometry (MS), and single-crystal X-ray analysis.
69 was synthesized and its structure solved by X-ray analysis.
70 olute stereochemistry has been determined by X-ray analysis.
71 in the transcription complex as suggested by X-ray analysis.
72 by electron microscopy and energy-dispersive X-ray analysis.
73 heses, were observed using energy dispersive X-ray analysis.
74 The disulfide complex was characterized by X-ray analysis.
78 uents) was determined through single-crystal X-ray analysis and 2D (NOESY, HSQC, HMBC) NMR experiment
79 tion were characterized by energy dispersive x-ray analysis and backscattered scanning electron micro
82 tablished by a combination of single-crystal X-ray analysis and comprehensive 2D NMR measurements.
83 ved to be sufficiently crystalline to enable X-ray analysis and determination of their solid-state co
84 ble molecular "scrolls" were investigated by X-ray analysis and electron microscopy, respectively.
86 validates the structural model derived from X-ray analysis and provides additional insight into apoE
87 The stage behavior was investigated using X-ray analysis and Quantum Mechanics/Molecular Mechanics
88 n electron microscopy with energy dispersive X-ray analysis and scanning transmission X-ray microscop
89 nteraction, was visualized by single-crystal X-ray analysis and supported by variable-temperature NMR
90 ng electron microscopy and energy-dispersive X-ray analysis and the particle size distributions using
92 hemistry was characterized by single-crystal X-ray analysis and was furthermore extended toward next
93 the structural features determined from the X-ray analysis and, consistent with the experimental abs
97 per duplex are localized and visible in the X-ray analysis, and nine are disordered and invisible.
98 tests, surface microscopy, energy-dispersive X-ray analysis, and Raman microscopy has led to the iden
99 ls have been characterized by single-crystal X-ray analysis, and the presence of inter- and intramole
100 ons were characterized in the solid state by X-ray analysis, and the strength of each interaction was
101 orophores were structurally characterized by X-ray analysis, and their photophysical properties studi
102 tructures were confirmed with single-crystal X-ray analysis, and their properties were determined by
103 nning electron microscopy, energy-dispersive X-ray analysis, and X-ray photoelectron spectroscopy ind
105 poses a difficult challenge to conventional X-ray analysis, because it was completely obscured with
107 CD-MOF has been confirmed by single-crystal X-ray analysis by determining the vacancies of K(+)-ion
115 ectron microscopy (HRTEM), energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM), sca
118 e products, as established by single-crystal X-ray analysis for substrates (S)-11c, (S)-19, and (S)-2
122 ral origin for these differing activities by X-ray analysis has not succeeded due to difficulties in
123 mplete bony bridging by 12 weeks as shown by X-ray analysis, histology and live micromolecular imagin
124 d complex and its structure determination by X-ray analysis; in addition, kinetic simulations using t
130 one of these domains has been determined by x-ray analysis, its connection to the other major domain
131 bitor 5, structure-based design supported by X-ray analysis led to the discovery of the potent and se
132 on via infrared spectroscopy, single crystal X-ray analysis, Mossbauer spectroscopy, and magnetic sus
143 ucture represents the first visualization by X-ray analysis of a murine Fc segment, and its CH2 domai
144 ium complex and fluorenyl group, as shown by X-ray analysis of a single crystal, and this facilitates
145 bidentate nature of binding is supported by X-ray analysis of an intermediate analogue, which experi
147 pported by molecular modeling studies and by X-ray analysis of BACE1 complexes with various ligands t
153 mately confirmed to be spiroleucettadine via X-ray analysis of crystalline spiroleucettadine and rein
161 ablished by successful cocrystallization and X-ray analysis of potent inhibitors with the TbetaR-I re
162 eochemistry was unequivocally established by X-ray analysis of precursor trans-(+)-5a as camphorsulfo
167 )4(C6H5CO2)4(C5H5N) (CH3OH)] was obtained by X-ray analysis of single crystals and shows that the com
169 his lack of correlation is explained through X-ray analysis of the azastilbene monomers and is shown
174 evealed by the combination of single-crystal X-ray analysis of the free host and the 1:2 host:calcium
175 atives, this being the first high-resolution X-ray analysis of the iron centres in any ferritin.The b
176 o aldehyde 15 (16:1 ratio) by single-crystal X-ray analysis of the major diastereomer of sulfamate 21
178 )H NOESY NMR, and is further corroborated by X-ray analysis of the product 1,4-bis(exo-1-chloro-2-nor
180 ation of (+)-2 was determined to be 2S,5R by X-ray analysis of the salt with (+)-camphoric acid.
188 ct sites in TTR, consistent with the data of x-ray analysis of TTR in complex with both ligands.
189 ectroscopy in solution and on single-crystal X-ray analysis of tweezer-oligomer complexes in the soli
192 a structural biology approach to complement X-ray analysis or electron microscopy, but also highligh
193 HPLC analysis was verified by single-crystal X-ray analysis or studies with carbamoyl derivatives of
195 ith the N-terminal domain, this combined NMR-X-ray analysis provides the first detailed and accurate
203 se materials were obtained by single-crystal X-ray analysis, revealing interesting aspects of conform
207 g electron microscopy with energy dispersive X-ray analysis (SEM/EDX), scanning transmission X-ray mi
210 isolated from this mixture in 5% yield, and X-ray analysis showed it to be the "supertetraphenylene"
213 oscopy in combination with energy-dispersive X-ray analysis showed that the site of Tc deposition was
215 ition adduct, with structural elucidation by X-ray analysis, showed that the mono-oxide was catalytic
219 anning electron microscopy/energy-dispersive X-ray analysis suggested a possible transformation of th
220 , and (+)-23 were obtained by single-crystal X-ray analysis, the assignment of the absolute stereoche
226 ve been well characterized by single crystal X-ray analysis; the mono-radicals have been distinguishe
227 structure of the compound was confirmed with X-ray analysis to demonstrate the strong charge separati
228 erties of the compounds were investigated by X-ray analysis, UV/vis spectroscopy, and electrochemistr
232 rystals of the hydroiodide salt suitable for X-ray analysis were obtained, and although there is some
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