[HTML][HTML] Cardiac transmembrane ion channels and action potentials: cellular physiology and arrhythmogenic behavior
Cardiac arrhythmias are among the leading causes of mortality. They often arise from
alterations in the electrophysiological properties of cardiac cells and their underlying ionic …
alterations in the electrophysiological properties of cardiac cells and their underlying ionic …
[HTML][HTML] Skeletal and cardiac muscle disorders caused by mutations in genes encoding intermediate filament proteins
L Maggi, M Mavroidis, S Psarras, Y Capetanaki… - International Journal of …, 2021 - mdpi.com
Intermediate filaments are major components of the cytoskeleton. Desmin and synemin,
cytoplasmic intermediate filament proteins and A-type lamins, nuclear intermediate filament …
cytoplasmic intermediate filament proteins and A-type lamins, nuclear intermediate filament …
[HTML][HTML] Dynamic effects of genetic variation on gene expression revealed following hypoxic stress in cardiomyocytes
One life-threatening outcome of cardiovascular disease is myocardial infarction, where
cardiomyocytes are deprived of oxygen. To study inter-individual differences in response to …
cardiomyocytes are deprived of oxygen. To study inter-individual differences in response to …
[HTML][HTML] Three-dimensional cell cultures: The bridge between in vitro and in vivo models
O Urzì, R Gasparro, E Costanzo, A De Luca… - International Journal of …, 2023 - mdpi.com
Although historically, the traditional bidimensional in vitro cell system has been widely used
in research, providing much fundamental information regarding cellular functions and …
in research, providing much fundamental information regarding cellular functions and …
[HTML][HTML] Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling
M Chintanaphol, BO Orgil, NR Alberson… - Reviews in …, 2022 - imrpress.com
Restrictive cardiomyopathy (RCM), a potentially devastating heart muscle disorder, is
characterized by diastolic dysfunction due to abnormal muscle relaxation and myocardial …
characterized by diastolic dysfunction due to abnormal muscle relaxation and myocardial …
[HTML][HTML] Genetic animal models for arrhythmogenic cardiomyopathy
B Gerull, A Brodehl - Frontiers in Physiology, 2020 - frontiersin.org
Arrhythmogenic cardiomyopathy has been clinically defined since the 1980s and causes
right or biventricular cardiomyopathy associated with ventricular arrhythmia. Although it is a …
right or biventricular cardiomyopathy associated with ventricular arrhythmia. Although it is a …
[HTML][HTML] Understanding arrhythmogenic cardiomyopathy: advances through the use of human pluripotent stem cell models
CJ Chua, J Morrissette-McAlmon, L Tung, KR Boheler - Genes, 2023 - mdpi.com
Cardiomyopathies (CMPs) represent a significant healthcare burden and are a major cause
of heart failure leading to premature death. Several CMPs are now recognized to have a …
of heart failure leading to premature death. Several CMPs are now recognized to have a …
Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20
A Gaertner, B Klauke, E Felski, A Kassner… - Human …, 2020 - Wiley Online Library
Mutations in RBM20 encoding the RNA‐binding motif protein 20 (RBM20) are associated
with an early onset and clinically severe forms of cardiomyopathies. Transcriptome analyses …
with an early onset and clinically severe forms of cardiomyopathies. Transcriptome analyses …
[HTML][HTML] Recent trends in stem cell-based therapies and applications of artificial intelligence in regenerative medicine
S Mukherjee, G Yadav, R Kumar - World journal of stem cells, 2021 - ncbi.nlm.nih.gov
Stem cells are undifferentiated cells that can self-renew and differentiate into diverse types
of mature and functional cells while maintaining their original identity. This profound …
of mature and functional cells while maintaining their original identity. This profound …
[HTML][HTML] The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy
A Gaertner, J Bloebaum, A Brodehl, B Klauke… - Genes, 2021 - mdpi.com
A major cause of heart failure is cardiomyopathies, with dilated cardiomyopathy (DCM) as
the most common form. Over 40 genes are linked to DCM, among them TTN and RBM20 …
the most common form. Over 40 genes are linked to DCM, among them TTN and RBM20 …