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However, these previous studies may have resulted in biased growth parameter estimates because these samples were not chosen at random and hence violated the assumptions of the method.
This correlations was not found in the control animals, mainly because these samples were almost entirely devoid of both rhamnose and galacturonic acid.
In systems with very big multidomain particles, the coercive force increases with a decrease in particle size [20]; this case was not observed for the samples considered in this work because these samples were synthesized by several surfactants.
Fibrosis grade F0 was considered to be the negative control because these samples were derived from patients with no finding of liver fibrosis.
Because these samples were collected between 1877 and 1951 (i.e., covering ca. 15 tiger generations) from wild tigers in China, Kazakhstan, Afghanistan, and Uzbekistan (see Table S1) it is unlikely they represent the sampling of a single extended family.
Because these samples were tested retrospectively, ascertaining the HEV IgG status of other family members was not possible.
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Because of hemolization these samples were only subjected to PCR.
The commercial PHB sample (sample B) and the C. necator PHB sample CN did not form nanofibers when using solutions with PHB concentrations of about 20% w/w, while the C. necator PHB sample RE produced nanofibers with droplets, because of which these samples were not tested with sodium chloride and Spirulina biomass.
The low-positive reactions from pigs in herd 1 might have been the result of nonspecific reactions because a few of these samples were from old sows, which might have more serologic interference.
These samples were selected because of their contrasting structures after 8 years of ageing (i.e., 2 years before the present study).
These samples were redundant because the sample of homologous regions ≥ 100 also included homologous regions ≥ 300 bp.
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CEO of Professional Science Editing for Scientists @ prosciediting.com