(Q38024282)

27 August 2017

title

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

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27 August 2017

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2

H A Katus

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27 August 2017

W Kloos

1

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27 August 2017

B Meder

series ordinal

3

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27 August 2017

publication date

1 September 2012

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27 August 2017

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27 August 2017

volume

37

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27 August 2017

issue

6

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27 August 2017

page(s)

612-617

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27 August 2017

cites work

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

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

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

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

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

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

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RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

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

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

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

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The myosin-interacting protein SMYD1 is essential for sarcomere organization

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

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Lessons from morpholino-based screening in zebrafish

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

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

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

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

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

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

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21 January 2018

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What Causes a Broken Heart—Molecular Insights into Heart Failure

21 January 2018

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

21 January 2018

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Control of cardiac growth by histone acetylation/deacetylation

21 January 2018

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

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Genetics of dilated cardiomyopathy

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12 December 2020

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

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

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10.1007/S00059-012-3651-8

Identifiers

DOI

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27 August 2017

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