Altered endothelial gene expression associated with hereditary haemorrhagic telangiectasia

Background Mutations in endoglin (ENG) and activin receptor‐like kinase 1 (ALK‐1 or ACVRL1) genes are the underlying basis of hereditary haemorrhagic telangiectasia (HHT) types 1 and 2, respectively. Both genes belong to the transforming growth factor‐β (TGF‐β) receptors superfamily and are express...

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Veröffentlicht in:	European journal of clinical investigation 2007-07, Vol.37 (7), p.580-588
Hauptverfasser:	Thomas, B., Eyries, M., Montagne, K., Martin, S., Agrapart, M., Simerman-François, R., Letarte, M., Soubrier, F.
Format:	Artikel
Sprache:	eng
Schlagworte:	Activin Receptors Antigens, CD Biological and medical sciences Blotting, Western Cells, Cultured Dermatology Endoglin Endothelium, Vascular - physiology expression profiling Gene Expression General aspects Humans Infant, Newborn Medical sciences Receptors, Cell Surface Rendu-Osler-Weber disease Telangiectasia, Hereditary Hemorrhagic - genetics Vascular disorders of the skin vascular hereditary disease
Online-Zugang:	Volltext
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