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A large-scale channel-shoal morphological system has been historically present in the outer bay.
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How or why this multiple coding system has been sustained and why morphological changes happen due to mutation in a single protein have also been subjects of intense debate.
This system has enabled studies of sequence-dependent structural changes of triple helical type II collagen monomers and of morphological changes of self-assembled fibrils [ 30– 30].
This α-helical coiled-coil peptide system has been purpose-designed to mimic some of the biochemical and morphological properties of ECM.
This expression system has the advantage that in addition to neuron-like membrane properties, the genetic and morphological homogeneity of these cells facilitate quantitative patch-clamp fluorometry.
Our study of the female reproductive system has complete taxon overlap with the molecular phylogeny, while only 38 species are shared with the morphological tree; i.e., some species had to be deleted for the pairwise comparison with the morphological tree.
A fundamental, yet unsolved, question is type and leverage of freedom such a system has, in search for an optimal architecture under altering sets of environmental and biological challenges (considering claims that morphological plasticity in corals is either strictly adoptive and/or stems from absence of genetic canalization in morphological traits [28], [29]).
This system has advantages.
Morphological classification systems have been established to assess the pathological response and prognosis after systemic primary therapy.
Several morphological scoring systems have been designed to select the most viable embryos in a cohort, by analyzing pronuclear-stage zygotes [ 43], cleavage-stage embryos [ 42], and blastocysts [ 44].
The system had worked.
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