List of works - Angeliki Asimaki

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

scientific article

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

scientific article

Altered desmosomal proteins in granulomatous myocarditis and potential pathogenic links to arrhythmogenic right ventricular cardiomyopathy.

scientific article

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

scientific article

Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell-cell adhesion

scientific article

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

scientific article

BIN1: A new biomarker to track ARVC? ⬇️

scientific article published on 03 March 2012

Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

scientific article published in February 2016

Cardiac sarcoidosis with severe involvement of the right ventricle: a case report

scientific article published on October 2015

Central role for GSK3β in the pathogenesis of arrhythmogenic cardiomyopathy

scientific article published on April 2016

Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.

scientific article

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

scientific article

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

scientific article

Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death

scientific article published on 16 December 2011

Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

scientific article published on 24 April 2010

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease

scientific article published on 14 November 2006

Development of dilated cardiomyopathy and impaired calcium homeostasis with cardiac-specific deletion of ESRRβ.

scientific article published on 27 January 2017

Disparate effects of different mutations in plakoglobin on cell mechanical behavior

scientific article

Electrical Coupling and Propagation in Engineered Ventricular Myocardium With Heterogeneous Expression of Connexin43 ⬇️

scientific article published on April 19, 2012

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

scientific article

End stage of arrhythmogenic cardiomyopathy with severe involvement of the interventricular septum.

scientific article published on 18 October 2012

Expression of cathepsin K and tartrate-resistant acid phosphatase is not confined to osteoclasts but is a general feature of multinucleated giant cells: systematic analysis.

scientific article published on 14 May 2013

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures

scientific article published on 02 February 2018

Gap junction remodeling in a case of arrhythmogenic right ventricular dysplasia due to plakophilin-2 mutation

scientific article published on 19 May 2008

Gap junctions and arrhythmogenic cardiomyopathy.

scientific article

Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome

scientific article published on 01 December 2018

Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.

scientific article published on June 2014

MY APPROACH to the patient with arrhythmogenic right ventricular cardiomyopathy (ARVC)

scientific article published on 02 November 2016

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

scientific article

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele

article

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

scientific article

Pathogenesis of Arrhythmogenic Cardiomyopathy

scientific article

Persistent lone atrial fibrillation: clinicopathologic study of 19 cases

scientific article published on 18 February 2014

Prolonged RV endocardial activation duration: a novel marker of arrhythmogenic right ventricular dysplasia/cardiomyopathy

scientific article published on 24 February 2009

Reduced plakoglobin immunoreactivity in arrhythmogenic cardiomyopathy: methodological considerations.

scientific article published on 17 May 2013

Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy

scientific article published on February 2014

Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene

scientific article

The role of endomyocardial biopsy in ARVC: looking beyond histology in search of new diagnostic markers.

scientific article

Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutations

scientific article published on 29 October 2008

[Left dominant arrhythmogenic cardiomyopathy caused by a novel nonsense mutation in desmoplakin]

scientific article published on 31 March 2011

List of works by Angeliki Asimaki

A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

Altered desmosomal proteins in granulomatous myocarditis and potential pathogenic links to arrhythmogenic right ventricular cardiomyopathy.

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis

Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell-cell adhesion

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

BIN1: A new biomarker to track ARVC? ⬇️

Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy

Cardiac sarcoidosis with severe involvement of the right ventricle: a case report

Central role for GSK3β in the pathogenesis of arrhythmogenic cardiomyopathy

Characterizing the Molecular Pathology of Arrhythmogenic Cardiomyopathy in Patient Buccal Mucosa Cells.

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy

Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death

Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

Desmoglein-2 mutations in arrhythmogenic right ventricular cardiomyopathy: a genotype-phenotype characterization of familial disease

Development of dilated cardiomyopathy and impaired calcium homeostasis with cardiac-specific deletion of ESRRβ.

Disparate effects of different mutations in plakoglobin on cell mechanical behavior

Electrical Coupling and Propagation in Engineered Ventricular Myocardium With Heterogeneous Expression of Connexin43 ⬇️

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human study.

End stage of arrhythmogenic cardiomyopathy with severe involvement of the interventricular septum.

Expression of cathepsin K and tartrate-resistant acid phosphatase is not confined to osteoclasts but is a general feature of multinucleated giant cells: systematic analysis.

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures

Gap junction remodeling in a case of arrhythmogenic right ventricular dysplasia due to plakophilin-2 mutation

Gap junctions and arrhythmogenic cardiomyopathy.

Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome

Identification of a new modulator of the intercalated disc in a zebrafish model of arrhythmogenic cardiomyopathy.

MY APPROACH to the patient with arrhythmogenic right ventricular cardiomyopathy (ARVC)

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null allele

Novel missense mutations in exon 15 of desmoglein-2: role of the intracellular cadherin segment in arrhythmogenic right ventricular cardiomyopathy?

Pathogenesis of Arrhythmogenic Cardiomyopathy

Persistent lone atrial fibrillation: clinicopathologic study of 19 cases

Prolonged RV endocardial activation duration: a novel marker of arrhythmogenic right ventricular dysplasia/cardiomyopathy

Reduced plakoglobin immunoreactivity in arrhythmogenic cardiomyopathy: methodological considerations.

Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy

Severe cardiac phenotype with right ventricular predominance in a large cohort of patients with a single missense mutation in the DES gene

The role of endomyocardial biopsy in ARVC: looking beyond histology in search of new diagnostic markers.

Unique epidermolytic bullous dermatosis with associated lethal cardiomyopathy related to novel desmoplakin mutations

[Left dominant arrhythmogenic cardiomyopathy caused by a novel nonsense mutation in desmoplakin]