Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement

Cardiac progenitor cells (CPCs) form cardiomyocytes, pericytes, smooth muscle and endothelial cells during embryonic development. Here, the authors characterize mouse CPCs marked by Nkx2.5 and Isl1 from E7.5 to E9.5 by single cell RNA-seq and ATAC-seq, showing fate transitions involve distinct open...

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Autores principales: Guangshuai Jia, Jens Preussner, Xi Chen, Stefan Guenther, Xuejun Yuan, Michail Yekelchyk, Carsten Kuenne, Mario Looso, Yonggang Zhou, Sarah Teichmann, Thomas Braun
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/f7864042a18d4c6f9b5af4ce0b06ab0a
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spelling oai:doaj.org-article:f7864042a18d4c6f9b5af4ce0b06ab0a2021-12-02T14:41:17ZSingle cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement10.1038/s41467-018-07307-62041-1723https://doaj.org/article/f7864042a18d4c6f9b5af4ce0b06ab0a2018-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-07307-6https://doaj.org/toc/2041-1723Cardiac progenitor cells (CPCs) form cardiomyocytes, pericytes, smooth muscle and endothelial cells during embryonic development. Here, the authors characterize mouse CPCs marked by Nkx2.5 and Isl1 from E7.5 to E9.5 by single cell RNA-seq and ATAC-seq, showing fate transitions involve distinct open chromatin state.Guangshuai JiaJens PreussnerXi ChenStefan GuentherXuejun YuanMichail YekelchykCarsten KuenneMario LoosoYonggang ZhouSarah TeichmannThomas BraunNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Guangshuai Jia
Jens Preussner
Xi Chen
Stefan Guenther
Xuejun Yuan
Michail Yekelchyk
Carsten Kuenne
Mario Looso
Yonggang Zhou
Sarah Teichmann
Thomas Braun
Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
description Cardiac progenitor cells (CPCs) form cardiomyocytes, pericytes, smooth muscle and endothelial cells during embryonic development. Here, the authors characterize mouse CPCs marked by Nkx2.5 and Isl1 from E7.5 to E9.5 by single cell RNA-seq and ATAC-seq, showing fate transitions involve distinct open chromatin state.
format article
author Guangshuai Jia
Jens Preussner
Xi Chen
Stefan Guenther
Xuejun Yuan
Michail Yekelchyk
Carsten Kuenne
Mario Looso
Yonggang Zhou
Sarah Teichmann
Thomas Braun
author_facet Guangshuai Jia
Jens Preussner
Xi Chen
Stefan Guenther
Xuejun Yuan
Michail Yekelchyk
Carsten Kuenne
Mario Looso
Yonggang Zhou
Sarah Teichmann
Thomas Braun
author_sort Guangshuai Jia
title Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
title_short Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
title_full Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
title_fullStr Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
title_full_unstemmed Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement
title_sort single cell rna-seq and atac-seq analysis of cardiac progenitor cell transition states and lineage settlement
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/f7864042a18d4c6f9b5af4ce0b06ab0a
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