Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contractile dysfunction of the cardiac chambers. The present work aimed to study the alterations in gene expression of ion channels involved in cardiomyocyte function. (p < 0.05). Furthermore, we performed an IPA analysis and we found a functional relationship between the different ion channels studied in this work. This study shows a differential expression of ion channel genes involved in cardiac contraction in DCM that might partly underlie the changes in left ventricular function observed in these patients. These results could be the basis for new genetic therapeutic approaches
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
BackgroundDilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of hea...
Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contractile dysfun...
BACKGROUND: Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contra...
Dilated cardiomyopathy (DCM) is a multifactorial disease characterized by left ventricular dilation ...
Disruptions in cardiac ion channels have shown to influence the impaired cardiac contraction in hear...
Cardiomyopathies represent a wide and heterogeneous group of diseases wherein a genetic cause has be...
Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has bee...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart failure (HF) o...
AbstractWe employed ABI high-density oligonucleotide microarrays containing 31,700 sixty-mer probes ...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
The recent advances in molecular biology and genetic engineering are producing relevant results in c...
The application of molecular genetics in cardiology is currently producing important results in the ...
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
BackgroundDilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of hea...
Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contractile dysfun...
BACKGROUND: Dilated cardiomyopathy (DCM) is characterized by idiopathic dilation and systolic contra...
Dilated cardiomyopathy (DCM) is a multifactorial disease characterized by left ventricular dilation ...
Disruptions in cardiac ion channels have shown to influence the impaired cardiac contraction in hear...
Cardiomyopathies represent a wide and heterogeneous group of diseases wherein a genetic cause has be...
Dilated cardiomyopathy (DCM) is a major cause of cardiac death and heart transplantation. It has bee...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
Patients with inherited dilated cardiomyopathy (DCM) frequently die with severe heart failure (HF) o...
AbstractWe employed ABI high-density oligonucleotide microarrays containing 31,700 sixty-mer probes ...
Objective: To investigate the global changes accompanying human dilated cardiomyopathy (DCM) we perf...
The recent advances in molecular biology and genetic engineering are producing relevant results in c...
The application of molecular genetics in cardiology is currently producing important results in the ...
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
Recent studies have demonstrated that genetic factors are likely to play a major role in the pathoge...
BackgroundDilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of hea...