Genetic cardiomyopathies. Lessons learned from humans, mice, and zebrafish (Q38024282)

27 August 2017

Genetic cardiomyopathies. Lessons learned from humans, mice, and zebrafish (English)

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27 August 2017

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H A Katus

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27 August 2017

W Kloos

1

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PubMed ID

22767018

27 August 2017

B Meder

series ordinal

3

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27 August 2017

1 September 2012

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27 August 2017

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27 August 2017

37

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27 August 2017

6

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27 August 2017

612-617

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27 August 2017

Dilated cardiomyopathy

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Lamin A/C deficiency as a cause of familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Heritable cardiac conduction and myocardial disease: from the clinic to the basic science laboratory and back to the clinic.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Structures of the lamin A/C R335W and E347K mutants: implications for dilated cardiolaminopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Identification of novel mutations in RBM20 in patients with dilated cardiomyopathy.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Truncations of titin causing dilated cardiomyopathy.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Genetics: broken giant linked to heart failure.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

BAG3 directly interacts with mutated alphaB-crystallin to suppress its aggregation and toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Animal models of cardiovascular diseases

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Fishing for the genetic basis of cardiovascular disease.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

In-vivo characterization of human dilated cardiomyopathy genes in zebrafish

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Integrin-linked kinase, a novel component of the cardiac mechanical stretch sensor, controls contractility in the zebrafish heart

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

The myosin-interacting protein SMYD1 is essential for sarcomere organization

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

A single serine in the carboxyl terminus of cardiac essential myosin light chain-1 controls cardiomyocyte contractility in vivo

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Lessons from morpholino-based screening in zebrafish

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

p53 activation by knockdown technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Nexilin mutations destabilize cardiac Z-disks and lead to dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Next generation sequencing for clinical diagnostics and personalised medicine: implications for the next generation cardiologist

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Next steps in cardiovascular disease genomic research--sequencing, epigenetics, and transcriptomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Mitochondrial DNA variant discovery and evaluation in human Cardiomyopathies through next-generation sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

21 January 2018

The epigenotype. 1942.

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

On the epigenetics of vascular regulation and disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Origins and Mechanisms of miRNAs and siRNAs

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Loss of cardiac microRNA-mediated regulation leads to dilated cardiomyopathy and heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

A cellular microRNA, let-7i, is a novel biomarker for clinical outcome in patients with dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

MiR423-5p as a circulating biomarker for heart failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Quantitative comparison of genome-wide DNA methylation mapping technologies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Distinct epigenomic features in end-stage failing human hearts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Chromatin remodeling in cardiovascular development and physiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

What causes a broken heart--molecular insights into heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Casein kinase-2α1 induces hypertrophic response by phosphorylation of histone deacetylase 2 S394 and its activation in the heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Control of cardiac growth by histone acetylation/deacetylation

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Homozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00059-012-3651-8

Genetics of dilated cardiomyopathy

21 January 2018

1 reference

12 December 2020

Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin

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12 December 2020

Altered microRNA expression associated with reduced catecholamine sensitivity in patients with chronic heart failure

1 reference

12 December 2020

Genetic diagnosis of familial dilated cardiomyopathy

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12 December 2020

Next-generation sequencing entering the clinical arena

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12 December 2020

10.1007/S00059-012-3651-8

Identifiers

DOI

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27 August 2017

1 reference

PubMed ID

22767018