hiPSC-CM Monolayer Maturation State Determines Drug Responsiveness in High Throughput Pro-Arrhythmia Screen

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Changing Metabolism in Differentiating Cardiac Progenitor Cells-Can Stem Cells Become Metabolically Flexible Cardiomyocytes?

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Q57072502-DCBCC8F5-B6A4-471E-8264-B578547CE43F

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hiPSC-CM Monolayer Maturation State Determines Drug Responsiveness in High Throughput Pro-Arrhythmia Screen

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http://www.wikidata.org/entity/Q42645439

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

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hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

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Item

label

hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

@en

hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

@nl

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hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

@en

hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

@nl

P1476

hiPSC-CM Monolayer Maturation ...... roughput Pro-Arrhythmia Screen

@en

P2093

André Monteiro da Rocha

http://www.w3.org/2001/XMLSchema#string

Guadalupe Guerrero-Serna

http://www.w3.org/2001/XMLSchema#string

Jiang Jiang

http://www.w3.org/2001/XMLSchema#string

Katherine Campbell

http://www.w3.org/2001/XMLSchema#string

Lakshmi Mundada

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Sergey Mironov

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Todd J Herron

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P2860

Differentiation of human embryonic stem cells and induced pluripotent stem cells to cardiomyocytes: a methods overview

Growth of engineered human myocardium with mechanical loading and vascular coculture

Engineering adolescence: maturation of human pluripotent stem cell-derived cardiomyocytes

Safety of non-antiarrhythmic drugs that prolong the QT interval or induce torsade de pointes: an overview.

Myosin light chain 2-based selection of human iPSC-derived early ventricular cardiac myocytes.

Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics.

High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currents.

Maximum diastolic potential of human induced pluripotent stem cell-derived cardiomyocytes depends critically on I(Kr).

Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine.

Robust cardiomyocyte differentiation from human pluripotent stem cells via temporal modulation of canonical Wnt signaling.

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s41598-017-13590-y

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13834

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scholarly article

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10.1038/S41598-017-13590-Y

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English

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http://www.w3.org/2001/XMLSchema#string

P478

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José Jalife

P577

2017-10-23T00:00:00Z

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1092262001

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29061979

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5653750

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hiPSC-CM Monolayer Maturation State Determines Drug Responsiveness in High Throughput Pro-Arrhythmia Screen

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hiPSC-CM Monolayer Maturation State Determines Drug Responsiveness in High Throughput Pro-Arrhythmia Screen

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type

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P6179

P698

P932