Abstract
In this article, D'Antonio-Chronowska, Donovan and colleagues differentiated 191 iPSC lines to generate iPSC-derived cardiovascular progenitor cells (iPSC-CVPCs). The iPSC-CVPC samples showed cellular heterogeneity due to varying fractions of cardiomyocytes (CMs) and epicardium-derived cells (EPDCs). Donor sex and expression levels of signature genes in iPSCs played a role in the relative proportions of CMs and EPDCs present in the derived CVPCs.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 924-938 |
| Number of pages | 15 |
| Journal | Stem Cell Reports |
| Volume | 13 |
| Issue number | 5 |
| DOIs | |
| State | Published - Nov 12 2019 |
| Externally published | Yes |
Keywords
- X chromosome erosion
- X chromosome inactivation
- iPSC
- iPSC differentiation
- iPSC-derived cardiomyocytes
- iPSC-derived cardiovascular progenitor cells
- iPSC-derived epicardium
- scRNA-seq
- single-cell transcriptomics
ASJC Scopus subject areas
- Biochemistry
- Genetics
- Developmental Biology
- Cell Biology
Fingerprint
Dive into the research topics of 'Association of Human iPSC Gene Signatures and X Chromosome Dosage with Two Distinct Cardiac Differentiation Trajectories'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS