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They probably originated from a more basal duplication of a "TSA ancestor", leading to the IGL/BX1 and TSA/TSA_like lineages.
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The observation that the two P. buchholzi GRs differ in their transactivation activity sensitivity may be a divergence in functional traits that helps explain the retention of two GRs in basal teleosts following the duplication of a GR in an ancestral teleost.
In the pancrustaceans, a basal duplication event generated the ancestral Dscam-hv and the ancestor of the rest of the Dscam-like clades.
A duplication event deep enough in the tree to explain the two Aegilops outliers as paralogs (i.e., a basal duplication) should be apparent in most, if not all, of the genera.
In spite of a large number of governing equations, the model has a quite simple mathematical structure: it is a duplication of a single visco-elastic model.
To exemplify, duplication of a single gene could result in severe phenotype like in MECP2 duplication syndrome which was associated with autism and mental retardation [57].
A dramatic result of numerous bi-complex duplications could be a duplication of a whole complex.
The duplication of an entire genome.
Thus, it appeared most likely that teleost NCX4 was a product of either the 3R WGD, or a duplication of NCX1 in a basal actinopterygian [ 20].
Afterward there was a duplication of the ceremony and a banquet for 350 people.
Furthermore, K5-Ets1 BT skin, but not Inv-Ets1 skin, showed an apparent duplication of the basal layer of the epidermis.
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