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1 resent a comprehensive complementary neutron small-angle and spin-echo study directly showing the pre
4 bright-field and polarised light microscopy, small-angle and wide-angle X-ray scattering, and steady-
5 t required endocyclic transition states with small angles between the bond being formed to the nucleo
6 uctive field, 11 (73%) patients had residual small angle esotropia (mean = 7 prism diopters) in ipsil
9 yer materials stacked at a relative twist of small angle have recently shown the emergence of flat en
10 re reflected by a strong transient signal in small-angle inelastic scattering, and nuclear structural
13 measurement techniques, spin echo modulated small angle neutron scattering (SEMSANS) has attracted a
16 scattering, small angle X-ray scattering and small angle neutron scattering data of the colloidal dis
20 ted with charged lipid bilayers, we employed Small Angle Neutron Scattering to probe lipid distributi
24 rdered phycobilisome structure, evident from small-angle neutron and X-ray scattering and cryo-transm
25 ed sampling MD we reproduce the experimental small-angle neutron and X-ray scattering profiles and th
26 at the same pressures on the General-Purpose Small-Angle Neutron Scattering (GP-SANS) instrument at O
27 characterized using confocal microscopy and small-angle neutron scattering (length scales of microme
29 for Small-Angle X-Ray Scattering (SAXS) and Small-Angle Neutron Scattering (SANS) characterizations.
30 utputs for scattering profiles obtained from small-angle neutron scattering (SANS) experiments of pol
32 a multi-physics approach towards analysis of small-angle neutron scattering (SANS) on graphene-based
34 action (ND), neutron reflectometry (NR), and small-angle neutron scattering (SANS), have already been
35 these deficiencies, making particular use of small-angle neutron scattering and exploiting the device
36 resolution studies using techniques such as small-angle neutron scattering and neutron reflection, t
38 pported by structural characterization using small-angle neutron scattering and X-ray diffraction.
39 In the present study neutron diffraction and small-angle neutron scattering measurements of adsorbed
44 formational equilibrium of this enzyme using small-angle neutron scattering, under conditions where w
49 tal context by using it to direct autonomous small-angle (SAXS) and grazing-incidence small-angle (GI
50 es were determined by numerical inversion of small angle scattering and isothermal magnetisation data
53 estoration of soluble protein structure from small-angle scattering data, we construct a general mult
57 domain Hck kinase previously determined from small-angle solution X-ray scattering to produce full-le
59 a highly tunable correlated system based on small-angle twisted bilayer-bilayer graphene (TBBG), con
62 face sensitive synchrotron grazing incidence small angle X-ray scattering (GISAXS) and specular X-ray
63 f symmetry Fd3m (Q227) which was verified by Small angle X-ray scattering (SAXS) and Transmission ele
64 crystal structures of MotB fragments to the small angle X-ray scattering (SAXS) data revealed that t
70 multi-domain constructs in combination with small angle X-ray scattering (SAXS) to determine the str
74 of the pore structure using a combination of small angle X-ray scattering (SAXS), low-pressure N2 and
76 combined x-ray crystallography of Pcore with small angle x-ray scattering (SAXS)-based ensemble model
85 entire ESCRT binding region of HD-PTP using small angle X-ray scattering and hydrodynamic analyses.
86 rmined the MBD1-3 conformational space using small angle X-ray scattering and identified changes in M
87 etween DNA and three prototypical AMPs using small angle X-ray scattering and molecular modeling.
90 ourier transform of static light scattering, small angle X-ray scattering and small angle neutron sca
91 bubbles was performed using a combination of small angle x-ray scattering and transmission electron m
95 sm, a molecular envelope was calculated from small angle X-ray scattering data for the Bacillus subti
100 Both unfolding experiments and independent small angle x-ray scattering measurements demonstrate th
103 nges while size-exclusion chromatography and small angle X-ray scattering studies indicated that hepa
106 ded from photon correlation spectroscopy and small angle X-ray scattering was confirmed by additional
108 from a combination of X-ray crystallography, small angle X-ray scattering, and complementary biophysi
109 ned data from crystallography, biochemistry, small angle X-ray scattering, and electron microscopy un
110 onformation, and function were examined with small angle x-ray scattering, circular dichroism, and a
112 Here, we use multiple approaches, including small angle X-ray scattering, hydrogen-deuterium exchang
113 using an integrative approach that combines small angle X-ray scattering, NMR spectroscopy, and mole
114 We also studied the complex in solution by small angle X-Ray scattering, nuclear magnetic resonance
115 ined with molecular dynamics simulations and small angle X-ray scattering, suggests that variability
116 x-ray crystallography, NMR spectroscopy, and small angle x-ray scattering, to characterize the struct
118 cence microscopy and spectroscopy as well as small angle X-ray scattering, we show that the encapsula
124 ted by the custom ligands and verified using small angle x-ray spectroscopy, allows us to calculate t
125 Specifically, we coupled a joint analysis of small-angle x-ray and neutron scattering experiments on
128 onent to the co-assembly, as corroborated by small-angle X-ray and neutron-scattering structural stud
130 WetSTEM), combined with UV/vis spectroscopy, small-angle X-ray diffraction (SAXRD) and multiscale mod
136 ructure of PbS NC SLs with grazing-incidence small-angle X-ray scattering (GISAXS) while using nuclea
142 cryogenic electron microscopy (cryo-EM) and small-angle X-ray scattering (SAXS) analyses of recombin
146 nformation of the RcRE RNA in solution using small-angle X-ray scattering (SAXS) and atomic force mic
147 oferritin (Bfr), using synchrotron radiation small-angle X-ray scattering (SAXS) and circular dichroi
149 zed Galpha(i) (miniGalpha(i)) in solution by small-angle X-ray scattering (SAXS) and exploited the sc
150 In this work, we propose the combination of small-angle X-ray scattering (SAXS) and high throughput,
151 e modification procedures in preparation for Small-Angle X-Ray Scattering (SAXS) and Small-Angle Neut
154 truction of homo-multimers, consideration of small-angle X-ray scattering (SAXS) data, and location o
157 g and the shape of the dimerization curve in small-angle X-ray scattering (SAXS) experiments using is
159 hoton-correlation spectroscopy (XPCS) in the small-angle X-ray scattering (SAXS) geometry to probe bo
161 enzyme kinetics, X-ray crystallography, and small-angle X-ray scattering (SAXS) methodologies to dem
167 canning calorimetry, limited proteolysis and small-angle X-ray scattering (SAXS) support the proper f
170 f minimally perturbing labels, time-resolved small-angle X-ray scattering (SAXS), all-atom simulation
172 clear Magnetic Resonance (NMR) spectroscopy, Small-angle X-ray Scattering (SAXS), and single-molecule
176 hes, including hydrodynamic measurements and small-angle X-ray scattering (SAXS), coupled with bioche
177 ural approach that combines the strengths of small-angle X-ray scattering (SAXS), crystallography, an
179 ation, we excluded this possibility by using small-angle X-ray scattering (SAXS), dynamic light scatt
181 thium storage mechanism are also revealed by small-angle X-ray scattering (SAXS), especially the clos
182 omatography, analytical ultracentrifugation, small-angle X-ray scattering (SAXS), molecular dynamics
183 ZrT(d) and Zr(25) in water were described by small-angle X-ray scattering (SAXS), pair distribution f
185 uorescence resonance energy transfer (FRET), small-angle x-ray scattering (SAXS), x-ray crystallograp
189 g size-exclusion chromatography coupled with small-angle X-ray scattering (SEC-SAXS) analysis, we inv
190 Size exclusion chromatography coupled to small-angle X-ray scattering (SEC-SAXS) of this hybrid m
191 d size-exclusion chromatography in line with small-angle X-ray scattering (SEC-SAXS) to analyze the f
196 Moreover, an APE2 Zf-GRF X-ray structure and small-angle X-ray scattering analyses show that the Zf-G
197 imer in the presence of NEIL1 and DNA, while small-angle X-ray scattering analysis confirmed the NEIL
199 orm, and inverse-tapered molecular "shapes." Small-angle X-ray scattering analysis of the self-assemb
202 AS (but otherwise structurally identical) by small-angle X-ray scattering and analytical ultracentrif
204 es of the behavior of 3 and 4 in solution by small-angle X-ray scattering and atomistic molecular dyn
206 beta-lactoglobulin (betaLG), were studied by small-angle x-ray scattering and both near- and far-UV c
207 lO4 was studied by in situ grazing-incidence small-angle X-ray scattering and complementary scanning
209 its heterotetrameric complex in solution by small-angle X-ray scattering and find that mutations tha
210 of the Ca(2+).CaM-GRK5 complex determined by small-angle X-ray scattering and negative-stain electron
211 d unphosphorylated rOPN were investigated by small-angle x-ray scattering and no significant changes
213 ion are analysed by simultaneous synchrotron small-angle X-ray scattering and Raman spectroscopy in a
215 ale sufficient for structural analysis using small-angle X-ray scattering and stochiometric analysis
216 ce-sensitive native centric simulations with small-angle X-ray scattering and time-resolved Forster r
220 ns over 200 ns by analysis of time-resolved, small-angle X-ray scattering data acquired during detona
221 a truncated version of RrCooJ, combined with small-angle X-ray scattering data and a modeling study o
222 ar weight of the complex was calculated from small-angle X-ray scattering data and was in good agreem
223 The structure was accurately modeled from small-angle x-ray scattering data by treating ColN as a
224 tetramers and one homopentamer) had solution small-angle X-ray scattering data consistent with the de
226 copy, Forster resonance energy transfer, and small-angle x-ray scattering data obtained under conditi
227 A low-resolution structure calculated from small-angle X-ray scattering data revealed a conformatio
231 of the double-tetrameric form, combined with small-angle X-ray scattering data, allows the localisati
232 ate the RNA secondary structure information, small-angle X-ray scattering data, and any readily avail
235 ger alpha3 chain constructs, spanning N6-N3, small-angle X-ray scattering demonstrates that the tande
238 to require multiple actin-binding sites, yet small-angle X-ray scattering experiments revealed that E
240 P2 structure by X-ray crystallography and by small-angle X-ray scattering in solution as well as that
243 l structure of full-length KGA and present a small-angle X-ray scattering model for full-length GLS2.
244 namic analysis of the ligand association and small-angle x-ray scattering of the dual domain in the a
245 ing analytical ultracentrifugation, NMR, and small-angle x-ray scattering on full-length ColN and its
246 ed, 82% have circular dichroism and solution small-angle X-ray scattering profiles consistent with th
247 n alternative interpretation of experimental small-angle X-ray scattering profiles of these systems,
249 pG(1), EspG(3), and EspG(5) chaperones using small-angle X-ray scattering reveals that EspG(1) and Es
261 tures of individual VSG domains, we employed small-angle X-ray scattering to elucidate the first two
264 scribe a label-free method based on spectral small-angle X-ray scattering with a polychromatic beam f
265 l changes resulting from binding, we applied small-angle x-ray scattering with contrast variation to
266 port our computational approach we performed small-angle X-ray scattering with purified E2 ectodomain
267 (circular dichroism, chaperone activity, and small-angle x-ray scattering) and in vivo tools (Caenorh
268 lution of U(70) in organic media reveals (by small-angle X-ray scattering) that differing supramolecu
269 complementary biophysical methods including small-angle x-ray scattering, analytical ultracentrifuga
270 OAS2 using an integrated approach involving small-angle x-ray scattering, analytical ultracentrifuga
271 Here, we used NMR spectroscopy, mutagenesis, small-angle X-ray scattering, and computational modeling
272 on resonance assays; and immunofluorescence, small-angle X-ray scattering, and MS-based analyses, we
273 des nuclear magnetic resonance spectroscopy, small-angle x-ray scattering, and multiscale simulations
274 light scattering, dynamic light scattering, small-angle x-ray scattering, and native mass spectromet
275 d and unbound state using mass spectrometry, small-angle X-ray scattering, and negative-stain electro
276 E) using negative stain electron microscopy, small-angle X-ray scattering, and selective deuteration/
277 irected mutagenesis, isothermal calorimetry, small-angle X-ray scattering, and X-ray crystallography
278 V039 using isothermal titration calorimetry, small-angle X-ray scattering, and X-ray crystallography.
280 the crystalline domain sizes measured using small-angle X-ray scattering, indicating that thermal ph
281 pectroscopy, analytical ultracentrifugation, small-angle X-ray scattering, molecular dynamics simulat
283 l for protein-intensive experiments, such as small-angle X-ray scattering, providing biochemical insi
284 the cellular data, biophysical measurements (small-angle X-ray scattering, single-molecule fluorescen
285 electron-spin resonance spectroscopy (PDS), small-angle x-ray scattering, targeted protein cross-lin
287 arrest, combining dynamic light scattering, small-angle x-ray scattering, tracer-based microrheology
289 scopy, isothermal titration calorimetry, and small-angle X-ray scattering, we show that in the homodi
290 g cryo-electron microscopy and time-resolved small-angle X-ray scattering, we show that lipopolysacch
291 d inhibit the cleavage of complement C3, and small-angle X-ray scattering-based modeling indicates th