Over the past decade, our understanding of cardiomyopathies has improved dramatically, due to improvements in screening and detection of gene defects in the human genome as well as a variety of novel animal models (mouse, zebrafish, and drosophila) and in silico computational models. These novel experimental tools have created a platform that is highly complementary to the naturally occurring cardiomyopathies in cats and dogs that had been available for some time. A fully integrative approach, which incorporates all these modalities, is likely required for significant steps forward in understanding the molecular underpinnings and pathogenesis of cardiomyopathies. Finally, novel technologies, including CRISPR/Cas9, which have already been pr...
Arrhythmogenic cardiomyopathy has been clinically defined since the 1980s and causes right or bivent...
One of the obstacles to a better understanding of the pathogenesis of human cardiomyopathies has bee...
Familial hypertrophic cardiomyopathy (FHC) is an autosomal-dominant disease that is both clinically ...
Over the past decade, our understanding of cardiomyopathies has improved dramatically, due to improv...
Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic mut...
n the global human population, the leading cause of non-communicable death is cardiovascular disease...
In the global human population, the leading cause of non-communicable death is cardiovascular diseas...
SUMMARY To assess the effects during cardiac development of mutations that cause human cardiomyopath...
Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic mut...
This article reports a coupled computational experimental approach to design small molecules aimed a...
: Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic m...
Arrhythmogenic cardiomyopathy has been clinically defined since the 1980s and causes right or bivent...
One of the obstacles to a better understanding of the pathogenesis of human cardiomyopathies has bee...
Familial hypertrophic cardiomyopathy (FHC) is an autosomal-dominant disease that is both clinically ...
Over the past decade, our understanding of cardiomyopathies has improved dramatically, due to improv...
Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic mut...
n the global human population, the leading cause of non-communicable death is cardiovascular disease...
In the global human population, the leading cause of non-communicable death is cardiovascular diseas...
SUMMARY To assess the effects during cardiac development of mutations that cause human cardiomyopath...
Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic mut...
This article reports a coupled computational experimental approach to design small molecules aimed a...
: Genetic cardiomyopathies are disorders of the cardiac muscle, most often explained by pathogenic m...
Arrhythmogenic cardiomyopathy has been clinically defined since the 1980s and causes right or bivent...
One of the obstacles to a better understanding of the pathogenesis of human cardiomyopathies has bee...
Familial hypertrophic cardiomyopathy (FHC) is an autosomal-dominant disease that is both clinically ...