(Q41713568)

7 October 2017

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title

The role of cytoskeletal proteins in cardiomyopathies (English)

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7 October 2017

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Towbin JA

1

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7 October 2017

publication date

1 February 1998

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Current Opinion in Cell Biology

7 October 2017

published in

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7 October 2017

volume

10

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7 October 2017

issue

1

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7 October 2017

page(s)

131-139

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Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

7 October 2017

cites work

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7 January 2021

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (2).

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7 January 2021

Hypertrophic cardiomyopathy

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7 January 2021

Molecular genetic aspects of cardiomyopathy

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7 January 2021

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

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7 January 2021

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

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7 January 2021

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3

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7 January 2021

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

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7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

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7 January 2021

A mouse model of familial hypertrophic cardiomyopathy

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7 January 2021

Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

1 reference

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7 January 2021

Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy

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7 January 2021

The troponin complex and regulation of muscle contraction

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7 January 2021

Impairment of muscle function caused by mutations of phosphorylation sites in myosin regulatory light chain.

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7 January 2021

Familial dilated cardiomyopathy in the United Kingdom

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7 January 2021

Identification of the Syrian hamster cardiomyopathy gene.

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7 January 2021

Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

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7 January 2021

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

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7 January 2021

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

1 reference

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7 January 2021

Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle

1 reference

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7 January 2021

The structural and functional diversity of dystrophin

1 reference

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7 January 2021

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

1 reference

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7 January 2021

1 reference

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7 January 2021

Dystrophin and its isoforms

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Dystrophin protects the sarcolemma from stresses developed during muscle contraction

1 reference

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7 January 2021

Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions

1 reference

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7 January 2021

Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse

1 reference

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7 January 2021

Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy

1 reference

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7 January 2021

A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart

1 reference

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7 January 2021

Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy

1 reference

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7 January 2021

A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Duchenne muscular dystrophy and dystrophin: sequence homology observations

1 reference

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7 January 2021

Nitric oxide synthase complexed with dystrophin and absent from skeletal muscle sarcolemma in Duchenne muscular dystrophy

1 reference

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7 January 2021

Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarcolemma and co-fractionates with dystrophin and dystrophin-associated glycoproteins

1 reference

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7 January 2021

Association of dystrophin and an integral membrane glycoprotein.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Membrane organization of the dystrophin-glycoprotein complex

1 reference

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7 January 2021

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

1 reference

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7 January 2021

HyperCKemic, proximal muscular dystrophies and the dystrophin membrane cytoskeleton, including dystrophinopathies, sarcoglycanopathies, and merosinopathies.

1 reference

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7 January 2021

Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophy.

1 reference

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7 January 2021

Mutations in the sarcoglycan genes in patients with myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Mechanotransduction across the cell surface and through the cytoskeleton

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

An additional exon in the human vinculin gene specifically encodes meta-vinculin-specific difference peptide. Cross-species comparison reveals variable and conserved motifs in the meta-vinculin insert

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Immunolocalization of meta-vinculin in human smooth and cardiac muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

Molecular genetics of long QT syndrome from genes to patients

1 reference

https://api.crossref.org/works/10.1016%2FS0955-0674%2898%2980096-3

7 January 2021

10.1016/S0955-0674(98)80096-3

Identifiers

DOI

1 reference

7 October 2017

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