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Human-induced pluripotent stem cell models of inherited cardiomyopathies

Human-induced pluripotent stem cell models of inherited cardiomyopathies

http://www.wikidata.org/entity/Q26852052

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Induced pluripotent stem cells for cardiovascular disease: from product-focused disease modeling to process-focused disease discovery Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy Prospects for In Vitro Myofilament Maturation in Stem Cell-Derived Cardiac Myocytes.Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia.Interleukin-18 deteriorates Fabry cardiomyopathy and contributes to the development of left ventricular hypertrophy in Fabry patients with GLA IVS4+919 G>A mutation Hold or fold--proteins in advanced heart failure and myocardial recovery.Optical-flow based non-invasive analysis of cardiomyocyte contractility.

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

http://www.wikidata.org/entity/Q26852052

description

2014 nî lūn-bûn

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2014 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2014 թվականի մայիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Current Opinion in Cardiology

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Human-induced pluripotent stem cell models of inherited cardiomyopathies

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Ioannis Karakikes

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Vittavat Termglinchan

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P2860

Clinical and genetic determinants of torsade de pointes risk

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

Embryonic stem cell lines derived from human blastocysts

Mechanisms of disease: molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy

Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells

A mouse model of familial hypertrophic cardiomyopathy

Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish

Patient-specific induced pluripotent stem cells as a model for familial dilated cardiomyopathy.

Screening drug-induced arrhythmia [corrected] using human induced pluripotent stem cell-derived cardiomyocytes and low-impedance microelectrode arrays.

Small molecule-mediated directed differentiation of human embryonic stem cells toward ventricular cardiomyocytes.

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Human Induced Pluripotent Stem Cells

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