Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q24288778

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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation 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 Genetics of sudden cardiac death syndromes Small heat shock proteins are necessary for heart migration and laterality determination in zebrafish.Multiple Loci are associated with dilated cardiomyopathy in Irish wolfhounds Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci Small heat shock proteins Hspb7 and Hspb12 regulate early steps of cardiac morphogenesis.Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.Downregulation of the tumor suppressor HSPB7, involved in the p53 pathway, in renal cell carcinoma by hypermethylation.Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population.A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers.The genomic architecture of sporadic heart failure Functional genomics applied to cardiovascular medicine.Common variant rs7597774 in ADD2 is associated with dilated cardiomyopathy in Chinese Han population The sarcomeric Z-disc and Z-discopathies.Common Variants for Heart Failure.Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease Non-iterative, regression-based estimation of haplotype associations with censored survival outcomes.Diabetes Susceptibility Genes Pdx1 and Clec16a Function in a Pathway Regulating Mitophagy in β-Cells.Small heat shock proteins in redox metabolism: implications for cardiovascular diseases.TNNT2 Gene Polymorphisms are Associated with Susceptibility to Idiopathic Dilated Cardiomyopathy in Kazak and Han Chinese Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals.Reductive stress linked to small HSPs, G6PD, and Nrf2 pathways in heart disease Variants of resistin gene and the risk of idiopathic dilated cardiomyopathy in Pakistan.HSPB7 interacts with dimerized FLNC and its absence results in progressive myopathy in skeletal muscles.Clinical and Genetic Determinants of Cardiomyopathy Risk among Hematopoietic Cell Transplantation Survivors Microarray analysis of port wine stains before and after pulsed dye laser treatment Genetics and genomics of dilated cardiomyopathy and systolic heart failure.Clinical considerations of heritable factors in common heart failure Genetic polymorphisms associated with heart failure: A literature review.Small heat shock proteins in ageing and age-related diseases.HSPB7 prevents cardiac conduction system defect through maintaining intercalated disc integrity.TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review.A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.Investigating DNA-, RNA-, and protein-based features as a means to discriminate pathogenic synonymous variants.

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

http://www.wikidata.org/entity/Q24288778

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2010 nî lūn-bûn

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2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Genetic association study iden ...... opathic dilated cardiomyopathy

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JOURNAL.PGEN.1001167

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Genetic association study iden ...... opathic dilated cardiomyopathy

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Anette Richter

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Arne Schillert

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Bernhard Maisch

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François Cambien

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P2860

Why most published research findings are false

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

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

HSPB7 is a SC35 speckle resident small heat shock protein

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

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

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

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e1001167

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scholarly article

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10.1371/JOURNAL.PGEN.1001167

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6

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Heinz Erich Wichmann

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Vera Regitz-Zagrosek

Christian Hengstenberg

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2010-10-01T00:00:00Z

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20975947

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