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A novel dominant mutation in plakoglobin causes Arrhythmogenic right ventricular cardiomyopathy
Angeliki Asimaki et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
Giorgia Beffagna et al.
BMC MEDICAL GENETICS (2007)
Cardiomyocyte expression of PPARγ leads to cardiac dysfunction in mice
Ni-Huiping Son et al.
JOURNAL OF CLINICAL INVESTIGATION (2007)
Connexin43 remodeling caused by inhibition of plakophilin-2 expression in cardiac cells
Eva M. Oxford et al.
CIRCULATION RESEARCH (2007)
A unique and specific interaction between αT-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs
Steven Goossens et al.
JOURNAL OF CELL SCIENCE (2007)
TGFβ, cardiac fibroblasts, and the fibrotic response
Andrew Leask
CARDIOVASCULAR RESEARCH (2007)
Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression
Srijita Sen-Chowdhry et al.
CIRCULATION (2007)
Microtubule plus-end-tracking proteins target gap junctions directly from the cell interior to adherens junctions
Robin M. Shaw et al.
CELL (2007)
Mutant desmocollin-2 causes arrhythmogenic right ventricular cardiomyopathy
Arnd Heuser et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Age- and training-dependent development of arrhythmogenic right ventricular cardiomyopathy in heterozygous plakoglobin-deficient mice
Paulus Kirchhof et al.
CIRCULATION (2006)
Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program
Domenico Corrado et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)
Desmosomal dysfunction due to mutations in desmoplakin causes arrhythmogenic right ventricular dysplasia/cardiomyopathy
Zhao Yang et al.
CIRCULATION RESEARCH (2006)
Functional interaction between peroxisome proliferator-activated receptor γ and β-catenin
Jiajian Liu et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Suppression of canonical Wnt/β-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathy
Eduardo Garcia-Gras et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
The β-catenin/T-cell factor/lymphocyte enhancer factor signaling pathway is required for normal and stress-induced cardiac hypertrophy
Xin Chen et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy
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CIRCULATION (2006)
The requirement for Perp in postnatal viability and epithelial integrity reflects an intrinsic role in stratified epithelia
Michelle R. Marques et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2006)
The right ventricle, outflow tract, and ventricular septum comprise a restricted expression domain within the secondary/anterior heart field
MP Verzi et al.
DEVELOPMENTAL BIOLOGY (2005)
Wnt5b partially inhibits canonical Wnt/β-catenin signaling pathway and promotes adipogenesis in 3T3-L1 preadipocytes
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BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Task force 8: Classification of sports
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JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
Apoptosis, pyroptosis, and necrosis: Mechanistic description of dead and dying eukaryotic cells
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INFECTION AND IMMUNITY (2005)
Regulatory mutations in transforming growth factor-β3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1
G Beffagna et al.
CARDIOVASCULAR RESEARCH (2005)
Thin: Physiological function and role in cardiomyopathy and failure
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HEART FAILURE REVIEWS (2005)
Remodeling of myocyte gap junctions in arrhythmogenic right ventricular cardiomyopathy due to a deletion in plakoglobin (Naxos disease)
SR Kaplan et al.
HEART RHYTHM (2004)
Cell shape, cytoskeletal tension, and RhoA regulate stem cell lineage commitment
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DEVELOPMENTAL CELL (2004)
Remodelling of gap junctions and connexin expression in heart disease
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BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES (2004)
Prevalence of right ventricular dysplasia-cardiomyopathy in a non-referral hospital
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INTERNATIONAL JOURNAL OF CARDIOLOGY (2004)
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
B Gerull et al.
NATURE GENETICS (2004)
Requirement of plakophilin 2 for heart morphogenesis and cardiac junction formation
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JOURNAL OF CELL BIOLOGY (2004)
Structural and molecular pathology of the heart in Carvajal syndrome
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CARDIOVASCULAR PATHOLOGY (2004)
Perp is a mediator of p53-dependent apoptosis in diverse cell types
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CURRENT BIOLOGY (2003)
Phospholamban: A crucial regulator of cardiac contractility
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NATURE REVIEWS MOLECULAR CELL BIOLOGY (2003)
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes
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EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Myotonic dystrophy and the heart
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HEART (2002)
Loss of desmoglein 2 suggests essential functions for early embryonic development and proliferation of embryonal stem cells
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EUROPEAN JOURNAL OF CELL BIOLOGY (2002)
TGF-β receptor-activated p38 MAP kinase mediates smad-independent TGF-β responses
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EMBO JOURNAL (2002)
The detection of cardiotropic viruses in the myocardium of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy
NE Bowles et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
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HUMAN MOLECULAR GENETICS (2001)
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma
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HUMAN MOLECULAR GENETICS (2000)
Gap junctions in cardiovascular disease
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CIRCULATION RESEARCH (2000)
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
G McKoy et al.
LANCET (2000)
No detection of enteroviral genome in the myocardium of patients with arrhythmogenic right ventricular cardiomyopathy
F Calabrese et al.
JOURNAL OF CLINICAL PATHOLOGY (2000)
Angiotensin II, adhesion, and cardiac fibrosis
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CARDIOVASCULAR RESEARCH (2000)
Arrhythmogenic right ventricular dysplasia/cardiomyopathy - Need for an international registry
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CIRCULATION (2000)
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