The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy. - Wikidata - awgldk - TriplyDB

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

http://www.wikidata.org/entity/Q34327150

about

Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation A novel custom resequencing array for dilated cardiomyopathy Importance of genetic evaluation and testing in pediatric cardiomyopathy Familial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivity Linking Genes to Cardiovascular Diseases: Gene Action and Gene-Environment Interactions.Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm.Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada.Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionals Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy E101K and M123V alpha-cardiac actin gene mutations are not associated with cardiomyopathy in Iranian population.Almanac 2011: cardiomyopathies. The national society journals present selected research that has driven recent advances in clinical cardiology.Poor prognosis of rare sarcomeric gene variants in patients with dilated cardiomyopathy The genetics of dilated cardiomyopathy.How do mutations in contractile proteins cause the primary familial cardiomyopathies?Genetic evaluation of dilated cardiomyopathy.Familial dilated cardiomyopathy. Clinical and genetic characteristics.Clinical utility gene card for: dilated cardiomyopathy (CMD).Haplotype sharing test maps genes for familial cardiomyopathies.A low prevalence of sarcomeric gene variants in a Chinese cohort with left ventricular non-compaction.Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy.Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience

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The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

http://www.wikidata.org/entity/Q34327150

description

2009 nî lūn-bûn

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2009 թուականի Մարտին հրատարակուած գիտական յօդուած

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2009 թվականի մարտին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

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name

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

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The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

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The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@nl

type

label

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

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The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@en

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@nl

prefLabel

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@ast

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@en

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@nl

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European Journal of Human Genetics

P1476

The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.

@en

P2093

Daniel Vega Møller

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Johanna Moolman-Smook

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Mads Kristian Ersbøll

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Michael Christiansen

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P2860

Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden

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10.1038/EJHG.2009.34

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Paal S Andersen

Paula Louise Hedley

Henning Bundgaard

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