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资源简介：
Determine mRNA expression levels in cultured cardiomyocytes derived from human iPS cells 1 sample
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创建时间：
2019-01-09
相关数据集
RNA-Seq of isogenic human iPS cell-derived cardiomyocytes with RBM20 mutations created by genome editing (WTB RNA-Seq)
RBM20 heterozygous (Het) mutation was created by genome editing in an iPS cell line generated from a healthy female patient. Those cells were differentiated into cardiomyocytes by modulating the WNT s
NIAID Data Ecosystem60
Gene expression analysis comparing rat neonatal cardiomyocytes and human iPSC-cardiomyocytes
Bulk RNA sequencing of rat neonatal cardiomyocytes and hiPSC-cardiomyocytes treated with vehicle or GPCR agonists for 60 minutes. Bulk RNA sequencing of rat neonatal cardiomyocytes and hiPSC-cardiomyo
NIAID Data Ecosystem30
Flow cytometry data from iPS-derived macrophages.
This page contains raw flow cytometry data from macrophages derived from three different iPS cell lines. The data are part of the manuscript "Transcriptional profiling of macrophages derived from mono
Figshare2014-07-28 更新10
Comparison of gene expression profiles of neonate rat cardiomyocytes (NRCMs) transfected with LacZ, 23k prolactin (PRL), or 16k PRL.
Recently, it is reported that multiple signaling pathways are involved with the pathogenesis of PPCM. Here, we show that 23k PRL activates PERK signaling. Overall design: Total 9 samples were derived
NIAID Data Ecosystem60
JMJD4 regulates PKM2 degradation of cardiomyocytes and is critical in the development of dilated cardiomyopathy. JMJD4 regulates PKM2 degradation of cardiomyocytes and is critical in the development of dilated cardiomyopathy
RNA-Seq results of adult mouse cardiomyocytes with Jmjd4 knockout and neonatal rat cardiomyocytes with Jmjd4 knockdown. To investigate the role of Jmjd4 in dilated cardiomyopathy, we performed gene ex
NIAID Data Ecosystem20
