Day23_exon3lines_Rep2
收藏NIAID Data Ecosystem2026-04-29 收录
下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP223003
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资源简介：
Haploinsufficiency of transcriptional regulators causes human congenital heart disease (CHD), predicting gene regulatory network (GRN) imbalances. Here, we define transcriptional responses to reduced transcription factor dosage in human iPSCs heterozygous or homozygous for loss of the CHD gene TBX5. Overall design: Single cell RNA sequencing of day 23 cells from exon3 lines (WTC11, TBX5Het and TBX5Hom) - biological replicate 2 Processed data are on the GSE137873 Series record.
创建时间：
2021-03-16
