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It has also been shown that variation in oxygen (O2) concentration plays a key role in the proliferation of cardiac MFBs.
Recently, it has been shown that variation in PP may correlate with variation in pulse oximetry plethysmographic (POP) waveform amplitude, as they both depend on the stroke volume.
In barley, it has been shown that variation in both expression levels and copy numbers of CBF genes is associated with low temperature tolerance differences amongst cultivars [ 12].
Furthermore, it has been shown that variation in GA levels can provide a mechanism for plant growth regulation, causing ROS levels to remain low after biotic or abiotic stress [ 13].
For instance, it has been shown that variation of short oligonucleotide usage is moderate in some fungi genomes and that parametric methods based on this type of criterion could be applied to them [ 50, 70, 71].
It has been shown that variation in the fraction of the recombining accessory genome correlates with variation in bacterial ecology (Newton and Bordenstein 2011; Rankin et al. 2011; Wiedenbeck and Cohan 2011; Baltrus 2013).
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Studies have been shown that variations in steel strength and concrete strength are different, and so are their respective probability distributions.
It has also been shown that variations in precipitation levels in the Amazon is regulated by SSTs in the Atlantic and Pacific oceans.
It has been shown that variations in parameter values (e.g. corresponding to mutations) can lead to only four different scenarios of dynamical behaviour of the network [ 52].
It has been shown that variations in the lengths of homopolymeric tracts are attributable to variations in the DNA template population and are not an artefact of the sequencing process, although this may be influenced by the length of repeat and the experimental conditions [ 33].
Methods of modelling and experimental results are presented and it is shown that variation of the adhesive mechanical properties with temperature is generally the most critical factor.
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