Genome-environment interactions in the molecular pathogenesis of dilated cardiomyopathy (Q36148725)

12 August 2017

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title

Genome-environment interactions in the molecular pathogenesis of dilated cardiomyopathy (English)

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12 August 2017

Poller W

1

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12 August 2017

Kühl U

2

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12 August 2017

Tschoepe C

3

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12 August 2017

Pauschinger M

4

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12 August 2017

Fechner H

5

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12 August 2017

Schultheiss HP

6

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12 August 2017

2 June 2005

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Journal of Molecular Medicine

12 August 2017

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12 August 2017

83

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12 August 2017

8

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12 August 2017

579-586

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https://scigraph.springernature.com/pub.10.1007/s00109-005-0664-2

12 August 2017

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cites work

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Persistent expression of cytokine in the chronic stage of viral myocarditis in mice

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Disruption of cardiac Ena-VASP protein localization in intercalated disks causes dilated cardiomyopathy.

21 January 2018

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Heterozygous inactivation of the vinculin gene predisposes to stress-induced cardiomyopathy

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Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin

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Desmin mutation responsible for idiopathic dilated cardiomyopathy

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Risk of cirrhosis and primary liver cancer in alpha 1-antitrypsin deficiency

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12 December 2020

Pancreatic expression of interferon-gamma protects mice from lethal coxsackievirus B3 infection and subsequent myocarditis

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First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy

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Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

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Prevalence of the parvovirus B19 genome in endomyocardial biopsy specimens

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Cardiomyopathies: from genetics to the prospect of treatment

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

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Missense mutations in desmin associated with familial cardiac and skeletal myopathy

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12 December 2020

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

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12 December 2020

Enhanced ERK-1/2 activation in mice susceptible to coxsackievirus-induced myocarditis

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12 December 2020

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

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12 December 2020

Protective role for interferon-beta in coxsackievirus B3 infection

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12 December 2020

A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency

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12 December 2020

Dilated cardiomyopathy caused by aberrant endoplasmic reticulum quality control in mutant KDEL receptor transgenic mice

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12 December 2020

Highly variable clinical course in severe alpha 1-antitrypsin deficiency--use of polymerase chain reaction for the detection of rare deficiency alleles

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12 December 2020

Mutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy

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12 December 2020

Detection of Coxsackie-B-virus-specific RNA sequences in myocardial biopsy samples from patients with myocarditis and dilated cardiomyopathy

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12 December 2020

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

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12 December 2020

Human coxsackie-adenovirus receptor is colocalized with integrins alpha(v)beta(3) and alpha(v)beta(5) on the cardiomyocyte sarcolemma and upregulated in dilated cardiomyopathy: implications for cardiotropic viral infections

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Active myocarditis in the spectrum of acute dilated cardiomyopathies. Clinical features, histologic correlates, and clinical outcome

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High prevalence of viral genomes and multiple viral infections in the myocardium of adults with "idiopathic" left ventricular dysfunction.

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Molecular Aspects of Myocarditis

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

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PULMONARY EMPHYSEMA AND ALPHA1-ANTITRYPSIN DEFICIENCY.

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Prognostic impact of matrix metalloproteinase gene polymorphisms in patients with heart failure according to the aetiology of left ventricular systolic dysfunction

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Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

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12 December 2020

Therapeutics targeting the innate immune system

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12 December 2020

Immunohistologic evidence of myocardial disease in apparently healthy relatives of patients with dilated cardiomyopathy

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12 December 2020

Immunosuppressive therapy for active lymphocytic myocarditis: virological and immunologic profile of responders versus nonresponders

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12 December 2020

Interferon-beta treatment eliminates cardiotropic viruses and improves left ventricular function in patients with myocardial persistence of viral genomes and left ventricular dysfunction

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The tyrosine kinase p56lck is essential in coxsackievirus B3-mediated heart disease

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Parvovirus B19 infection mimicking acute myocardial infarction.

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12 December 2020

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12 December 2020

Association of beta-adrenergic receptor polymorphisms and progression to heart failure in patients with idiopathic dilated cardiomyopathy.

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12 December 2020

Fatal parvovirus myocarditis in a 5-year-old girl

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12 December 2020

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

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12 December 2020

Molecular and cellular aspects of troponin cardiomyopathies

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12 December 2020

A novel mutation, Ser143Pro, in the lamin A/C gene is common in finnish patients with familial dilated cardiomyopathy

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12 December 2020

High prevalence of cardiac parvovirus B19 infection in patients with isolated left ventricular diastolic dysfunction.

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12 December 2020

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12 December 2020

CD46 is a cellular receptor for group B adenoviruses

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12 December 2020

Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-up.

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12 December 2020

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy.

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12 December 2020

The role of enterovirus replication in the development of acute and chronic heart muscle disease in different immunocompetent mouse strains

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12 December 2020

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12 December 2020

Titin mutations as the molecular basis for dilated cardiomyopathy

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12 December 2020

Molecular pathogenesis of liver disease in alpha1-antitrypsin deficiency

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12 December 2020

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

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12 December 2020

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

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12 December 2020

Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human

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12 December 2020

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

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12 December 2020

10.1007/S00109-005-0664-2

Identifiers

DOI

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12 August 2017

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