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1  charge distribution from the Te ions at the crystallographic 8 f sites to the neighboring Co and O i
2 ing of the crystalline series shows that the crystallographic a-axis, along the channel, can be varie
3 below T C for magnetic fields applied in the crystallographic ab-plane.
4                   When particles assemble in crystallographic alignment, expulsion of the intervening
5                                   Subsequent crystallographic analyses of AChE complexes with the TZ2
6 putational model of the nucleosome, based on crystallographic analyses of the structure and elasticit
7                                NMR and X-ray crystallographic analyses of the tetrafluorinated methyl
8                                              Crystallographic analyses with succinate, fumarate, L-ma
9 se complexes could be characterized by X-ray crystallographic analysis and employed as catalysts for
10                                    The X-ray crystallographic analysis confirms that while CIP and CI
11                                 Furthermore, crystallographic analysis demonstrated atomic accuracy t
12                                              Crystallographic analysis demonstrated that the Crwn-THF
13 insights provide simple and accurate optical crystallographic analysis for liquid-dispersed nanomater
14                                     An X-ray crystallographic analysis has shown the compound to be a
15                                              Crystallographic analysis of 35 different peptide sequen
16 steric inhibitors, a finding rationalized by crystallographic analysis of allosterically inhibited L-
17 nimized insulin receptors (IRs) have enabled crystallographic analysis of insulin-bound "micro-recept
18                               Traditionally, crystallographic analysis of macromolecules has depended
19 ency to form fibrils were coupled with X-ray crystallographic analysis of nine TTR.ligand complexes.
20  lysozyme, and has been employed for routine crystallographic analysis of organic and inorganic mater
21 annot phosphorylate PtdIns(4,5)P2 Therefore, crystallographic analysis of the yeast and plant enzymes
22                                        X-ray crystallographic analysis of these scaffold nucleoporins
23                                              Crystallographic analysis provided insights into the inh
24                                        X-ray crystallographic analysis revealed that Abeta42 binding
25                                              Crystallographic analysis reveals architectural features
26                                        X-ray crystallographic analysis reveals that 12 adopts a simil
27                                          The crystallographic analysis reveals that the thiolate liga
28                                          Our crystallographic analysis unveiled the exact position of
29 repare single crystals suitable for accurate crystallographic analysis was missing.
30 tional significance that extend recent x-ray crystallographic analysis.
31 es that was unambiguously confirmed by X-ray crystallographic analysis.
32                              We report X-ray crystallographic and (19) F NMR studies of the G-protein
33                                              Crystallographic and AFM data were used to build a struc
34                Here we report on a series of crystallographic and biochemical analyses of an evolutio
35                                              Crystallographic and biochemical studies on the Pseudomo
36                      Here, we report through crystallographic and biochemical studies that K-80003 bi
37 rward approach to the discrimination between crystallographic and biological dimers by docking the tw
38 to the fungus Candida albicans Complementary crystallographic and biophysical characterization of Bsp
39                                This combined crystallographic and computational study provides valuab
40                     Consistent with previous crystallographic and cryo-EM studies, the obtained force
41                                              Crystallographic and docking studies revealed the main i
42                              Here we present crystallographic and electron microscopic structures of
43                         Here, we present our crystallographic and enzymatic studies of TTPA.
44                             Here, we present crystallographic and functional data showing that the K(
45                              Here, we report crystallographic and functional studies of the TRIM5alph
46       Targeted modifications to CP2 based on crystallographic and mass spectrometry analyses results
47                   We report here on an X-ray crystallographic and molecular modeling investigation in
48                                              Crystallographic and mutagenesis studies elucidated a ke
49                                              Crystallographic and native ion-mobility mass spectromet
50                                              Crystallographic and quantum chemical studies reveal tha
51                                              Crystallographic and small-angle X-ray scattering (SAXS)
52                 This article describes X-ray crystallographic and solution-state NMR studies of pepti
53                                        X-ray crystallographic and spectroscopic analyses demonstrate
54                                 We use X-ray crystallographic and spectroscopic approaches to show th
55                                          The crystallographic and spectroscopic characteristics of li
56                                              Crystallographic and spectroscopic characterization toge
57 e transport domains consistent with previous crystallographic and spectroscopic studies.
58 nd Selectfluor is presented, together with a crystallographic and spectroscopic study.
59 experimental data obtained in spectroscopic, crystallographic, and calorimetric measurements during e
60               Comparisons of their magnetic, crystallographic, and computational characterization to
61 heir microstructures by photophysical, X-ray crystallographic, and computational means.
62 and studied them using biochemical, kinetic, crystallographic, and computational studies.
63 plexes were assigned by using spectroscopic, crystallographic, and magnetic analyses.
64                   Results from calorimetric, crystallographic, and theoretical analyses suggest that
65 -dependent surface energy and the subsequent crystallographic anisotropy via ab-initio calculations b
66                         We describe here the crystallographic application of "atom replacement" mimet
67                        Using biophysical and crystallographic approaches, we identify that PrimPol po
68 ntations of the nanocrystals, as well as the crystallographic axes of the ensuing triclinic colloidal
69 it ferroelectric behavior along two distinct crystallographic axes.
70 culations and experimentally by a normalized crystallographic B-factor analysis.
71 redict related data (NMR order parameter, or crystallographic B-factor).
72                              Analyses of the crystallographic B-factors indicated several regions wit
73                           Significantly, the crystallographic binding poses are distinguished not onl
74                              Here we combine crystallographic, biochemical and genetic analyses to sh
75                                    Trends in crystallographic bond lengths and angles shed light on t
76 oscale AFM results confirm the alteration of crystallographic characteristics, and the ability of dis
77 stinct, has allowed for the isolation, X-ray crystallographic characterization and comprehensive spec
78       Herein we report the spectroscopic and crystallographic characterization of [(N4Py)Fe(III) -O-C
79 ssemblies can also form, as evidenced by the crystallographic characterization of a Pt10L5 complex an
80 R, infra-red, (57) Fe-Mossbauer, EPR), X-ray crystallographic characterization of the cluster in both
81                                              Crystallographic characterization showed the two hydride
82                            However, standard crystallographic characterization through diffraction yi
83                       A combination of x-ray crystallographic, computational and electrophysiological
84 t the influence of other receptor domains or crystallographic conditions.
85               However, the resultant reduced crystallographic control in mussels raises concerns for
86 allography are of comparable quality to cryo-crystallographic data and can be routinely collected at
87 n interaction were designed, guided by X-ray crystallographic data and molecular dynamics simulations
88                                        Using crystallographic data and the virtual screening of a che
89                              Biochemical and crystallographic data demonstrate a mechanism in which d
90      Here MS, thioflavin T fluorescence, and crystallographic data demonstrate that while the X-ray s
91                                       Serial crystallographic data for molecular replacement already
92                                          The crystallographic data identified most of the monosacchar
93 the handling of MOF crystals and analysis of crystallographic data obtained from single-crystal X-ray
94 irm the current picture derived from NMR and crystallographic data of domain docking upon ATP binding
95                   Furthermore, we report the crystallographic data of the chiral [Ru(I)H(CO)((S,S)-f-
96        Our analysis of a pilot collection of crystallographic data sets demonstrates that the informa
97 plete glycoprotein was achieved by combining crystallographic data with molecular modeling.
98 ment reported here are consistent with X-ray crystallographic data, and suggest that crystal packing
99 ties that are derived from spectroscopic and crystallographic data.
100 ructural conservation and localisation using crystallographic data.
101 x are revealed by the combination of NMR and crystallographic data.
102  epitaxial nature, low strain character, and crystallographic defect content of the resultant solid G
103 tions can change at kinks with no observable crystallographic defect.
104 fness is 'defect-driven', i.e., dominated by crystallographic defects such as bridging site vacancies
105                                              Crystallographic defects such as dislocations can signif
106         These novel H2 O2 solvates have high crystallographic densities (1.96 and 2.03 g cm(-3) , res
107 provide an experimentally validated complete crystallographic detail of a highly strained BiFeO3 that
108 mal motion and low occupancies, the reliable crystallographic determination of the guest can be very
109  meningitidis Structural analysis with X-ray crystallographic diffraction data to 2.0-A revealed that
110 s in cells, and that both occurs through the crystallographic dimer interface.
111 basis than previously suggested by the MLA10 crystallographic dimer.
112 niform and random orientation of the lattice crystallographic direction enabled by a photoalignment t
113 way to realize designed micropatterning of a crystallographic direction of a soft, cubic liquid-cryst
114       Uniform and patterned orientation of a crystallographic direction of ordered materials is of fu
115 , acetylene molecules react along a specific crystallographic direction that is perpendicular to thos
116 ctures were tested along the [001] austenite crystallographic direction using a custom designed magne
117 ansport Jc of 10(5) A/cm(2) at 15 T for main crystallographic directions of the applied field, which
118  where it contracts and expands in different crystallographic directions when hosting the inserted Mg
119      The NWs form along the <11-20> 2H-MoTe2 crystallographic directions with lengths in the micromet
120  kappa, located at ~15 K at zero-H along all crystallographic directions, moves gradually toward lowe
121 e reaction or lithium diffusion in different crystallographic directions.
122 h is fully incommensurate (ICM) in all three crystallographic directions.
123 locities of optical phonons in the different crystallographic directions.
124  validated by both the Harvey-Gray method of crystallographic-distance-to-force-constant correlation
125 ogress in experimental investigations on the crystallographic, dynamic and kinetic aspects of substra
126 e of the whole molecule, alone or within the crystallographic environment.
127 ch structural changes were suppressed in the crystallographic environment.
128                                              Crystallographic evidence for the protonation of nearby
129                      Furthermore, we provide crystallographic evidence of an organometallic aryl-Co(I
130                                              Crystallographic evidence suggests that IREDs may be abl
131  and high frame-rate detector allows typical crystallographic experiments to be performed at room-tem
132 ystals expressing the (001), (012), or (110) crystallographic face.
133                                              Crystallographic, full spectroscopic characterization, a
134 ut is packed as a high 70% solvent content, crystallographic heptamer.
135 acroscopic etch pit hexagonal profile to the crystallographic hexagon.
136                        The bases are labeled crystallographic hexagons.
137 s and coactivator peptides, examined through crystallographic, hydrogen-deuterium exchange mass spect
138 e we report a fundamental study coupling the crystallographic imaging capability of laboratory diffra
139         The nanoparticles' ability to remove crystallographic imperfections renders them more durable
140                                              Crystallographic imperfections significantly alter mater
141    We selected the nucleants on the basis of crystallographic information and assembled them onto 707
142 g, as well as the functional significance of crystallographic interprotomer interfaces.
143                                  Comparative crystallographic investigation of CB[7].Diam(NMe3)2, CB[
144                                              Crystallographic investigations indicate that the S672R
145 ty in primary sequence and cofactor content, crystallographic, kinetic, and mass spectrometry analyse
146 ginates from chirality interplay between the crystallographic lattice and geometric morphology at dif
147  110 cm(3)/g by cobalt insertion in the MoS2 crystallographic lattice, which induces the formation of
148                With this strategy, different crystallographic lattices using the same particles can b
149 f ENAM mutation on the enamel structure at a crystallographic level.
150 lly preferred binding modes that differ from crystallographic ligands.
151                                High pressure crystallographic measurements confirm uniform compressio
152                            Our time-resolved crystallographic measurements with a 10-second delay cap
153      Using low-temperature magnetisation and crystallographic measurements, we show here for the firs
154 c coordinates of real systems beyond average crystallographic measurements.
155              Notably, the recent progress in crystallographic methods led to a breakthrough in elucid
156 tlenecks to structure determination by X-ray crystallographic methods-that of crystal growth.
157 he extent of cavitation, the orientation and crystallographic misorientation of each boundary is char
158 zed glycosyltransfer and present an improved crystallographic model for inhibition of the PBP1b glyco
159 n of this MDFF model with an earlier-derived crystallographic model for the planar assembly, the indu
160 es (both in the physical crystals and in the crystallographic model) and (2) crystallographic twinnin
161  C-terminal domain is in good agreement with crystallographic models derived from ExoU in complex wit
162                       Knowledge of the basic crystallographic modes of slip is critical to understand
163 ain with phosphorylated XRCC1 peptides using crystallographic, NMR, and fluorescence polarization stu
164                                     Possible crystallographic nomenclatures, to be used to describe l
165 nt a hierarchy of assembly criteria based on crystallographic observations and subsequently quantify
166                                          The crystallographic observations are reinforced by protein-
167 ades, borides have been primarily studied as crystallographic oddities.
168            The printed films exhibit similar crystallographic order and chemistry as the original pow
169                               We explore how crystallographic order and orientation affect the tribol
170 s in the xenolith had the same chemistry and crystallographic orientation as those for inclusions in
171                       This revealed a strong crystallographic orientation dependence of the sliding p
172 he elastic and shear moduli as a function of crystallographic orientation gleaned from experiments an
173 and sensitivity of this metal's stiffness to crystallographic orientation help explain why the existi
174                                          The crystallographic orientation of a metal affects its surf
175 ric properties through composition, size and crystallographic orientation of domains made it possible
176 oxidation state, the coordination number and crystallographic orientation of metal sites, and bonding
177 s strongly influences the angular spread and crystallographic orientation of TES-ADT spherulites.
178 ications are achieved based on the patterned crystallographic orientation of the cubic blue phase, so
179 rably enhance the conductance in a preferred crystallographic orientation of the layered solid.
180 e show that Li-metal texturing (preferential crystallographic orientation) occurs during electrochemi
181 ard/soft nanocomposites often exhibit random crystallographic orientations and monomorphological equi
182 lar complexes aligned along several discrete crystallographic orientations and that, consequently, co
183 at sites of high stored energy and they have crystallographic orientations from those present in the
184 omprised of different materials with varying crystallographic orientations on the overall thermal bou
185 ly scattered by Umklapp processes in all the crystallographic orientations.
186 various perovskite substrates with different crystallographic orientations.
187 st tissue biopsies, and related this to both crystallographic parameters measured previously in the s
188    Such microstructure depends on the shape, crystallographic phase and orientation, and interfacing
189                                      The non-crystallographic phase problem arises in numerous scient
190 dge dislocations that glide on two different crystallographic planes.
191 th preferred orientation between hk0 and 00l crystallographic planes.
192 g of lithium electrocrystallization from the crystallographic point of view provides significant insi
193 ns successfully reverted back to near-native crystallographic poses after being perturbed.
194 e without the GIST term was wrong, and three crystallographic poses differed from both predictions.
195                                              Crystallographic preferred orientation (CPO) of post-per
196         Quantitative characterization of the crystallographic properties from enamel with known genot
197 oscopy and multiple conformer simulations of crystallographic protomers as described in the companion
198 o determine which structure fits two sets of crystallographic raw data best.
199 ducts is also observed, but the mechanism of crystallographic realignment is unknown.
200         We have employed quantum refinement (crystallographic refinement enhanced with quantum-mechan
201 o be similar to the oxidation, with the same crystallographic relationship between the two phases.
202  the confined nanovoids has been observed at crystallographic resolution, leading to a highly efficie
203 nalized metal-organic framework, MFM-188, at crystallographic resolution.
204                                        X-ray crystallographic screening identified three distinct "ho
205                  To fill this gap, we report crystallographic, sedimentation-velocity, and kinetics d
206 ead to more complex defect structures, e.g., crystallographic shear planes or modules with differing
207  while the higher temperature (Wadsley-Roth, crystallographic shear structure) H-phase shows high int
208               Here, we identify two possible crystallographic signatures of geometric frustration: ex
209 rder, but that correlated disorder has clear crystallographic signatures.
210 and Li are completely disordered on a common crystallographic site (3c).
211 es associated with shearing on nine distinct crystallographic slip modes in the hexagonal omega-Zr cr
212                                          Our crystallographic, small angle x-ray scattering, and NMR
213                                              Crystallographic, spectroscopic, and computational analy
214 unusual hydrogen bond donor, as confirmed by crystallographic, spectroscopic, and computational metho
215                                              Crystallographic, spectroscopic, and computational studi
216                                              Crystallographic, spectroscopic, and DFT studies reveal
217                Our results from mutagenesis, crystallographic, spectroscopic, and kinetic experiments
218                                    Moreover, crystallographic structural analysis of isomaltase predi
219 , the ferric enterobactin complex has eluded crystallographic structural characterization.
220 as a model system, we have used solution and crystallographic structural methods to delineate the ran
221                                              Crystallographic structural studies during the developme
222 ools; and clustering on the basis of similar crystallographic structure (for example, zeolite structu
223 the enzyme active site could be explained by crystallographic structure analysis, which highlighted t
224  as Fe3 O4 and CoFe2 O4 , which have similar crystallographic structure and lattice constants as NiFe
225                                          Its crystallographic structure determination is the first fo
226                          One way to depict a crystallographic structure is by a periodic (di)graph, i
227 tein, which had been used to solve the X-ray crystallographic structure of 5-LOX, and examined the bi
228                                          The crystallographic structure of a rice (Oryza sativa) cell
229 ing with a comparative analysis of the X-ray crystallographic structure of compound 5 in complex with
230                   We determined the electron crystallographic structure of H(+),K(+)-ATPase at 6.5 A
231                 This paper reports the X-ray crystallographic structure of oligomers formed by a pept
232 n solubility and function, we determined the crystallographic structure of one such LGK mutant.
233                                          The crystallographic structure of RbkR from Thermoplasma aci
234                    We report the first X-ray crystallographic structure of the "head-to-middle" preny
235                          Here we present the crystallographic structure of the Arabidopsis TPL N-term
236                    Here we present the X-ray crystallographic structure of the human alpha4beta2 nico
237                            Here we present a crystallographic structure of the minimal adhesive fragm
238  precluded conclusive determination of their crystallographic structure to date, but here we analyze
239 hips and used alternate conformations from a crystallographic structure to grow a fragment into a mor
240 -diazabicyclo[2.2.2]octane (DABCO), an X-ray crystallographic structure was obtained.
241                                    The X-ray crystallographic structures confirm the mutual columnar
242           This is consistent with time-lapse crystallographic structures following insertion of Sp-dC
243                            Twenty-five X-ray crystallographic structures have been obtained to confir
244  the role of loop motion in TCR binding, and crystallographic structures have raised questions about
245     A Bayesian inference method for refining crystallographic structures is presented.
246  packaged by the nucleoprotein N) we present crystallographic structures of HMPV N in its assembled R
247                This paper presents the X-ray crystallographic structures of oligomers formed by a 20-
248 s a beta-hairpin is described, and the X-ray crystallographic structures of oligomers it forms are re
249                                Novel protein crystallographic structures of the prototypical PC famil
250                Here, we determined the X-ray crystallographic structures of two catalytically inactiv
251                              High-resolution crystallographic structures provide invaluable insight o
252                                    The X-ray crystallographic structures reveal that the stabilized t
253       Through biochemical analyses and X-ray crystallographic structures we show that to hydrolyze th
254 s that combine high-accuracy priors (such as crystallographic structures) with medium-resolution cryo
255 paper describes the design, synthesis, X-ray crystallographic structures, and biophysical and biologi
256 ule Na3 Cit not only helps to manipulate the crystallographic structures, but also to initiate the tr
257 as identified in some DNA polymerase product crystallographic structures, but its role is not known.
258 mbination of atomic-resolution protein X-ray crystallographic structures, ligand-dependent LBD stabil
259 4 of BRD4 as revealed by peptide binding and crystallographic studies and enhances BRD4's stability b
260                                              Crystallographic studies and mutational analyses have co
261                      The comparison of X-ray crystallographic studies at low and high temperatures an
262 the molecular basis of this regulation using crystallographic studies augmented by computational anal
263                                  Docking and crystallographic studies corroborate favorable binding t
264                          Mutant yeast and co-crystallographic studies demonstrate binding to the bc1
265                                     To date, crystallographic studies have focused on conserved trans
266 pecies, but previous spectroscopic and X-ray crystallographic studies have not been able to unambiguo
267                               Recent EPR and crystallographic studies have observed that oxidized Pdx
268   However, in contradiction, biochemical and crystallographic studies have shown that heme decreases
269                   We present biochemical and crystallographic studies indicating that irrespective of
270                                        X-ray crystallographic studies of CorA show similar conformati
271                                              Crystallographic studies of GTF180-DeltaN show that at t
272                       Mass spectrometric and crystallographic studies of Pt(II) binding to the RecA i
273 y NMR (including DOSY) experiments and X-ray crystallographic studies of several model lithio interme
274                        On the basis of X-ray crystallographic studies of the complex of hCA II with 4
275                                              Crystallographic studies of the CRBN-DDB1-CC-885-GSPT1 c
276                                        X-ray crystallographic studies of the isolated DHO and of the
277 formatic, biochemical, mutational, and X-ray crystallographic studies on the unicellular alga Chlamyd
278                                              Crystallographic studies revealed that the specificity o
279  modeling, along with enzymatic, genetic and crystallographic studies, have established a mechanism-o
280                              Mutagenesis and crystallographic studies, including the structure of BT3
281 wever, by combining genetic, biochemical and crystallographic studies, we demonstrate that MTM and PK
282 d by deuterium labeling experiment and X-ray crystallographic studies.
283 ination of biochemical experiments and X-ray crystallographic studies.
284 FAM) distorts DNA into a U-turn, as shown by crystallographic studies.
285                             This first X-ray crystallographic study of a single human CCT subunit in
286                   Through a combined NMR and crystallographic study on the histidine kinase HK853 and
287                                   Our recent crystallographic study showed that CaM embraces helices
288  enzyme, particularly in light of a previous crystallographic study that placed the cofactor-binding
289             This allowed a comparative X-ray crystallographic study to delineate the successive struc
290           Thus, we conclude that there is no crystallographic support for a dinuclear Cu site in pMMO
291 ent structure-guided optimization using this crystallographic surrogate.
292                    When molecular motion and crystallographic symmetry are both accounted for, the J(
293 he DQF J splitting is influenced by both the crystallographic symmetry of the system and the presence
294  perovskite films, featuring strong uniaxial-crystallographic texture, micrometer-grain morphology, h
295               We report the pressure-induced crystallographic transitions and optical behavior of MAP
296 athing'-typically occur through well-defined crystallographic transitions.
297 s and in the crystallographic model) and (2) crystallographic twinning.
298                                              Crystallographic unit cells can be assembled into a regu
299                      In contrast to previous crystallographic views, we found that the selectivity fi
300 -49-Asn, and Arg-126-Lys, we inferred that a crystallographic water acts as a general base during GSH

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