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

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 Growth Factor-β/Bone Morphogenetic Protein-9 expre...

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Detalles Bibliográficos
Autores principales: Galaris, Georgios, Montagne, Kévin, Thalgott, Jérémy H., Goujon, Geoffroy J. P. E., van den Driesche, Sander, Martin, Sabrina, Mager, Hans-Jurgen J., Mummery, Christine L., Rabelink, Ton J., Lebrin, Franck
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396348/
https://www.ncbi.nlm.nih.gov/pubmed/34445652
http://dx.doi.org/10.3390/ijms22168948

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396348/
https://www.ncbi.nlm.nih.gov/pubmed/34445652
http://dx.doi.org/10.3390/ijms22168948

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