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Additionally, the role of oocyte polarity on influencing superficial epithelial cell fate in early frog and fish development is addressed.
In addition, comparing data between frog and fish (within the same apparatus under identical conditions) offers a powerful "evo-devo" perspective in which conservation and divergence of results between vertebrates can be studied.
More importantly, there is strong co-localization of Xin with known intercalated disc components, such as β-catenin, N-cadherin and plakoglobin in the mouse, chicken, frog and fish hearts.
The p.Pro52, p.Cys53 and p.Ala55 residues were also completely conserved in platypus (Ornithorhynchus anatinus), frog and fish.
The Ush1g-Otop2-Otop3 locus is markedly different in frog and fish lineages compared to the other vertebrates studied.
A profile HMM was constructed from the alignment of known OR sequences from human, frog, and fish using the HMMER software package (http://hmmer.janelia.org).org
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PARP12-like protein exhibits expansion in different lineages through duplications (e.g. in frog and fishes, Table 1).
It feeds mostly upon rodents, but it also preys upon frogs and fish.
(Grass snakes do eat frogs and fish, but not usually enough to impact their populations).
There are five separate ponds with frogs and fish; herons and mallards are visitors.
In frogs and fish, the optic tectum receives direct excitatory input from the contralateral retina (the retinotectal projection).
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