(Q34974147)

5 August 2017

title

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

1 reference

5 August 2017

main subject

dilated cardiomyopathy

1 reference

Idiopathic dilated cardiomyopathy

inferred from title

1 reference

Luisa Mestroni

14

0 references

author name string

Arthur M Feldman

1

1 reference

5 August 2017

Rene L Begay

2

1 reference

5 August 2017

Tijana Knezevic

3

1 reference

5 August 2017

Valerie D Myers

4

1 reference

5 August 2017

Dobromir B Slavov

5

1 reference

5 August 2017

Weizhong Zhu

6

1 reference

5 August 2017

Katherine Gowan

7

1 reference

5 August 2017

Sharon L Graw

8

1 reference

5 August 2017

Kenneth L Jones

9

1 reference

5 August 2017

Douglas G Tilley

10

1 reference

5 August 2017

Ryan C Coleman

11

1 reference

5 August 2017

Paul Walinsky

12

1 reference

5 August 2017

Joseph Y Cheung

13

1 reference

5 August 2017

Kamel Khalili

15

1 reference

5 August 2017

Mathew R G Taylor

16

1 reference

5 August 2017

publication date

1 November 2014

1 reference

Journal of Cellular Physiology

5 August 2017

published in

1 reference

5 August 2017

volume

229

1 reference

5 August 2017

issue

11

1 reference

5 August 2017

page(s)

1697-1702

1 reference

Genetic evaluation of dilated cardiomyopathy

5 August 2017

cites work

1 reference

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8 July 2018

1 reference

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BAG3: a multifaceted protein that regulates major cell pathways

8 July 2018

1 reference

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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8 July 2018

Myofibrillar myopathies

1 reference

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

8 July 2018

1 reference

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8 July 2018

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Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation

8 July 2018

1 reference

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8 July 2018

1 reference

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Genetic evaluation of familial cardiomyopathy

8 July 2018

1 reference

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Manipulation of death pathways in desmin-related cardiomyopathy

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4296028

8 July 2018

Dilated cardiomyopathy

1 reference

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Fast and SNP-tolerant detection of complex variants and splicing in short reads

8 July 2018

1 reference

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Caught in the middle: the role of Bag3 in disease

8 July 2018

1 reference

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Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

8 July 2018

1 reference

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Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline

8 July 2018

1 reference

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Mutation in BAG3 causes severe dominant childhood muscular dystrophy

8 July 2018

1 reference

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Molecular pathology of myofibrillar myopathies.

8 July 2018

1 reference

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BAG3 deficiency results in fulminant myopathy and early lethality

8 July 2018

1 reference

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Sarcomeric protein mutations in dilated cardiomyopathy

8 July 2018

1 reference

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From A to Z and back? Multicompartment proteins in the sarcomere.

8 July 2018

1 reference

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

8 July 2018

1 reference

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Guidelines for the study of familial dilated cardiomyopathies. Collaborative Research Group of the European Human and Capital Mobility Project on Familial Dilated Cardiomyopathy.

8 July 2018

1 reference

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Reduced beta 1 receptor messenger RNA abundance in the failing human heart

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4296028

Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes

8 July 2018

1 reference

Converging pathways and principles in heart development and disease: CV@CSH.

21 January 2018

1 reference

Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy

21 January 2018

1 reference

Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up

21 January 2018

1 reference

21 January 2018

1 reference

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

21 January 2018

1 reference

Autophagy is altered in skeletal and cardiac muscle of spontaneously hypertensive rats.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4296028

A Novel Locus for Dilated Cardiomyopathy, Diffuse Myocardial Fibrosis, and Sudden Death on Chromosome 10q25-26

26 October 2018

1 reference

Autophagy in desmin-related cardiomyopathy: thoughts at the halfway point

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24623017

12 December 2020

inferred from PubMed ID database lookup

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24623017

12 December 2020

inferred from PubMed ID database lookup

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24623017

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/JCP.24615

1 reference

5 August 2017

1 reference

5 August 2017

1 reference