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We assumed that the ferromagnetic behavior observed in the nanowires before thermal heat treatment was attributed to (Co related-) organic residue on the surface of the nanowires synthesized via the aqueous solution method[15, 20, 37].
Likely, flower color fade under pH 4.0 treatment was attributed to decreased anthocyanin content and increased pH value of petal, which were coordinately regulated by nine anthocyanin biosynthetic genes and a vacuolar Na+/H+ antiporter1 gene (NHX1), respectively.
The deterioration of mechanical properties after the elevated temperature treatment was attributed to the formation of a thick compound layer (~6 µm) on the surface followed by an α-Case (~20 µm) and phase transformation in the bulk microstructure from fully equiaxed to bimodal with coarse grains (~5 times higher average grain size value).
The enhancement due to the TiCl4 treatment was attributed to the formation of an amorphous TiO2 thin layer, which separated the uncovered surface of TiO2 nanoparticles from the electrolyte, and reduced the surface states of the TiO2 nanocrystals and the quantum dots.
Amelioration of the disease after this treatment was attributed to the antiproliferative action of IFN-γ and to the ability of this cytokine to downregulate IL-1, which is involved in bone resorption [ 10].
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Changes after exposure of unwashed samples exposed before vacuum treatment were attributed to reactions involving volatile species.
Furthermore, the unexpected drop of diffusivity after one TiCl4 treatment is attributed to the involvement of surface diffusion in untreated TiO2 matrix.
In patients with high cholesterol and hypomagnesaemia, magnesium treatment is attributed to increasing the effectiveness of statin pharmaceuticals by shifting the equilibrium to the formation of a Mg+2-ATP complex which is a necessary intermediate in the cholesterol biosynthetic pathway [24].
The side effects of GA treatment were attributed to the degradation of the GA-derived cross-links and the continuous release of aldehydes contributing to prolong toxic effects Schmidt and Baier (2000).
The randomization result provided by the system is attributed in 80%% of the cases; otherwise the other treatment is attributed.
Table 2b indicates that the most commonly reported adverse effects of ITP treatment were attributed to the use of steroids.
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