Sinoatrial node cardiomyocytes derived from human pluripotent cells function as a biological pacemaker-Reference-Cited by-同舟云学术

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Sinoatrial node cardiomyocytes derived from human pluripotent cells function as a biological pacemaker

Published:2016-12-12 Issue:1 Volume:35 Page:56-68
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Protze Stephanie I,Liu Jie,Nussinovitch Udi,Ohana Lily,Backx Peter H,Gepstein Lior,Keller Gordon M

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/nbt.3745.pdf

Reference48 articles.

1. Yang, L. et al. Human cardiovascular progenitor cells develop from a KDR+ embryonic-stem-cell-derived population. Nature 453, 524–528 (2008).

2. Laflamme, M.A. et al. Cardiomyocytes derived from human embryonic stem cells in pro-survival factors enhance function of infarcted rat hearts. Nat. Biotechnol. 25, 1015–1024 (2007).

3. Kattman, S.J. et al. Stage-specific optimization of activin/nodal and BMP signaling promotes cardiac differentiation of mouse and human pluripotent stem cell lines. Cell Stem Cell 8, 228–240 (2011).

4. Burridge, P.W. et al. Chemically defined generation of human cardiomyocytes. Nat. Methods 11, 855–860 (2014).

5. He, J.Q., Ma, Y., Lee, Y., Thomson, J.A. & Kamp, T.J. Human embryonic stem cells develop into multiple types of cardiac myocytes: action potential characterization. Circ. Res. 93, 32–39 (2003).

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1. Single-cell transcriptome analysis reveals CD34 as a novel marker of human sinoatrial node pacemaker cardiomyocytes;2024-09-07

2. A new paradigm for generating high-quality cardiac pacemaker cells from mouse pluripotent stem cells;Signal Transduction and Targeted Therapy;2024-09-06

3. Differentiation of Sinoatrial-like Cardiomyocytes as a Biological Pacemaker Model;International Journal of Molecular Sciences;2024-08-23

4. Stem cell-derived cardiomyocytes expressing a dominant negative pacemaker HCN4 channel do not reduce the risk of graft-related arrhythmias;Frontiers in Cardiovascular Medicine;2024-07-09

5. Chamber-specific contractile responses of atrial and ventricular hiPSC-cardiomyocytes to GPCR and ion channel targeting compounds: A microphysiological system for cardiac drug development;Journal of Pharmacological and Toxicological Methods;2024-07

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