The atrioventricular canal defect (AVCD) is a congenital heart defect (CHD) frequently associated with extracardiac anomalies (75%). Previous observations from a personal series of patients with AVCD and "polydactyly syndromes" showed that the distinct morphology and combination of AVCD features in some of these syndromes is reminiscent of the cardiac phenotype found in heterotaxy, a malformation complex previously associated with functional cilia abnormalities and aberrant Hedgehog (Hh) signaling. Hh signaling coordinates multiple aspects of left-right lateralization and cardiovascular growth. Being active at the venous pole the secondary heart field (SHF) is essential for normal development of dorsal mesenchymal protrusion and AVCD format...
Hypoplastic left heart syndrome (HLHS) is a complex congenital heart defect characterized by severe ...
Les malformations cardiaques sont des anomalies congénitales fréquentes puisqu’elles concernent 1 na...
By using a candidate gene approach, we have identified novel single-nucleotide polymorphisms specifi...
Atrioventricular canal defect (AVCD) is a common congenital heart defect (CHD), representing 7.4% of...
Atrioventricular canal defect (AVCD) represents a quite common congenital heart defect (CHD) account...
An incomplete septation of the ventricles in the vertebrate heart that disturbes the strict separati...
AbstractThe Hedgehog signaling pathway is critical for a significant number of developmental pattern...
The Hedgehog (HH) signalling pathway is one of the major pathways controlling cell differentiation a...
Congenital heart malformations are the most common type of defects found at birth. About 1% of infan...
About half of people with trisomy 21 have a congenital heart defect (CHD), whereas the remainder hav...
The evolutionarily conserved hedgehog (Hh) pathway is essential for organogenesis and plays critical...
Atrioventricular canal defect (AVCD) is a congenital heart defect, which occurs in 2.9 % of all cong...
Congenital heart disease (CHD) affects up to 1% of live births. Although a genetic etiology is indic...
A recessive lethal insertional mutation on chromosome 13 has been identified in a transgenic mouse l...
AbstractThe Sonic hedgehog (Shh)-null mouse was initially described as a phenotypic mimic of Tetralo...
Hypoplastic left heart syndrome (HLHS) is a complex congenital heart defect characterized by severe ...
Les malformations cardiaques sont des anomalies congénitales fréquentes puisqu’elles concernent 1 na...
By using a candidate gene approach, we have identified novel single-nucleotide polymorphisms specifi...
Atrioventricular canal defect (AVCD) is a common congenital heart defect (CHD), representing 7.4% of...
Atrioventricular canal defect (AVCD) represents a quite common congenital heart defect (CHD) account...
An incomplete septation of the ventricles in the vertebrate heart that disturbes the strict separati...
AbstractThe Hedgehog signaling pathway is critical for a significant number of developmental pattern...
The Hedgehog (HH) signalling pathway is one of the major pathways controlling cell differentiation a...
Congenital heart malformations are the most common type of defects found at birth. About 1% of infan...
About half of people with trisomy 21 have a congenital heart defect (CHD), whereas the remainder hav...
The evolutionarily conserved hedgehog (Hh) pathway is essential for organogenesis and plays critical...
Atrioventricular canal defect (AVCD) is a congenital heart defect, which occurs in 2.9 % of all cong...
Congenital heart disease (CHD) affects up to 1% of live births. Although a genetic etiology is indic...
A recessive lethal insertional mutation on chromosome 13 has been identified in a transgenic mouse l...
AbstractThe Sonic hedgehog (Shh)-null mouse was initially described as a phenotypic mimic of Tetralo...
Hypoplastic left heart syndrome (HLHS) is a complex congenital heart defect characterized by severe ...
Les malformations cardiaques sont des anomalies congénitales fréquentes puisqu’elles concernent 1 na...
By using a candidate gene approach, we have identified novel single-nucleotide polymorphisms specifi...