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Though the molecular architecture of many native RNA structures has been characterized, the structures of folding intermediates are poorly defined.
We characterized the structures of single ZnO nanorods grown for 4 h on Si 001) wafer and FTO glass substrates by using TEM and energy dispersive X-ray spectroscopy (EDX) analysis.
Benthic ecologists have characterized the structures of burrows using methods such as resin casting and X-radio-graphy; these detailed measurements can be used to calculate the depth-dependence of burrow surface areas without implementing a stochastic approach.
By using different and complementary microscopy approaches (AFM, FESEM and TEM), light scattering and electrophoretic mobility techniques, we characterized the structures of the complexes formed at different charge ratios and Chitosan molecular weight.
We have recently characterized the structures of novel phosphorylated dihydroceramide (PDHC) lipids produced by this organism [1].
Before describing the kinetics of RSC-nucleosome remodeling, we first characterized the structures of RSC, RSC-DNA and RSC-nucleosome complexes to assess the reaction stoichiometry and to get a broad overview of the reaction mechanism.
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Whereas FGFR1 FGFR3 have been structurally characterized, the structure of the FGFR4 kinase domain has not yet been reported.
Dedekind (1893) famously proved, for example, that the second-order formulation of the Peano Axioms characterized the structure of the natural number system.
Murata et al. characterized the structure of this model system using X-ray absorption fine structure (XAFS) and X-ray photoelectron spectroscopy (XPS).
We have characterized the structure of chemical vapor deposition-grown polycrystalline cubic SiC films by quantitative transmission electron microscopy.
We also generated and characterized the structure of a mouse- chimeric amelogenin containing the MQP repeats.
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