Prediction of putative small molecules for manipulation of enriched signalling pathways in hESC-derived early cardiovascular progenitors by bioinformatics analysis.
作者:
关键词
DEGsHippoMESP1-negative cellsPI3K/AktWntbioinformaticsbioinformatics analysiscardiac cell typescardiac regenerative medicinecardiogenesiscardiovascular systemcell fate decisionscell proliferationcellular biophysicsdifferentially expressed genesenriched signalling pathwaysenzymesgene expression signaturegene ontologygeneticshESC-derived CPCshESC-derived early cardiovascular progenitorshuman embryonic stem cells-derived MESP1+ cellshuman pluripotent stem cell-derived cardiovascular progenitor cellslab-on-a-chipmesoderm posterior1+ cellsmicroarray datamolecular biophysicsontologies (artificial intelligence)pathway enrichment analysisputative regulatory small moleculestranscriptional regulatory factorstransforming growth factor-β
DOI
10.1049/iet-syb.2018.5037
PMID
33444476
发布时间
2022-02-18
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IET systems biology
77-83页
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