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Article

Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in mice

2 Dec 2014

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25463264
DOI: 10.1038/ncomms6515

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mybpc3 gene therapy for neonatal cardiomyopathy enables long-term disease prevention in micePMID 25463264Read ↗

The impact of non-cardiomyocyte <i>MYBPC3</i> expression on the development of hypertrophic cardiomyopathySemantic proximity Read ↗

Targeting the population for gene therapy with MYBPC3.Semantic proximity Read ↗

MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correctionSemantic proximity Read ↗

Abnormal ventricular wall patterning precedes and drives MYBPC3 hypertrophic cardiomyopathySemantic proximity Read ↗

Transcriptome Analysis of Cardiac Hypertrophic Growth in MYBPC3-Null Mice Suggests Early Responders in Hypertrophic RemodelingSemantic proximity Read ↗

MYBPC3 deficiency in cardiac fibroblasts drives their activation and contributes to fibrosisSemantic proximity Read ↗

MYBPC3 deficiency in cardiac fibroblasts drives their activation and contributes to fibrosis.Semantic proximity Read ↗

Homology-Directed Repair of an MYBPC3 gene mutation in a rat model of hypertrophic cardiomyopathySemantic proximity Read ↗

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.Semantic proximity Read ↗

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.Semantic proximity Read ↗

An integration-free iPSC line ZZUNEUi028-A derived from a patient with hypertrophic cardiomyopathy carrying a heterozygous mutation (c. 1504 C > T) in MYBPC3 gene.Semantic proximity Read ↗

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