Lista de obras - Angeliki Asimaki - Dominio Público Uruguay

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

artículo científico publicado en 2011

A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2007

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

artículo científico publicado en 2011

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

artículo científico publicado en 2006

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

artículo científico publicado en 2014

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

artículo científico publicado en 2006

BIN1: A new biomarker to track ARVC? ⬇️

artículo científico publicado el 3 de marzo de 2012

Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy.

artículo científico publicado en 2016

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

artículo científico publicado en 2015

Central role for GSK3β in the pathogenesis of arrhythmogenic cardiomyopathy

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2007

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

artículo científico publicado en 2006

Connexin43 mutation causes heterogeneous gap junction loss and sudden infant death

artículo científico publicado en 2011

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

artículo científico publicado en 2010

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

artículo científico publicado en 2006

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

artículo científico publicado en 2017

Disparate effects of different mutations in plakoglobin on cell mechanical behavior

artículo científico publicado en 2008

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

artículo científico publicado el 19 de abril de 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 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.

artículo científico publicado en 2013

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

artículo científico publicado en 2018

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

artículo científico publicado en 2008

Gap junctions and arrhythmogenic cardiomyopathy.

artículo científico publicado en 2011

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.

artículo científico publicado en 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

artículo científico publicado en 2011

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?

artículo científico publicado en 2010

Pathogenesis of Arrhythmogenic Cardiomyopathy

artículo científico publicado en 2015

Persistent lone atrial fibrillation: clinicopathologic study of 19 cases

artículo científico publicado en 2014

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

artículo científico publicado en 2009

Reduced plakoglobin immunoreactivity in arrhythmogenic cardiomyopathy: methodological considerations.

artículo científico publicado en 2013

Remodeling of cell-cell junctions in arrhythmogenic cardiomyopathy

artículo científico publicado en 2014

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

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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

articulo cientifico

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

artículo científico publicado en 2011

Lista de obras de 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]