(Q28253008)

1

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Saskia Schlossarek

6

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Birgit Geertz

3

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Ingke Braren

11

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Elisabeth Krämer

5

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Hugo A. Katus

12

object named as

Hugo A Katus

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author name string

Doreen Stimpel

2

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Florian Weinberger

4

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Julia Mourot-Filiatre

7

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Andrea Stoehr

8

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Alexander Dutsch

9

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Paul J M Wijnker

10

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Oliver J Müller

13

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Thomas Voit

14

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Thomas Eschenhagen

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

15

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language of work or name

English

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publication date

2 December 2014

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published in

Nature Communications

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volume

5

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page(s)

5515

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

MYBPC3 in hypertrophic cardiomyopathy: from mutation identification to RNA-based correction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Cardiac myosin-binding protein C in hypertrophic cardiomyopathy: mechanisms and therapeutic opportunities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

How do MYBPC3 mutations cause hypertrophic cardiomyopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Nonsense-mediated mRNA decay and ubiquitin-proteasome system regulate cardiac myosin-binding protein C mutant levels in cardiomyopathic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Defective proteolytic systems in Mybpc3-targeted mice with cardiac hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Ubiquitin-proteasome system and hereditary cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Adrenergic stress reveals septal hypertrophy and proteasome impairment in heterozygous Mybpc3-targeted knock-in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Sudden deaths in young competitive athletes: analysis of 1866 deaths in the United States, 1980-2006.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

A case of compound mutations in the MYBPC3 gene associated with biventricular hypertrophy and neonatal death.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Rescue of cardiomyopathy through U7snRNA-mediated exon skipping in Mybpc3-targeted knock-in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Repair of Mybpc3 mRNA by 5'-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Contractile abnormalities and altered drug response in engineered heart tissue from Mybpc3-targeted knock-in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Percutaneous cardiac recirculation-mediated gene transfer of an inhibitory phospholamban peptide reverses advanced heart failure in large animals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Cardiac AAV9-S100A1 gene therapy rescues post-ischemic heart failure in a preclinical large animal model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Calcium Upregulation by Percutaneous Administration of Gene Therapy in Cardiac Disease (CUPID): a phase 2 trial of intracoronary gene therapy of sarcoplasmic reticulum Ca2+-ATPase in patients with advanced heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Pharmacological treatment options for hypertrophic cardiomyopathy: high time for evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Mechanisms of disease: hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Allele-specific silencing of mutant Myh6 transcripts in mice suppresses hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Cardiac myosin binding protein-C: a novel sarcomeric target for gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Effect of genome size on AAV vector packaging

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Adeno-associated virus (AAV) serotype 9 provides global cardiac gene transfer superior to AAV1, AAV6, AAV7, and AAV8 in the mouse and rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Robust cardiomyocyte-specific gene expression following systemic injection of AAV: in vivo gene delivery follows a Poisson distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Rapid and highly efficient inducible cardiac gene knockout in adult mice using AAV-mediated expression of Cre recombinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Hypertrophic cardiomyopathy in cardiac myosin binding protein-C knockout mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Asymmetric septal hypertrophy in heterozygous cMyBP-C null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Adeno-associated virus antibody profiles in newborns, children, and adolescents

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Impact of ANKRD1 mutations associated with hypertrophic cardiomyopathy on contraction parameters of engineered heart tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

Hypertrophic cardiomyopathy: prognostic factors and survival analysis in 128 Egyptian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

7 January 2021

Homozygosity for a novel splice site mutation in the cardiac myosin-binding protein C gene causes severe neonatal hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

7 January 2021

Next-generation sequencing (NGS) as a fast molecular diagnosis tool for left ventricular noncompaction in an infant with compound mutations in the MYBPC3 gene

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

7 January 2021

Transgenic over-expression of a motor protein at high levels results in severe cardiac pathology

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

7 January 2021

Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS6515

7 January 2021

Identifiers

DOI

10.1038/NCOMMS6515

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

ADS bibcode

2014NatCo...5.5515M

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1016814386

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

25463264

1 reference

Consolidated OpenCitations Corpus – April 2017