The genes of nuclear factor of activated T-cells (NFATC) play a key role both in heart valves formation and immune response. The genes belong to transcriptional factors and lead to myocardial hypertrophy in postnatal period that is confirmed by experimental models on animals. The purpose of this study was to reveale NFATC1 and NFATC4 genes expression level in the blood of 30 children with congenital heart diseases (CHD), 15 of them had bicuspid aortic valve, 15 had CHD without valve anomalies and 15 healthy children of the control group. No patients had signs of heart failure. At the first sage of Doppler heart ultrasound study a significant increase of the left ventricle posterior wall and ventricular septum thickness in comparison with CH...
The molecular mechanisms leading to premature development of aortic valve stenosis (AS) in individua...
: Bicuspid aortic valve (BAV) is the most frequent congenital heart disease, with an incidence of ap...
The study investigated the role of genetic polymorphisms in four genes of the calcineurin pathway on...
Aim. The nuclear factor of activated T-cells (NFATc 1-4) family gene expression against the backgrou...
Congenital malformations are the most common cause of death in infancy in the United States. Of thes...
Bicuspid aortic valve is one of the most common congenital heart diseases with low manifestation in ...
The aim of the study was to determine the possibility of association of the single nucleotide polymo...
One major intracellular signaling pathway involved in heart failure employs the phosphatase calcineu...
This overview provides insight into the underlying genetic mechanism of the high incidence of cardia...
ObjectiveBicuspid aortic valve, the most common congenital cardiac malformation, is caused by fusion...
Despite significant progress in the prevention and treatment of cardiovascular diseases, heart failu...
Bicuspid aortic valve (BAV) is a common congenital heart malformation frequently associated with the...
International audienceCalcific aortic valve disease (CAVD) is a significant cause of illness and dea...
Bicuspid aortic valve (BAV) is the most common congenital heart defect, affecting 1-2% of the popula...
Aims The present study aims to characterize the genetic risk architecture of bicuspid aortic valve (...
The molecular mechanisms leading to premature development of aortic valve stenosis (AS) in individua...
: Bicuspid aortic valve (BAV) is the most frequent congenital heart disease, with an incidence of ap...
The study investigated the role of genetic polymorphisms in four genes of the calcineurin pathway on...
Aim. The nuclear factor of activated T-cells (NFATc 1-4) family gene expression against the backgrou...
Congenital malformations are the most common cause of death in infancy in the United States. Of thes...
Bicuspid aortic valve is one of the most common congenital heart diseases with low manifestation in ...
The aim of the study was to determine the possibility of association of the single nucleotide polymo...
One major intracellular signaling pathway involved in heart failure employs the phosphatase calcineu...
This overview provides insight into the underlying genetic mechanism of the high incidence of cardia...
ObjectiveBicuspid aortic valve, the most common congenital cardiac malformation, is caused by fusion...
Despite significant progress in the prevention and treatment of cardiovascular diseases, heart failu...
Bicuspid aortic valve (BAV) is a common congenital heart malformation frequently associated with the...
International audienceCalcific aortic valve disease (CAVD) is a significant cause of illness and dea...
Bicuspid aortic valve (BAV) is the most common congenital heart defect, affecting 1-2% of the popula...
Aims The present study aims to characterize the genetic risk architecture of bicuspid aortic valve (...
The molecular mechanisms leading to premature development of aortic valve stenosis (AS) in individua...
: Bicuspid aortic valve (BAV) is the most frequent congenital heart disease, with an incidence of ap...
The study investigated the role of genetic polymorphisms in four genes of the calcineurin pathway on...