Sentence examples for be explained by inheritance from inspiring English sources

Similar to developing pollen, this observation may in part be explained by inheritance of wild type mitochondria with functional MIRO1 from the diploid megasporocyte.

Even though a substantial proportion of myopia cases can be explained by inheritance [ 15], it does not exclude strong environmental etiology, especially in East Asia [ 16].

The major reason for the clustering result appears to be the high fraction of vertically transmitted microbes associated with a specific host genotype: TRFLP peak size sharing analysis suggested that 51-67% of bacterial TRFLP signals observed in young Zea plants could be explained by inheritance through seed.

The formation of biaxially oriented polycrystals can be explained by the inheritance of octahedral TiO6 blocks from the layered to regular perovskites.

Within this context metamorphism during the early stages of orogenesis can be explained by the inheritance of elevated geothermal gradients produced by lithospheric thinning and sediment loading during formation of the basin.

Such a disparity cannot be explained by mitochondrial inheritance, genetic imprinting, or epigenetic factors because, on average, these should be similar for siblings and fraternal twins sharing the same biological parents.

The monophyly of eukaryote STC homologues could be explained by vertical inheritance from a common tetrahymanol-synthesizing eukaryotic ancestor.

In more practical terms, it should now be understood that even "core" proteins can have a more complex evolutionary history than can be explained by vertical inheritance.

Given the relatively recent bacterial origins established for archaeal class I RNRs, class I presence in eukaryotes cannot be explained by vertical inheritance from the common ancestor of eukaryotes and archaea.

Importantly, the non-mendelian distribution revealed in the MMP9 −/−:Plg −/− F2 offspring cannot be explained by linked inheritance between MMP9 and Plg because these genes are localized to chromosome 2H3 and 17E, respectively (Degen et al., 1990; Leco et al., 1997).

Our findings are consistent with both loss- and gain-of-function disorders among the PCP mutants, and suggest that the wide range of NTD-like phenotypes that are associated with human PCP mutations might be explained by the inheritance of different combinations of mutant alleles in different individuals.