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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

http://www.wikidata.org/entity/Q34930971

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Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes Afford New Opportunities in Inherited Cardiovascular Disease Modeling Importance of genetic evaluation and testing in pediatric cardiomyopathy Genetics and disease of ventricular muscle.Cardiac disease and arrhythmogenesis: Mechanistic insights from mouse models Heart failure: advanced development in genetics and epigenetics The genetics of dilated cardiomyopathy: a prioritized candidate gene study of LMNA, TNNT2, TCAP, and PLN Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation Genetic determinants of myocardial dysfunction.Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells Inpatient detection of cardiac-inherited disease: the impact of improving family history taking Next-generation sequencing: from understanding biology to personalized medicine.Familial dilated cardiomyopathy diagnosis is commonly overlooked at the time of transplant listing.RAF1 mutations in childhood-onset dilated cardiomyopathy Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation.Cardiac troponin T (TNNT2) mutations in chinese dilated cardiomyopathy patients Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing.DCM-related tropomyosin mutants E40K/E54K over-inhibit the actomyosin interaction and lead to a decrease in the number of cycling cross-bridges.Familial dilated cardiomyopathy: Current challenges and future directions Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report Genetics and heart failure: a concise guide for the clinician Assessment of LMNA copy number variation in 58 probands with dilated cardiomyopathy A novel human R25C-phospholamban mutation is associated with super-inhibition of calcium cycling and ventricular arrhythmia Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy.A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.The mutations associated with dilated cardiomyopathy New Genetic Insights into Congenital Heart Disease.Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy Cell-cell junction remodeling in the heart: possible role in cardiac conduction system function and arrhythmias?An uncommon clinical presentation of relapsing dilated cardiomyopathy with identification of sequence variations in MYNPC3, KCNH2 and mitochondrial tRNA cysteine Genetic testing for dilated cardiomyopathy in clinical practice.Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy.Contemporary strategies in the diagnosis and management of heart failure Periodontitis in Chronic Heart Failure Diagnosis, prevalence, and screening of familial dilated cardiomyopathy.Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy Genetics and epigenetics of arrhythmia and heart failure.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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J.JACC.2011.01.015

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Journal of the American College of Cardiology

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Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.

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Jill D Siegfried

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Ray E Hershberger

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P2860

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

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

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

Tcap gene mutations in hypertrophic cardiomyopathy and 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 ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

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

Exome sequencing identifies the cause of a mendelian disorder

Targeted capture and massively parallel sequencing of 12 human exomes

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