Dystrophin deficiency markedly increases enterovirus-induced cardiomyopathy: a genetic predisposition to viral heart disease (Q34138862)

31 July 2017

Dystrophin deficiency markedly increases enterovirus-induced cardiomyopathy: a genetic predisposition to viral heart disease (English)

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31 July 2017

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Dingding Xiong

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31 July 2017

Gil-Hwan Lee

2

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31 July 2017

Cornel Badorff

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31 July 2017

Andrea Dorner

4

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31 July 2017

Sang Lee

5

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31 July 2017

Paul Wolf

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31 July 2017

Kirk U Knowlton

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31 July 2017

language of work or name

English

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publication date

15 July 2002

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31 July 2017

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31 July 2017

8

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31 July 2017

8

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31 July 2017

872-877

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https://scigraph.springernature.com/pub.10.1038/nm737

31 July 2017

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cites work

The Genetic Basis for Cardiomyopathy

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Viral infection and the pathogenesis of dilated cardiomyopathy

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

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The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy

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

21 January 2018

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

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

21 January 2018

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Enteroviral protease 2A directly cleaves dystrophin and is inhibited by a dystrophin-based substrate analogue

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Dissociation of sarcoglycans and the dystrophin carboxyl terminus from the sarcolemma in enteroviral cardiomyopathy

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Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

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Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex

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Recombinant truncated dystrophin minigenes: construction, expression, and adenoviral delivery

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Expression of recombinant dystrophin and its localization to the cell membrane

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Dystrophin protects the sarcolemma from stresses developed during muscle contraction

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

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Forced expression of dystrophin deletion constructs reveals structure-function correlations.

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Viral interactions with the host-cell cytoskeleton: the role of retroviral proteases

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Human immunodeficiency virus type 1 protease cleaves the intermediate filament proteins vimentin, desmin, and glial fibrillary acidic protein

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

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

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7 January 2021

Etiologies of cardiomyopathy and heart failure

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7 January 2021

Serial left ventricular wall measurements in Duchenne's muscular dystrophy

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7 January 2021

Echocardiography in duchenne muscular dystrophy

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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

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7 January 2021

2A proteinase of human rhinovirus cleaves cytokeratin 8 in infected HeLa cells

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7 January 2021

The role of CD8+ T lymphocytes in coxsackievirus B3-induced myocarditis

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7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/NM737

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