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

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

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

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Genetics of Human and Canine Dilated Cardiomyopathy Keep your heart in shape: molecular chaperone networks for treating heart disease Genome-wide association studies of late-onset cardiovascular disease BAG3: a new player in the heart failure paradigm The genetics of dilated cardiomyopathy: a prioritized candidate gene study of LMNA, TNNT2, TCAP, and PLN An exploration of heat tolerance in mice utilizing mRNA and microRNA expression analysis Prioritizing causal disease genes using unbiased genomic features Genetic determinants of myocardial dysfunction.A BAG3 Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy.The Hybrid Mouse Diversity Panel: a resource for systems genetics analyses of metabolic and cardiovascular traits.Alterations in cardiac DNA methylation in human dilated cardiomyopathy Small heat shock proteins Hspb7 and Hspb12 regulate early steps of cardiac morphogenesis.Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish Downregulation of the tumor suppressor HSPB7, involved in the p53 pathway, in renal cell carcinoma by hypermethylation.Genetic polymorphism G894T and the prognosis of heart failure outpatients The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation.Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population.Epigenomes: the missing heritability in human cardiovascular disease?Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy Mapping genetic contributions to cardiac pathology induced by Beta-adrenergic stimulation in mice Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population Genetic variants are not associated with outcome in patients with coronary artery disease and left ventricular dysfunction: results of the Genetic Substudy of the Surgical Treatment for Ischemic Heart Failure (STICH) trials The sarcomeric Z-disc and Z-discopathies.Genetics of common forms of heart failure: challenges and potential solutions.Common Variants for Heart Failure.Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease Genetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model.Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.RNAseq analysis of heart tissue from mice treated with atenolol and isoproterenol reveals a reciprocal transcriptional response.Small heat shock proteins in redox metabolism: implications for cardiovascular diseases.A novel miR-371a-5p-mediated pathway, leading to BAG3 upregulation in cardiomyocytes in response to epinephrine, is lost in Takotsubo cardiomyopathy TNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han Chinese Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction Genetic mutations and mechanisms in dilated cardiomyopathy Almanac 2011: cardiomyopathies. The national society journals present selected research that has driven recent advances in clinical cardiology.Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.BAG3 regulates contractility and Ca(2+) homeostasis in adult mouse ventricular myocytes Clinical and Genetic Determinants of Cardiomyopathy Risk among Hematopoietic Cell Transplantation Survivors

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

http://www.wikidata.org/entity/Q24601469

description

2011 nî lūn-bûn

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2011 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2011 թվականի մայիսին 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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name

A genome-wide association stud ...... due to dilated cardiomyopathy

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A genome-wide association stud ...... due to dilated cardiomyopathy

@en

A genome-wide association stud ...... due to dilated cardiomyopathy

@nl

type

label

A genome-wide association stud ...... due to dilated cardiomyopathy

@ast

A genome-wide association stud ...... due to dilated cardiomyopathy

@en

A genome-wide association stud ...... due to dilated cardiomyopathy

@nl

prefLabel

A genome-wide association stud ...... due to dilated cardiomyopathy

@ast

A genome-wide association stud ...... due to dilated cardiomyopathy

@en

A genome-wide association stud ...... due to dilated cardiomyopathy

@nl

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European Heart Journal

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Angharad M Roberts

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Bernhard Maisch

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Carole Proust

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P2860

Identification and characterization of cvHsp. A novel human small stress protein selectively expressed in cardiovascular and insulin-sensitive tissues

Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy

Protein quality control during aging involves recruitment of the macroautophagy pathway by BAG3

Mutations in the ANKRD1 gene encoding CARP are responsible for human dilated cardiomyopathy

The human genome encodes 10 alpha-crystallin-related small heat shock proteins: HspB1-10

Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation

Genome-wide association study of intracranial aneurysm identifies three new risk loci

WGAViewer: software for genomic annotation of whole genome association studies

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10.1093/EURHEARTJ/EHR105

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9

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32

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Vera Regitz-Zagrosek

Christian Hengstenberg

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Eloisa Arbustini

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2011-05-01T00:00:00Z

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genome-wide association study

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3086901

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