Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional Deficits

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Isogenic Pairs of hiPSC-CMs with Hypertrophic Cardiomyopathy/LVNC-Associated ACTC1 E99K Mutation Unveil Differential Functional Deficits

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scientific article published on 01 November 2018

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wetenschappelijk artikel

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наукова стаття, опублікована в жовтні 2018

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Isogenic Pairs of hiPSC-CMs wi ...... fferential Functional Deficits

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Arne Hansen

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Chris Denning

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Diogo Mosqueira

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Elizabeth Scott

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Ingra Mannhardt

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Lorenzo Monserrat

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Thomas Eschenhagen

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Thomas Owen

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P2860

Calsequestrin 2 and arrhythmias

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Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

Functional consequences of a mutation in an expressed human alpha-cardiac actin at a site implicated in familial hypertrophic cardiomyopathy

Human actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitro

Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy

Shared genetic causes of cardiac hypertrophy in children and adults

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

Contemporary definitions and classification of the cardiomyopathies: an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and F

Random monoallelic expression: regulating gene expression one allele at a time

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1226-1243

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scholarly article

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10.1016/J.STEMCR.2018.10.006

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English

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Asha Patel

Roberto Barriales-Villa

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2018-11-01T00:00:00Z

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30392975

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6235010

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