(Q36501691)

14 August 2017

1 reference

title

Dilated cardiomyopathy: a tale of cytoskeletal proteins and beyond (English)

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14 August 2017

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dilated cardiomyopathy

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1

Jeffrey A Towbin

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14 August 2017

Neil E Bowles

2

1 reference

14 August 2017

9 June 2006

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Journal of Cardiovascular Electrophysiology

14 August 2017

1 reference

14 August 2017

17

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14 August 2017

8

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14 August 2017

919-926

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Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

14 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Heart transplant and left ventricular assist device costs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The role of cytoskeletal proteins in cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Architecture and function in the muscle sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

To the heart of myofibril assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Desmin cytoskeleton: a potential regulator of muscle mitochondrial behavior and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Intermediate filament structure and assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Specific interaction of the potassium channel beta-subunit minK with the sarcomeric protein T-cap suggests a T-tubule-myofibril linking system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Localization of sodium channels in intercalated disks modulates cardiac conduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Voltage-gated sodium channel (SkM1) content in dystrophin-deficient muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The Incidence of Pediatric Cardiomyopathy in Two Regions of the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The Epidemiology of Childhood Cardiomyopathy in Australia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Idiopathic dilated cardiomyopathy in children: prognostic indicators and outcome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Incidence and epidemiology of heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Muscular dystrophies: genes to pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Cardiomyopathy in dystrophin-deficient hearts is prevented by expression of a neuronal nitric oxide synthase transgene in the myocardium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Neuronal nitric oxide synthase and dystrophin-deficient muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Role of contraction-induced injury in the mechanisms of muscle damage in muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Loss of dystrophin causes aberrant mechanotransduction in skeletal muscle fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The genetic basis for cardiac remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Molecular mechanisms of inherited cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Molecular and cell biology of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Sarcoglycans in vascular smooth and striated muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Smooth muscle cell-extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Identification of the Syrian hamster cardiomyopathy gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Delineation of genomic deletion in cardiomyopathic hamster

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Comparative biochemical analysis suggests that vinculin and metavinculin cooperate in muscular adhesion sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Spectrin, alpha-actinin, and dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

At the crossroads of myocardial signaling: the role of Z-discs in intracellular signaling and cardiac function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Decreased expression of the cardiac LIM domain protein MLP in chronic human heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

The giant protein titin: a major player in myocardial mechanics, signaling, and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Nuclear lamins: their structure, assembly, and interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

A novel X-linked gene, G4.5. is responsible for Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Role for alpha-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Mutations in ZASP define a novel form of muscular dystrophy in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Dystrophin disruption in enterovirus-induced myocarditis and dilated cardiomyopathy: from bench to bedside

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

Molecular normalization of dystrophin in the failing left and right ventricle of patients treated with either pulsatile or continuous flow-type ventricular assist devices.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.2006.00530.X

10.1111/J.1540-8167.2006.00530.X

21 January 2018

Identifiers

DOI

1 reference

14 August 2017

1 reference

PubMed ID

16764708