Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8768487 | Seminars in Perinatology | 2018 | 9 Pages |
Abstract
DA closure is crucial for the transition from fetal to neonatal life. This closure is supported by changes to the DA's signaling and structural properties that distinguish it from neighboring vessels. Examining transcriptional differences between these vessels is key to identifying genes or pathways responsible for DA closure. Several microarray studies have explored the DA transcriptome in animal models but varied experimental designs have led to conflicting results. Thorough transcriptomic analysis of the human DA has yet to be performed. A clear picture of the DA transcriptome is key to guiding future research endeavors, both to allow more targeted treatments in the clinical setting, and to understand the basic biology of DA function. In this review, we use a cross-species cross-platform analysis to consider all available published rodent microarray data and novel human RNAseq data in order to provide high priority candidate genes for consideration in future DA studies.
Keywords
UniProtPDAFDRRNA-seqRMAFPKMGEOECMAortaDuctus arteriosusMolecular functioncellular componentKEGG یا Kyoto Encyclopedia of Genes and Genomes Kyoto Encyclopedia of Genes and GenomesDAVIDMicroarrayRINDEGRNA Integrity Numberbiological processFragments per kilobase of transcript per million mapped readsExtracellular matrixfalse discovery rateGene ontologyDatabase for Annotation, Visualization, and Integrated DiscoveryTranscriptional profilingGene Expression OmnibusDifferentially expressed gene
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Authors
Michael T. Yarboro, Matthew D. MD, Jennifer L. PhD, Elaine L. PhD, Tao MD, PhD, Cris G. Ebby, Jason Z. MD, Ronald I. MD, Jeff MD,