Hypertrophic cardiomyopathy (HCM) is the most prevalent inherited arrhythmia (irregular heartbeat), affecting 1:500 individuals and the primary cause of sudden cardiac arrest (SCA) in youth and young adults, including elite athletes. HCM presents with an enlargement of the ventricles/septal wall, disarray of cardiomyocyte (contracting heart cells) alignment, and electrically inactive fibrotic tissue deposition. These variations to the typical cardiac composition produce substrates for chaotic electrical activity across the myocardium (the heart's muscular tissue), preventing normal contraction and relaxation cycles. Various mutations have been identified in genes encoding cardiac contractile proteins. Of concern, some patients harbouring TN...
Modelling disease with hPSCs is hindered because the impact on cell phenotype from genetic variabili...
E192K missense mutation of TPM1 has been found in different types of cardiomyopathies (e.g., hypertr...
Chronic diseases are the primary cause of mortality worldwide, accounting for 67% of deaths. One of ...
Hypertrophic cardiomyopathy (HCM) is a prevalent genetic cardiovascular disease affecting 1:500 indi...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy with a variety of causative mutatio...
Aims: Sarcomeric gene mutations frequently underlie hypertrophic cardiomyopathy (HCM), a prevalent a...
Cardiac arrhythmias can arise due to a host of both genetic and acquired factors. Specifically, the ...
The study of inherited human cardiovascular diseases has been hampered by limited access to cardiac ...
Hypertrophic cardiomyopathy (HCM) is the most common cardiomyopathy, estimated to affect 1:250 peopl...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a devastating, heritable cardiac arr...
Tese de doutoramento, Ciências Biomédicas (Biologia Celular e Molecular), Universidade de Lisboa, Fa...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a potentially lethal inherited cardi...
Hypertrophic cardiomyopathy (HCM) is a primary disorder of contractility in heart muscle. To gain me...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
The ACTC E99K mutation is associated with hypertrophic cardiomyopathy (HCM- predominantly apical) an...
Modelling disease with hPSCs is hindered because the impact on cell phenotype from genetic variabili...
E192K missense mutation of TPM1 has been found in different types of cardiomyopathies (e.g., hypertr...
Chronic diseases are the primary cause of mortality worldwide, accounting for 67% of deaths. One of ...
Hypertrophic cardiomyopathy (HCM) is a prevalent genetic cardiovascular disease affecting 1:500 indi...
Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy with a variety of causative mutatio...
Aims: Sarcomeric gene mutations frequently underlie hypertrophic cardiomyopathy (HCM), a prevalent a...
Cardiac arrhythmias can arise due to a host of both genetic and acquired factors. Specifically, the ...
The study of inherited human cardiovascular diseases has been hampered by limited access to cardiac ...
Hypertrophic cardiomyopathy (HCM) is the most common cardiomyopathy, estimated to affect 1:250 peopl...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a devastating, heritable cardiac arr...
Tese de doutoramento, Ciências Biomédicas (Biologia Celular e Molecular), Universidade de Lisboa, Fa...
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a potentially lethal inherited cardi...
Hypertrophic cardiomyopathy (HCM) is a primary disorder of contractility in heart muscle. To gain me...
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with ...
The ACTC E99K mutation is associated with hypertrophic cardiomyopathy (HCM- predominantly apical) an...
Modelling disease with hPSCs is hindered because the impact on cell phenotype from genetic variabili...
E192K missense mutation of TPM1 has been found in different types of cardiomyopathies (e.g., hypertr...
Chronic diseases are the primary cause of mortality worldwide, accounting for 67% of deaths. One of ...