Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy. (Q27314792)

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English	Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy.	scientific article

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31 March 2020

Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic Cardiomyopathy (English)

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31 March 2020

hypertrophic cardiomyopathy

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1

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31 March 2020

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31 March 2020

Risto-Pekka Pölönen

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31 March 2020

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Chandra Prajapati

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31 March 2020

Kristiina Rajala

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31 March 2020

Mari Pekkanen-Mattila

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31 March 2020

Jyrki Rasku

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31 March 2020

Kim Larsson

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31 March 2020

Katriina Aalto-Setälä

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28 December 2015

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31 March 2020

Stem Cells International

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31 March 2020

2016

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31 March 2020

1684792

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31 March 2020

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Creative Commons Attribution 4.0 International

1 January 2016

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April 2022 Public Data File from Crossref

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Europe PubMed Central

11 June 2022

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Animal and in silico models for the study of sarcomeric cardiomyopathies

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21 March 2017

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

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Endothelin-1 induces myofibrillar disarray and contractile vector variability in hypertrophic cardiomyopathy-induced pluripotent stem cell-derived cardiomyocytes

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Perturbed length-dependent activation in human hypertrophic cardiomyopathy with missense sarcomeric gene mutations

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

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21 March 2017

Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic function

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21 March 2017

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

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21 March 2017

Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction

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21 March 2017

Genetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypes

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21 March 2017

Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations

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Sarcomere mutation-specific expression patterns in human hypertrophic cardiomyopathy

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Hypertrophic cardiomyopathy: present and future, with translation into contemporary cardiovascular medicine

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Serum supplemented culture medium masks hypertrophic phenotypes in human pluripotent stem cell derived cardiomyocytes

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Video image-based analysis of single human induced pluripotent stem cell derived cardiomyocyte beating dynamics using digital image correlation.

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Drug screening using a library of human induced pluripotent stem cell-derived cardiomyocytes reveals disease-specific patterns of cardiotoxicity

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

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Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population

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Distinct electrophysiological and mechanical beating phenotypes of long QT syndrome type 1-specific cardiomyocytes carrying different mutations.

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Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

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A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

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Identifiers

10.1155/2016/1684792

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Europe PubMed Central

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31 March 2020

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PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

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31 March 2020

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31 March 2020

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