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As previously reported in Arabidopsis, this can be attributed to secondary siRNA in the 21-nucleotide register with the cleavage site for miR393 [ 64].
It could be attributed to secondary siRNA in the 21-nucleotide register with the cleavage site for miRNAs, as reported by Ronemus and De Paola [ 43, 44].
This finding could be attributed to secondary siRNA in the 21-nt register with the cleavage site for miRNAs as previously reported [ 36].
While the actives are unknown at this stage, the activity recorded in this study may be attributed to secondary metabolites [ 41].
This might be attributed to secondary or tertiary structure restrictions (e.g., steric hindrance), sequence specificity of insertion, or an inability to detect introns at these locations in the environment.
It was sliced 21 nucleotides downstream the canonical cleavage site, which could be attributed to secondary siRNA in the 21-nucleotide register with the cleavage site for miRNAs, as reported by Ronemus and De Paola [ 46, 47].
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Based on these analysis, the formation of branched nanorods was attributed to secondary nucleation at the crystal imperfections.
The peaks in the range of 3288 3335 cm−1 were attributed to secondary amide.
The primary form typically presents with soft tissue masses in the first or second decade of life, whereas the secondary form occurs mainly in patients with chronic renal failure, and has been attributed to secondary hyperparathyroidism [49].
Altered calcium release has been attributed to secondary modification of RyR function through CaMKII-dependent phosphorylation; oxidation or nitrosylation, described in heart failure, may also be present.
In addition, a high h and high π indicated high levels of divergence within three regions, which was attributed to secondary contact between previously differentiated allopatric lineages.
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