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Our analysis uncovered that the occurrence of these errors is favored by the existence of multiple aromatic or condensed ring systems with a small number of substitutions and the presence of conjugated environments.
But our analysis uncovered something different: The key problem wasn't work-family conflict but long hours across the board.
Our analysis uncovered a network of transcription factors that potentially dysregulate several genes in MS or one or more of its disease subtypes.
Additionally, our analysis uncovered B3 genes from other families that have underwent recent duplication in different chromosomes, as well as old duplication events (Table S6).
Some examples, drawn from the families our analysis uncovered, follow.
Our analysis uncovered a topology in accordance with expansion in the vertebrate lineage.
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Moreover, our analysis uncovers the unskilled answerer profile, which has not received much attention in the context of Q&A systems.
Our analysis uncovers the transcriptional circuits that function in establishing distinct mesenchymal compartments downstream of HAND2 and upstream of SHH signaling.
In our analysis, uncovering correlation is limited to identifying genes that experience similar selective regimes.
Our analysis uncovers possible miRNA sequence alterations as a potential reason for differential activity, and we identify an association between RAS signaling and miRNA processing in which miRNAs may attenuate their own biogenesis.
Our analysis uncovers a highly ordered developmental program that correlates with the spore morphological changes and reveals the spatial and temporal molecular events fundamental to reconstruct a cell.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com