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1 4)Cu accumulation sites by energy dispersive x-ray analysis.
2 s were determined by DFT calculations and/or X-ray analysis.
3 em have been characterized by single-crystal X-ray analysis.
4 formations were determined by single-crystal X-ray analysis.
5 nambiguously characterized by single-crystal X-ray analysis.
6 em have been characterized by single-crystal X-ray analysis.
7 n mass spectrometry (MS), and single-crystal X-ray analysis.
8 was synthesized and its structure solved by X-ray analysis.
9 olute stereochemistry has been determined by X-ray analysis.
10 as unambiguously confirmed by single-crystal X-ray analysis.
11 by electron microscopy and energy-dispersive X-ray analysis.
12 heses, were observed using energy dispersive X-ray analysis.
13 The disulfide complex was characterized by X-ray analysis.
14 prepared and characterized by single crystal X-ray analysis.
15 2.0]heptane was determined by single crystal X-ray analysis.
16 mplexes were characterized by single-crystal X-ray analysis.
17 py, X-ray diffraction, and energy-dispersive X-ray analysis.
18 that can be recalcitrant to high resolution X-ray analysis.
19 ulphur mapping by cryo-SEM/energy-dispersive X-ray analysis.
20 ives have been isolated and characterized by X-ray analysis.
21 sphatidylcholine that had been determined by X-ray analysis.
22 ding block 2 are confirmed by single-crystal X-ray analysis.
23 abicyclo[3.2.1]octane has been reassigned by X-ray analysis.
24 electron diffraction, and energy dispersive X-ray analysis.
25 c molecule, whose structure was confirmed by X-ray analysis.
26 eochemistry of an aldol product confirmed by X-ray analysis.
27 9, and 11 were unambiguously established by X-ray analysis.
28 unprecedented geometry, as revealed from the X-ray analysis.
29 lly characterized by means of single-crystal X-ray analysis.
30 g from the core that was deleted for NMR and X-ray analysis.
31 ization, electrospray mass spectrometry, and X-ray analysis.
32 e high-resolution structure of the enzyme by x-ray analysis.
33 ctivity filter (TVGYG) of KcsA identified by x-ray analysis.
34 ng diffraction-quality crystals suitable for x-ray analysis.
35 ton NMR spectroscopy, mass spectrometry, and X-ray analysis.
36 erivatives was prepared and characterized by X-ray analysis.
37 alline forms as determined by single-crystal X-ray analysis.
38 talline (reactive) salts suitable for direct X-ray analysis.
39 t types was corroborated by a single-crystal X-ray analysis.
40 structure was confirmed on the basis of its X-ray analysis.
41 ion of 2D NMR experiments and single-crystal X-ray analysis.
42 les has been established by a single-crystal X-ray analysis.
43 borate (11c) was confirmed by single-crystal X-ray analysis.
44 adiazines were established by single-crystal X-ray analysis.
45 d characterized through NMR spectroscopy and X-ray analysis.
46 f the arms were determined by single-crystal X-ray analysis.
47 diphosphonate cavitand 13 by single-crystal X-ray analysis.
48 and 12 have been confirmed by single-crystal X-ray analysis.
49 unequivocally determined by a single-crystal X-ray analysis.
50 C NMR, mass spectrometry, and single-crystal X-ray analysis.
51 to a structure similar to those obtained by x-ray analysis.
52 l structure of PGHS-2 holoenzyme obtained by x-ray analysis.
53 onfiguration was confirmed by single-crystal X-ray analysis.
54 pic methods, accurate mass measurements, and X-ray analysis.
55 enyldiimide N'-oxide as indicated by NMR and X-ray analysis.
56 btaining crystals with a volume suitable for x-ray analysis.
57 state for 5, as determined by single crystal X-ray analysis.
58 ctroscopic methods, including single crystal X-ray analysis.
59 tively), whose structures were determined by X-ray analysis.
60 nfiguration was determined by single-crystal X-ray analysis.
61 oxynucleoside triphosphate, as determined by x-ray analysis.
62 2) also forms crystals that are suitable for X-ray analysis.
63 tal structure compared to LT-BM according to X-ray analysis.
64 lose agreement with the results obtained via X-ray analysis.
65 nd the structure confirmed by single-crystal X-ray analysis.
66 enzene rings, respectively, according to the X-ray analysis.
67 acterized by mass spectrometry, FIB/SIMS and X-ray analysis.
68 by spectroscopic methods and single crystal X-ray analysis.
69 alkenylpyrazole compound 5c was confirmed by X-ray analysis.
70 ere confirmed and assigned by single-crystal X-ray analysis.
71 ature and characterized using single-crystal X-ray analysis.
72 lly characterized supported by NMR, EPR, and X-ray analysis.
73 phore unambiguously proven by single-crystal X-ray analysis.
74 -Mn complex formed after hydride transfer by X-ray analysis.
75 ctroscopic data as well as by single crystal X-ray analysis.
76 med by DFT quantum chemical calculations and X-ray analysis.
77 f 3 was determined via 13a by single-crystal X-ray analysis.
78 or into crystalline derivatives suitable for X-ray analysis.
79 in the transcription complex as suggested by X-ray analysis.
80 ng electron microscopy and energy dispersive X-ray analysis.
81 e ligand and characterized by single crystal X-ray analysis.
82 ructure, both of which were characterized by X-ray analysis.
83 re NMR (17.1 +/- 0.8 kcal/mol) estimates and X-ray analysis.
84 re isostructural according to single crystal X-ray analysis.
85 MR spectroscopy, intermediate isolation, and X-ray analysis.
86 RMS, HPLC, and in the cases of 2b and 5b, by X-ray analysis.
87 nd 5-15 H2O were confirmed by single-crystal X-ray analysis.
88 a diborane complex has been established from X-ray analysis.
89 hich was further confirmed by single-crystal X-ray analysis.
90 key products are confirmed by single-crystal X-ray analysis.
91 Both structures are verified by X-ray analysis.
95 uents) was determined through single-crystal X-ray analysis and 2D (NOESY, HSQC, HMBC) NMR experiment
96 tion were characterized by energy dispersive x-ray analysis and backscattered scanning electron micro
101 tablished by a combination of single-crystal X-ray analysis and comprehensive 2D NMR measurements.
102 ved to be sufficiently crystalline to enable X-ray analysis and determination of their solid-state co
103 ble molecular "scrolls" were investigated by X-ray analysis and electron microscopy, respectively.
106 validates the structural model derived from X-ray analysis and provides additional insight into apoE
107 The stage behavior was investigated using X-ray analysis and Quantum Mechanics/Molecular Mechanics
108 n electron microscopy with energy dispersive X-ray analysis and scanning transmission X-ray microscop
109 nteraction, was visualized by single-crystal X-ray analysis and supported by variable-temperature NMR
110 ng electron microscopy and energy-dispersive X-ray analysis and the particle size distributions using
113 hemistry was characterized by single-crystal X-ray analysis and was furthermore extended toward next
114 the structural features determined from the X-ray analysis and, consistent with the experimental abs
115 ed ring has been confirmed by single-crystal X-ray analysis, and cis is found to be the major product
120 per duplex are localized and visible in the X-ray analysis, and nine are disordered and invisible.
121 tests, surface microscopy, energy-dispersive X-ray analysis, and Raman microscopy has led to the iden
122 ls have been characterized by single-crystal X-ray analysis, and the presence of inter- and intramole
123 ons were characterized in the solid state by X-ray analysis, and the strength of each interaction was
124 orophores were structurally characterized by X-ray analysis, and their photophysical properties studi
125 tructures were confirmed with single-crystal X-ray analysis, and their properties were determined by
126 nning electron microscopy, energy-dispersive X-ray analysis, and X-ray photoelectron spectroscopy ind
127 racterized by multinuclear NMR spectroscopy, X-ray analysis, as well as their calculated NICS values,
129 poses a difficult challenge to conventional X-ray analysis, because it was completely obscured with
131 CD-MOF has been confirmed by single-crystal X-ray analysis by determining the vacancies of K(+)-ion
139 nning electron microscopy, energy dispersive X-ray analysis, cyclic voltammetry, and electrochemical
140 Benzotriazepin-2-one crystallization and X-ray analysis demonstrated that in spite the absence of
142 tron Microscopy (SEM) with Energy Dispersive X-Ray Analysis (EDX) and Fourier-transform infrared spec
143 ion, as shown via previous energy-dispersive X-ray analysis (EDX) elemental mapping and crystal struc
146 ectron microscopy (HRTEM), energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM), sca
147 electron microscopy (SEM), Energy Dispersive X-Ray Analysis (EDX), Fourier-transform infrared spectro
149 ctron microscopy (SEM) and energy dispersive X-ray analysis (EDXA) revealed that the SiO(2) gel was d
152 e products, as established by single-crystal X-ray analysis for substrates (S)-11c, (S)-19, and (S)-2
155 microscopy, combined with energy-dispersive X-ray analysis (for elemental compositions) methods, dif
156 material was fully characterized, including X-ray analysis, Fourier transform infrared, scanning and
159 ral origin for these differing activities by X-ray analysis has not succeeded due to difficulties in
160 mplete bony bridging by 12 weeks as shown by X-ray analysis, histology and live micromolecular imagin
161 d complex and its structure determination by X-ray analysis; in addition, kinetic simulations using t
168 one of these domains has been determined by x-ray analysis, its connection to the other major domain
169 bitor 5, structure-based design supported by X-ray analysis led to the discovery of the potent and se
170 on via infrared spectroscopy, single crystal X-ray analysis, Mossbauer spectroscopy, and magnetic sus
184 ucture represents the first visualization by X-ray analysis of a murine Fc segment, and its CH2 domai
186 ium complex and fluorenyl group, as shown by X-ray analysis of a single crystal, and this facilitates
187 bidentate nature of binding is supported by X-ray analysis of an intermediate analogue, which experi
190 pported by molecular modeling studies and by X-ray analysis of BACE1 complexes with various ligands t
196 mately confirmed to be spiroleucettadine via X-ray analysis of crystalline spiroleucettadine and rein
199 e inhibitory activities were rationalized by X-ray analysis of kinase/flavonoid crystal structures; t
206 ablished by successful cocrystallization and X-ray analysis of potent inhibitors with the TbetaR-I re
207 eochemistry was unequivocally established by X-ray analysis of precursor trans-(+)-5a as camphorsulfo
212 )4(C6H5CO2)4(C5H5N) (CH3OH)] was obtained by X-ray analysis of single crystals and shows that the com
215 his lack of correlation is explained through X-ray analysis of the azastilbene monomers and is shown
217 unknown properties of human DIPP1.We provide X-ray analysis of the catalytic core of DIPP1 in crystal
218 is conclusion was independently supported by X-ray analysis of the complex with (+)-R-2,2'-dihydroxy-
222 evealed by the combination of single-crystal X-ray analysis of the free host and the 1:2 host:calcium
223 atives, this being the first high-resolution X-ray analysis of the iron centres in any ferritin.The b
224 o aldehyde 15 (16:1 ratio) by single-crystal X-ray analysis of the major diastereomer of sulfamate 21
226 )H NOESY NMR, and is further corroborated by X-ray analysis of the product 1,4-bis(exo-1-chloro-2-nor
230 ation of (+)-2 was determined to be 2S,5R by X-ray analysis of the salt with (+)-camphoric acid.
239 ct sites in TTR, consistent with the data of x-ray analysis of TTR in complex with both ligands.
240 ectroscopy in solution and on single-crystal X-ray analysis of tweezer-oligomer complexes in the soli
243 a structural biology approach to complement X-ray analysis or electron microscopy, but also highligh
244 HPLC analysis was verified by single-crystal X-ray analysis or studies with carbamoyl derivatives of
247 ith the N-terminal domain, this combined NMR-X-ray analysis provides the first detailed and accurate
259 se materials were obtained by single-crystal X-ray analysis, revealing interesting aspects of conform
263 ysical evaluation (STD-NMR/ITC), followed by X-ray analysis, reveals a highly interesting binding mod
264 g electron microscopy with energy dispersive X-ray analysis (SEM/EDX), scanning transmission X-ray mi
267 isolated from this mixture in 5% yield, and X-ray analysis showed it to be the "supertetraphenylene"
270 sonance experiments, molecular modeling, and X-ray analysis showed that the resulting hydantoin-based
271 oscopy in combination with energy-dispersive X-ray analysis showed that the site of Tc deposition was
273 ition adduct, with structural elucidation by X-ray analysis, showed that the mono-oxide was catalytic
278 anning electron microscopy/energy-dispersive X-ray analysis suggested a possible transformation of th
280 , and (+)-23 were obtained by single-crystal X-ray analysis, the assignment of the absolute stereoche
286 ve been well characterized by single crystal X-ray analysis; the mono-radicals have been distinguishe
287 structure of the compound was confirmed with X-ray analysis to demonstrate the strong charge separati
289 erties of the compounds were investigated by X-ray analysis, UV/vis spectroscopy, and electrochemistr
290 anning electron microscopy-energy dispersive X-ray analysis validated the presence of VD(3) and Fe in
295 g electron microscopy with energy-dispersive X-ray analysis we show that two GLS importers, NPF2.10/G
296 rystals of the hydroiodide salt suitable for X-ray analysis were obtained, and although there is some
298 y atomic force microscopy and single-crystal X-ray analysis which we combined to derive a structural