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1 ficant neutron scattering techniques, namely small angle scattering.
2 ic and dynamic light scattering, and neutron small angle scattering.
3 d transmission electron microscopy and X-ray small angle scattering.
4 ormidable challenge, particularly when using small-angle scattering.
5 es were determined by numerical inversion of small angle scattering and isothermal magnetisation data
9 ains-determined by X-ray crystallography and small angle scattering-as well as kinetics experiments d
12 rr complex is experimentally determined from small angle scattering data to present the first structu
13 idual amino acid side chains, implied by the small angle scattering data, could have significant effe
16 a generally useful tool for the analysis of small-angle scattering data from concentrated macromolec
19 ir ligands; SASBDB, a primary repository for small-angle scattering data of various macromolecular co
20 the VEGF-E/VEGFR-2 ECD complex derived from small-angle scattering data provided evidence for homoty
21 structure at room temperature to explain the small-angle scattering data, as it is consistent with a
22 estoration of soluble protein structure from small-angle scattering data, we construct a general mult
25 Three examples are given of application to small-angle scattering from pressure-induced unfolding o
26 flectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctional
28 14 A using a synchrotron X-ray source and a small-angle scattering instrument adapted for single cry
32 24I, derived using electron microscopy (EM), small-angle scattering (neutron and X-ray), and detailed
34 this respect, experimental information from small-angle scattering of X-ray radiation in solution (S
36 of probing ultrastructure ordering, such as small-angle scattering of X-rays or neutrons, can be app
37 een developed that allows observation of the small angle scattering profile of an integral membrane p
38 However, to date the quantification in the small angle scattering regime is severely limited by the
39 eat spacings (5.0 nm at 55 degrees C) in the small-angle scattering region which first appears at app
43 atial beam modulation, allows for mapping of small-angle scattering signals and hence addressing micr
45 idopsis thaliana; AtCESA1CatD) determined by small-angle scattering techniques and provides the first
50 with statistical coil ensemble modeling and small-angle scattering, to analyze the conformational be
51 er solution, the micelle contribution to the small angle scattering vanishes, and the molecular weigh
55 we introduce an imaging method that combines small-angle scattering with tensor tomography to probe n
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