AbstractAbnormalities of cardiomyocyte Ca2+ homeostasis and excitation–contraction (E–C) coupling are early events in the pathogenesis of hypertrophic cardiomyopathy (HCM) and concomitant determinants of the diastolic dysfunction and arrhythmias typical of the disease. T-tubule remodelling has been reported to occur in HCM but little is known about its role in the E–C coupling alterations of HCM. Here, the role of T-tubule remodelling in the electro-mechanical dysfunction associated to HCM is investigated in the Δ160E cTnT mouse model that expresses a clinically-relevant HCM mutation. Contractile function of intact ventricular trabeculae is assessed in Δ160E mice and wild-type siblings. As compared with wild-type, Δ160E trabeculae show prol...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in different genes mainl...
Mutations in thin filament regulatory proteins that cause hypertrophic cardiomyopathy (HCM) increase...
AbstractCardiomyocytes from failing hearts exhibit spatially nonuniform or dyssynchronous sarcoplasm...
AbstractAbnormalities of cardiomyocyte Ca2+ homeostasis and excitation–contraction (E–C) coupling ar...
Background-In cardiomyocytes from patients with hypertrophic cardiomyopathy, mechanical dysfunction ...
AbstractHypertrophic cardiomyopathy (HCM) is frequently caused by mutations in MYBPC3 encoding cardi...
Chronic mechanical load variation triggers a wide range of responses in the heart, a part of which i...
AbstractIn mammalian cardiac ventricular myocytes, Ca influx and release occur predominantly at t-tu...
Right ventricle (RV) dysfunction is an independent predictor of patient survival in heart failure (H...
Hypertrophic cardiomyopathy (HCM) is the most common mendelian heart disease, with a prevalence of 1...
Hypertrophic cardiomyopathy (HCM) is the most common monogenic cardiovascular disease carrying a sig...
Familial hypertrophic cardiomyopathy (HCM), a leading cause of sudden cardiac death, is primarily ca...
An arginine (R) to a glycine (G) mutation at position 145 in the highly reserved inhibitory domain o...
AbstractHuman familial hypertrophic cardiomyopathy is the most common Mendelian cardiovascular disea...
AbstractRecent work has demonstrated that cardiomyocyte Ca2+release is desynchronized in several pat...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in different genes mainl...
Mutations in thin filament regulatory proteins that cause hypertrophic cardiomyopathy (HCM) increase...
AbstractCardiomyocytes from failing hearts exhibit spatially nonuniform or dyssynchronous sarcoplasm...
AbstractAbnormalities of cardiomyocyte Ca2+ homeostasis and excitation–contraction (E–C) coupling ar...
Background-In cardiomyocytes from patients with hypertrophic cardiomyopathy, mechanical dysfunction ...
AbstractHypertrophic cardiomyopathy (HCM) is frequently caused by mutations in MYBPC3 encoding cardi...
Chronic mechanical load variation triggers a wide range of responses in the heart, a part of which i...
AbstractIn mammalian cardiac ventricular myocytes, Ca influx and release occur predominantly at t-tu...
Right ventricle (RV) dysfunction is an independent predictor of patient survival in heart failure (H...
Hypertrophic cardiomyopathy (HCM) is the most common mendelian heart disease, with a prevalence of 1...
Hypertrophic cardiomyopathy (HCM) is the most common monogenic cardiovascular disease carrying a sig...
Familial hypertrophic cardiomyopathy (HCM), a leading cause of sudden cardiac death, is primarily ca...
An arginine (R) to a glycine (G) mutation at position 145 in the highly reserved inhibitory domain o...
AbstractHuman familial hypertrophic cardiomyopathy is the most common Mendelian cardiovascular disea...
AbstractRecent work has demonstrated that cardiomyocyte Ca2+release is desynchronized in several pat...
Hypertrophic cardiomyopathy (HCM) is a genetic disorder caused by mutations in different genes mainl...
Mutations in thin filament regulatory proteins that cause hypertrophic cardiomyopathy (HCM) increase...
AbstractCardiomyocytes from failing hearts exhibit spatially nonuniform or dyssynchronous sarcoplasm...