BMP10 functions independently from BMP9 for the development of a proper arteriovenous network

Hereditary hemorrhagic telangiectasia (HHT) is a genetic vascular disorder characterized by the presence of arteriovenous malformation (AVM) in multiple organs. HHT is caused by mutations in genes encoding major constituents for transforming growth factor-β (TGF-β) family signaling: endoglin (ENG),...

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Detalles Bibliográficos
Autores principales: Choi, Hyunwoo, Kim, Bo-Gyeong, Kim, Yong Hwan, Lee, Se-Jin, Lee, Young Jae, Oh, S. Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2022
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908740/
https://www.ncbi.nlm.nih.gov/pubmed/36348215
http://dx.doi.org/10.1007/s10456-022-09859-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908740/
https://www.ncbi.nlm.nih.gov/pubmed/36348215
http://dx.doi.org/10.1007/s10456-022-09859-0

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