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Erbium diffusion coefficient in the SRSO layer has been deduced using the Einstein equation of self-diffusivity.
A generalized Nash model (GNM) has been deduced using the Laplace transform and the principle of mathematical induction.
The cleavage rate constant of the carbon chlorine bond has been deduced using the voltammetric data in conjunction with convolution analysis and the results have been verified by simulating the experimental voltammogram under the frame work of EC mechanism.
Much information about the roles of ABC transporters has been deduced using loss of function mutants isolated in genetic screens [ 20] and the pressing need for complementary biochemical studies of plant ABC transporters was outlined by François Lefèvre, using ABC sub-class G as an exemplar [ 24].
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The specific surface areas of the nanoparticles have been deduced using the relationship S = 6/dρ, where S is the specific surface area, d is the mean particle size and ρ is the material density.
The 'IDs' have been deduced using NCBI BLAST searches, and have not been experimentally verified.
Proteins sequences from the Genoscope database have been deduced using an automated method [ 25].
Most of these structural changes have been deduced using radiolabeled monosaccharides and sulfate as biosynthetic precursors in various cellular systems.
The interacting residues of various proteins of β-grasp fold with their interacting molecules have been deduced using custom made PERL scripts.
One of possible models of this epitaxy structure has been deduced with using its crystal structure proposed in a previous paper, which well matches its X-ray diffraction patterns.
One of the possible models of this epitaxy structure, which matched its X-ray diffraction patterns well, has been deduced by using the crystal structure proposed in a previous paper.
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