| Literature DB >> 27717505 |
Christopher E Slagle1, Frank L Conlon2.
Abstract
Congenital heart defects remain a leading cause of infant mortality in the western world, despite decades of research focusing on cardiovascular development and disease. With the recent emergence of several high-throughput technologies including RNA sequencing, chromatin-immunoprecipitation-coupled sequencing, mass-spectrometry-based proteomics analyses, and the numerous variations of these strategies, investigations into cardiac development have been transformed from candidate-based studies into whole-genome, -transcriptome, and -proteome undertakings. In this review, we discuss several reports that have emerged from our laboratory and others over the past 5 years that emphasize the versatility of large dataset-based investigations of cardiogenic transcription factors, from phenotypic validations and new gene implications to the identification of novel roles of well-studied transcriptional regulators.Entities:
Keywords: cardiovascular development; chromatin; congenital heart disease; high-throughput sequencing; proteomics; transcription factor
Mesh:
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Year: 2016 PMID: 27717505 PMCID: PMC5828029 DOI: 10.1016/j.tig.2016.09.002
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639