In contrast, the cytoplasmic loop domain and the C-terminus domain are divergent and variable in length and sequence, allowing for the functional differences among the different connexins and the connexon types [ 31- 33].
This result implies that when evaluating hormone treatment, the importance of divergent outcome variables will also differ among individuals.
Our analyses revealed differences among individuals in terms of motives, which implies that in an evaluation of hormone treatment, the importance of divergent outcome variables will also differ among individuals.
Divergent outcome variables, specifically those that have low loadings on the first principal component and that mostly vary because of sources other than the target construct, can be readily identified and excluded.
This hypothesis is an example of the view that genetically divergent ecotypes and variable phenotypes due to plasticity are opposing strategies to evolve local adaptation.
When compared to untreated controls, 5-Aza C-treated lines exhibited reduced immuno-staining of 5mC on pachytene chromosomes, and Methylation Sensitive Amplified Polymorphism (MSAP) profiles that were both divergent and more variable.
The additional intron splice site of the 8-exon structure is also conserved, although the extra exon encodes a highly divergent sequence of variable length, termed the CD loop.
Compared with the two conserved domains, the N- and C-terminal regions are variable and divergent.
Divergent selection can impose variable genome-wide effects.
The orthologues of these three serpins show divergent RCL sequences, with variable P1/P1'sites affecting specificity for putative target proteinases.
