Cargando…

A combinatorial oligogenic basis for the phenotypic plasticity between late-onset dilated and arrhythmogenic cardiomyopathy in a single family

INTRODUCTION: Primary dilated cardiomyopathy (DCM) and arrhythmogenic right ventricular cardiomyopathy (ARVC) are the two common and distinct forms of hereditary cardiomyopathies caused by defined pathogenic variants (PVs) typically in different sets of genes. DCM is characterized by left ventricula...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pourebrahim, Kimia, Marian, John Garrity, Tan, Yanli, Chang, Jeffrey T., Marian, Ali J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8594872/ https://www.ncbi.nlm.nih.gov/pubmed/34790974 http://dx.doi.org/10.20517/jca.2021.15

Ejemplares similares

Oligogenic Cardiomyopathy
por: Marian, Ali J.
Publicado: (2022)

Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy
por: Bainbridge, Matthew Neil, et al.
Publicado: (2017)

Risk prediction of late-onset Alzheimer’s disease implies an oligogenic architecture
por: Zhang, Qian, et al.
Publicado: (2020)

MicroRNAs in Hypertrophic, Arrhythmogenic and Dilated Cardiomyopathy
por: Chiti, Enrica, et al.
Publicado: (2021)

Hypertrophic, Dilated, and Arrhythmogenic Cardiomyopathy: Where Are We?
por: El Hadi, Hamza, et al.
Publicado: (2023)

Arrhythmogenic Right Ventricular Cardiomyopathy: Characterization of Left Ventricular Phenotype and Differential Diagnosis With Dilated Cardiomyopathy
por: Cipriani, Alberto, et al.
Publicado: (2020)

Arrhythmogenic Phenotype in Dilated Cardiomyopathy: Natural History and Predictors of Life‐Threatening Arrhythmias
por: Spezzacatene, Anita, et al.
Publicado: (2015)

Deletion of the Lmna gene in fibroblasts causes senescence-associated dilated cardiomyopathy by activating the double-stranded DNA damage response and induction of senescence-associated secretory phenotype
por: Rouhi, Leila, et al.
Publicado: (2022)

Risk stratification in cardiomyopathies (dilated, hypertrophic, and arrhythmogenic cardiomyopathy) by cardiac magnetic resonance imaging
por: Guglielmo, Marco, et al.
Publicado: (2021)

Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
por: Campuzano, Oscar, et al.
Publicado: (2020)

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell–Cell Adhesion Structures
por: Begay, Rene L., et al.
Publicado: (2018)

Risk stratification and subclinical phenotyping of dilated and/or arrhythmogenic cardiomyopathy mutation-positive relatives: CVON eDETECT consortium
por: Roudijk, R. W., et al.
Publicado: (2021)

The genetic basis for adult-onset idiopathic dilated cardiomyopathy in people of African descent
por: Tsabedze, Nqoba, et al.
Publicado: (2023)

Arrhythmogenic cardiomyopathy
por: Pilichou, Kalliopi, et al.
Publicado: (2016)

Scaling up oligogenic diseases research with OLIDA: the Oligogenic Diseases Database
por: Nachtegael, Charlotte, et al.
Publicado: (2022)

Possibly Late-Onset Arrhythmogenic Right Ventricular Cardiomyopathy: Unique Triglyceride Deposition by Analysis of Lipid Contents
por: Yamamoto, Kentaro, et al.
Publicado: (2019)

Arrhythmogenic Noncompaction Cardiomyopathy: Is There an Echocardiographic Phenotypic Overlap of Two Distinct Cardiomyopathies?
por: Aras, Dursun, et al.
Publicado: (2015)

Arrhythmogenic Cardiomyopathy: A Disease or Merely a Phenotype?
por: Protonotarios, Alexandros, et al.
Publicado: (2020)

The phenotypic and genetic features of arrhythmogenic cardiomyopathy in the pediatric population
por: Kofeynikova, Olga, et al.
Publicado: (2023)

Pharmacological suppression of the WNT signaling pathway attenuates age-dependent expression of the phenotype in a mouse model of arrhythmogenic cardiomyopathy
por: Cheedipudi, Sirisha M., et al.
Publicado: (2021)

Pregnancy in arrhythmogenic cardiomyopathy
por: Wichter, Thomas, et al.
Publicado: (2021)

Scarring/arrhythmogenic cardiomyopathy
por: Corrado, Domenico, et al.
Publicado: (2023)

Late presentation of arrhythmogenic right ventricular cardiomyopathy: a case report
por: Papaioannou, Georgios I, et al.
Publicado: (2009)

Arrhythmogenic Cardiomyopathy as a Late Complication of COVID-19-Induced Myocarditis
por: Campoamor, David, et al.
Publicado: (2022)

Better late than never: assessment of arrhythmogenic cardiomyopathy in an elderly patient
por: Barriuso, Ignacio, et al.
Publicado: (2023)

Arrhythmogenic Ventricular Cardiomyopathy: Challenges With Complex Genetics and Variable Phenotypes
por: Rawal, Aranyak S., et al.
Publicado: (2021)

Genetic Basis and Genotype–Phenotype Correlations in Han Chinese Patients with Idiopathic Dilated Cardiomyopathy
por: Zhang, Xin-Lin, et al.
Publicado: (2020)

Autophagy and Endoplasmic Reticulum Stress during Onset and Progression of Arrhythmogenic Cardiomyopathy
por: Pitsch, Mark, et al.
Publicado: (2021)

Highly malignant disease in childhood-onset arrhythmogenic right ventricular cardiomyopathy
por: Smedsrud, Marit Kristine, et al.
Publicado: (2022)

Left Ventricular Dysfunction in Arrhythmogenic Cardiomyopathy: Association With Exercise Exposure, Genetic Basis, and Prognosis
por: Lie, Øyvind H., et al.
Publicado: (2021)

Late evolution of arrhythmogenic cardiomyopathy in patients with initial presentation as idiopathic ventricular fibrillation
por: Blom, Lennart J., et al.
Publicado: (2018)

Arrhythmogenic right ventricular cardiomyopathy
por: Cho, Yongkeun
Publicado: (2018)

Arrhythmogenic left ventricular cardiomyopathy
por: Mirmomen, Seyedeh Mojdeh, et al.
Publicado: (2020)

Natural History of Arrhythmogenic Cardiomyopathy
por: Mattesi, Giulia, et al.
Publicado: (2020)

Metabolic Signature of Arrhythmogenic Cardiomyopathy
por: Volani, Chiara, et al.
Publicado: (2021)

Arrhythmogenic left ventricular cardiomyopathy
por: Corrado, Domenico, et al.
Publicado: (2022)

What’s New in Arrhythmogenic Cardiomyopathies
por: Çimen, Tolga, et al.
Publicado: (2022)

Arrhythmogenic Right Ventricular Cardiomyopathy
por: Dolkar, Tsering, et al.
Publicado: (2022)

Shared Genetic Etiology of Primary Dilated Cardiomyopathy and Ischemic Dilated Cardiomyopathy
por: Sun, Yang, et al.
Publicado: (2021)

Oligogenic basis of sporadic ALS: The example of SOD1 p.Ala90Val mutation
por: Kuuluvainen, Liina, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_iomdt2p8494qdsmo71cf5v8le2