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Studies exploring differences in gene expression in multiple primate tissues have yielded lists of genes, which are differentially expressed in closely related species (Khaitovich et al. 2005), but it is less clear which regulatory changes drive these differences.
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Scientific papers published at the time did not say what primate tissues were used to make the vaccine, Mr. Hooper wrote.
Adhesion of endothelial cells was markedly enhanced on human and primate tissues.
Placing comparative sequence analysis of the TNF promoter from multiple primate species in the context of known primate phylogeny demonstrates that specific single nucleotide positions are characteristic of different primate taxa (Figure 6).
Similar, but less steep, miRNA conservation profiles have been distinguished in alignments of multiple primate species [8].
We demonstrated that DRBP76 exhibits intrinsically distinct subcellular distribution in primate tissues in the absence of known stimuli.
We also performed expression pattern analysis in multiple primate species, and examined between-species and between-paralogs expression divergences.
The gene copy number analysis showed that there had been parallel gene duplications/losses in multiple primate lineages.
However, because these associations correspond to multiple, potentially unrelated phenotypes, it remains unknown which of them are responsible for the persistence of ABO types in multiple primate species.
Taken together, during the evolution of primates, along with parallel gene duplications and/or losses, positive selection has been acting on multiple primate lineages leading to the rapid protein sequence changes of RHOXF2.
As the major function of RHOXF2 in primates is male reproduction, we speculate that the observed strong selection in multiple primate lineages is likely to be related to sperm competition in promiscuous mating systems [ 49, 50].
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