Quantitative proteomics and systems analysis of cultured H9C2 cardiomyoblasts during differentiation over time supports a ‘function follows form’ model of differentiation-Reference-Cited by-同舟云学术

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Quantitative proteomics and systems analysis of cultured H9C2 cardiomyoblasts during differentiation over time supports a ‘function follows form’ model of differentiation

Published:2018 Issue:3 Volume:14 Page:181-196
ISSN:2515-4184
Container-title:Molecular Omics
language:en
Short-container-title:Mol. Omics

Author:

Kankeu Cynthia¹²³⁴,Clarke Kylie¹²³⁴,Van Haver Delphi⁵⁶⁷⁴⁸^ORCID,Gevaert Kris⁵⁶⁷⁴⁸^ORCID,Impens Francis⁵⁶⁷⁴⁸^ORCID,Dittrich Anna⁹¹⁰¹¹¹²^ORCID,Roderick H. Llewelyn¹²³⁴^ORCID,Passante Egle¹³¹⁴¹⁵¹⁶^ORCID,Huber Heinrich J.¹²³⁴¹⁷^ORCID

Affiliation:

1. Department of Cardiovascular Sciences

2. KU Leuven

3. 3000 Leuven

4. Belgium

5. Department of Biochemistry

6. Ghent University

7. Ghent

8. VIB-UGent Center for Medical Biotechnology

9. Department for Systems Biology

10. Institute of Biology

11. Otto-von-Guericke University Magdeburg

12. Germany

13. School of Pharmacy and Biomedical Sciences

14. Univ. of Central Lancashire

15. Preston

16. UK

17. Laboratory for Systems Theory and Automatic Control

Abstract

The rat cardiomyoblast cell line H9C2 has emerged as a valuable tool for studying cardiac development, mechanisms of disease and toxicology.

Funder

Bijzonder Onderzoeksfonds

Publisher

Royal Society of Chemistry (RSC)

Subject

Genetics,Molecular Biology,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/MO/C8MO00036K

Reference56 articles.

1. Re-employment of developmental transcription factors in adult heart disease

2. Properties of a clonal muscle cell line from rat heart

3. Cozzarelli Prize Winner: Robust cardiomyocyte differentiation from human pluripotent stem cells via temporal modulation of canonical Wnt signaling

4. Human Induced Pluripotent Stem Cells as a Platform for Personalized and Precision Cardiovascular Medicine

5. Morphological, biochemical, and electrophysiological characterization of a clonal cell (H9c2) line from rat heart.

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1. Regulation of mitochondrial calcium uniporter expression and calcium-dependent cell signaling by lncRNA Tug1 in cardiomyocytes;American Journal of Physiology-Cell Physiology;2023-10-01

2. The retinoic acid response is a minor component of the cardiac phenotype in H9c2 myoblast differentiation;BMC Genomics;2023-08-02

3. Natural guanine derivatives exert PARP-inhibitory and cytoprotective effects in a model of cardiomyocyte damage under oxidative stress;Биохимия;2023-06-15

4. Natural Guanine Derivatives Exert PARP-Inhibitory and Cytoprotective Effects in a Model of Cardiomyocyte Damage under Oxidative Stress;Biochemistry (Moscow);2023-06

5. Titanium Dioxide (E171) Induces Toxicity in H9c2 Rat Cardiomyoblasts and Ex Vivo Rat Hearts;Cardiovascular Toxicology;2022-05-28

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