The role of β-catenin in cardiac diseases

B Ni, M Sun, J Zhao, J Wang, Z Cao - Frontiers in Pharmacology, 2023 - frontiersin.org
The Wnt/β-catenin signaling pathway is a classical Wnt pathway that regulates the stability
and nuclear localization of β-catenin and plays an important role in adult heart development …

Non coding RNAs as regulators of wnt/β-catenin and hippo pathways in arrhythmogenic cardiomyopathy

M Piquer-Gil, S Domenech-Dauder… - Biomedicines, 2022 - mdpi.com
Arrhythmogenic cardiomyopathy (ACM) is an inherited cardiomyopathy histologically
characterized by the replacement of myocardium by fibrofatty infiltration, cardiomyocyte loss …

[HTML][HTML] Clinical profile and long-term follow-up of a cohort of patients with desmoplakin cardiomyopathy

R Bariani, M Cason, I Rigato, A Cipriani, R Celeghin… - Heart Rhythm, 2022 - Elsevier
Background Desmoplakin (DSP) genetic variants have been reported in arrhythmogenic
cardiomyopathy with particular regard to predominant left ventricular (LV) involvement …

Arrhythmogenic Cardiomyopathy: from Preclinical Models to Genotype–phenotype Correlation and Pathophysiology

X Fan, G Yang, F Duru, M Grilli, I Akin, X Zhou… - Stem Cell Reviews and …, 2023 - Springer
Arrhythmogenic cardiomyopathy (ACM) is a hereditary myocardial disease characterized by
the replacement of the ventricular myocardium with fibrous fatty deposits. ACM is usually …

[HTML][HTML] Novel plasma biomarkers predicting biventricular involvement in arrhythmogenic right ventricular cardiomyopathy

D Akdis, L Chen, AM Saguner, N Zhang… - American Heart …, 2022 - Elsevier
Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart
muscle disease characterized by fibrofatty replacement of the myocardium and ventricular …

Transcriptomic hallmarks of mortality reveal universal and specific mechanisms of aging, chronic disease, and rejuvenation

A Tyshkovskiy, D Kholdina, K Ying, M Davitadze… - bioRxiv, 2024 - biorxiv.org
Health is strongly affected by aging and lifespan-modulating interventions, but the molecular
mechanisms of mortality regulation remain unclear. Here, we conducted an RNA-seq …

[HTML][HTML] In Vivo Approaches to Understand Arrhythmogenic Cardiomyopathy: Perspectives on Animal Models

G Risato, R Brañas Casas, M Cason, M Bueno Marinas… - Cells, 2024 - mdpi.com
Arrhythmogenic cardiomyopathy (AC) is a hereditary cardiac disorder characterized by the
gradual replacement of cardiomyocytes with fibrous and adipose tissue, leading to …

A Comprehensive Analysis of Non-Desmosomal Rare Genetic Variants in Arrhythmogenic Cardiomyopathy: Integrating in Padua Cohort Literature-Derived Data

M Bueno Marinas, M Cason, R Bariani… - International Journal of …, 2024 - mdpi.com
Arrhythmogenic cardiomyopathy (ACM) is an inherited myocardial disease at risk of sudden
death. Genetic testing impacts greatly in ACM diagnosis, but gene-disease associations …

Arrhythmogenic cardiomyopathy: the ongoing search for mechanism-driven therapies meets extracellular vesicles

C Basso, T Zaglia, K Pilichou - European Heart Journal, 2021 - academic.oup.com
Graphical Abstract Curative therapy in AC: outstanding questions. Upper panel: delivery of
CDC-derived EVs seems to attenuate AC in desmoglein-2 mutant mice, thus being …

Role of galectin-3 in the pathogenesis of arrhythmogenic cardiomyopathy—It's complicated

SP Chelko, JE Saffitz - Heart Rhythm, 2021 - heartrhythmjournal.com
The familial nonischemic cardiomyopathies are complex disorders of altered cardiac
structure, contractile function, and electrophysiology. They often are caused by mendelian …