Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy - Wikidata - awgldk - TriplyDB

Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy

Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy

http://www.wikidata.org/entity/Q34974147

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BAG3: a new player in the heart failure paradigm Genetic determinants of myocardial dysfunction.GENETIC CAUSES OF DILATED CARDIOMYOPATHY.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 Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene.A novel miR-371a-5p-mediated pathway, leading to BAG3 upregulation in cardiomyocytes in response to epinephrine, is lost in Takotsubo cardiomyopathy BAG3 regulates contractility and Ca(2+) homeostasis in adult mouse ventricular myocytes Cardiac Dysfunction in HIV-1 Transgenic Mouse: Role of Stress and BAG3 Bcl-2-associated athanogene 3 protects the heart from ischemia/reperfusion injury Adeno-associated Virus Serotype 9 - Driven Expression of BAG3 Improves Left Ventricular Function in Murine Hearts with Left Ventricular Dysfunction Secondary to a Myocardial Infarction.The Role of the Multifunctional BAG3 Protein in Cellular Protein Quality Control and in Disease.A BAG3 chaperone complex maintains cardiomyocyte function during proteotoxic stress.Loss-of-function mutations in co-chaperone BAG3 destabilize small HSPs and cause cardiomyopathy.BAG3 plays a central role in proteostasis in the heart.Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy.Haplo-insufficiency of Bcl2-associated Athanogene 3 in Mice Results in Progressive Left Ventricular Dysfunction, β-Adrenergic Insensitivity and Increased Apoptosis.Hearing loss, coloboma and left ventricular enlargement in a boy with an interstitial 10q26 deletion.The role of heat shock proteins and co-chaperones in heart failure.The Multifunctional Protein BAG3: A Novel Therapeutic Target in Cardiovascular Disease.Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency

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Decreased levels of BAG3 in a family with a rare variant and in idiopathic dilated cardiomyopathy

http://www.wikidata.org/entity/Q34974147

description

2014 nî lūn-bûn

@nan

2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

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Journal of Cellular Physiology

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Decreased levels of BAG3 in a ...... opathic dilated cardiomyopathy

@en

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Arthur M Feldman

http://www.w3.org/2001/XMLSchema#string

Dobromir B Slavov

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Douglas G Tilley

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Joseph Y Cheung

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Kamel Khalili

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Katherine Gowan

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Kenneth L Jones

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Mathew R G Taylor

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Paul Walinsky

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Rene L Begay

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P2860

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

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

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

BAG3 and Hsc70 interact with actin capping protein CapZ to maintain myofibrillar integrity under mechanical stress

Myofibrillar myopathies

Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients

BAG3 deficiency results in fulminant myopathy and early lethality

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Dilated cardiomyopathy.

P304

1697-1702

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scholarly article

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10.1002/JCP.24615

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11

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229

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2014-11-01T00:00:00Z

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24623017

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4296028

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