Thresholds of Endoglin Expression in Endothelial Cells Explains Vascular Etiology in Hereditary Hemorrhagic Telangiectasia Type 1

Autor: Hans-Jurgen J Mager, Sabrina Martin, Georgios Galaris, Geoffroy J P E Goujon, Ton J. Rabelink, Franck Lebrin, Kevin Montagne, Sander van den Driesche, Jérémy H. Thalgott, Christine L. Mummery

Publikováno v: International Journal of Molecular Sciences
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8948, p 8948 (2021)
International Journal of Molecular Sciences, 22(16). MDPI

Hereditary Hemorrhagic Telangiectasia type 1 (HHT1) is an autosomal dominant inherited disease characterized by arteriovenous malformations and hemorrhage. HHT1 is caused by mutations in ENDOGLIN, which encodes an ancillary receptor for Transforming

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