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The initial form-related adaptation (observed change in functional space) can challenge strain-adaptive nature of tissues to meet functional demands with increasing age into adulthood.
This observation would be in agreement with the rapid adaptation observed for promoters of genes involved in immune response – genes which are statistically over-represented among genes with TE-derived HS sites.
The so-called staircase-of-eye-movements effect, Groh reasons, would predict some of the symptoms — at least the trailing, after-imaging, and poor darkness adaptation — observed in H.P.P.D. patients.
This may explain an adaptation observed in some Brachyhypopomus species that restrict the lower end of the frequency spectrum to near-body pulses allowing only higher frequencies to dissipate widely.
This ancestral dichotomy, where both annual and perennial ancestors are recombined with W1 accessions, undoubtedly contributes to the high levels of diversity and broad adaptation observed within the indica subpopulation (Garris et al. 2005; Huang et al. 2012c).
Together, the intention specific adaptation observed at these two stages indicates that right STS and aIPS regions do not simply function as part of a serial, unidirectional network.
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We thus assessed whether this explains differences among octopods from polar, temperate, subtropical or tropical climates and in particular the functional adaptations observed in cold-adapted Antarctic octopods [ 16].
Furthermore, the observed protein expression differences would then largely reflect functional adaptations observed in species phenotypes.
If this is true, then differences in protein expression may largely reflect functional adaptations observed in species phenotypes.
These local adaptations observed as differences in protein levels may be related to genetic or epigenetic changes in the queens of the different populations.
Hence, abnormally elevated NO levels may contribute to the physiological adaptations observed in Mb-knockout mice.
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