Animals have frequently been used as models for human disorders and mutations. Following advances in genetic testing and treatment options, and the decreasing cost of these technologies in the clinic, mutations in both companion and commercial animals are now being investigated. A recent review highlighted the genes associated with both human and non-human dilated cardiomyopathy. Cardiac troponin T and dystrophin were observed to be associated with both human and turkey (troponin T) and canine (dystrophin) dilated cardiomyopathies. This review gives an overview of the work carried out in cardiac troponin T and dystrophin to date in both human and animal dilated cardiomyopathy
Background: Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mut...
Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mutations, incl...
ObjectivesWe performed genetic investigations of cardiac troponin T (TNNT2) and troponin C (TNNC1) i...
Animals have frequently been used as models for human disorders and mutations. Following advances in...
Animals have frequently been used as models for human disorders and mutations. Following advances in...
Key points: Mutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) ca...
BACKGROUND: Dilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of h...
n the global human population, the leading cause of non-communicable death is cardiovascular disease...
BACKGROUND Dilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of...
Rationale: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
RATIONALE: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
The demonstrated number 1 killer in the world is cardiovascular disease, with inherited cardiomyopat...
BackgroundDilated cardiomyopathy is a myocardial disease occurring in humans and domestic animals an...
Cardiac disease is a leading cause of death for both humans and dogs. Genetic cardiomyopathies, incl...
BackgroundDilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of hea...
Background: Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mut...
Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mutations, incl...
ObjectivesWe performed genetic investigations of cardiac troponin T (TNNT2) and troponin C (TNNC1) i...
Animals have frequently been used as models for human disorders and mutations. Following advances in...
Animals have frequently been used as models for human disorders and mutations. Following advances in...
Key points: Mutations in genes encoding cardiac troponin I (TNNI3) and cardiac troponin T (TNNT2) ca...
BACKGROUND: Dilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of h...
n the global human population, the leading cause of non-communicable death is cardiovascular disease...
BACKGROUND Dilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of...
Rationale: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
RATIONALE: Idiopathic dilated cardiomyopathy (DCM) is inherited in approximately one third of cases,...
The demonstrated number 1 killer in the world is cardiovascular disease, with inherited cardiomyopat...
BackgroundDilated cardiomyopathy is a myocardial disease occurring in humans and domestic animals an...
Cardiac disease is a leading cause of death for both humans and dogs. Genetic cardiomyopathies, incl...
BackgroundDilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of hea...
Background: Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mut...
Hypertrophic (HCM) and dilated (DCM) cardiomyopathies result from sarcomeric protein mutations, incl...
ObjectivesWe performed genetic investigations of cardiac troponin T (TNNT2) and troponin C (TNNC1) i...