Endothelial cilia dysfunction in pathogenesis of hereditary hemorrhagic telangiectasia

Hereditary hemorrhagic telangiectasia (HHT) is associated with defective capillary network, leading to dilated superficial vessels and arteriovenous malformations (AVMs) in which arteries connect directly to the veins. Loss or haploinsufficiency of components of TGF-β signaling, ALK1, ENG, SMAD4, an...

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Detalles Bibliográficos
Autores principales: Eisa-Beygi, Shahram, Burrows, Patricia E., Link, Brian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686338/
https://www.ncbi.nlm.nih.gov/pubmed/36438574
http://dx.doi.org/10.3389/fcell.2022.1037453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686338/
https://www.ncbi.nlm.nih.gov/pubmed/36438574
http://dx.doi.org/10.3389/fcell.2022.1037453

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