Suggestions(1)
Exact(3)
All strains originating from the Wistar rat (Table S2) shared the same allele at all these three positions indicating inheritance of an ancestral haplotype.
Several sequences from other Metazoa and Fungi code for proteins similar to those encoded by SmTRC1, suggesting that such elements have a common ancestry, and indicating inheritance through vertical transmission before separation of the Eumetazoa, Fungi and Plants.
The human genome contained a deleteriously mutated gene remnant corresponding to TCHHL2 (Fig. S5), indicating inheritance of this gene from a common ancestor of mammals (26) and independent inactivations of this gene in the evolutionary lineages leading to cetaceans and humans.
Similar(57)
The few older tor ages have no systematic explanation, and may indicate inheritance from an earlier cycle of bedrock near-exposure.
They are the result of convergent evolution, which is the acquisition of the same biological trait in unrelated lineages--and, thus, do not indicate inheritance of the trait from a shared ancestor.
Data from phylogenetic analysis of the Transposase_21 domain suggests a common ancestry for such elements, and indicates inheritance through vertical transmission before the separation of Eumetazoa, Fungi and Plants.
Averaged values above 0.7 or below −0.7 thresholds were indicative of a non-random SNP segregation at that locus, indicating preferential inheritance from a 16D or ER18 parent, respectively.
To date, there have been no reported data indicating the inheritance of psychological stress-induced gene expression.
In this case, the masks from are used and new labels for the substructures are introduced (indicating clonal inheritance of subcolonies or cells).
Genetic analysis revealed a previously unpublished ITGB4 loss-of-function mutation; the affected calf was homozygous for a 4.4 kb deletion involving exons 17 to 22, and the dam carried a single copy of the deletion indicating recessive inheritance.
Only one family has been reported in which Marfan syndrome was found in two affected cousins homozygous for a FBN1 mutation while the four normal parents were heterozygous carriers, indicating recessive inheritance of the syndrome (De Vries et al., 2007).
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com