Mechanism of spontaneous excitability in human embryonic stem cell derived cardiomyocytes. - Wikidata - awgldk - TriplyDB

Mechanism of spontaneous excitability in human embryonic stem cell derived cardiomyocytes.

Mechanism of spontaneous excitability in human embryonic stem cell derived cardiomyocytes.

http://www.wikidata.org/entity/Q44970476

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Cardiac applications for human pluripotent stem cells Mechanisms underlying the cardiac pacemaker: the role of SK4 calcium-activated potassium channels Autonomous beating rate adaptation in human stem cell-derived cardiomyocytes.Induced regeneration--the progress and promise of direct reprogramming for heart repair.Genetic engineering of somatic cells to study and improve cardiac function Survival and maturation of human embryonic stem cell-derived cardiomyocytes in rat hearts Optimization of direct fibroblast reprogramming to cardiomyocytes using calcium activity as a functional measure of success Screening drug-induced arrhythmia [corrected] using human induced pluripotent stem cell-derived cardiomyocytes and low-impedance microelectrode arrays.Characterization of contracting cardiomyocyte colonies in the primary culture of neonatal rat myocardial cells: a model of in vitro cardiomyogenesis.Excitability constraints on voltage-gated sodium channels Pluripotent stem cell derived cardiomyocytes for cardiac repair.Stepwise chemically induced cardiomyocyte specification of human embryonic stem cells.High purity human-induced pluripotent stem cell-derived cardiomyocytes: electrophysiological properties of action potentials and ionic currents.De novo myocardial regeneration: advances and pitfalls.Human pluripotent stem cell-derived cardiomyocytes: response to TTX and lidocain reveals strong cell to cell variability Adhesion proteins, stem cells, and arrhythmogenesis.Rhythmic beating of stem cell-derived cardiac cells requires dynamic coupling of electrophysiology and Ca cycling.Transcriptome-guided functional analyses reveal novel biological properties and regulatory hierarchy of human embryonic stem cell-derived ventricular cardiomyocytes crucial for maturation The promise of human embryonic stem cells in aging-associated diseases.Mechanism of automaticity in cardiomyocytes derived from human induced pluripotent stem cells.Cell and gene therapy for arrhythmias: Repair of cardiac conduction damage Strategies for enrichment and selection of stem cell-derived tissue precursors.Slow conduction in mixed cultured strands of primary ventricular cells and stem cell-derived cardiomyocytes.Modulation of hERG potassium channel gating normalizes action potential duration prolonged by dysfunctional KCNQ1 potassium channel Differentiation pathways in human embryonic stem cell-derived cardiomyocytes.Human pluripotent stem cells: Prospects and challenges as a source of cardiomyocytes for in vitro modeling and cell-based cardiac repair.Inhibition of cardiomyocytes differentiation of mouse embryonic stem cells by CD38/cADPR/Ca2+ signaling pathway.Stem cells as biological heart pacemakers.Cardiac repair by embryonic stem-derived cells Engineered heart tissues and induced pluripotent stem cells: Macro- and microstructures for disease modeling, drug screening, and translational studies.beta(1)- and beta(2)-adrenoceptor responses in cardiomyocytes derived from human embryonic stem cells: comparison with failing and non-failing adult human heart.Automated Electrophysiological and Pharmacological Evaluation of Human Pluripotent Stem Cell-Derived Cardiomyocytes.SK4 Ca2+ activated K+ channel is a critical player in cardiac pacemaker derived from human embryonic stem cells.Pluripotent stem cells for cardiac regeneration: overview of recent advances & emerging trends.Human embryonic stem cells and cardiac repair Cardiac tissue engineering using stem cells.Cardiac differentiation of human pluripotent stem cells Stem cell therapy is proarrhythmic.Electrophysiological and contractile function of cardiomyocytes derived from human embryonic stem cells.Engraftment of human embryonic stem cell derived cardiomyocytes improves conduction in an arrhythmogenic in vitro model.

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Mechanism of spontaneous excitability in human embryonic stem cell derived cardiomyocytes.

http://www.wikidata.org/entity/Q44970476

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

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name

Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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type

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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JPHYSIOL.2004.068213

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The Journal of Physiology

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Mechanism of spontaneous excit ...... m cell derived cardiomyocytes.

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P2093

Elizabeth A Schroder

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

Gil Arbel

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

Ido Perlman

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

Ilanit Itzhaki

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

Irit Huber

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Izhak Kehat

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Janos Magyar

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

Jonathan Satin

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

Lior Gepstein

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Oren Caspi

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P2860

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels

Human embryonic stem cells can differentiate into myocytes with structural and functional properties of cardiomyocytes

The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart.

Changes in membrane properties of chick embryonic hearts during development.

Establishment of ionic channels and signalling cascades in the embryonic stem cell-derived primitive endoderm and cardiovascular system.

Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent.

Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems.

An unexpected requirement for brain-type sodium channels for control of heart rate in the mouse sinoatrial node.

Derivation and potential applications of human embryonic stem cells.

Cyclic variation of intracellular calcium: a critical factor for cardiac pacemaker cell dominance.

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