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Time-resolved orientation measurements were made in situ through a novel X-ray rheometer coupled with a two-dimensional electronic X-ray camera, and using an intense X-ray source at the LURE synchrotron.
Both, the principal strand axis and the β-sheet plane orientations are required to resolve the orientation of β-sheet peptide in a model membrane.
It is also impossible to resolve the orientation and position in space with a single station.
Diffusion MRI (dMRI) is widely used to measure microstructural features of brain white matter, but commonly used dMRI measures have limited capacity to resolve the orientation structure of complex fiber architectures.
For resolved shear stress, orientation populations favoring tension and compression do not show any great difference.
Modeling of these mutations into the G296D model introduces local steric clashes around residues 443 and 444 that, when resolved, alter the orientation of the beta-sheet linker in which they are contained.
Recursive estimation improves the accuracy of resolving individual orientations and yields inherently smooth tracts despite the presence of noise and uncertainty.
Since the drag and lift forces are both shape factor- and orientation-dependent, coupled particle rotation equations are resolved to update particle orientation.
Harmonophore orientation is resolved in 3D from a sub-set of polarization-resolved SHG holograms.
Spatially resolved maps of crystal orientation and GB misorientation angles were measured by electron backscattering diffraction (EBSD).
The particular resonances in Figure 5(a), well resolved for some intermediate orientation angles, are marked as I, IIa, and IIb. Figure 5(b) presents the related dependences of the measured longitudinal relaxation rates (T_{1}^{-1}) on the B-field orientation at room temperature.
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