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Immune system responses have also been shown for fish [49, 50].
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Of note, if there are some examples of neofunctionalization events affecting the biochemical function of genes after the vertebrate WGD, much less numerous specific examples of that sort were shown for fish duplicated genes [ 22- 24].
Through the regulation of HOX genes, MOZ also influences ES cells with respect to body segment identity specification [ 65] and similar roles in development through HOX gene regulation have been shown for BRPF1 in zebra fish [ 66].
We did not detect any associated loss of diversity (as measured by haplotype diversity and nucleotide diversity) from West to East (longitude), as has been shown for a number of other fish species inhabiting the Baltic Sea [15].
Differences between fish species have been shown for tissue distribution of ER subtypes as well as differences in ER affinities for environmental oestrogens ([ 59- 61]).
The cumulative distribution of ACRs is shown for Daphnia and fish in Fig. 2.
Changes in cardiovascular parameters between days 1 and 5 are shown for both a single fish and a population.
Control neuron dialyzed with 0.5 mM EGTA (black; 47 boutons from 3 fish) is shown for comparison.
Up-regulation was shown for lectins and genes with reported induction in pathogen infected fish.
These images are shown for a single control (left) and ω-conotoxin GVIA-treated (right) fish.
Overexploitation of stocks has already been shown to select for smaller fish.
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