t/endoglin

Endoglin

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Global prevalence of hereditary hemorrhagic telangiectasia-associated variants estimated by analysis of large-scale genomic databases.
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Generation of ENG p.Met1Val mutant LUMCi029-A-2 for modeling Hereditary Hemorrhagic Telangiectasia type 1.
Endoglin
Disruption of endothelial stability directly impacts vascular neighboring cells in Hereditary Hemorrhagic Telangiectasia
Endoglin
Platelet-derived growth factor receptor β F7 mutations result in and exacerbate the severity of vascular dysplasia in the brain arteriovenous malformation through enhancing angiogenesis.
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Genotype-driven cerebrovascular risk across age and sex in hereditary hemorrhagic telangiectasia.
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Pulmonary hypertension associated with hereditary haemorrhagic telangiectasia: from genetics to clinical management.
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Genotype-phenotype correlations and protein domain-level predictors of cerebrovascular malformations in hereditary hemorrhagic telangiectasia.
Endoglin
Secretory products from regulatory macrophages modulate senescence in human endothelial cells: implications for cardiovascular aging and diseases.
Endoglin
VE-cadherin NOT-gated CD93 CAR T cells discriminate between AML and healthy endothelial cells
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