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An important task is to determine to what extent these differences can be attributed to different analysis methods and to what extent to different data.
In previous works with enzymes of P. echinulatum [ 18], high relationships of FPA/ β-glucosidase were obtained; these differences can be attributed to the different inducer substrate or the different substrate used to β-glucosidase determination.
These observed differences can be attributed to different types of micropores generated by shrinkage effects during carbon liberation from the parent zeolite host.
These differences can be attributed to different climatic conditions, enrollment criteria, case definitions and testing platforms.
The small differences can be attributed to different LC systems with unique system dead volumes.
These differences can be attributed to different methods of detection of VEGF expression, such as immunohistochemistry, ELISA, and RT-PCR [ 1, 4].
These differences can be attributed to the different nature of the information provided by these modalities.
One possible explanation for these differences can be attributed to the different methods used for the assessment of TIMP3 expression.
These differences can be attributed to the different components in the PM mixture to which OPESR and OPDTT are sensitive.
The differences can be attributed to the different reactants, conditions, and mechanisms [ 18], which will be further investigated in follow-up studies.
These differences can be attributed to the method of extraction and the different trademarks used in these studies.
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