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- Publisher Website: 10.1016/j.ddmod.2012.11.001
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Article: Cardiac tissue engineering using human stem cell-derived cardiomyocytes for disease modeling and drug discovery
Title | Cardiac tissue engineering using human stem cell-derived cardiomyocytes for disease modeling and drug discovery |
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Authors | |
Issue Date | 2012 |
Publisher | Elsevier Ltd, Trends Journals. The Journal's web site is located at http://www.elsevier.com/locate/ddmod |
Citation | Drug Discovery Today: Disease Models, 2012, v. 9 n. 4, p. e219-e227 How to Cite? |
Abstract | Cardiovascular disease (CVD) is the most prevalent health problem in the world, and the high mortality rate associated with irreversibly injured heart muscle motivates an urgent need for the development of novel therapies to treat damaged myocardium. Recently, human engineered cardiac tissues (hECT) have been created using cardiomyocytes (CM) derived from human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC). Although a healthy adult phenotype remains elusive, such hECT display structural and functional properties that recapitulate key aspects of natural human myocardium, including dose related responses to compounds with known chronotropic, inotropic and arrhythmogenic effects. Thus, hECT offer the advantage over traditional in vitro culture models of providing a biomimetic 3D environment for the study of myocardial physiopathology, and may be used to generate preclinical models for the development and screening of therapies for CVD. © 2012 Elsevier Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/143052 |
ISSN | 2023 SCImago Journal Rankings: 0.665 |
DC Field | Value | Language |
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dc.contributor.author | Turnbull, IC | en_US |
dc.contributor.author | Lieu, DK | en_US |
dc.contributor.author | Li, RA | - |
dc.contributor.author | Costa, K | - |
dc.date.accessioned | 2011-10-28T03:05:26Z | - |
dc.date.available | 2011-10-28T03:05:26Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | Drug Discovery Today: Disease Models, 2012, v. 9 n. 4, p. e219-e227 | - |
dc.identifier.issn | 1740-6757 | - |
dc.identifier.uri | http://hdl.handle.net/10722/143052 | - |
dc.description.abstract | Cardiovascular disease (CVD) is the most prevalent health problem in the world, and the high mortality rate associated with irreversibly injured heart muscle motivates an urgent need for the development of novel therapies to treat damaged myocardium. Recently, human engineered cardiac tissues (hECT) have been created using cardiomyocytes (CM) derived from human embryonic stem cells (hESC) and human induced pluripotent stem cells (hiPSC). Although a healthy adult phenotype remains elusive, such hECT display structural and functional properties that recapitulate key aspects of natural human myocardium, including dose related responses to compounds with known chronotropic, inotropic and arrhythmogenic effects. Thus, hECT offer the advantage over traditional in vitro culture models of providing a biomimetic 3D environment for the study of myocardial physiopathology, and may be used to generate preclinical models for the development and screening of therapies for CVD. © 2012 Elsevier Ltd. All rights reserved. | - |
dc.language | eng | en_US |
dc.publisher | Elsevier Ltd, Trends Journals. The Journal's web site is located at http://www.elsevier.com/locate/ddmod | en_US |
dc.relation.ispartof | Drug Discovery Today: Disease Models | - |
dc.title | Cardiac tissue engineering using human stem cell-derived cardiomyocytes for disease modeling and drug discovery | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li, RA: ronaldli@hkucc.hku.hk | en_US |
dc.identifier.authority | Li, RA=rp01352 | en_US |
dc.identifier.doi | 10.1016/j.ddmod.2012.11.001 | - |
dc.identifier.scopus | eid_2-s2.0-84876675545 | - |
dc.identifier.hkuros | 197128 | en_US |
dc.identifier.volume | 9 | - |
dc.identifier.issue | 4 | - |
dc.identifier.spage | e219 | - |
dc.identifier.epage | e227 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1740-6757 | - |