Vascular malformations result from improper blood vessel responses to molecular and mechanical signals. Two studies now show that endothelial cell migration and cell shape changes are perturbed in mutants lacking the TGFβ/BMP co-receptor endoglin, leading to arteriovenous shunts. Endoglin coordinates endothelial cell responses to ligand-receptor signalling and flow-mediated mechanical cues
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Mutations in endoglin, a TGFβ/BMP coreceptor, are causal for hereditary hemorrhagic telangiectasia (...
Genetic studies show that TGFß superfamily members are essential for vascular development, although ...
The hierarchical organization of properly sized blood vessels ensures the correct distribution of bl...
Mechanical cues and biochemical stimulations impact cell functions throughout the body. We investiga...
<div><p>ENDOGLIN (ENG) is a co-receptor for transforming growth factor-β (TGF-β) family members that...
Endoglin is an accessory receptor for transforming growth factor beta (TGFbeta) in endothelial cells...
AbstractMutations in endoglin, a TGFβ/BMP coreceptor, are causal for hereditary hemorrhagic telangie...
ENDOGLIN (ENG) is a co-receptor for transforming growth factor-β (TGF-β) family members that is high...
Endoglin is an accessory receptor for transforming growth factor beta (TGF beta ) in endothelial cel...
Rationale: ENG (endoglin) is a coreceptor for BMP (bone morphogenetic protein) 9/10 and is strongly ...
Rationale: ENG (endoglin) is a coreceptor for BMP (bone morphogenetic protein) 9/10 and is strongly ...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Mutations in endoglin, a TGFβ/BMP coreceptor, are causal for hereditary hemorrhagic telangiectasia (...
Genetic studies show that TGFß superfamily members are essential for vascular development, although ...
The hierarchical organization of properly sized blood vessels ensures the correct distribution of bl...
Mechanical cues and biochemical stimulations impact cell functions throughout the body. We investiga...
<div><p>ENDOGLIN (ENG) is a co-receptor for transforming growth factor-β (TGF-β) family members that...
Endoglin is an accessory receptor for transforming growth factor beta (TGFbeta) in endothelial cells...
AbstractMutations in endoglin, a TGFβ/BMP coreceptor, are causal for hereditary hemorrhagic telangie...
ENDOGLIN (ENG) is a co-receptor for transforming growth factor-β (TGF-β) family members that is high...
Endoglin is an accessory receptor for transforming growth factor beta (TGF beta ) in endothelial cel...
Rationale: ENG (endoglin) is a coreceptor for BMP (bone morphogenetic protein) 9/10 and is strongly ...
Rationale: ENG (endoglin) is a coreceptor for BMP (bone morphogenetic protein) 9/10 and is strongly ...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder in humans that is cha...
Mutations in endoglin, a TGFβ/BMP coreceptor, are causal for hereditary hemorrhagic telangiectasia (...